ZDB-GENE-000125-4 30120 10683 dlc GO:0001756 somitogenesis PATO:0001507 disrupted abnormal ZDB-GENE-000125-4 30120 10683 dlc GO:0001757 somite specification PATO:0001507 disrupted abnormal ZDB-GENE-000125-4 30120 10683 dlc GO:0002244 hematopoietic progenitor cell differentiation PATO:0001236 process quality abnormal ZDB-GENE-000125-4 30120 10683 dlc GO:0003140 determination of left/right asymmetry in lateral mesoderm PATO:0001507 disrupted abnormal ZDB-GENE-000125-4 30120 10683 dlc GO:0007398 ectoderm development PATO:0001507 disrupted abnormal ZDB-GENE-000125-4 30120 10683 dlc GO:0048368 lateral mesoderm development PATO:0001507 disrupted abnormal ZDB-GENE-000125-4 30120 10683 dlc GO:0048514 blood vessel morphogenesis PATO:0001507 disrupted abnormal ZDB-GENE-000125-4 30120 10683 dlc GO:0060218 hematopoietic stem cell differentiation PATO:0001507 disrupted abnormal ZDB-GENE-000125-4 30120 10683 dlc GO:0061056 sclerotome development PATO:0001236 process quality abnormal ZDB-GENE-000125-4 30120 10683 dlc ZFA:0000007 blood PATO:0001997 decreased amount abnormal ZDB-GENE-000125-4 30120 10683 dlc ZFA:0001462 somite border BFO:0000050 part_of ZFA:0000073 somite 5 PATO:0001332 amorphous abnormal ZDB-GENE-000125-4 30120 10683 dlc ZFA:0000155 somite PATO:0000001 quality abnormal ZDB-GENE-000125-4 30120 10683 dlc ZFA:0000155 somite PATO:0000051 morphology abnormal ZDB-GENE-000125-4 30120 10683 dlc ZFA:0000155 somite PATO:0000052 shape abnormal ZDB-GENE-000125-4 30120 10683 dlc ZFA:0001462 somite border BFO:0000050 part_of ZFA:0000733 somite 7 PATO:0001332 amorphous abnormal ZDB-GENE-000125-4 30120 10683 dlc ZFA:0001462 somite border BFO:0000050 part_of ZFA:0000858 somite 8 PATO:0001332 amorphous abnormal ZDB-GENE-000125-4 30120 10683 dlc ZFA:0001462 somite border BFO:0000050 part_of ZFA:0000982 somite 6 PATO:0001332 amorphous abnormal ZDB-GENE-000125-4 30120 10683 dlc ZFA:0001462 somite border BFO:0000050 part_of ZFA:0000983 somite 9 PATO:0001332 amorphous abnormal ZDB-GENE-000125-4 30120 10683 dlc ZFA:0001117 post-vent region PATO:0000001 quality abnormal ZDB-GENE-000125-4 30120 10683 dlc ZFA:0001285 intersegmental vessel PATO:0000646 malformed abnormal ZDB-GENE-000125-4 30120 10683 dlc ZFA:0001462 somite border PATO:0000330 irregular spatial pattern abnormal ZDB-GENE-000125-4 30120 10683 dlc ZFA:0001462 somite border PATO:0001617 deformed abnormal ZDB-GENE-000125-4 30120 10683 dlc ZFA:0009014 hematopoietic stem cell PATO:0001997 decreased amount abnormal ZDB-GENE-000201-18 30728 80714 pbx4 GO:0001755 neural crest cell migration PATO:0001507 disrupted abnormal ZDB-GENE-000201-18 30728 80714 pbx4 GO:0003007 heart morphogenesis PATO:0002302 decreased process quality abnormal ZDB-GENE-000201-18 30728 80714 pbx4 GO:0003139 secondary heart field specification PATO:0002052 decreased occurrence abnormal ZDB-GENE-000201-18 30728 80714 pbx4 GO:0003143 embryonic heart tube morphogenesis PATO:0002302 decreased process quality abnormal ZDB-GENE-000201-18 30728 80714 pbx4 GO:0003232 bulbus arteriosus development PATO:0001236 process quality abnormal ZDB-GENE-000201-18 30728 80714 pbx4 GO:0003319 cardioblast migration to the midline involved in heart rudiment formation PATO:0002052 decreased occurrence abnormal ZDB-GENE-000201-18 30728 80714 pbx4 GO:0003342 proepicardium development PATO:0002052 decreased occurrence abnormal ZDB-GENE-000201-18 30728 80714 pbx4 GO:0007492 endoderm development PATO:0001507 disrupted abnormal ZDB-GENE-000201-18 30728 80714 pbx4 GO:0048798 swim bladder inflation PATO:0000297 arrested abnormal ZDB-GENE-000201-18 30728 80714 pbx4 GO:0055008 cardiac muscle tissue morphogenesis PATO:0002302 decreased process quality abnormal ZDB-GENE-000201-18 30728 80714 pbx4 ZFA:0000007 blood PATO:0002269 accumulation abnormal BSPO:0000070 anatomical region BFO:0000050 part_of ZFA:0000471 atrium ZDB-GENE-000201-18 30728 80714 pbx4 ZFA:0000008 brain PATO:0000001 quality abnormal ZDB-GENE-000201-18 30728 80714 pbx4 ZFA:0009316 cardiac muscle cell BFO:0000050 part_of ZFA:0000009 cardiac ventricle PATO:0000470 increased amount abnormal ZDB-GENE-000201-18 30728 80714 pbx4 ZFA:0000009 cardiac ventricle PATO:0000051 morphology abnormal ZDB-GENE-000201-18 30728 80714 pbx4 ZFA:0000009 cardiac ventricle PATO:0000646 malformed abnormal ZDB-GENE-000201-18 30728 80714 pbx4 ZFA:0000017 endoderm PATO:0000051 morphology abnormal ZDB-GENE-000201-18 30728 80714 pbx4 ZFA:0000029 hindbrain PATO:0000001 quality abnormal ZDB-GENE-000201-18 30728 80714 pbx4 ZFA:0000042 midbrain hindbrain boundary PATO:0000646 malformed abnormal ZDB-GENE-000201-18 30728 80714 pbx4 ZFA:0000045 neural crest PATO:0000001 quality abnormal ZDB-GENE-000201-18 30728 80714 pbx4 ZFA:0000054 pericardium PATO:0001450 edematous abnormal ZDB-GENE-000201-18 30728 80714 pbx4 ZFA:0000076 swim bladder PATO:0001241 physical object quality abnormal ZDB-GENE-000201-18 30728 80714 pbx4 ZFA:0000084 yolk PATO:0000001 quality abnormal ZDB-GENE-000201-18 30728 80714 pbx4 ZFA:0000095 pharyngeal arch 3-7 skeleton PATO:0000001 quality abnormal ZDB-GENE-000201-18 30728 80714 pbx4 ZFA:0000107 eye PATO:0000587 decreased size abnormal ZDB-GENE-000201-18 30728 80714 pbx4 ZFA:0000114 heart PATO:0000001 quality abnormal ZDB-GENE-000201-18 30728 80714 pbx4 ZFA:0000123 liver PATO:0001921 mislocalised anteriorly abnormal ZDB-GENE-000201-18 30728 80714 pbx4 ZFA:0000141 pectoral fin bud PATO:0001483 aplastic abnormal ZDB-GENE-000201-18 30728 80714 pbx4 ZFA:0000292 surface structure PATO:0000001 quality abnormal ZDB-GENE-000201-18 30728 80714 pbx4 ZFA:0000360 heart tube PATO:0000646 malformed abnormal ZDB-GENE-000201-18 30728 80714 pbx4 ZFA:0000445 optic tectum PATO:0000587 decreased size abnormal ZDB-GENE-000201-18 30728 80714 pbx4 ZFA:0009316 cardiac muscle cell BFO:0000050 part_of ZFA:0000471 atrium PATO:0000470 increased amount abnormal ZDB-GENE-000201-18 30728 80714 pbx4 ZFA:0000948 rhombomere 3 PATO:0000051 morphology abnormal ZDB-GENE-000201-18 30728 80714 pbx4 ZFA:0000948 rhombomere 3 PATO:0000587 decreased size abnormal ZDB-GENE-000201-18 30728 80714 pbx4 ZFA:0005198 RoL2 BFO:0000050 part_of ZFA:0001032 rhombomere 4 PATO:0000628 mislocalised abnormal ZDB-GENE-000201-18 30728 80714 pbx4 ZFA:0001078 thymus PATO:0001483 aplastic abnormal ZDB-GENE-000201-18 30728 80714 pbx4 ZFA:0001114 head PATO:0000587 decreased size abnormal ZDB-GENE-000201-18 30728 80714 pbx4 ZFA:0001161 pectoral fin PATO:0000001 quality abnormal ZDB-GENE-000201-18 30728 80714 pbx4 ZFA:0001161 pectoral fin PATO:0001483 aplastic abnormal ZDB-GENE-000201-18 30728 80714 pbx4 ZFA:0001205 Meckel's cartilage PATO:0000642 fused with abnormal ZFA:0001400 ceratohyal cartilage ZDB-GENE-000201-18 30728 80714 pbx4 ZFA:0001205 Meckel's cartilage PATO:0000587 decreased size abnormal ZDB-GENE-000201-18 30728 80714 pbx4 ZFA:0001249 exocrine pancreas PATO:0001921 mislocalised anteriorly abnormal ZDB-GENE-000201-18 30728 80714 pbx4 ZFA:0001260 endocrine pancreas PATO:0001921 mislocalised anteriorly abnormal ZDB-GENE-000201-18 30728 80714 pbx4 ZFA:0001319 myocardium PATO:0000646 malformed abnormal ZDB-GENE-000201-18 30728 80714 pbx4 ZFA:0001319 myocardium PATO:0001924 mislocalised medially abnormal ZDB-GENE-000201-18 30728 80714 pbx4 ZFA:0001383 fin bud PATO:0001483 aplastic abnormal ZDB-GENE-000201-18 30728 80714 pbx4 ZFA:0001399 palatoquadrate cartilage PATO:0000642 fused with abnormal ZFA:0001422 hyosymplectic cartilage ZDB-GENE-000201-18 30728 80714 pbx4 ZFA:0001399 palatoquadrate cartilage PATO:0000587 decreased size abnormal ZDB-GENE-000201-18 30728 80714 pbx4 ZFA:0001400 ceratohyal cartilage PATO:0000587 decreased size abnormal ZDB-GENE-000201-18 30728 80714 pbx4 ZFA:0001422 hyosymplectic cartilage PATO:0000587 decreased size abnormal ZDB-GENE-000201-18 30728 80714 pbx4 ZFA:0001516 ceratobranchial cartilage PATO:0000462 absent abnormal ZDB-GENE-000201-18 30728 80714 pbx4 ZFA:0005198 RoL2 PATO:0000470 increased amount abnormal ZDB-GENE-000201-18 30728 80714 pbx4 ZFA:0009003 cranial neural crest cell PATO:0000628 mislocalised abnormal ZDB-GENE-000201-18 30728 80714 pbx4 ZFA:0009149 Mauthner neuron PATO:0000462 absent abnormal ZDB-GENE-000201-18 30728 80714 pbx4 ZFA:0009316 cardiac muscle cell PATO:0000470 increased amount abnormal ZDB-GENE-000201-9 30630 3730 anos1a GO:0007411 axon guidance PATO:0001507 disrupted abnormal ZDB-GENE-000201-9 30630 3730 anos1a GO:0021772 olfactory bulb development PATO:0001507 disrupted abnormal ZDB-GENE-000201-9 30630 3730 anos1a GO:0048883 neuromast primordium migration PATO:0000502 delayed abnormal ZDB-GENE-000201-9 30630 3730 anos1a GO:0048918 posterior lateral line nerve development PATO:0001507 disrupted abnormal ZDB-GENE-000201-9 30630 3730 anos1a GO:0060384 innervation PATO:0001507 disrupted abnormal ZDB-GENE-000201-9 30630 3730 anos1a GO:0097155 fasciculation of sensory neuron axon PATO:0001507 disrupted abnormal ZDB-GENE-000201-9 30630 3730 anos1a ZFA:0000048 olfactory placode PATO:0000937 disorganized abnormal ZDB-GENE-000201-9 30630 3730 anos1a ZFA:0000175 posterior lateral line nerve PATO:0000574 decreased length abnormal ZDB-GENE-000201-9 30630 3730 anos1a ZFA:0000357 glomerular layer PATO:0001483 aplastic abnormal ZDB-GENE-000201-9 30630 3730 anos1a ZFA:0009276 GABAergic neuron BFO:0000050 part_of ZFA:0000402 olfactory bulb PATO:0001997 decreased amount abnormal ZDB-GENE-000201-9 30630 3730 anos1a ZFA:0009301 dopaminergic neuron BFO:0000050 part_of ZFA:0000402 olfactory bulb PATO:0001997 decreased amount abnormal ZDB-GENE-000201-9 30630 3730 anos1a ZFA:0000402 olfactory bulb PATO:0000937 disorganized abnormal ZDB-GENE-000201-9 30630 3730 anos1a ZFA:0000554 olfactory epithelium PATO:0000937 disorganized abnormal ZDB-GENE-000201-9 30630 3730 anos1a ZFA:0000554 olfactory epithelium PATO:0001786 split abnormal ZDB-GENE-000201-9 30630 3730 anos1a ZFA:0000940 posterior lateral line neuromast PATO:0000646 malformed abnormal ZDB-GENE-000201-9 30630 3730 anos1a ZFA:0000940 posterior lateral line neuromast PATO:0001997 decreased amount abnormal ZDB-GENE-000201-9 30630 3730 anos1a ZFA:0001157 posterior lateral line primordium PATO:0000411 circular abnormal ZDB-GENE-000201-9 30630 3730 anos1a ZFA:0001157 posterior lateral line primordium PATO:0001870 crescent-shaped abnormal ZDB-GENE-000201-9 30630 3730 anos1a ZFA:0001472 anterior lateral line neuromast PATO:0001997 decreased amount abnormal ZDB-GENE-000201-9 30630 3730 anos1a GO:0030424 axon BFO:0000050 part_of ZFA:0009125 olfactory receptor cell PATO:0000574 decreased length abnormal ZDB-GENE-000201-9 30630 3730 anos1a GO:0030424 axon BFO:0000050 part_of ZFA:0009125 olfactory receptor cell PATO:0000937 disorganized abnormal ZDB-GENE-000201-9 30630 3730 anos1a ZFA:0009125 olfactory receptor cell PATO:0000060 spatial pattern abnormal ZDB-GENE-000201-9 30630 3730 anos1a ZFA:0009367 neuromast hair cell PATO:0001997 decreased amount abnormal ZDB-GENE-000208-17 30248 125972 calr3a ZFA:0000243 neuromast PATO:0001997 decreased amount abnormal ZDB-GENE-000208-18 30617 7389 urod GO:0004853 uroporphyrinogen decarboxylase activity PATO:0000911 decreased rate abnormal ZDB-GENE-000208-18 30617 7389 urod GO:0006778 porphyrin-containing compound metabolic process PATO:0001507 disrupted abnormal ZDB-GENE-000208-18 30617 7389 urod ZFA:0000007 blood PATO:0000001 quality abnormal ZDB-GENE-000208-18 30617 7389 urod ZFA:0000114 heart PATO:0000001 quality abnormal ZDB-GENE-000208-18 30617 7389 urod ZFA:0001094 whole organism PATO:0000718 lethal (sensu genetics) abnormal ZDB-GENE-000208-18 30617 7389 urod ZFA:0001439 anatomical system PATO:0000001 quality abnormal ZDB-GENE-000208-18 30617 7389 urod ZFA:0009256 nucleate erythrocyte PATO:0000018 fluorescence abnormal ZDB-GENE-000208-18 30617 7389 urod ZFA:0009256 nucleate erythrocyte PATO:0001868 autofluorescence abnormal ZDB-GENE-000208-18 30617 7389 urod ZFA:0009256 nucleate erythrocyte PATO:0001926 increased fluorescence abnormal ZDB-GENE-000208-20 30115 83881 mixl1 GO:0001706 endoderm formation PATO:0001236 process quality abnormal ZDB-GENE-000208-20 30115 83881 mixl1 GO:0001714 endodermal cell fate specification PATO:0001507 disrupted abnormal ZDB-GENE-000208-20 30115 83881 mixl1 GO:0007492 endoderm development PATO:0001507 disrupted abnormal ZDB-GENE-000208-20 30115 83881 mixl1 ZFA:0000008 brain PATO:0000001 quality abnormal ZDB-GENE-000208-20 30115 83881 mixl1 ZFA:0009139 endodermal cell BFO:0000050 part_of ZFA:0000017 endoderm PATO:0001997 decreased amount abnormal ZDB-GENE-000208-20 30115 83881 mixl1 ZFA:0000054 pericardium PATO:0001450 edematous abnormal ZDB-GENE-000208-20 30115 83881 mixl1 ZFA:0000071 shield PATO:0002106 poorly differentiated abnormal ZDB-GENE-000208-20 30115 83881 mixl1 ZFA:0000084 yolk PATO:0000586 increased size abnormal ZDB-GENE-000208-20 30115 83881 mixl1 ZFA:0000106 extension PATO:0000591 increased thickness abnormal ZDB-GENE-000208-20 30115 83881 mixl1 ZFA:0000110 fourth ventricle PATO:0001478 collapsed abnormal ZDB-GENE-000208-20 30115 83881 mixl1 ZFA:0000111 germ ring PATO:0002106 poorly differentiated abnormal ZDB-GENE-000208-20 30115 83881 mixl1 ZFA:0000112 gut PATO:0001483 aplastic abnormal ZDB-GENE-000208-20 30115 83881 mixl1 ZFA:0000114 heart PATO:0000001 quality abnormal ZDB-GENE-000208-20 30115 83881 mixl1 ZFA:0000114 heart PATO:0000051 morphology abnormal ZDB-GENE-000208-20 30115 83881 mixl1 ZFA:0000114 heart PATO:0000403 cleft abnormal ZDB-GENE-000208-20 30115 83881 mixl1 ZFA:0000114 heart PATO:0001473 duplicated abnormal ZDB-GENE-000208-20 30115 83881 mixl1 ZFA:0000159 tectal ventricle PATO:0001478 collapsed abnormal ZDB-GENE-000208-20 30115 83881 mixl1 ZFA:0000360 heart tube PATO:0001473 duplicated abnormal ZDB-GENE-000208-20 30115 83881 mixl1 ZFA:0000360 heart tube PATO:0001784 bifurcated abnormal ZDB-GENE-000208-20 30115 83881 mixl1 ZFA:0000396 nervous system PATO:0000001 quality abnormal ZDB-GENE-000208-20 30115 83881 mixl1 ZFA:0001259 forebrain ventricle PATO:0001478 collapsed abnormal ZDB-GENE-000208-20 30115 83881 mixl1 ZFA:0001439 anatomical system PATO:0000001 quality abnormal ZDB-GENE-000208-23 561679 1302 col11a2 GO:0001958 endochondral ossification PATO:0001507 disrupted abnormal ZDB-GENE-000208-23 561679 1302 col11a2 GO:0002062 chondrocyte differentiation PATO:0000502 delayed abnormal ZDB-GENE-000208-23 561679 1302 col11a2 ZFA:0000107 eye PATO:0000628 mislocalised abnormal ZDB-GENE-000208-23 561679 1302 col11a2 ZFA:0000135 notochord PATO:0000967 undulate abnormal ZDB-GENE-000208-23 561679 1302 col11a2 ZFA:0000250 opercle PATO:0001545 inflexible abnormal ZDB-GENE-000208-23 561679 1302 col11a2 ZFA:0000351 olfactory region PATO:0000645 hypoplastic abnormal ZDB-GENE-000208-23 561679 1302 col11a2 ZFA:0000547 mouth PATO:0000462 absent abnormal ZDB-GENE-000208-23 561679 1302 col11a2 ZFA:0000547 mouth PATO:0001906 movement quality abnormal ZDB-GENE-000208-23 561679 1302 col11a2 ZFA:0001114 head PATO:0000587 decreased size abnormal ZDB-GENE-000208-23 561679 1302 col11a2 ZFA:0001114 head PATO:0000646 malformed abnormal ZDB-GENE-000208-23 561679 1302 col11a2 ZFA:0009084 chondrocyte BFO:0000050 part_of ZFA:0001205 Meckel's cartilage PATO:0000051 morphology abnormal ZDB-GENE-000208-23 561679 1302 col11a2 ZFA:0009084 chondrocyte BFO:0000050 part_of ZFA:0001205 Meckel's cartilage PATO:0000411 circular abnormal ZDB-GENE-000208-23 561679 1302 col11a2 ZFA:0009084 chondrocyte BFO:0000050 part_of ZFA:0001205 Meckel's cartilage PATO:0000584 hypertrophic abnormal ZDB-GENE-000208-23 561679 1302 col11a2 ZFA:0001205 Meckel's cartilage PATO:0000587 decreased size abnormal ZDB-GENE-000208-23 561679 1302 col11a2 ZFA:0001205 Meckel's cartilage PATO:0000628 mislocalised abnormal ZDB-GENE-000208-23 561679 1302 col11a2 ZFA:0001205 Meckel's cartilage PATO:0000646 malformed abnormal ZDB-GENE-000208-23 561679 1302 col11a2 ZFA:0009084 chondrocyte BFO:0000050 part_of ZFA:0001227 mandibular arch skeleton PATO:0001501 immature abnormal ZDB-GENE-000208-23 561679 1302 col11a2 ZFA:0001227 mandibular arch skeleton PATO:0000051 morphology abnormal ZDB-GENE-000208-23 561679 1302 col11a2 ZFA:0001227 mandibular arch skeleton PATO:0001545 inflexible abnormal ZDB-GENE-000208-23 561679 1302 col11a2 ZFA:0001227 mandibular arch skeleton PATO:0001598 protruding abnormal ZDB-GENE-000208-23 561679 1302 col11a2 ZFA:0001227 mandibular arch skeleton PATO:0001906 movement quality abnormal ZDB-GENE-000208-23 561679 1302 col11a2 ZFA:0001239 ceratobranchial 5 bone PATO:0000025 composition abnormal ZDB-GENE-000208-23 561679 1302 col11a2 ZFA:0001273 ventral mandibular arch PATO:0000051 morphology abnormal ZDB-GENE-000208-23 561679 1302 col11a2 ZFA:0001273 ventral mandibular arch PATO:0000574 decreased length abnormal ZDB-GENE-000208-23 561679 1302 col11a2 ZFA:0001273 ventral mandibular arch PATO:0000600 increased width abnormal ZDB-GENE-000208-23 561679 1302 col11a2 ZFA:0001306 pharyngeal arch PATO:0001483 aplastic abnormal ZDB-GENE-000208-23 561679 1302 col11a2 ZFA:0001321 neurocranial trabecula PATO:0000587 decreased size abnormal ZDB-GENE-000208-23 561679 1302 col11a2 ZFA:0001321 neurocranial trabecula PATO:0000646 malformed abnormal ZDB-GENE-000208-23 561679 1302 col11a2 ZFA:0001400 ceratohyal cartilage PATO:0000628 mislocalised abnormal ZDB-GENE-000208-23 561679 1302 col11a2 ZFA:0001400 ceratohyal cartilage PATO:0000646 malformed abnormal ZDB-GENE-000208-23 561679 1302 col11a2 ZFA:0001405 ethmoid cartilage PATO:0000587 decreased size abnormal ZDB-GENE-000208-23 561679 1302 col11a2 ZFA:0001458 cranial cartilage PATO:0000937 disorganized abnormal ZDB-GENE-000208-23 561679 1302 col11a2 ZFA:0001460 pharyngeal arch cartilage PATO:0000937 disorganized abnormal ZDB-GENE-000208-23 561679 1302 col11a2 ZFA:0001516 ceratobranchial cartilage PATO:0000587 decreased size abnormal ZDB-GENE-000208-23 561679 1302 col11a2 ZFA:0001633 perichordal connective tissue PATO:0000051 morphology abnormal ZDB-GENE-000208-23 561679 1302 col11a2 GO:0005581 collagen trimer BFO:0000050 part_of ZFA:0007117 Meckel's cartilage-palatoquadrate cartilage joint PATO:0000330 irregular spatial pattern abnormal ZDB-GENE-000208-23 561679 1302 col11a2 GO:0005581 collagen trimer BFO:0000050 part_of ZFA:0007117 Meckel's cartilage-palatoquadrate cartilage joint PATO:0000591 increased thickness abnormal ZDB-GENE-000208-23 561679 1302 col11a2 ZFA:0007117 Meckel's cartilage-palatoquadrate cartilage joint PATO:0000051 morphology abnormal ZDB-GENE-000208-23 561679 1302 col11a2 ZFA:0007117 Meckel's cartilage-palatoquadrate cartilage joint PATO:0000587 decreased size abnormal ZDB-GENE-000208-23 561679 1302 col11a2 ZFA:0007117 Meckel's cartilage-palatoquadrate cartilage joint PATO:0001906 movement quality abnormal ZDB-GENE-000208-23 561679 1302 col11a2 ZFA:0009084 chondrocyte PATO:0000937 disorganized abnormal ZDB-GENE-000208-25 30584 655 bmp7a GO:0001702 gastrulation with mouth forming second PATO:0000001 quality abnormal ZDB-GENE-000208-25 30584 655 bmp7a GO:0001702 gastrulation with mouth forming second PATO:0001507 disrupted abnormal ZDB-GENE-000208-25 30584 655 bmp7a GO:0009953 dorsal/ventral pattern formation PATO:0001507 disrupted abnormal ZDB-GENE-000208-25 30584 655 bmp7a GO:0009957 epidermal cell fate specification PATO:0001507 disrupted abnormal ZDB-GENE-000208-25 30584 655 bmp7a GO:0021703 locus ceruleus development PATO:0001507 disrupted abnormal ZDB-GENE-000208-25 30584 655 bmp7a GO:0036342 post-anal tail morphogenesis PATO:0001561 having extra processual parts abnormal GO:0036342 post-anal tail morphogenesis ZDB-GENE-000208-25 30584 655 bmp7a GO:0036342 post-anal tail morphogenesis PATO:0001507 disrupted abnormal ZDB-GENE-000208-25 30584 655 bmp7a ZFA:0000022 floor plate PATO:0000600 increased width abnormal ZDB-GENE-000208-25 30584 655 bmp7a ZFA:0000045 neural crest PATO:0000586 increased size abnormal ZDB-GENE-000208-25 30584 655 bmp7a ZFA:0000077 tail bud PATO:0000051 morphology abnormal ZDB-GENE-000208-25 30584 655 bmp7a ZFA:0000077 tail bud PATO:0001617 deformed abnormal ZDB-GENE-000208-25 30584 655 bmp7a ZFA:0000077 tail bud PATO:0001922 mislocalised posteriorly abnormal ZDB-GENE-000208-25 30584 655 bmp7a ZFA:0000077 tail bud PATO:0002495 dorsal orientation abnormal ZDB-GENE-000208-25 30584 655 bmp7a ZFA:0000077 tail bud PATO:0002501 ventral orientation abnormal ZDB-GENE-000208-25 30584 655 bmp7a ZFA:0000084 yolk PATO:0040044 ruptured abnormal ZDB-GENE-000208-25 30584 655 bmp7a ZFA:0000115 heart rudiment PATO:0000651 unfused from abnormal ZFA:0000115 heart rudiment ZDB-GENE-000208-25 30584 655 bmp7a ZFA:0000135 notochord PATO:0000001 quality abnormal ZDB-GENE-000208-25 30584 655 bmp7a ZFA:0000135 notochord PATO:0000600 increased width abnormal ZDB-GENE-000208-25 30584 655 bmp7a ZFA:0000138 otic placode PATO:0000937 disorganized abnormal ZDB-GENE-000208-25 30584 655 bmp7a ZFA:0000138 otic placode PATO:0001483 aplastic abnormal ZDB-GENE-000208-25 30584 655 bmp7a ZFA:0000150 pronephric duct PATO:0000645 hypoplastic abnormal ZDB-GENE-000208-25 30584 655 bmp7a BSPO:0000068 ventral side BFO:0000050 part_of ZFA:0000155 somite PATO:0000642 fused with abnormal BSPO:0000068 ventral side BFO:0000050 part_of ZFA:0000155 somite ZDB-GENE-000208-25 30584 655 bmp7a ZFA:0000155 somite PATO:0002463 extends to abnormal BSPO:0000068 ventral side BFO:0000050 part_of ZFA:0001115 trunk ZDB-GENE-000208-25 30584 655 bmp7a ZFA:0000155 somite PATO:0000411 circular abnormal ZDB-GENE-000208-25 30584 655 bmp7a ZFA:0000155 somite PATO:0000600 increased width abnormal ZDB-GENE-000208-25 30584 655 bmp7a BSPO:0000013 anterior-posterior axis BFO:0000050 part_of ZFA:0000255 paraxial mesoderm PATO:0000574 decreased length abnormal ZDB-GENE-000208-25 30584 655 bmp7a ZFA:0000255 paraxial mesoderm PATO:0002002 has extra parts of type abnormal ZFA:0000003 adaxial cell ZDB-GENE-000208-25 30584 655 bmp7a ZFA:0000255 paraxial mesoderm PATO:0000051 morphology abnormal ZDB-GENE-000208-25 30584 655 bmp7a BSPO:0000000 left side BFO:0000050 part_of ZFA:0000823 rhombomere 5 PATO:0000642 fused with abnormal BSPO:0000007 right side BFO:0000050 part_of ZFA:0000823 rhombomere 5 ZDB-GENE-000208-25 30584 655 bmp7a ZFA:0000948 rhombomere 3 PATO:0000573 increased length abnormal ZDB-GENE-000208-25 30584 655 bmp7a BSPO:0000013 anterior-posterior axis BFO:0000050 part_of ZFA:0001094 whole organism PATO:0000573 increased length abnormal ZDB-GENE-000208-25 30584 655 bmp7a BSPO:0000072 posterior region BFO:0000050 part_of ZFA:0001094 whole organism PATO:0000620 wholly dorsalized abnormal ZDB-GENE-000208-25 30584 655 bmp7a BSPO:0000072 posterior region BFO:0000050 part_of ZFA:0001094 whole organism PATO:0000936 truncated abnormal ZDB-GENE-000208-25 30584 655 bmp7a ZFA:0001094 whole organism PATO:0002002 has extra parts of type abnormal ZFA:0001117 post-vent region ZDB-GENE-000208-25 30584 655 bmp7a ZFA:0001094 whole organism PATO:0000052 shape abnormal ZDB-GENE-000208-25 30584 655 bmp7a ZFA:0001094 whole organism PATO:0000169 viability abnormal ZDB-GENE-000208-25 30584 655 bmp7a ZFA:0001094 whole organism PATO:0000620 wholly dorsalized abnormal ZDB-GENE-000208-25 30584 655 bmp7a ZFA:0001094 whole organism PATO:0000718 lethal (sensu genetics) abnormal ZDB-GENE-000208-25 30584 655 bmp7a ZFA:0001094 whole organism PATO:0000947 elliptic abnormal ZDB-GENE-000208-25 30584 655 bmp7a ZFA:0001094 whole organism PATO:0001422 dead abnormal ZDB-GENE-000208-25 30584 655 bmp7a ZFA:0001094 whole organism PATO:0001891 ovate abnormal ZDB-GENE-000208-25 30584 655 bmp7a ZFA:0001094 whole organism PATO:0030001 dorsalized abnormal ZDB-GENE-000208-25 30584 655 bmp7a ZFA:0001115 trunk PATO:0001485 condensed abnormal ZDB-GENE-000208-25 30584 655 bmp7a ZFA:0001115 trunk PATO:0001787 rotational curvature abnormal ZDB-GENE-000208-25 30584 655 bmp7a ZFA:0001117 post-vent region PATO:0002002 has extra parts of type abnormal ZFA:0000077 tail bud ZDB-GENE-000208-25 30584 655 bmp7a ZFA:0001117 post-vent region PATO:0002002 has extra parts of type abnormal ZFA:0000135 notochord ZDB-GENE-000208-25 30584 655 bmp7a ZFA:0001117 post-vent region PATO:0001483 aplastic abnormal ZDB-GENE-000208-25 30584 655 bmp7a ZFA:0001135 neural tube PATO:0000051 morphology abnormal ZDB-GENE-000208-25 30584 655 bmp7a ZFA:0001161 pectoral fin PATO:0000628 mislocalised abnormal ZDB-GENE-000208-25 30584 655 bmp7a ZFA:0009248 neuron BFO:0000050 part_of ZFA:0007035 spinal cord neural rod PATO:0000470 increased amount abnormal ZDB-GENE-000208-25 30584 655 bmp7a ZFA:0009248 neuron BFO:0000050 part_of ZFA:0007035 spinal cord neural rod PATO:0001923 mislocalised laterally abnormal ZDB-GENE-000208-25 30584 655 bmp7a ZFA:0009004 trunk neural crest cell PATO:0001997 decreased amount abnormal ZDB-GENE-000208-25 30584 655 bmp7a ZFA:0009044 blood cell PATO:0001997 decreased amount abnormal ZDB-GENE-000208-25 30584 655 bmp7a ZFA:0009150 Rohon-Beard neuron PATO:0001997 decreased amount abnormal ZDB-GENE-000208-25 30584 655 bmp7a ZFA:0009325 erythroid lineage cell PATO:0000462 absent abnormal ZDB-GENE-000208-4 30096 7545 zic1 GO:0021854 hypothalamus development PATO:0001236 process quality abnormal ZDB-GENE-000208-4 30096 7545 zic1 GO:0034653 retinoic acid catabolic process PATO:0000911 decreased rate abnormal ZDB-GENE-000208-4 30096 7545 zic1 GO:0048853 forebrain morphogenesis PATO:0001236 process quality abnormal ZDB-GENE-000208-4 30096 7545 zic1 GO:0060059 embryonic retina morphogenesis in camera-type eye PATO:0001236 process quality abnormal ZDB-GENE-000208-4 30096 7545 zic1 ZFA:0000050 optic vesicle PATO:0000636 wholly ventralized abnormal ZDB-GENE-000208-4 30096 7545 zic1 ZFA:0000101 diencephalon PATO:0001241 physical object quality abnormal ZDB-GENE-000208-4 30096 7545 zic1 ZFA:0000109 forebrain PATO:0001241 physical object quality abnormal ZDB-GENE-000208-4 30096 7545 zic1 ZFA:0000137 optic stalk PATO:0000646 malformed abnormal ZDB-GENE-000208-4 30096 7545 zic1 ZFA:0000144 retinal pigmented epithelium PATO:0000628 mislocalised abnormal ZDB-GENE-000208-4 30096 7545 zic1 ZFA:0000152 retina PATO:0000646 malformed abnormal ZDB-GENE-000208-4 30096 7545 zic1 ZFA:0000152 retina PATO:0001241 physical object quality abnormal ZDB-GENE-000208-4 30096 7545 zic1 ZFA:0001202 optic cup PATO:0001241 physical object quality abnormal ZDB-GENE-000208-4 30096 7545 zic1 ZFA:0001284 optic fissure PATO:0000609 closure incomplete abnormal ZDB-GENE-000209-3 30769 6091 robo1 GO:0003160 endocardium morphogenesis PATO:0002302 decreased process quality abnormal ZDB-GENE-000209-3 30769 6091 robo1 GO:0055008 cardiac muscle tissue morphogenesis PATO:0002302 decreased process quality abnormal ZDB-GENE-000209-3 30769 6091 robo1 GO:0060975 cardioblast migration to the midline involved in heart field formation PATO:0002302 decreased process quality abnormal ZDB-GENE-000209-3 30769 6091 robo1 ZFA:0000059 postoptic commissure PATO:0000600 increased width abnormal ZDB-GENE-000209-3 30769 6091 robo1 ZFA:0001319 myocardium PATO:0000628 mislocalised abnormal ZDB-GENE-000209-3 30769 6091 robo1 ZFA:0009000 cell BFO:0000050 part_of ZFA:0001320 endocardium PATO:0000646 malformed abnormal ZDB-GENE-000209-3 30769 6091 robo1 ZFA:0001320 endocardium PATO:0000628 mislocalised abnormal ZDB-GENE-000209-4 30770 64221 robo3 GO:0001964 startle response PATO:0001507 disrupted abnormal ZDB-GENE-000209-4 30770 64221 robo3 GO:0007634 optokinetic behavior PATO:0001507 disrupted abnormal ZDB-GENE-000209-4 30770 64221 robo3 GO:0008345 larval locomotory behavior PATO:0000078 rhythm quality abnormal ZDB-GENE-000209-4 30770 64221 robo3 GO:0009612 response to mechanical stimulus PATO:0001507 disrupted abnormal ZDB-GENE-000209-4 30770 64221 robo3 GO:0009646 response to absence of light PATO:0001507 disrupted abnormal ZDB-GENE-000209-4 30770 64221 robo3 GO:0010996 response to auditory stimulus PATO:0001507 disrupted abnormal ZDB-GENE-000209-4 30770 64221 robo3 GO:0016199 axon midline choice point recognition PATO:0001507 disrupted abnormal ZDB-GENE-000209-4 30770 64221 robo3 GO:0050881 musculoskeletal movement PATO:0000001 quality abnormal ZDB-GENE-000209-4 30770 64221 robo3 GO:0050885 neuromuscular process controlling balance PATO:0000001 quality abnormal ZDB-GENE-000209-4 30770 64221 robo3 GO:0050885 neuromuscular process controlling balance PATO:0001507 disrupted abnormal ZDB-GENE-000209-4 30770 64221 robo3 GO:0050957 equilibrioception PATO:0001507 disrupted abnormal ZDB-GENE-000209-4 30770 64221 robo3 GO:0071679 commissural neuron axon guidance PATO:0001507 disrupted abnormal ZDB-GENE-000209-4 30770 64221 robo3 ZFA:0000059 postoptic commissure PATO:0000599 decreased width abnormal ZDB-GENE-000209-4 30770 64221 robo3 ZFA:0000059 postoptic commissure PATO:0000600 increased width abnormal ZDB-GENE-000209-4 30770 64221 robo3 ZFA:0001094 whole organism PATO:0000169 viability abnormal ZDB-GENE-000209-4 30770 64221 robo3 ZFA:0001094 whole organism PATO:0000718 lethal (sensu genetics) abnormal ZDB-GENE-000209-4 30770 64221 robo3 ZFA:0001094 whole organism PATO:0002076 movement behavioral quality abnormal ZDB-GENE-000209-4 30770 64221 robo3 ZFA:0001117 post-vent region PATO:0001906 movement quality abnormal ZDB-GENE-000209-4 30770 64221 robo3 GO:0030424 axon BFO:0000050 part_of ZFA:0001659 diencephalic nucleus PATO:0002168 displaced to abnormal BSPO:0000082 lateral region BFO:0000050 part_of ZFA:0000029 hindbrain ZDB-GENE-000209-4 30770 64221 robo3 ZFA:0001692 hindbrain commissure PATO:0000937 disorganized abnormal ZDB-GENE-000209-4 30770 64221 robo3 GO:0030424 axon BFO:0000050 part_of ZFA:0009149 Mauthner neuron PATO:0000628 mislocalised abnormal ZDB-GENE-000210-17 30065 1994 elavl1b ZFA:0000009 cardiac ventricle PATO:0001571 dilated abnormal ZDB-GENE-000210-17 30065 1994 elavl1b ZFA:0000009 cardiac ventricle PATO:0001581 decreased contractility abnormal ZDB-GENE-000210-17 30065 1994 elavl1b ZFA:0000029 hindbrain PATO:0001571 dilated abnormal ZDB-GENE-000210-17 30065 1994 elavl1b ZFA:0000054 pericardium PATO:0001450 edematous abnormal ZDB-GENE-000210-17 30065 1994 elavl1b ZFA:0000109 forebrain PATO:0001571 dilated abnormal ZDB-GENE-000210-17 30065 1994 elavl1b ZFA:0000114 heart PATO:0001624 decreased functionality abnormal ZDB-GENE-000210-17 30065 1994 elavl1b ZFA:0000128 midbrain PATO:0001571 dilated abnormal ZDB-GENE-000210-17 30065 1994 elavl1b ZFA:0000471 atrium PATO:0001571 dilated abnormal ZDB-GENE-000210-19 30077 5950 rbp4 GO:0001889 liver development PATO:0001507 disrupted abnormal ZDB-GENE-000210-19 30077 5950 rbp4 ZFA:0000008 brain PATO:0000051 morphology abnormal ZDB-GENE-000210-19 30077 5950 rbp4 ZFA:0000084 yolk PATO:0000327 low brightness abnormal ZDB-GENE-000210-19 30077 5950 rbp4 ZFA:0000084 yolk PATO:0000586 increased size abnormal ZDB-GENE-000210-19 30077 5950 rbp4 ZFA:0000106 extension PATO:0000574 decreased length abnormal ZDB-GENE-000210-19 30077 5950 rbp4 ZFA:0000124 liver primordium PATO:0001473 duplicated abnormal ZDB-GENE-000210-19 30077 5950 rbp4 ZFA:0001094 whole organism PATO:0000718 lethal (sensu genetics) abnormal ZDB-GENE-000210-19 30077 5950 rbp4 ZFA:0001117 post-vent region PATO:0000051 morphology abnormal ZDB-GENE-000210-20 30068 847 cat GO:0008283 cell population proliferation BFO:0000066 occurs_in ZFA:0000152 retina PATO:0002051 increased occurrence abnormal ZDB-GENE-000210-21 30072 3624 inhbaa GO:0031101 fin regeneration PATO:0001507 disrupted abnormal ZDB-GENE-000210-23 30066 4212 meis2b GO:0001947 heart looping PATO:0001507 disrupted abnormal ZDB-GENE-000210-23 30066 4212 meis2b GO:0003209 cardiac atrium morphogenesis PATO:0002302 decreased process quality abnormal ZDB-GENE-000210-23 30066 4212 meis2b GO:0003317 cardioblast cell midline fusion PATO:0001507 disrupted abnormal ZDB-GENE-000210-23 30066 4212 meis2b GO:0007507 heart development PATO:0001507 disrupted abnormal ZDB-GENE-000210-23 30066 4212 meis2b GO:0060047 heart contraction PATO:0000381 decreased frequency abnormal ZDB-GENE-000210-23 30066 4212 meis2b GO:0061371 determination of heart left/right asymmetry PATO:0001507 disrupted abnormal ZDB-GENE-000210-23 30066 4212 meis2b ZFA:0000054 pericardium PATO:0001450 edematous abnormal ZDB-GENE-000210-23 30066 4212 meis2b ZFA:0000114 heart PATO:0000140 position abnormal ZDB-GENE-000210-23 30066 4212 meis2b ZFA:0000114 heart PATO:0001624 decreased functionality abnormal ZDB-GENE-000210-23 30066 4212 meis2b GO:0061337 cardiac conduction BFO:0000066 occurs_in ZFA:0000471 atrium PATO:0002302 decreased process quality abnormal ZDB-GENE-000210-23 30066 4212 meis2b ZFA:0000471 atrium PATO:0000586 increased size abnormal ZDB-GENE-000210-23 30066 4212 meis2b ZFA:0000471 atrium PATO:0002057 increased area abnormal ZDB-GENE-000210-23 30066 4212 meis2b ZFA:0001094 whole organism PATO:0001591 curvature abnormal ZDB-GENE-000210-23 30066 4212 meis2b ZFA:0001114 head PATO:0000587 decreased size abnormal ZDB-GENE-000210-23 30066 4212 meis2b ZFA:0001114 head PATO:0001958 increased variability of size abnormal ZDB-GENE-000210-23 30066 4212 meis2b GO:0008283 cell population proliferation BFO:0000066 occurs_in ZFA:0001374 atrial myocardium PATO:0002051 increased occurrence abnormal ZDB-GENE-000210-31 30076 7421 vdra GO:0043931 ossification involved in bone maturation PATO:0000502 delayed abnormal ZDB-GENE-000210-31 30076 7421 vdra GO:0070509 calcium ion import PATO:0002302 decreased process quality abnormal ZDB-GENE-000210-31 30076 7421 vdra GO:0071425 hematopoietic stem cell proliferation PATO:0001507 disrupted abnormal ZDB-GENE-000210-31 30076 7421 vdra ZFA:0005028 ventral wall of dorsal aorta PATO:0002002 has extra parts of type abnormal ZFA:0009014 hematopoietic stem cell ZDB-GENE-000210-31 30076 7421 vdra ZFA:0005028 ventral wall of dorsal aorta PATO:0002001 has fewer parts of type abnormal ZFA:0009354 hematopoietic multipotent progenitor cell ZDB-GENE-000210-31 30076 7421 vdra ZFA:0005028 ventral wall of dorsal aorta PATO:0002002 has extra parts of type abnormal ZFA:0009354 hematopoietic multipotent progenitor cell ZDB-GENE-000210-32 30083 4831 nme2b.1 GO:0001525 angiogenesis PATO:0001507 disrupted abnormal ZDB-GENE-000210-32 30083 4831 nme2b.1 GO:0006171 cAMP biosynthetic process PATO:0000911 decreased rate abnormal ZDB-GENE-000210-32 30083 4831 nme2b.1 GO:0006183 GTP biosynthetic process PATO:0000911 decreased rate abnormal ZDB-GENE-000210-32 30083 4831 nme2b.1 GO:0060047 heart contraction PATO:0000911 decreased rate abnormal ZDB-GENE-000210-32 30083 4831 nme2b.1 GO:0060047 heart contraction PATO:0001236 process quality abnormal ZDB-GENE-000210-32 30083 4831 nme2b.1 ZFA:0000054 pericardium PATO:0001450 edematous abnormal ZDB-GENE-000210-32 30083 4831 nme2b.1 ZFA:0000099 brain vasculature PATO:0000646 malformed abnormal ZDB-GENE-000210-32 30083 4831 nme2b.1 ZFA:0000107 eye PATO:0000587 decreased size abnormal ZDB-GENE-000210-32 30083 4831 nme2b.1 ZFA:0000114 heart PATO:0000025 composition abnormal ZDB-GENE-000210-32 30083 4831 nme2b.1 ZFA:0000114 heart PATO:0001581 decreased contractility abnormal ZDB-GENE-000210-32 30083 4831 nme2b.1 ZFA:0000114 heart PATO:0001624 decreased functionality abnormal ZDB-GENE-000210-32 30083 4831 nme2b.1 ZFA:0001285 intersegmental vessel PATO:0000646 malformed abnormal ZDB-GENE-000210-32 30083 4831 nme2b.1 ZFA:0005020 central artery PATO:0000646 malformed abnormal ZDB-GENE-000210-32 30083 4831 nme2b.1 ZFA:0005025 dorsal longitudinal anastomotic vessel PATO:0000646 malformed abnormal ZDB-GENE-000210-32 30083 4831 nme2b.1 ZFA:0005034 parachordal vessel PATO:0001483 aplastic abnormal ZDB-GENE-000210-32 30083 4831 nme2b.1 ZFA:0005035 subintestinal vein PATO:0000462 absent abnormal ZDB-GENE-000210-32 30083 4831 nme2b.1 ZFA:0005035 subintestinal vein PATO:0000646 malformed abnormal ZDB-GENE-000210-33 30084 4831 nme2b.2 GO:0006183 GTP biosynthetic process PATO:0000911 decreased rate abnormal ZDB-GENE-000210-34 30085 4832 nme3 GO:0001947 heart looping PATO:0001236 process quality abnormal ZDB-GENE-000210-34 30085 4832 nme3 GO:0007368 determination of left/right symmetry PATO:0001236 process quality abnormal ZDB-GENE-000210-34 30085 4832 nme3 GO:0060047 heart contraction BFO:0000066 occurs_in ZFA:0000009 cardiac ventricle PATO:0001236 process quality abnormal ZDB-GENE-000210-34 30085 4832 nme3 ZFA:0000054 pericardium PATO:0001450 edematous abnormal ZDB-GENE-000210-34 30085 4832 nme3 ZFA:0000151 pronephros PATO:0001673 cystic abnormal ZDB-GENE-000210-34 30085 4832 nme3 CHEBI:17489 3',5'-cyclic AMP BFO:0000050 part_of ZFA:0001094 whole organism PATO:0001997 decreased amount abnormal ZDB-GENE-000210-34 30085 4832 nme3 ZFA:0001117 post-vent region PATO:0001592 increased curvature abnormal ZDB-GENE-000210-34 30085 4832 nme3 GO:0005929 cilium BFO:0000050 part_of ZFA:0001558 pronephric tubule PATO:0000574 decreased length abnormal ZDB-GENE-000210-35 30086 29922 nme7 ZFA:0001117 post-vent region PATO:0001592 increased curvature abnormal ZDB-GENE-000223-14 404602 401 phox2a GO:0003358 noradrenergic neuron development PATO:0001507 disrupted abnormal ZDB-GENE-000223-14 404602 401 phox2a GO:0021703 locus ceruleus development PATO:0001507 disrupted abnormal ZDB-GENE-000223-14 404602 401 phox2a ZFA:0000013 cranial ganglion PATO:0000587 decreased size abnormal ZDB-GENE-000223-14 404602 401 phox2a ZFA:0000107 eye PATO:0002181 displaced abnormal ZDB-GENE-000223-14 404602 401 phox2a ZFA:0000396 nervous system PATO:0000001 quality abnormal ZDB-GENE-000223-14 404602 401 phox2a ZFA:0000450 trochlear motor nucleus PATO:0000587 decreased size abnormal ZDB-GENE-000223-14 404602 401 phox2a ZFA:0009248 neuron BFO:0000050 part_of ZFA:0000539 locus coeruleus PATO:0000462 absent abnormal ZDB-GENE-000223-14 404602 401 phox2a ZFA:0000539 locus coeruleus PATO:0001999 lacks parts or has fewer parts of type abnormal ZFA:0009248 neuron ZDB-GENE-000223-14 404602 401 phox2a ZFA:0000553 oculomotor nucleus PATO:0000587 decreased size abnormal ZDB-GENE-000223-14 404602 401 phox2a ZFA:0001094 whole organism PATO:0001422 dead abnormal ZDB-GENE-000223-14 404602 401 phox2a ZFA:0009214 norepinephrine secreting cell BFO:0000050 part_of ZFA:0001306 pharyngeal arch PATO:0000462 absent abnormal ZDB-GENE-000223-14 404602 401 phox2a ZFA:0001306 pharyngeal arch PATO:0002001 has fewer parts of type abnormal ZFA:0009248 neuron ZDB-GENE-000308-1 30967 10643 igf2bp3 GO:0000910 cytokinesis PATO:0001507 disrupted abnormal ZDB-GENE-000308-1 30967 10643 igf2bp3 GO:0036090 cleavage furrow ingression PATO:0001507 disrupted abnormal ZDB-GENE-000308-1 30967 10643 igf2bp3 GO:0040016 embryonic cleavage PATO:0001507 disrupted abnormal ZDB-GENE-000308-1 30967 10643 igf2bp3 ZFA:0000084 yolk PATO:0000957 opacity abnormal ZDB-GENE-000308-1 30967 10643 igf2bp3 ZFA:0000088 yolk syncytial layer PATO:0001602 distended abnormal ZDB-GENE-000308-1 30967 10643 igf2bp3 GO:0005884 actin filament BFO:0000050 part_of ZFA:0000093 blastomere PATO:0001997 decreased amount abnormal ZDB-GENE-000308-1 30967 10643 igf2bp3 GO:0043487 regulation of RNA stability BFO:0000066 occurs_in ZFA:0000093 blastomere PATO:0001507 disrupted abnormal ZDB-GENE-000308-1 30967 10643 igf2bp3 ZFA:0000093 blastomere PATO:0000411 circular abnormal ZDB-GENE-000308-1 30967 10643 igf2bp3 ZFA:0000093 blastomere PATO:0001531 cellular adhesivity abnormal ZDB-GENE-000308-1 30967 10643 igf2bp3 ZFA:0000242 male organism PATO:0001470 proportionality to abnormal ZFA:0000303 female organism ZDB-GENE-000308-1 30967 10643 igf2bp3 GO:0007369 gastrulation BFO:0000066 occurs_in ZFA:0001094 whole organism PATO:0002302 decreased process quality abnormal ZDB-GENE-000308-1 30967 10643 igf2bp3 ZFA:0001094 whole organism PATO:0001422 dead abnormal ZDB-GENE-000308-1 30967 10643 igf2bp3 ZFA:0001094 whole organism PATO:0001617 deformed abnormal ZDB-GENE-000308-1 30967 10643 igf2bp3 GO:0032154 cleavage furrow BFO:0000050 part_of ZFA:0001175 blastodisc PATO:0000141 structure abnormal ZDB-GENE-000308-1 30967 10643 igf2bp3 GO:0032154 cleavage furrow BFO:0000050 part_of ZFA:0001175 blastodisc PATO:0000470 increased amount abnormal ZDB-GENE-000308-1 30967 10643 igf2bp3 ZFA:0001176 blastoderm PATO:0000587 decreased size abnormal ZDB-GENE-000308-1 30967 10643 igf2bp3 GO:0060471 cortical granule exocytosis BFO:0000066 occurs_in ZFA:0005772 fertilized egg PATO:0001507 disrupted abnormal ZDB-GENE-000308-1 30967 10643 igf2bp3 GO:0006915 apoptotic process BFO:0000066 occurs_in ZFA:0009288 primordial germ cell PATO:0002304 increased process quality abnormal ZDB-GENE-000308-1 30967 10643 igf2bp3 ZFA:0009288 primordial germ cell PATO:0000060 spatial pattern abnormal ZDB-GENE-000308-1 30967 10643 igf2bp3 ZFA:0009288 primordial germ cell PATO:0001997 decreased amount abnormal ZDB-GENE-000322-1 58114 70 actc1b GO:0001966 thigmotaxis PATO:0002302 decreased process quality abnormal ZDB-GENE-000322-1 58114 70 actc1b GO:0036268 swimming PATO:0002302 decreased process quality abnormal ZDB-GENE-000322-1 58114 70 actc1b GO:0036269 swimming behavior PATO:0001236 process quality abnormal ZDB-GENE-000322-1 58114 70 actc1b GO:0110165 cellular anatomical entity BFO:0000050 part_of ZFA:0001089 myoseptum PATO:0001629 aggregated abnormal ZDB-GENE-000322-1 58114 70 actc1b ZFA:0005145 muscle PATO:0000051 morphology abnormal ZDB-GENE-000322-1 58114 70 actc1b GO:0005739 mitochondrion BFO:0000050 part_of ZFA:0005277 skeletal muscle PATO:0000470 increased amount abnormal ZDB-GENE-000322-1 58114 70 actc1b GO:0030017 sarcomere BFO:0000050 part_of ZFA:0005277 skeletal muscle PATO:0000591 increased thickness abnormal ZDB-GENE-000322-1 58114 70 actc1b GO:0110165 cellular anatomical entity BFO:0000050 part_of ZFA:0005277 skeletal muscle PATO:0001629 aggregated abnormal ZDB-GENE-000322-1 58114 70 actc1b ZFA:0009115 skeletal muscle cell BFO:0000050 part_of ZFA:0005277 skeletal muscle PATO:0000937 disorganized abnormal ZDB-GENE-000322-1 58114 70 actc1b ZFA:0005277 skeletal muscle PATO:0000937 disorganized abnormal ZDB-GENE-000322-1 58114 70 actc1b ZFA:0009115 skeletal muscle cell PATO:0001444 broken abnormal ZDB-GENE-000322-3 58084 7140 tnnt3a ZFA:0005145 muscle BFO:0000050 part_of ZFA:0001115 trunk PATO:0001372 refractivity abnormal ZDB-GENE-000322-3 58084 7140 tnnt3a GO:0030017 sarcomere BFO:0000050 part_of ZFA:0005277 skeletal muscle PATO:0000937 disorganized abnormal ZDB-GENE-000322-3 58084 7140 tnnt3a GO:0005884 actin filament BFO:0000050 part_of ZFA:0009117 fast muscle cell PATO:0000937 disorganized abnormal ZDB-GENE-000322-3 58084 7140 tnnt3a GO:0005884 actin filament BFO:0000050 part_of ZFA:0009117 fast muscle cell PATO:0001566 distributed abnormal ZDB-GENE-000322-3 58084 7140 tnnt3a GO:0030016 myofibril BFO:0000050 part_of ZFA:0009117 fast muscle cell PATO:0000639 degenerate abnormal ZDB-GENE-000328-3 58073 8325 fzd8a GO:0002088 lens development in camera-type eye PATO:0001507 disrupted abnormal ZDB-GENE-000328-3 58073 8325 fzd8a GO:0003407 neural retina development PATO:0000502 delayed abnormal ZDB-GENE-000328-3 58073 8325 fzd8a GO:0010842 retina layer formation PATO:0000502 delayed abnormal ZDB-GENE-000328-3 58073 8325 fzd8a GO:0021520 spinal cord motor neuron cell fate specification PATO:0001507 disrupted abnormal ZDB-GENE-000328-3 58073 8325 fzd8a GO:0021530 spinal cord oligodendrocyte cell fate specification PATO:0001507 disrupted abnormal ZDB-GENE-000328-3 58073 8325 fzd8a GO:0048703 embryonic viscerocranium morphogenesis PATO:0002302 decreased process quality abnormal ZDB-GENE-000328-3 58073 8325 fzd8a GO:0061386 closure of optic fissure PATO:0000502 delayed abnormal ZDB-GENE-000328-3 58073 8325 fzd8a GO:1990009 retinal cell apoptotic process PATO:0002051 increased occurrence abnormal ZDB-GENE-000328-3 58073 8325 fzd8a ZFA:0000024 retinal ganglion cell layer PATO:0000600 increased width abnormal ZDB-GENE-000328-3 58073 8325 fzd8a ZFA:0009169 glioblast (sensu Vertebrata) BFO:0000050 part_of ZFA:0000075 spinal cord PATO:0000462 absent abnormal ZDB-GENE-000328-3 58073 8325 fzd8a ZFA:0009169 glioblast (sensu Vertebrata) BFO:0000050 part_of ZFA:0000075 spinal cord PATO:0001997 decreased amount abnormal ZDB-GENE-000328-3 58073 8325 fzd8a ZFA:0009247 secondary motor neuron BFO:0000050 part_of ZFA:0000075 spinal cord PATO:0001997 decreased amount abnormal ZDB-GENE-000328-3 58073 8325 fzd8a ZFA:0009292 radial glial cell BFO:0000050 part_of ZFA:0000075 spinal cord PATO:0000937 disorganized abnormal ZDB-GENE-000328-3 58073 8325 fzd8a ZFA:0009292 radial glial cell BFO:0000050 part_of ZFA:0000075 spinal cord PATO:0001997 decreased amount abnormal ZDB-GENE-000328-3 58073 8325 fzd8a ZFA:0009301 dopaminergic neuron BFO:0000050 part_of ZFA:0000101 diencephalon PATO:0000470 increased amount abnormal ZDB-GENE-000328-3 58073 8325 fzd8a ZFA:0000107 eye PATO:0000587 decreased size abnormal ZDB-GENE-000328-3 58073 8325 fzd8a ZFA:0000119 retinal inner nuclear layer PATO:0000600 increased width abnormal ZDB-GENE-000328-3 58073 8325 fzd8a GO:0051301 cell division BFO:0000066 occurs_in ZFA:0000152 retina PATO:0002052 decreased occurrence abnormal ZDB-GENE-000328-3 58073 8325 fzd8a GO:0051726 regulation of cell cycle BFO:0000066 occurs_in ZFA:0000152 retina PATO:0000502 delayed abnormal ZDB-GENE-000328-3 58073 8325 fzd8a ZFA:0009000 cell BFO:0000050 part_of ZFA:0000152 retina PATO:0001997 decreased amount abnormal ZDB-GENE-000328-3 58073 8325 fzd8a ZFA:0000152 retina PATO:0000587 decreased size abnormal ZDB-GENE-000328-3 58073 8325 fzd8a ZFA:0000152 retina PATO:0000592 decreased thickness abnormal ZDB-GENE-000328-3 58073 8325 fzd8a ZFA:0000152 retina PATO:0002247 degree of pigmentation abnormal ZDB-GENE-000328-3 58073 8325 fzd8a GO:0072659 protein localization to plasma membrane BFO:0000066 occurs_in ZFA:0001106 pharyngeal pouch PATO:0002052 decreased occurrence abnormal ZDB-GENE-000328-3 58073 8325 fzd8a ZFA:0001106 pharyngeal pouch PATO:0000646 malformed abnormal ZDB-GENE-000328-3 58073 8325 fzd8a ZFA:0001284 optic fissure PATO:0000610 open abnormal ZDB-GENE-000328-3 58073 8325 fzd8a ZFA:0001516 ceratobranchial cartilage PATO:0000646 malformed abnormal ZDB-GENE-000328-5 58043 3225 hoxc9a GO:0001946 lymphangiogenesis PATO:0000297 arrested abnormal ZDB-GENE-000328-5 58043 3225 hoxc9a ZFA:0005110 thoracic duct PATO:0000645 hypoplastic abnormal ZDB-GENE-000328-5 58043 3225 hoxc9a ZFA:0009395 vascular lymphangioblast PATO:0000645 hypoplastic abnormal ZDB-GENE-000329-2 58044 3217 hoxb7a GO:0009790 embryo development PATO:0000502 delayed abnormal ZDB-GENE-000329-2 58044 3217 hoxb7a ZFA:0001094 whole organism PATO:0002251 decreased pigmentation abnormal ZDB-GENE-000329-2 58044 3217 hoxb7a ZFA:0001117 post-vent region PATO:0000617 bent abnormal ZDB-GENE-000329-2 58044 3217 hoxb7a ZFA:0001117 post-vent region PATO:0002364 shortened abnormal ZDB-GENE-000329-4 58065 4853 notch2 GO:0001944 vasculature development PATO:0001236 process quality abnormal ZDB-GENE-000329-4 58065 4853 notch2 GO:0001946 lymphangiogenesis PATO:0001507 disrupted abnormal ZDB-GENE-000329-4 58065 4853 notch2 GO:0031018 endocrine pancreas development PATO:0001507 disrupted abnormal ZDB-GENE-000329-4 58065 4853 notch2 GO:0035883 enteroendocrine cell differentiation PATO:0001507 disrupted abnormal ZDB-GENE-000329-4 58065 4853 notch2 GO:0042593 glucose homeostasis PATO:0001507 disrupted abnormal ZDB-GENE-000329-4 58065 4853 notch2 ZFA:0005944 mural cell BFO:0000050 part_of ZFA:0000014 dorsal aorta PATO:0001997 decreased amount abnormal ZDB-GENE-000329-4 58065 4853 notch2 ZFA:0005944 mural cell BFO:0000050 part_of ZFA:0000099 brain vasculature PATO:0001997 decreased amount abnormal ZDB-GENE-000329-4 58065 4853 notch2 ZFA:0000250 opercle PATO:0000406 curved abnormal ZDB-GENE-000329-4 58065 4853 notch2 ZFA:0000250 opercle PATO:0000599 decreased width abnormal ZDB-GENE-000329-4 58065 4853 notch2 ZFA:0001260 endocrine pancreas PATO:0000587 decreased size abnormal ZDB-GENE-000329-4 58065 4853 notch2 ZFA:0005944 mural cell BFO:0000050 part_of ZFA:0001285 intersegmental vessel PATO:0001997 decreased amount abnormal ZDB-GENE-000329-4 58065 4853 notch2 ZFA:0001399 palatoquadrate cartilage PATO:0000936 truncated abnormal ZDB-GENE-000329-4 58065 4853 notch2 ZFA:0001422 hyosymplectic cartilage PATO:0001154 elongated abnormal ZDB-GENE-000329-4 58065 4853 notch2 ZFA:0001422 hyosymplectic cartilage PATO:0001617 deformed abnormal ZDB-GENE-000329-4 58065 4853 notch2 ZFA:0005110 thoracic duct PATO:0000462 absent abnormal ZDB-GENE-000329-4 58065 4853 notch2 ZFA:0005110 thoracic duct PATO:0001442 wholeness abnormal ZDB-GENE-000329-4 58065 4853 notch2 ZFA:0009102 pancreatic B cell PATO:0001997 decreased amount abnormal ZDB-GENE-000329-4 58065 4853 notch2 ZFA:0009102 pancreatic B cell PATO:0002058 decreased area abnormal ZDB-GENE-000329-5 58066 4854 notch3 GO:0002244 hematopoietic progenitor cell differentiation PATO:0001236 process quality abnormal ZDB-GENE-000329-5 58066 4854 notch3 GO:0014003 oligodendrocyte development PATO:0000297 arrested abnormal ZDB-GENE-000329-5 58066 4854 notch3 GO:0022015 radial glial cell division in pallium PATO:0002051 increased occurrence abnormal ZDB-GENE-000329-5 58066 4854 notch3 GO:0030097 hemopoiesis PATO:0001236 process quality abnormal ZDB-GENE-000329-5 58066 4854 notch3 GO:0035633 maintenance of blood-brain barrier PATO:0001507 disrupted abnormal ZDB-GENE-000329-5 58066 4854 notch3 GO:0039014 cell differentiation involved in pronephros development PATO:0001507 disrupted abnormal ZDB-GENE-000329-5 58066 4854 notch3 GO:0048538 thymus development PATO:0001236 process quality abnormal ZDB-GENE-000329-5 58066 4854 notch3 GO:0048709 oligodendrocyte differentiation PATO:0001236 process quality abnormal ZDB-GENE-000329-5 58066 4854 notch3 GO:0060218 hematopoietic stem cell differentiation PATO:0001236 process quality abnormal ZDB-GENE-000329-5 58066 4854 notch3 GO:0061056 sclerotome development PATO:0001236 process quality abnormal ZDB-GENE-000329-5 58066 4854 notch3 GO:0008219 cell death BFO:0000066 occurs_in ZFA:0000029 hindbrain PATO:0000912 increased rate abnormal ZDB-GENE-000329-5 58066 4854 notch3 ZFA:0005314 blood vessel BFO:0000050 part_of ZFA:0000079 telencephalon PATO:0001482 prominent abnormal ZDB-GENE-000329-5 58066 4854 notch3 ZFA:0005314 blood vessel BFO:0000050 part_of ZFA:0000079 telencephalon PATO:0001571 dilated abnormal ZDB-GENE-000329-5 58066 4854 notch3 ZFA:0005314 blood vessel BFO:0000050 part_of ZFA:0000079 telencephalon PATO:0001714 increased diameter abnormal ZDB-GENE-000329-5 58066 4854 notch3 ZFA:0005944 mural cell BFO:0000050 part_of ZFA:0000099 brain vasculature PATO:0001997 decreased amount abnormal ZDB-GENE-000329-5 58066 4854 notch3 GO:0098722 asymmetric stem cell division BFO:0000066 occurs_in ZFA:0000109 forebrain PATO:0002051 increased occurrence abnormal ZDB-GENE-000329-5 58066 4854 notch3 ZFA:0000151 pronephros PATO:0001396 cellular quality abnormal ZDB-GENE-000329-5 58066 4854 notch3 ZFA:0005250 capillary BFO:0000050 part_of ZFA:0000445 optic tectum PATO:0001957 decreased variability of size abnormal ZDB-GENE-000329-5 58066 4854 notch3 ZFA:0005314 blood vessel BFO:0000050 part_of ZFA:0000445 optic tectum PATO:0001957 decreased variability of size abnormal ZDB-GENE-000329-5 58066 4854 notch3 ZFA:0001083 ventricular zone BFO:0000050 part_of ZFA:0000505 dorsal telencephalon PATO:0002002 has extra parts of type abnormal ZFA:0009292 radial glial cell ZDB-GENE-000329-5 58066 4854 notch3 ZFA:0009292 radial glial cell BFO:0000050 part_of ZFA:0000505 dorsal telencephalon PATO:0002102 proliferative abnormal ZDB-GENE-000329-5 58066 4854 notch3 ZFA:0001094 whole organism PATO:0000406 curved abnormal ZDB-GENE-000329-5 58066 4854 notch3 ZFA:0000007 blood BFO:0000050 part_of ZFA:0001261 ventricular system PATO:0000628 mislocalised abnormal ZDB-GENE-000329-5 58066 4854 notch3 ZFA:0001267 cranial vasculature PATO:0002105 hemorrhagic abnormal ZDB-GENE-000329-5 58066 4854 notch3 ZFA:0009112 pericyte BFO:0000050 part_of ZFA:0005297 cranial blood vessel PATO:0001997 decreased amount abnormal ZDB-GENE-000329-5 58066 4854 notch3 ZFA:0005297 cranial blood vessel PATO:0002286 decreased branchiness abnormal ZDB-GENE-000329-5 58066 4854 notch3 ZFA:0005304 caudal fin blood vessel PATO:0001444 broken abnormal ZDB-GENE-000329-5 58066 4854 notch3 ZFA:0005304 caudal fin blood vessel PATO:0001714 increased diameter abnormal ZDB-GENE-000329-5 58066 4854 notch3 ZFA:0005304 caudal fin blood vessel PATO:0002105 hemorrhagic abnormal ZDB-GENE-000329-5 58066 4854 notch3 ZFA:0005304 caudal fin blood vessel PATO:0002181 displaced abnormal ZDB-GENE-000329-5 58066 4854 notch3 GO:0044838 cell quiescence BFO:0000066 occurs_in ZFA:0009292 radial glial cell PATO:0001236 process quality abnormal ZDB-GENE-000329-9 58037 89 actn3a GO:0008015 blood circulation PATO:0002302 decreased process quality abnormal ZDB-GENE-000329-9 58037 89 actn3a ZFA:0000009 cardiac ventricle PATO:0001581 decreased contractility abnormal ZDB-GENE-000329-9 58037 89 actn3a ZFA:0000114 heart PATO:0001624 decreased functionality abnormal ZDB-GENE-000329-9 58037 89 actn3a ZFA:0000471 atrium PATO:0001571 dilated abnormal ZDB-GENE-000330-4 58038 112755 stx1b GO:0001966 thigmotaxis PATO:0002052 decreased occurrence abnormal ZDB-GENE-000330-4 58038 112755 stx1b GO:0050881 musculoskeletal movement PATO:0001845 irregular rhythm abnormal ZDB-GENE-000330-4 58038 112755 stx1b GO:0050881 musculoskeletal movement PATO:0001860 decreased coordination abnormal ZDB-GENE-000330-4 58038 112755 stx1b GO:0050881 musculoskeletal movement PATO:0002630 episodic abnormal ZDB-GENE-000330-4 58038 112755 stx1b GO:0019228 neuronal action potential BFO:0000066 occurs_in ZFA:0000445 optic tectum PATO:0000380 increased frequency abnormal ZDB-GENE-000330-4 58038 112755 stx1b GO:0019228 neuronal action potential BFO:0000066 occurs_in ZFA:0000445 optic tectum PATO:0001845 irregular rhythm abnormal ZDB-GENE-000330-4 58038 112755 stx1b GO:0098908 regulation of neuronal action potential BFO:0000066 occurs_in ZFA:0000445 optic tectum PATO:0002302 decreased process quality abnormal ZDB-GENE-000330-5 57925 994 cdc25b GO:0001756 somitogenesis PATO:0001624 decreased functionality abnormal ZDB-GENE-000330-5 57925 994 cdc25b GO:0007049 cell cycle PATO:0000297 arrested abnormal ZDB-GENE-000330-5 57925 994 cdc25b GO:0008283 cell population proliferation PATO:0002052 decreased occurrence abnormal ZDB-GENE-000330-5 57925 994 cdc25b ZFA:0000054 pericardium PATO:0001450 edematous abnormal ZDB-GENE-000330-5 57925 994 cdc25b ZFA:0000107 eye PATO:0000587 decreased size abnormal ZDB-GENE-000330-5 57925 994 cdc25b ZFA:0001094 whole organism PATO:0000052 shape abnormal ZDB-GENE-000330-5 57925 994 cdc25b ZFA:0001094 whole organism PATO:0000718 lethal (sensu genetics) abnormal ZDB-GENE-000330-5 57925 994 cdc25b ZFA:0001094 whole organism PATO:0001422 dead abnormal ZDB-GENE-000330-5 57925 994 cdc25b ZFA:0001114 head PATO:0000587 decreased size abnormal ZDB-GENE-000330-5 57925 994 cdc25b GO:0035282 segmentation BFO:0000066 occurs_in ZFA:0001117 post-vent region PATO:0000297 arrested abnormal ZDB-GENE-000330-5 57925 994 cdc25b ZFA:0001477 portion of tissue PATO:0000647 necrotic abnormal ZDB-GENE-000330-5 57925 994 cdc25b ZFA:0009090 pigment cell PATO:0001997 decreased amount abnormal ZDB-GENE-000330-8 58024 8161 coil GO:0000387 spliceosomal snRNP assembly PATO:0002302 decreased process quality abnormal ZDB-GENE-000330-8 58024 8161 coil GO:0006915 apoptotic process PATO:0002051 increased occurrence abnormal ZDB-GENE-000330-8 58024 8161 coil GO:0008283 cell population proliferation PATO:0002052 decreased occurrence abnormal ZDB-GENE-000330-8 58024 8161 coil GO:0009790 embryo development PATO:0000297 arrested abnormal ZDB-GENE-000330-8 58024 8161 coil GO:0030576 Cajal body organization PATO:0002302 decreased process quality abnormal ZDB-GENE-000330-8 58024 8161 coil GO:0045292 mRNA cis splicing, via spliceosome PATO:0002052 decreased occurrence abnormal ZDB-GENE-000330-8 58024 8161 coil ZFA:0009000 cell BFO:0000050 part_of ZFA:0001094 whole organism PATO:0000638 apoptotic abnormal ZDB-GENE-000330-8 58024 8161 coil ZFA:0009000 cell BFO:0000050 part_of ZFA:0001094 whole organism PATO:0001422 dead abnormal ZDB-GENE-000330-8 58024 8161 coil GO:0015030 Cajal body BFO:0000050 part_of ZFA:0009000 cell PATO:0001997 decreased amount abnormal ZDB-GENE-000330-8 58024 8161 coil GO:0030532 small nuclear ribonucleoprotein complex BFO:0000050 part_of ZFA:0009000 cell PATO:0001630 dispersed abnormal ZDB-GENE-000330-9 58026 5664 psen2 GO:0001756 somitogenesis PATO:0001507 disrupted abnormal ZDB-GENE-000330-9 58026 5664 psen2 GO:0014032 neural crest cell development PATO:0001507 disrupted abnormal ZDB-GENE-000330-9 58026 5664 psen2 ZFA:0000008 brain PATO:0001853 hydrocephalic abnormal ZDB-GENE-000330-9 58026 5664 psen2 ZFA:0000029 hindbrain PATO:0001853 hydrocephalic abnormal ZDB-GENE-000330-9 58026 5664 psen2 ZFA:0000110 fourth ventricle PATO:0000586 increased size abnormal ZDB-GENE-000330-9 58026 5664 psen2 ZFA:0000128 midbrain PATO:0001853 hydrocephalic abnormal ZDB-GENE-000330-9 58026 5664 psen2 ZFA:0000159 tectal ventricle PATO:0000586 increased size abnormal ZDB-GENE-000330-9 58026 5664 psen2 ZFA:0001094 whole organism PATO:0000587 decreased size abnormal ZDB-GENE-000330-9 58026 5664 psen2 ZFA:0009091 melanocyte BFO:0000050 part_of ZFA:0001115 trunk PATO:0001997 decreased amount abnormal ZDB-GENE-000330-9 58026 5664 psen2 ZFA:0009091 melanocyte BFO:0000050 part_of ZFA:0001117 post-vent region PATO:0001997 decreased amount abnormal ZDB-GENE-000330-9 58026 5664 psen2 ZFA:0009091 melanocyte BFO:0000050 part_of ZFA:0001463 melanophore stripe PATO:0002251 decreased pigmentation abnormal ZDB-GENE-000330-9 58026 5664 psen2 ZFA:0005178 DoLA PATO:0000470 increased amount abnormal ZDB-GENE-000330-9 58026 5664 psen2 ZFA:0009091 melanocyte PATO:0000060 spatial pattern abnormal ZDB-GENE-000330-9 58026 5664 psen2 ZFA:0009091 melanocyte PATO:0001997 decreased amount abnormal ZDB-GENE-000330-9 58026 5664 psen2 ZFA:0009165 neural crest cell PATO:0001997 decreased amount abnormal ZDB-GENE-000330-9 58026 5664 psen2 ZFA:0009248 neuron PATO:0000470 increased amount abnormal ZDB-GENE-000403-1 57931 8312 axin1 GO:0001947 heart looping PATO:0001507 disrupted abnormal ZDB-GENE-000403-1 57931 8312 axin1 GO:0007368 determination of left/right symmetry PATO:0001507 disrupted abnormal ZDB-GENE-000403-1 57931 8312 axin1 GO:0007632 visual behavior PATO:0001507 disrupted abnormal ZDB-GENE-000403-1 57931 8312 axin1 GO:0008015 blood circulation PATO:0001507 disrupted abnormal ZDB-GENE-000403-1 57931 8312 axin1 GO:0021794 thalamus development PATO:0001236 process quality abnormal ZDB-GENE-000403-1 57931 8312 axin1 GO:0021794 thalamus development PATO:0002302 decreased process quality abnormal ZDB-GENE-000403-1 57931 8312 axin1 GO:0021881 Wnt-activated signaling pathway involved in forebrain neuron fate commitment PATO:0001507 disrupted abnormal ZDB-GENE-000403-1 57931 8312 axin1 GO:0030900 forebrain development PATO:0001507 disrupted abnormal ZDB-GENE-000403-1 57931 8312 axin1 GO:0048048 embryonic eye morphogenesis PATO:0001507 disrupted abnormal ZDB-GENE-000403-1 57931 8312 axin1 GO:0050673 epithelial cell proliferation PATO:0002051 increased occurrence abnormal ZDB-GENE-000403-1 57931 8312 axin1 GO:0060070 canonical Wnt signaling pathway PATO:0002051 increased occurrence abnormal ZDB-GENE-000403-1 57931 8312 axin1 GO:0061381 cell migration in diencephalon PATO:0000502 delayed abnormal ZDB-GENE-000403-1 57931 8312 axin1 GO:0071632 optomotor response PATO:0001507 disrupted abnormal ZDB-GENE-000403-1 57931 8312 axin1 ZFA:0000008 brain PATO:0000001 quality abnormal ZDB-GENE-000403-1 57931 8312 axin1 ZFA:0009127 photoreceptor cell BFO:0000050 part_of ZFA:0000019 epiphysis PATO:0000470 increased amount abnormal ZDB-GENE-000403-1 57931 8312 axin1 ZFA:0009248 neuron BFO:0000050 part_of ZFA:0000019 epiphysis PATO:0000470 increased amount abnormal ZDB-GENE-000403-1 57931 8312 axin1 ZFA:0000019 epiphysis PATO:0000586 increased size abnormal ZDB-GENE-000403-1 57931 8312 axin1 ZFA:0000022 floor plate PATO:0000001 quality abnormal ZDB-GENE-000403-1 57931 8312 axin1 ZFA:0000047 peripheral olfactory organ PATO:0000462 absent abnormal ZDB-GENE-000403-1 57931 8312 axin1 ZFA:0000048 olfactory placode PATO:0001483 aplastic abnormal ZDB-GENE-000403-1 57931 8312 axin1 ZFA:0000050 optic vesicle PATO:0000462 absent abnormal ZDB-GENE-000403-1 57931 8312 axin1 ZFA:0000054 pericardium PATO:0001450 edematous abnormal ZDB-GENE-000403-1 57931 8312 axin1 ZFA:0000059 postoptic commissure PATO:0001483 aplastic abnormal ZDB-GENE-000403-1 57931 8312 axin1 BSPO:0000029 antero-lateral region BFO:0000050 part_of ZFA:0000060 prechordal plate PATO:0000587 decreased size abnormal ZDB-GENE-000403-1 57931 8312 axin1 ZFA:0000079 telencephalon PATO:0000587 decreased size abnormal ZDB-GENE-000403-1 57931 8312 axin1 ZFA:0000079 telencephalon PATO:0001483 aplastic abnormal ZDB-GENE-000403-1 57931 8312 axin1 ZFA:0000107 eye PATO:0000001 quality abnormal ZDB-GENE-000403-1 57931 8312 axin1 ZFA:0000107 eye PATO:0000462 absent abnormal ZDB-GENE-000403-1 57931 8312 axin1 ZFA:0000107 eye PATO:0000587 decreased size abnormal ZDB-GENE-000403-1 57931 8312 axin1 ZFA:0000107 eye PATO:0001483 aplastic abnormal ZDB-GENE-000403-1 57931 8312 axin1 ZFA:0000107 eye PATO:0002291 agenesis abnormal ZDB-GENE-000403-1 57931 8312 axin1 ZFA:0000109 forebrain PATO:0000001 quality abnormal ZDB-GENE-000403-1 57931 8312 axin1 ZFA:0000109 forebrain PATO:0000462 absent abnormal ZDB-GENE-000403-1 57931 8312 axin1 ZFA:0000109 forebrain PATO:0000587 decreased size abnormal ZDB-GENE-000403-1 57931 8312 axin1 ZFA:0000114 heart PATO:0001199 linear abnormal ZDB-GENE-000403-1 57931 8312 axin1 ZFA:0009053 sensory neuron BFO:0000050 part_of ZFA:0000162 trigeminal placode PATO:0001921 mislocalised anteriorly abnormal ZDB-GENE-000403-1 57931 8312 axin1 ZFA:0000162 trigeminal placode PATO:0000586 increased size abnormal ZDB-GENE-000403-1 57931 8312 axin1 ZFA:0000396 nervous system PATO:0000001 quality abnormal ZDB-GENE-000403-1 57931 8312 axin1 ZFA:0000571 presumptive telencephalon PATO:0001483 aplastic abnormal ZDB-GENE-000403-1 57931 8312 axin1 ZFA:0000574 presumptive diencephalon PATO:0000586 increased size abnormal ZDB-GENE-000403-1 57931 8312 axin1 ZFA:0000653 dorsal thalamus PATO:0001396 cellular quality abnormal ZDB-GENE-000403-1 57931 8312 axin1 ZFA:0009034 epithelial cell BFO:0000050 part_of ZFA:0000706 posterior intestine PATO:0000470 increased amount abnormal ZDB-GENE-000403-1 57931 8312 axin1 ZFA:0009034 epithelial cell BFO:0000050 part_of ZFA:0001076 intestinal bulb PATO:0000470 increased amount abnormal ZDB-GENE-000403-1 57931 8312 axin1 ZFA:0001094 whole organism PATO:0002000 lacks all parts of type abnormal ZFA:0000079 telencephalon ZDB-GENE-000403-1 57931 8312 axin1 ZFA:0001094 whole organism PATO:0002000 lacks all parts of type abnormal ZFA:0000107 eye ZDB-GENE-000403-1 57931 8312 axin1 ZFA:0001094 whole organism PATO:0000718 lethal (sensu genetics) abnormal ZDB-GENE-000403-1 57931 8312 axin1 ZFA:0001108 anterior commissure PATO:0001483 aplastic abnormal ZDB-GENE-000403-1 57931 8312 axin1 ZFA:0001282 adenohypophysis PATO:0000587 decreased size abnormal ZDB-GENE-000403-1 57931 8312 axin1 ZFA:0001317 endocardial cushion PATO:0000644 hyperplastic abnormal ZDB-GENE-000403-1 57931 8312 axin1 ZFA:0001318 cardiac jelly PATO:0000595 increased volume abnormal ZDB-GENE-000403-1 57931 8312 axin1 ZFA:0001338 intestine PATO:0000051 morphology abnormal ZDB-GENE-000403-1 57931 8312 axin1 ZFA:0001338 intestine PATO:0000591 increased thickness abnormal ZDB-GENE-000403-1 57931 8312 axin1 ZFA:0001360 parapineal organ PATO:0000140 position abnormal ZDB-GENE-000403-1 57931 8312 axin1 ZFA:0009242 primary neuron BFO:0000050 part_of ZFA:0001366 tract of the postoptic commissure PATO:0000051 morphology abnormal ZDB-GENE-000403-1 57931 8312 axin1 ZFA:0005126 intestinal bulb epithelium PATO:0000591 increased thickness abnormal ZDB-GENE-000403-1 57931 8312 axin1 ZFA:0005126 intestinal bulb epithelium PATO:0000937 disorganized abnormal ZDB-GENE-000403-1 57931 8312 axin1 ZFA:0005126 intestinal bulb epithelium PATO:0001396 cellular quality abnormal ZDB-GENE-000403-1 57931 8312 axin1 ZFA:0005757 mid diencephalic organizer PATO:0000591 increased thickness abnormal ZDB-GENE-000403-1 57931 8312 axin1 ZFA:0005757 mid diencephalic organizer PATO:0001396 cellular quality abnormal ZDB-GENE-000403-1 57931 8312 axin1 ZFA:0005852 replacement tooth 4V PATO:0001501 immature abnormal ZDB-GENE-000403-1 57931 8312 axin1 ZFA:0007001 dorso-rostral cluster PATO:0000462 absent abnormal ZDB-GENE-000403-1 57931 8312 axin1 ZFA:0009399 intestinal epithelial cell PATO:0002102 proliferative abnormal ZDB-GENE-000403-2 58080 8313 axin2 ZFA:0000054 pericardium PATO:0000586 increased size abnormal ZDB-GENE-000405-1 58138 5087 pbx1a GO:0001944 vasculature development PATO:0001507 disrupted abnormal ZDB-GENE-000405-1 58138 5087 pbx1a GO:0048795 swim bladder morphogenesis PATO:0001236 process quality abnormal ZDB-GENE-000405-1 58138 5087 pbx1a GO:0048798 swim bladder inflation PATO:0000297 arrested abnormal ZDB-GENE-000405-1 58138 5087 pbx1a ZFA:0000076 swim bladder PATO:0000051 morphology abnormal ZDB-GENE-000405-1 58138 5087 pbx1a ZFA:0000076 swim bladder PATO:0001241 physical object quality abnormal ZDB-GENE-000405-1 58138 5087 pbx1a ZFA:0009327 neutrophil BFO:0000050 part_of ZFA:0000094 blood island PATO:0001997 decreased amount abnormal ZDB-GENE-000405-1 58138 5087 pbx1a ZFA:0000254 pancreas primordium PATO:0001241 physical object quality abnormal ZDB-GENE-000405-1 58138 5087 pbx1a ZFA:0001306 pharyngeal arch PATO:0001241 physical object quality abnormal ZDB-GENE-000405-1 58138 5087 pbx1a ZFA:0009256 nucleate erythrocyte PATO:0001997 decreased amount abnormal ZDB-GENE-000406-10 58025 891 ccnb1 GO:0000278 mitotic cell cycle PATO:0001507 disrupted abnormal ZDB-GENE-000406-10 58025 891 ccnb1 GO:0009790 embryo development PATO:0000297 arrested abnormal ZDB-GENE-000406-10 58025 891 ccnb1 GO:0051301 cell division PATO:0000297 arrested abnormal ZDB-GENE-000406-10 58025 891 ccnb1 GO:0051301 cell division PATO:0000911 decreased rate abnormal ZDB-GENE-000406-10 58025 891 ccnb1 GO:0051301 cell division PATO:0001492 growth rate abnormal ZDB-GENE-000406-10 58025 891 ccnb1 ZFA:0000012 central nervous system PATO:0000639 degenerate abnormal ZDB-GENE-000406-10 58025 891 ccnb1 ZFA:0000012 central nervous system PATO:0000647 necrotic abnormal ZDB-GENE-000406-10 58025 891 ccnb1 GO:0051301 cell division BFO:0000066 occurs_in ZFA:0000086 EVL PATO:0000911 decreased rate abnormal ZDB-GENE-000406-10 58025 891 ccnb1 ZFA:0000135 notochord PATO:0000001 quality abnormal ZDB-GENE-000406-10 58025 891 ccnb1 ZFA:0000396 nervous system PATO:0000001 quality abnormal ZDB-GENE-000406-10 58025 891 ccnb1 GO:0051301 cell division BFO:0000066 occurs_in ZFA:0000711 DEL PATO:0000911 decreased rate abnormal ZDB-GENE-000406-10 58025 891 ccnb1 GO:0000085 mitotic G2 phase BFO:0000066 occurs_in ZFA:0001094 whole organism PATO:0000498 increased duration abnormal ZDB-GENE-000406-10 58025 891 ccnb1 GO:0000087 mitotic M phase BFO:0000066 occurs_in ZFA:0001094 whole organism PATO:0000498 increased duration abnormal ZDB-GENE-000406-10 58025 891 ccnb1 GO:0030264 nuclear fragmentation involved in apoptotic nuclear change BFO:0000066 occurs_in ZFA:0001094 whole organism PATO:0002051 increased occurrence abnormal ZDB-GENE-000406-10 58025 891 ccnb1 GO:0051325 interphase BFO:0000066 occurs_in ZFA:0001094 whole organism PATO:0002052 decreased occurrence abnormal ZDB-GENE-000406-10 58025 891 ccnb1 ZFA:0009000 cell BFO:0000050 part_of ZFA:0001094 whole organism PATO:0000327 low brightness abnormal ZDB-GENE-000406-10 58025 891 ccnb1 ZFA:0001094 whole organism PATO:0000169 viability abnormal ZDB-GENE-000406-10 58025 891 ccnb1 ZFA:0001094 whole organism PATO:0000574 decreased length abnormal ZDB-GENE-000406-10 58025 891 ccnb1 ZFA:0001094 whole organism PATO:0000647 necrotic abnormal ZDB-GENE-000406-10 58025 891 ccnb1 ZFA:0001094 whole organism PATO:0000718 lethal (sensu genetics) abnormal ZDB-GENE-000406-10 58025 891 ccnb1 ZFA:0001094 whole organism PATO:0000957 opacity abnormal ZDB-GENE-000406-10 58025 891 ccnb1 ZFA:0001114 head PATO:0000407 flat abnormal ZDB-GENE-000406-10 58025 891 ccnb1 ZFA:0001114 head PATO:0000587 decreased size abnormal ZDB-GENE-000406-10 58025 891 ccnb1 ZFA:0001114 head PATO:0000638 apoptotic abnormal ZDB-GENE-000406-10 58025 891 ccnb1 ZFA:0001117 post-vent region PATO:0000587 decreased size abnormal ZDB-GENE-000406-10 58025 891 ccnb1 ZFA:0001678 immature eye PATO:0000587 decreased size abnormal ZDB-GENE-000406-6 57970 22818 copz1 ZFA:0000035 lens PATO:0000001 quality abnormal ZDB-GENE-000406-6 57970 22818 copz1 ZFA:0000107 eye PATO:0000001 quality abnormal ZDB-GENE-000406-6 57970 22818 copz1 ZFA:0000107 eye PATO:0000587 decreased size abnormal ZDB-GENE-000406-6 57970 22818 copz1 ZFA:0000107 eye PATO:0000639 degenerate abnormal ZDB-GENE-000406-6 57970 22818 copz1 ZFA:0000107 eye PATO:0002251 decreased pigmentation abnormal ZDB-GENE-000406-6 57970 22818 copz1 ZFA:0000112 gut PATO:0000645 hypoplastic abnormal ZDB-GENE-000406-6 57970 22818 copz1 ZFA:0000123 liver PATO:0000645 hypoplastic abnormal ZDB-GENE-000406-6 57970 22818 copz1 ZFA:0000144 retinal pigmented epithelium PATO:0000639 degenerate abnormal ZDB-GENE-000406-6 57970 22818 copz1 ZFA:0000282 sensory system PATO:0000001 quality abnormal ZDB-GENE-000406-6 57970 22818 copz1 ZFA:0001114 head PATO:0000587 decreased size abnormal ZDB-GENE-000406-6 57970 22818 copz1 ZFA:0001114 head PATO:0000599 decreased width abnormal ZDB-GENE-000406-8 58069 145873 mespaa GO:0060972 left/right pattern formation PATO:0015003 decreased efficacy abnormal ZDB-GENE-000406-8 58069 145873 mespaa GO:0061371 determination of heart left/right asymmetry PATO:0015003 decreased efficacy abnormal ZDB-GENE-000406-8 58069 145873 mespaa ZFA:0001094 whole organism PATO:0000647 necrotic abnormal ZDB-GENE-000406-9 58070 55897 mespba GO:0060972 left/right pattern formation PATO:0015003 decreased efficacy abnormal ZDB-GENE-000406-9 58070 55897 mespba GO:0061371 determination of heart left/right asymmetry PATO:0015003 decreased efficacy abnormal ZDB-GENE-000412-1 58118 627 bdnf GO:0006919 activation of cysteine-type endopeptidase activity involved in apoptotic process PATO:0002051 increased occurrence abnormal ZDB-GENE-000412-1 58118 627 bdnf GO:0007409 axonogenesis PATO:0001507 disrupted abnormal ZDB-GENE-000412-1 58118 627 bdnf GO:0040011 locomotion PATO:0002302 decreased process quality abnormal ZDB-GENE-000412-1 58118 627 bdnf ZFA:0000054 pericardium PATO:0001851 swollen abnormal ZDB-GENE-000412-1 58118 627 bdnf ZFA:0000076 swim bladder PATO:0001483 aplastic abnormal ZDB-GENE-000412-1 58118 627 bdnf ZFA:0000107 eye PATO:0000587 decreased size abnormal ZDB-GENE-000412-1 58118 627 bdnf ZFA:0000435 cranial nerve II PATO:0001483 aplastic abnormal ZDB-GENE-000412-1 58118 627 bdnf GO:0036269 swimming behavior BFO:0000066 occurs_in ZFA:0001094 whole organism PATO:0002302 decreased process quality abnormal ZDB-GENE-000412-1 58118 627 bdnf ZFA:0001114 head PATO:0000587 decreased size abnormal ZDB-GENE-000412-1 58118 627 bdnf ZFA:0001261 ventricular system PATO:0000586 increased size abnormal ZDB-GENE-000412-1 58118 627 bdnf ZFA:0001273 ventral mandibular arch PATO:0000646 malformed abnormal ZDB-GENE-000412-1 58118 627 bdnf GO:0043005 neuron projection BFO:0000050 part_of ZFA:0009052 motor neuron PATO:0000936 truncated abnormal ZDB-GENE-000426-1 100005469 2335 fn1a GO:0002088 lens development in camera-type eye PATO:0001507 disrupted abnormal ZDB-GENE-000426-1 100005469 2335 fn1a GO:0003007 heart morphogenesis PATO:0001507 disrupted abnormal ZDB-GENE-000426-1 100005469 2335 fn1a GO:0003146 heart jogging PATO:0001507 disrupted abnormal ZDB-GENE-000426-1 100005469 2335 fn1a GO:0003157 endocardium development PATO:0001507 disrupted abnormal ZDB-GENE-000426-1 100005469 2335 fn1a GO:0010842 retina layer formation PATO:0001507 disrupted abnormal ZDB-GENE-000426-1 100005469 2335 fn1a GO:0048546 digestive tract morphogenesis PATO:0001507 disrupted abnormal ZDB-GENE-000426-1 100005469 2335 fn1a GO:0070307 lens fiber cell development PATO:0001507 disrupted abnormal ZDB-GENE-000426-1 100005469 2335 fn1a GO:0070309 lens fiber cell morphogenesis PATO:0001507 disrupted abnormal ZDB-GENE-000426-1 100005469 2335 fn1a ZFA:0000008 brain PATO:0000001 quality abnormal ZDB-GENE-000426-1 100005469 2335 fn1a GO:0002040 sprouting angiogenesis BFO:0000066 occurs_in ZFA:0000014 dorsal aorta PATO:0001236 process quality abnormal ZDB-GENE-000426-1 100005469 2335 fn1a ZFA:0000014 dorsal aorta PATO:0000586 increased size abnormal ZDB-GENE-000426-1 100005469 2335 fn1a ZFA:0000017 endoderm PATO:0000600 increased width abnormal ZDB-GENE-000426-1 100005469 2335 fn1a ZFA:0000029 hindbrain PATO:0000001 quality abnormal ZDB-GENE-000426-1 100005469 2335 fn1a ZFA:0000029 hindbrain PATO:0000051 morphology abnormal ZDB-GENE-000426-1 100005469 2335 fn1a GO:0005634 nucleus BFO:0000050 part_of ZFA:0000035 lens PATO:0000470 increased amount abnormal ZDB-GENE-000426-1 100005469 2335 fn1a ZFA:0009000 cell BFO:0000050 part_of ZFA:0000035 lens PATO:0001802 loose abnormal ZDB-GENE-000426-1 100005469 2335 fn1a ZFA:0000035 lens PATO:0001505 separated from abnormal ZFA:0000152 retina ZDB-GENE-000426-1 100005469 2335 fn1a ZFA:0000035 lens PATO:0000051 morphology abnormal ZDB-GENE-000426-1 100005469 2335 fn1a ZFA:0000035 lens PATO:0000141 structure abnormal ZDB-GENE-000426-1 100005469 2335 fn1a ZFA:0000054 pericardium PATO:0001450 edematous abnormal ZDB-GENE-000426-1 100005469 2335 fn1a ZFA:0000072 somite 1 PATO:0000051 morphology abnormal ZDB-GENE-000426-1 100005469 2335 fn1a ZFA:0000076 swim bladder PATO:0000587 decreased size abnormal ZDB-GENE-000426-1 100005469 2335 fn1a ZFA:0000106 extension PATO:0002364 shortened abnormal ZDB-GENE-000426-1 100005469 2335 fn1a ZFA:0000107 eye PATO:0000587 decreased size abnormal ZDB-GENE-000426-1 100005469 2335 fn1a ZFA:0000110 fourth ventricle PATO:0000587 decreased size abnormal ZDB-GENE-000426-1 100005469 2335 fn1a ZFA:0000114 heart PATO:0000001 quality abnormal ZDB-GENE-000426-1 100005469 2335 fn1a ZFA:0000114 heart PATO:0000051 morphology abnormal ZDB-GENE-000426-1 100005469 2335 fn1a ZFA:0000128 midbrain PATO:0000001 quality abnormal ZDB-GENE-000426-1 100005469 2335 fn1a ZFA:0000128 midbrain PATO:0000051 morphology abnormal ZDB-GENE-000426-1 100005469 2335 fn1a ZFA:0000155 somite PATO:0000639 degenerate abnormal ZDB-GENE-000426-1 100005469 2335 fn1a ZFA:0000360 heart tube PATO:0001473 duplicated abnormal ZDB-GENE-000426-1 100005469 2335 fn1a ZFA:0000360 heart tube PATO:0002180 straight abnormal ZDB-GENE-000426-1 100005469 2335 fn1a ZFA:0000396 nervous system PATO:0000001 quality abnormal ZDB-GENE-000426-1 100005469 2335 fn1a ZFA:0000728 somite 2 PATO:0000051 morphology abnormal ZDB-GENE-000426-1 100005469 2335 fn1a ZFA:0000732 somite 3 PATO:0000051 morphology abnormal ZDB-GENE-000426-1 100005469 2335 fn1a ZFA:0000857 somite 4 PATO:0000051 morphology abnormal ZDB-GENE-000426-1 100005469 2335 fn1a ZFA:0001094 whole organism PATO:0000169 viability abnormal ZDB-GENE-000426-1 100005469 2335 fn1a ZFA:0001094 whole organism PATO:0000718 lethal (sensu genetics) abnormal ZDB-GENE-000426-1 100005469 2335 fn1a GO:0005614 interstitial matrix BFO:0000050 part_of ZFA:0001115 trunk PATO:0000051 morphology abnormal ZDB-GENE-000426-1 100005469 2335 fn1a ZFA:0001115 trunk PATO:0002364 shortened abnormal ZDB-GENE-000426-1 100005469 2335 fn1a ZFA:0001128 pharyngeal pouch 1 PATO:0001999 lacks parts or has fewer parts of type abnormal ZFA:0001128 pharyngeal pouch 1 ZDB-GENE-000426-1 100005469 2335 fn1a ZFA:0001205 Meckel's cartilage PATO:0000574 decreased length abnormal ZDB-GENE-000426-1 100005469 2335 fn1a ZFA:0001261 ventricular system PATO:0001478 collapsed abnormal ZDB-GENE-000426-1 100005469 2335 fn1a ZFA:0001338 intestine PATO:0000587 decreased size abnormal ZDB-GENE-000426-1 100005469 2335 fn1a GO:0006694 steroid biosynthetic process BFO:0000066 occurs_in ZFA:0001345 interrenal gland PATO:0002052 decreased occurrence abnormal ZDB-GENE-000426-1 100005469 2335 fn1a ZFA:0001345 interrenal gland PATO:0000628 mislocalised abnormal ZDB-GENE-000426-1 100005469 2335 fn1a BSPO:0000000 left side BFO:0000050 part_of ZFA:0001346 interrenal primordium PATO:0000651 unfused from abnormal BSPO:0000007 right side BFO:0000050 part_of ZFA:0001346 interrenal primordium ZDB-GENE-000426-1 100005469 2335 fn1a GO:0016477 cell migration BFO:0000066 occurs_in ZFA:0001346 interrenal primordium PATO:0001507 disrupted abnormal ZDB-GENE-000426-1 100005469 2335 fn1a ZFA:0001346 interrenal primordium PATO:0000051 morphology abnormal ZDB-GENE-000426-1 100005469 2335 fn1a ZFA:0001346 interrenal primordium PATO:0000140 position abnormal ZDB-GENE-000426-1 100005469 2335 fn1a ZFA:0001399 palatoquadrate cartilage PATO:0000574 decreased length abnormal ZDB-GENE-000426-1 100005469 2335 fn1a ZFA:0001400 ceratohyal cartilage PATO:0000574 decreased length abnormal ZDB-GENE-000426-1 100005469 2335 fn1a ZFA:0001458 cranial cartilage PATO:0000051 morphology abnormal ZDB-GENE-000426-1 100005469 2335 fn1a ZFA:0001458 cranial cartilage PATO:0000587 decreased size abnormal ZDB-GENE-000426-1 100005469 2335 fn1a ZFA:0001458 cranial cartilage PATO:0000937 disorganized abnormal ZDB-GENE-000426-1 100005469 2335 fn1a ZFA:0001611 pharyngeal arch 2 PATO:0000051 morphology abnormal ZDB-GENE-000426-1 100005469 2335 fn1a ZFA:0001611 pharyngeal arch 2 PATO:0000937 disorganized abnormal ZDB-GENE-000426-1 100005469 2335 fn1a GO:0048598 embryonic morphogenesis BFO:0000066 occurs_in ZFA:0001612 pharyngeal arch 1 PATO:0001507 disrupted abnormal ZDB-GENE-000426-1 100005469 2335 fn1a ZFA:0001612 pharyngeal arch 1 PATO:0000051 morphology abnormal ZDB-GENE-000426-1 100005469 2335 fn1a ZFA:0001612 pharyngeal arch 1 PATO:0000937 disorganized abnormal ZDB-GENE-000426-1 100005469 2335 fn1a ZFA:0001683 corneal epithelium PATO:0000051 morphology abnormal ZDB-GENE-000426-1 100005469 2335 fn1a ZFA:0001683 corneal epithelium PATO:0000967 undulate abnormal ZDB-GENE-000426-1 100005469 2335 fn1a ZFA:0005035 subintestinal vein PATO:0000051 morphology abnormal ZDB-GENE-000426-1 100005469 2335 fn1a ZFA:0005801 interrenal vessel PATO:0000462 absent abnormal ZDB-GENE-000426-1 100005469 2335 fn1a ZFA:0005802 interrenal angiogenic sprout PATO:0000462 absent abnormal ZDB-GENE-000427-3 58147 5024 p2rx3a GO:0008219 cell death PATO:0002051 increased occurrence abnormal ZDB-GENE-000427-3 58147 5024 p2rx3a ZFA:0000295 trigeminal ganglion PATO:0000646 malformed abnormal ZDB-GENE-000427-3 58147 5024 p2rx3a ZFA:0001273 ventral mandibular arch PATO:0000646 malformed abnormal ZDB-GENE-000427-3 58147 5024 p2rx3a ZFA:0001306 pharyngeal arch PATO:0000646 malformed abnormal ZDB-GENE-000427-3 58147 5024 p2rx3a ZFA:0001400 ceratohyal cartilage PATO:0000646 malformed abnormal ZDB-GENE-000427-3 58147 5024 p2rx3a ZFA:0001516 ceratobranchial cartilage PATO:0000585 hypotrophic abnormal ZDB-GENE-000427-3 58147 5024 p2rx3a ZFA:0001555 epibranchial ganglion PATO:0000646 malformed abnormal ZDB-GENE-000427-3 58147 5024 p2rx3a ZFA:0001611 pharyngeal arch 2 PATO:0000051 morphology abnormal ZDB-GENE-000427-3 58147 5024 p2rx3a ZFA:0001612 pharyngeal arch 1 PATO:0000051 morphology abnormal ZDB-GENE-000427-7 57936 57057 tbx20 GO:0001568 blood vessel development PATO:0001507 disrupted abnormal ZDB-GENE-000427-7 57936 57057 tbx20 GO:0001947 heart looping PATO:0001507 disrupted abnormal ZDB-GENE-000427-7 57936 57057 tbx20 GO:0002040 sprouting angiogenesis PATO:0002052 decreased occurrence abnormal ZDB-GENE-000427-7 57936 57057 tbx20 GO:0008015 blood circulation PATO:0000297 arrested abnormal ZDB-GENE-000427-7 57936 57057 tbx20 GO:0008015 blood circulation PATO:0001507 disrupted abnormal ZDB-GENE-000427-7 57936 57057 tbx20 GO:0030097 hemopoiesis PATO:0001507 disrupted abnormal ZDB-GENE-000427-7 57936 57057 tbx20 GO:0035844 cloaca development PATO:0001507 disrupted abnormal ZDB-GENE-000427-7 57936 57057 tbx20 GO:0060038 cardiac muscle cell proliferation PATO:0002302 decreased process quality abnormal ZDB-GENE-000427-7 57936 57057 tbx20 GO:0060047 heart contraction PATO:0000078 rhythm quality abnormal ZDB-GENE-000427-7 57936 57057 tbx20 GO:0060047 heart contraction PATO:0002018 decreased magnitude abnormal ZDB-GENE-000427-7 57936 57057 tbx20 GO:0072359 circulatory system development PATO:0001507 disrupted abnormal ZDB-GENE-000427-7 57936 57057 tbx20 ZFA:0000007 blood PATO:0002269 accumulation abnormal ZFA:0000154 sinus venosus ZDB-GENE-000427-7 57936 57057 tbx20 GO:0060038 cardiac muscle cell proliferation BFO:0000066 occurs_in ZFA:0000009 cardiac ventricle PATO:0002302 decreased process quality abnormal ZDB-GENE-000427-7 57936 57057 tbx20 ZFA:0009316 cardiac muscle cell BFO:0000050 part_of ZFA:0000009 cardiac ventricle PATO:0001997 decreased amount abnormal ZDB-GENE-000427-7 57936 57057 tbx20 ZFA:0000009 cardiac ventricle PATO:0000587 decreased size abnormal ZDB-GENE-000427-7 57936 57057 tbx20 ZFA:0000009 cardiac ventricle PATO:0001579 contractility abnormal ZDB-GENE-000427-7 57936 57057 tbx20 ZFA:0000009 cardiac ventricle PATO:0001779 decreased strength abnormal ZDB-GENE-000427-7 57936 57057 tbx20 ZFA:0000028 heart primordium PATO:0000645 hypoplastic abnormal ZDB-GENE-000427-7 57936 57057 tbx20 ZFA:0000054 pericardium PATO:0001450 edematous abnormal ZDB-GENE-000427-7 57936 57057 tbx20 ZFA:0000114 heart PATO:0000001 quality abnormal ZDB-GENE-000427-7 57936 57057 tbx20 ZFA:0000114 heart PATO:0000587 decreased size abnormal ZDB-GENE-000427-7 57936 57057 tbx20 ZFA:0000114 heart PATO:0001581 decreased contractility abnormal ZDB-GENE-000427-7 57936 57057 tbx20 ZFA:0000114 heart PATO:0001602 distended abnormal ZDB-GENE-000427-7 57936 57057 tbx20 ZFA:0000360 heart tube PATO:0000051 morphology abnormal ZDB-GENE-000427-7 57936 57057 tbx20 ZFA:0000360 heart tube PATO:0000587 decreased size abnormal ZDB-GENE-000427-7 57936 57057 tbx20 ZFA:0001094 whole organism PATO:0001422 dead abnormal ZDB-GENE-000427-7 57936 57057 tbx20 ZFA:0001285 intersegmental vessel PATO:0000051 morphology abnormal ZDB-GENE-000427-7 57936 57057 tbx20 ZFA:0001285 intersegmental vessel PATO:0000574 decreased length abnormal ZDB-GENE-000427-7 57936 57057 tbx20 ZFA:0001285 intersegmental vessel PATO:0001483 aplastic abnormal ZDB-GENE-000427-7 57936 57057 tbx20 ZFA:0005024 trunk vasculature PATO:0000051 morphology abnormal ZDB-GENE-000427-7 57936 57057 tbx20 ZFA:0005035 subintestinal vein PATO:0000051 morphology abnormal ZDB-GENE-000427-7 57936 57057 tbx20 ZFA:0005035 subintestinal vein PATO:0000574 decreased length abnormal ZDB-GENE-000427-7 57936 57057 tbx20 ZFA:0005035 subintestinal vein PATO:0001997 decreased amount abnormal ZDB-GENE-000427-7 57936 57057 tbx20 ZFA:0005061 ventricular myocardium PATO:0000592 decreased thickness abnormal ZDB-GENE-000427-7 57936 57057 tbx20 ZFA:0005077 vascular cord PATO:0000051 morphology abnormal ZDB-GENE-000427-7 57936 57057 tbx20 ZFA:0005781 cloaca PATO:0000051 morphology abnormal ZDB-GENE-000427-7 57936 57057 tbx20 ZFA:0009316 cardiac muscle cell PATO:0001997 decreased amount abnormal ZDB-GENE-000501-1 58137 10658 celf1 GO:0003146 heart jogging PATO:0001507 disrupted abnormal ZDB-GENE-000501-1 58137 10658 celf1 GO:0006402 mRNA catabolic process PATO:0001507 disrupted abnormal ZDB-GENE-000501-1 58137 10658 celf1 GO:0048557 embryonic digestive tract morphogenesis PATO:0001236 process quality abnormal ZDB-GENE-000501-1 58137 10658 celf1 GO:0060971 embryonic heart tube left/right pattern formation PATO:0001507 disrupted abnormal ZDB-GENE-000501-1 58137 10658 celf1 GO:0070306 lens fiber cell differentiation PATO:0001236 process quality abnormal ZDB-GENE-000501-1 58137 10658 celf1 GO:0008283 cell population proliferation BFO:0000066 occurs_in ZFA:0000017 endoderm PATO:0002302 decreased process quality abnormal ZDB-GENE-000501-1 58137 10658 celf1 GO:0016477 cell migration BFO:0000066 occurs_in ZFA:0000017 endoderm PATO:0001236 process quality abnormal ZDB-GENE-000501-1 58137 10658 celf1 ZFA:0009000 cell BFO:0000050 part_of ZFA:0000017 endoderm PATO:0001997 decreased amount abnormal ZDB-GENE-000501-1 58137 10658 celf1 GO:0031941 filamentous actin BFO:0000050 part_of ZFA:0000035 lens PATO:0000937 disorganized abnormal ZDB-GENE-000501-1 58137 10658 celf1 ZFA:0000035 lens PATO:0000963 opaque abnormal ZDB-GENE-000501-1 58137 10658 celf1 ZFA:0000107 eye PATO:0000587 decreased size abnormal ZDB-GENE-000501-1 58137 10658 celf1 ZFA:0000112 gut PATO:0000052 shape abnormal ZDB-GENE-000501-1 58137 10658 celf1 ZFA:0000112 gut PATO:0000646 malformed abnormal ZDB-GENE-000501-1 58137 10658 celf1 ZFA:0000124 liver primordium PATO:0002290 aplastic/hypoplastic abnormal ZDB-GENE-000501-1 58137 10658 celf1 ZFA:0000155 somite PATO:0000052 shape abnormal ZDB-GENE-000501-1 58137 10658 celf1 ZFA:0000155 somite PATO:0000616 asymmetrical abnormal ZDB-GENE-000501-1 58137 10658 celf1 ZFA:0000254 pancreas primordium PATO:0002290 aplastic/hypoplastic abnormal ZDB-GENE-000501-1 58137 10658 celf1 GO:0016477 cell migration BFO:0000066 occurs_in ZFA:0009139 endodermal cell PATO:0000502 delayed abnormal ZDB-GENE-000501-1 58137 10658 celf1 GO:0016477 cell migration BFO:0000066 occurs_in ZFA:0009139 endodermal cell PATO:0001236 process quality abnormal ZDB-GENE-000501-1 58137 10658 celf1 GO:0005634 nucleus BFO:0000050 part_of ZFA:0009401 lens fiber cell PATO:0000467 present abnormal ZDB-GENE-000502-1 58145 657 bmpr1aa GO:0001947 heart looping PATO:0000502 delayed abnormal ZDB-GENE-000502-1 58145 657 bmpr1aa GO:0001947 heart looping PATO:0001507 disrupted abnormal ZDB-GENE-000502-1 58145 657 bmpr1aa GO:0003146 heart jogging PATO:0001507 disrupted abnormal ZDB-GENE-000502-1 58145 657 bmpr1aa GO:0009953 dorsal/ventral pattern formation PATO:0001507 disrupted abnormal ZDB-GENE-000502-1 58145 657 bmpr1aa GO:0060047 heart contraction PATO:0000297 arrested abnormal ZDB-GENE-000502-1 58145 657 bmpr1aa GO:0060971 embryonic heart tube left/right pattern formation PATO:0001507 disrupted abnormal ZDB-GENE-000502-1 58145 657 bmpr1aa GO:0071907 determination of digestive tract left/right asymmetry PATO:0001507 disrupted abnormal ZDB-GENE-000502-1 58145 657 bmpr1aa ZFA:0000094 blood island PATO:0000587 decreased size abnormal ZDB-GENE-000502-1 58145 657 bmpr1aa ZFA:0000114 heart PATO:0000133 orientation abnormal BSPO:0000017 left-right axis BFO:0000050 part_of ZFA:0001094 whole organism ZDB-GENE-000502-1 58145 657 bmpr1aa ZFA:0000114 heart PATO:0001653 aligned with abnormal BSPO:0000075 central region BFO:0000050 part_of ZFA:0001094 whole organism ZDB-GENE-000502-1 58145 657 bmpr1aa ZFA:0000360 heart tube PATO:0001653 aligned with abnormal BSPO:0000075 central region BFO:0000050 part_of ZFA:0001094 whole organism ZDB-GENE-000502-1 58145 657 bmpr1aa ZFA:0000360 heart tube PATO:0000051 morphology abnormal ZDB-GENE-000502-1 58145 657 bmpr1aa ZFA:0001069 ventral fin fold PATO:0000587 decreased size abnormal ZDB-GENE-000502-1 58145 657 bmpr1aa ZFA:0001094 whole organism PATO:0001422 dead abnormal ZDB-GENE-000502-1 58145 657 bmpr1aa ZFA:0001117 post-vent region PATO:0000587 decreased size abnormal ZDB-GENE-000502-1 58145 657 bmpr1aa ZFA:0001338 intestine PATO:0000133 orientation abnormal BSPO:0000017 left-right axis BFO:0000050 part_of ZFA:0001094 whole organism ZDB-GENE-000508-1 58074 1638 dct GO:0006582 melanin metabolic process PATO:0001507 disrupted abnormal ZDB-GENE-000508-1 58074 1638 dct GO:0010842 retina layer formation PATO:0001507 disrupted abnormal ZDB-GENE-000508-1 58074 1638 dct ZFA:0000107 eye PATO:0002251 decreased pigmentation abnormal ZDB-GENE-000508-1 58074 1638 dct ZFA:0000144 retinal pigmented epithelium PATO:0002251 decreased pigmentation abnormal ZDB-GENE-000508-1 58074 1638 dct CHEBI:89634 Melanin BFO:0000050 part_of ZFA:0001094 whole organism PATO:0001997 decreased amount abnormal ZDB-GENE-000508-1 58074 1638 dct ZFA:0009091 melanocyte BFO:0000050 part_of ZFA:0001114 head PATO:0000330 irregular spatial pattern abnormal ZDB-GENE-000509-1 58098 406 bmal1a ZFA:0001285 intersegmental vessel PATO:0002364 shortened abnormal ZDB-GENE-000509-3 58092 4088 smad3a GO:0008283 cell population proliferation BFO:0000066 occurs_in ZFA:0000008 brain PATO:0002304 increased process quality abnormal ZDB-GENE-000509-3 58092 4088 smad3a ZFA:0000022 floor plate PATO:0000462 absent abnormal ZDB-GENE-000509-3 58092 4088 smad3a ZFA:0000033 intermediate cell mass of mesoderm PATO:0000586 increased size abnormal ZDB-GENE-000509-3 58092 4088 smad3a GO:0008283 cell population proliferation BFO:0000066 occurs_in ZFA:0001058 caudal fin PATO:0002304 increased process quality abnormal ZDB-GENE-000509-3 58092 4088 smad3a BSPO:0000013 anterior-posterior axis BFO:0000050 part_of ZFA:0001094 whole organism PATO:0000406 curved abnormal ZDB-GENE-000509-3 58092 4088 smad3a BSPO:0000013 anterior-posterior axis BFO:0000050 part_of ZFA:0001094 whole organism PATO:0002364 shortened abnormal ZDB-GENE-000509-3 58092 4088 smad3a BSPO:0000071 anterior region BFO:0000050 part_of ZFA:0001094 whole organism PATO:0000936 truncated abnormal ZDB-GENE-000509-3 58092 4088 smad3a ZFA:0001094 whole organism PATO:0000574 decreased length abnormal ZDB-GENE-000509-3 58092 4088 smad3a ZFA:0009052 motor neuron PATO:0001997 decreased amount abnormal ZDB-GENE-000509-3 58092 4088 smad3a ZFA:0009248 neuron PATO:0000639 degenerate abnormal ZDB-GENE-000511-1 58150 9464 hand2 GO:0001755 neural crest cell migration PATO:0001507 disrupted abnormal ZDB-GENE-000511-1 58150 9464 hand2 GO:0001947 heart looping PATO:0001507 disrupted abnormal ZDB-GENE-000511-1 58150 9464 hand2 GO:0003007 heart morphogenesis PATO:0001236 process quality abnormal ZDB-GENE-000511-1 58150 9464 hand2 GO:0003007 heart morphogenesis PATO:0001507 disrupted abnormal ZDB-GENE-000511-1 58150 9464 hand2 GO:0003318 cell migration to the midline involved in heart development PATO:0000502 delayed abnormal ZDB-GENE-000511-1 58150 9464 hand2 GO:0003318 cell migration to the midline involved in heart development PATO:0001236 process quality abnormal ZDB-GENE-000511-1 58150 9464 hand2 GO:0007507 heart development PATO:0001507 disrupted abnormal ZDB-GENE-000511-1 58150 9464 hand2 GO:0008078 mesodermal cell migration PATO:0001507 disrupted abnormal ZDB-GENE-000511-1 58150 9464 hand2 GO:0030878 thyroid gland development PATO:0001507 disrupted abnormal ZDB-GENE-000511-1 58150 9464 hand2 GO:0035138 pectoral fin morphogenesis PATO:0001507 disrupted abnormal ZDB-GENE-000511-1 58150 9464 hand2 GO:0036306 embryonic heart tube elongation PATO:0001507 disrupted abnormal ZDB-GENE-000511-1 58150 9464 hand2 GO:0048484 enteric nervous system development PATO:0001507 disrupted abnormal ZDB-GENE-000511-1 58150 9464 hand2 GO:0048565 digestive tract development PATO:0001507 disrupted abnormal ZDB-GENE-000511-1 58150 9464 hand2 GO:0051145 smooth muscle cell differentiation PATO:0001507 disrupted abnormal ZDB-GENE-000511-1 58150 9464 hand2 GO:0055007 cardiac muscle cell differentiation PATO:0001507 disrupted abnormal ZDB-GENE-000511-1 58150 9464 hand2 GO:0060047 heart contraction PATO:0000911 decreased rate abnormal ZDB-GENE-000511-1 58150 9464 hand2 GO:0060047 heart contraction PATO:0001507 disrupted abnormal ZDB-GENE-000511-1 58150 9464 hand2 GO:0060047 heart contraction PATO:0001783 decreased intensity abnormal ZDB-GENE-000511-1 58150 9464 hand2 GO:0060914 heart formation PATO:0001507 disrupted abnormal ZDB-GENE-000511-1 58150 9464 hand2 GO:0071908 determination of intestine left/right asymmetry PATO:0001507 disrupted abnormal ZDB-GENE-000511-1 58150 9464 hand2 ZFA:0000009 cardiac ventricle PATO:0000052 shape abnormal ZDB-GENE-000511-1 58150 9464 hand2 ZFA:0000009 cardiac ventricle PATO:0000141 structure abnormal ZDB-GENE-000511-1 58150 9464 hand2 ZFA:0000009 cardiac ventricle PATO:0000587 decreased size abnormal ZDB-GENE-000511-1 58150 9464 hand2 ZFA:0005490 myocardial precursor BFO:0000050 part_of ZFA:0000028 heart primordium PATO:0001997 decreased amount abnormal ZDB-GENE-000511-1 58150 9464 hand2 ZFA:0000028 heart primordium PATO:0000651 unfused from abnormal ZFA:0000028 heart primordium ZDB-GENE-000511-1 58150 9464 hand2 ZFA:0000054 pericardium PATO:0001450 edematous abnormal ZDB-GENE-000511-1 58150 9464 hand2 ZFA:0000108 fin PATO:0000001 quality abnormal ZDB-GENE-000511-1 58150 9464 hand2 ZFA:0000114 heart PATO:0000001 quality abnormal ZDB-GENE-000511-1 58150 9464 hand2 ZFA:0000114 heart PATO:0000051 morphology abnormal ZDB-GENE-000511-1 58150 9464 hand2 ZFA:0000114 heart PATO:0000646 malformed abnormal ZDB-GENE-000511-1 58150 9464 hand2 ZFA:0000115 heart rudiment PATO:0001784 bifurcated abnormal ZDB-GENE-000511-1 58150 9464 hand2 ZFA:0000121 lateral plate mesoderm PATO:0000599 decreased width abnormal ZDB-GENE-000511-1 58150 9464 hand2 ZFA:0000123 liver PATO:0001473 duplicated abnormal ZDB-GENE-000511-1 58150 9464 hand2 ZFA:0000140 pancreas PATO:0001473 duplicated abnormal ZDB-GENE-000511-1 58150 9464 hand2 ZFA:0000141 pectoral fin bud PATO:0000587 decreased size abnormal ZDB-GENE-000511-1 58150 9464 hand2 ZFA:0000191 dentary PATO:0000052 shape abnormal ZDB-GENE-000511-1 58150 9464 hand2 ZFA:0000292 surface structure PATO:0000001 quality abnormal ZDB-GENE-000511-1 58150 9464 hand2 ZFA:0000360 heart tube PATO:0001483 aplastic abnormal ZDB-GENE-000511-1 58150 9464 hand2 ZFA:0000471 atrium PATO:0000052 shape abnormal ZDB-GENE-000511-1 58150 9464 hand2 ZFA:0000471 atrium PATO:0000587 decreased size abnormal ZDB-GENE-000511-1 58150 9464 hand2 ZFA:0001072 thyroid follicle PATO:0001997 decreased amount abnormal ZDB-GENE-000511-1 58150 9464 hand2 ZFA:0001081 thyroid primordium PATO:0000587 decreased size abnormal ZDB-GENE-000511-1 58150 9464 hand2 ZFA:0009248 neuron BFO:0000050 part_of ZFA:0001155 enteric nervous system PATO:0001997 decreased amount abnormal ZDB-GENE-000511-1 58150 9464 hand2 ZFA:0001161 pectoral fin PATO:0000001 quality abnormal ZDB-GENE-000511-1 58150 9464 hand2 ZFA:0001205 Meckel's cartilage PATO:0000574 decreased length abnormal ZDB-GENE-000511-1 58150 9464 hand2 ZFA:0009118 smooth muscle cell BFO:0000050 part_of ZFA:0001338 intestine PATO:0000051 morphology abnormal ZDB-GENE-000511-1 58150 9464 hand2 ZFA:0009248 neuron BFO:0000050 part_of ZFA:0001338 intestine PATO:0001997 decreased amount abnormal ZDB-GENE-000511-1 58150 9464 hand2 ZFA:0001439 anatomical system PATO:0000001 quality abnormal ZDB-GENE-000511-1 58150 9464 hand2 ZFA:0005057 epicardium PATO:0001483 aplastic abnormal ZDB-GENE-000511-1 58150 9464 hand2 ZFA:0009316 cardiac muscle cell PATO:0002264 organization quality abnormal ZDB-GENE-000511-2 57923 29108 pycard GO:0097153 cysteine-type endopeptidase activity involved in apoptotic process PATO:0002052 decreased occurrence abnormal ZDB-GENE-000511-2 57923 29108 pycard ZFA:0009354 hematopoietic multipotent progenitor cell BFO:0000050 part_of ZFA:0005898 caudal hematopoietic tissue PATO:0001997 decreased amount abnormal ZDB-GENE-000511-2 57923 29108 pycard ZFA:0009256 nucleate erythrocyte PATO:0000470 increased amount abnormal ZDB-GENE-000511-2 57923 29108 pycard ZFA:0009327 neutrophil PATO:0001997 decreased amount abnormal ZDB-GENE-000511-8 58153 30061 slc40a1 GO:0008015 blood circulation PATO:0000297 arrested abnormal ZDB-GENE-000511-8 58153 30061 slc40a1 GO:0030282 bone mineralization PATO:0002052 decreased occurrence abnormal ZDB-GENE-000511-8 58153 30061 slc40a1 GO:0035162 embryonic hemopoiesis PATO:0001507 disrupted abnormal ZDB-GENE-000511-8 58153 30061 slc40a1 GO:0042541 hemoglobin biosynthetic process PATO:0001507 disrupted abnormal ZDB-GENE-000511-8 58153 30061 slc40a1 GO:0042541 hemoglobin biosynthetic process PATO:0002052 decreased occurrence abnormal ZDB-GENE-000511-8 58153 30061 slc40a1 GO:0043473 pigmentation PATO:0001507 disrupted abnormal ZDB-GENE-000511-8 58153 30061 slc40a1 ZFA:0000007 blood PATO:0000001 quality abnormal ZDB-GENE-000511-8 58153 30061 slc40a1 ZFA:0000107 eye PATO:0002251 decreased pigmentation abnormal ZDB-GENE-000511-8 58153 30061 slc40a1 GO:0030282 bone mineralization BFO:0000066 occurs_in ZFA:0000737 cranium PATO:0002052 decreased occurrence abnormal ZDB-GENE-000511-8 58153 30061 slc40a1 ZFA:0001069 ventral fin fold PATO:0001798 kinked abnormal ZDB-GENE-000511-8 58153 30061 slc40a1 ZFA:0001115 trunk PATO:0002251 decreased pigmentation abnormal ZDB-GENE-000511-8 58153 30061 slc40a1 GO:0030282 bone mineralization BFO:0000066 occurs_in ZFA:0001189 vertebra PATO:0002052 decreased occurrence abnormal ZDB-GENE-000511-8 58153 30061 slc40a1 ZFA:0001285 intersegmental vessel PATO:0000587 decreased size abnormal ZDB-GENE-000511-8 58153 30061 slc40a1 ZFA:0001439 anatomical system PATO:0000001 quality abnormal ZDB-GENE-000511-8 58153 30061 slc40a1 ZFA:0005025 dorsal longitudinal anastomotic vessel PATO:0000141 structure abnormal ZDB-GENE-000511-8 58153 30061 slc40a1 ZFA:0009044 blood cell PATO:0001997 decreased amount abnormal ZDB-GENE-000511-8 58153 30061 slc40a1 GO:0005634 nucleus BFO:0000050 part_of ZFA:0009256 nucleate erythrocyte PATO:0000051 morphology abnormal ZDB-GENE-000511-8 58153 30061 slc40a1 ZFA:0009256 nucleate erythrocyte PATO:0000052 shape abnormal ZDB-GENE-000511-8 58153 30061 slc40a1 ZFA:0009256 nucleate erythrocyte PATO:0000328 low saturation abnormal ZDB-GENE-000511-8 58153 30061 slc40a1 ZFA:0009256 nucleate erythrocyte PATO:0000586 increased size abnormal ZDB-GENE-000511-8 58153 30061 slc40a1 ZFA:0009256 nucleate erythrocyte PATO:0001501 immature abnormal ZDB-GENE-000511-8 58153 30061 slc40a1 ZFA:0009256 nucleate erythrocyte PATO:0001997 decreased amount abnormal ZDB-GENE-000516-1 58035 6468 fbxw4 ZFA:0009019 neuronal stem cell BFO:0000050 part_of ZFA:0000013 cranial ganglion PATO:0000470 increased amount abnormal ZDB-GENE-000516-1 58035 6468 fbxw4 ZFA:0009248 neuron BFO:0000050 part_of ZFA:0000013 cranial ganglion PATO:0002102 proliferative abnormal ZDB-GENE-000516-1 58035 6468 fbxw4 ZFA:0000013 cranial ganglion PATO:0002011 neoplastic abnormal ZDB-GENE-000516-1 58035 6468 fbxw4 ZFA:0000204 esophagus PATO:0002104 inflamed abnormal ZDB-GENE-000516-1 58035 6468 fbxw4 ZFA:0000641 cranial nerve PATO:0002011 neoplastic abnormal ZDB-GENE-000516-1 58035 6468 fbxw4 ZFA:0001076 intestinal bulb PATO:0002104 inflamed abnormal ZDB-GENE-000516-1 58035 6468 fbxw4 ZFA:0001094 whole organism PATO:0002129 neoplastic, invasive abnormal ZDB-GENE-000516-1 58035 6468 fbxw4 ZFA:0009090 pigment cell PATO:0000330 irregular spatial pattern abnormal ZDB-GENE-000526-1 58146 23493 hey2 GO:0000278 mitotic cell cycle PATO:0001309 duration abnormal ZDB-GENE-000526-1 58146 23493 hey2 GO:0001947 heart looping PATO:0001507 disrupted abnormal ZDB-GENE-000526-1 58146 23493 hey2 GO:0001947 heart looping PATO:0002052 decreased occurrence abnormal ZDB-GENE-000526-1 58146 23493 hey2 GO:0008015 blood circulation PATO:0000297 arrested abnormal ZDB-GENE-000526-1 58146 23493 hey2 GO:0008015 blood circulation PATO:0000462 absent abnormal ZDB-GENE-000526-1 58146 23493 hey2 GO:0008015 blood circulation PATO:0001507 disrupted abnormal ZDB-GENE-000526-1 58146 23493 hey2 GO:0048514 blood vessel morphogenesis PATO:0001507 disrupted abnormal ZDB-GENE-000526-1 58146 23493 hey2 GO:0060047 heart contraction PATO:0000911 decreased rate abnormal ZDB-GENE-000526-1 58146 23493 hey2 ZFA:0000005 artery PATO:0000462 absent abnormal ZDB-GENE-000526-1 58146 23493 hey2 ZFA:0000008 brain PATO:0002105 hemorrhagic abnormal ZDB-GENE-000526-1 58146 23493 hey2 GO:0008283 cell population proliferation BFO:0000066 occurs_in ZFA:0000009 cardiac ventricle PATO:0002051 increased occurrence abnormal ZDB-GENE-000526-1 58146 23493 hey2 ZFA:0009316 cardiac muscle cell BFO:0000050 part_of ZFA:0000009 cardiac ventricle PATO:0000470 increased amount abnormal ZDB-GENE-000526-1 58146 23493 hey2 ZFA:0009316 cardiac muscle cell BFO:0000050 part_of ZFA:0000009 cardiac ventricle PATO:0001485 condensed abnormal ZDB-GENE-000526-1 58146 23493 hey2 ZFA:0000009 cardiac ventricle PATO:0000587 decreased size abnormal ZDB-GENE-000526-1 58146 23493 hey2 ZFA:0009181 vascular associated smooth muscle cell BFO:0000050 part_of ZFA:0000014 dorsal aorta PATO:0001997 decreased amount abnormal ZDB-GENE-000526-1 58146 23493 hey2 ZFA:0000014 dorsal aorta PATO:0000462 absent abnormal ZDB-GENE-000526-1 58146 23493 hey2 ZFA:0000014 dorsal aorta PATO:0000608 closed abnormal ZDB-GENE-000526-1 58146 23493 hey2 ZFA:0000014 dorsal aorta PATO:0001478 collapsed abnormal ZDB-GENE-000526-1 58146 23493 hey2 ZFA:0000014 dorsal aorta PATO:0001483 aplastic abnormal ZDB-GENE-000526-1 58146 23493 hey2 ZFA:0000054 pericardium PATO:0001450 edematous abnormal ZDB-GENE-000526-1 58146 23493 hey2 ZFA:0000082 vein PATO:0000051 morphology abnormal ZDB-GENE-000526-1 58146 23493 hey2 GO:0030017 sarcomere BFO:0000050 part_of ZFA:0000114 heart PATO:0000586 increased size abnormal ZDB-GENE-000526-1 58146 23493 hey2 ZFA:0009316 cardiac muscle cell BFO:0000050 part_of ZFA:0000114 heart PATO:0000586 increased size abnormal ZDB-GENE-000526-1 58146 23493 hey2 ZFA:0000114 heart PATO:0000001 quality abnormal ZDB-GENE-000526-1 58146 23493 hey2 ZFA:0000114 heart PATO:0000586 increased size abnormal ZDB-GENE-000526-1 58146 23493 hey2 ZFA:0000149 primitive heart tube PATO:0000052 shape abnormal ZDB-GENE-000526-1 58146 23493 hey2 GO:0008283 cell population proliferation BFO:0000066 occurs_in ZFA:0000173 bulbus arteriosus PATO:0002051 increased occurrence abnormal ZDB-GENE-000526-1 58146 23493 hey2 ZFA:0009316 cardiac muscle cell BFO:0000050 part_of ZFA:0000173 bulbus arteriosus PATO:0000470 increased amount abnormal ZDB-GENE-000526-1 58146 23493 hey2 ZFA:0000173 bulbus arteriosus PATO:0001154 elongated abnormal ZDB-GENE-000526-1 58146 23493 hey2 GO:0008283 cell population proliferation BFO:0000066 occurs_in ZFA:0000471 atrium PATO:0002051 increased occurrence abnormal ZDB-GENE-000526-1 58146 23493 hey2 ZFA:0009316 cardiac muscle cell BFO:0000050 part_of ZFA:0000471 atrium PATO:0000470 increased amount abnormal ZDB-GENE-000526-1 58146 23493 hey2 ZFA:0009316 cardiac muscle cell BFO:0000050 part_of ZFA:0000471 atrium PATO:0001485 condensed abnormal ZDB-GENE-000526-1 58146 23493 hey2 ZFA:0000471 atrium PATO:0000586 increased size abnormal ZDB-GENE-000526-1 58146 23493 hey2 ZFA:0000477 posterior cardinal vein PATO:0000051 morphology abnormal ZDB-GENE-000526-1 58146 23493 hey2 ZFA:0001267 cranial vasculature PATO:0001444 broken abnormal ZDB-GENE-000526-1 58146 23493 hey2 ZFA:0001285 intersegmental vessel PATO:0000462 absent abnormal ZDB-GENE-000526-1 58146 23493 hey2 ZFA:0001285 intersegmental vessel PATO:0001478 collapsed abnormal ZDB-GENE-000526-1 58146 23493 hey2 ZFA:0001346 interrenal primordium PATO:0002268 centered abnormal ZDB-GENE-000526-1 58146 23493 hey2 ZFA:0009316 cardiac muscle cell BFO:0000050 part_of ZFA:0001374 atrial myocardium PATO:0000470 increased amount abnormal ZDB-GENE-000526-1 58146 23493 hey2 ZFA:0009316 cardiac muscle cell BFO:0000050 part_of ZFA:0001374 atrial myocardium PATO:0001790 decreased mass density abnormal ZDB-GENE-000526-1 58146 23493 hey2 ZFA:0001439 anatomical system PATO:0000001 quality abnormal ZDB-GENE-000526-1 58146 23493 hey2 ZFA:0005035 subintestinal vein PATO:0001478 collapsed abnormal ZDB-GENE-000526-1 58146 23493 hey2 ZFA:0009316 cardiac muscle cell BFO:0000050 part_of ZFA:0005061 ventricular myocardium PATO:0000470 increased amount abnormal ZDB-GENE-000526-1 58146 23493 hey2 ZFA:0009316 cardiac muscle cell BFO:0000050 part_of ZFA:0005061 ventricular myocardium PATO:0001788 increased mass density abnormal ZDB-GENE-000526-1 58146 23493 hey2 ZFA:0005309 pronephric glomerular capillary PATO:0000462 absent abnormal ZDB-GENE-000526-1 58146 23493 hey2 ZFA:0009044 blood cell PATO:0002269 accumulation abnormal ZFA:0005024 trunk vasculature ZDB-GENE-000526-1 58146 23493 hey2 GO:0008283 cell population proliferation BFO:0000066 occurs_in ZFA:0009316 cardiac muscle cell PATO:0002051 increased occurrence abnormal ZDB-GENE-000526-1 58146 23493 hey2 ZFA:0009316 cardiac muscle cell PATO:0000470 increased amount abnormal ZDB-GENE-000605-1 58126 861 runx1 GO:0030097 hemopoiesis PATO:0001507 disrupted abnormal ZDB-GENE-000605-1 58126 861 runx1 GO:0030099 myeloid cell differentiation PATO:0001236 process quality abnormal ZDB-GENE-000605-1 58126 861 runx1 GO:0030851 granulocyte differentiation PATO:0000911 decreased rate abnormal ZDB-GENE-000605-1 58126 861 runx1 GO:0030851 granulocyte differentiation PATO:0002052 decreased occurrence abnormal ZDB-GENE-000605-1 58126 861 runx1 GO:0042221 response to chemical PATO:0001530 behavioral quality of a process abnormal ZDB-GENE-000605-1 58126 861 runx1 GO:0042730 fibrinolysis PATO:0002051 increased occurrence abnormal ZDB-GENE-000605-1 58126 861 runx1 GO:0051917 regulation of fibrinolysis PATO:0001507 disrupted abnormal ZDB-GENE-000605-1 58126 861 runx1 GO:0060216 definitive hemopoiesis PATO:0001236 process quality abnormal ZDB-GENE-000605-1 58126 861 runx1 GO:0060216 definitive hemopoiesis PATO:0001507 disrupted abnormal ZDB-GENE-000605-1 58126 861 runx1 ZFA:0009324 myeloid cell BFO:0000050 part_of ZFA:0000094 blood island PATO:0000462 absent abnormal ZDB-GENE-000605-1 58126 861 runx1 ZFA:0009324 myeloid cell BFO:0000050 part_of ZFA:0000094 blood island PATO:0001997 decreased amount abnormal ZDB-GENE-000605-1 58126 861 runx1 ZFA:0009354 hematopoietic multipotent progenitor cell BFO:0000050 part_of ZFA:0000094 blood island PATO:0000462 absent abnormal ZDB-GENE-000605-1 58126 861 runx1 ZFA:0009142 B cell BFO:0000050 part_of ZFA:0000436 spleen PATO:0001997 decreased amount abnormal ZDB-GENE-000605-1 58126 861 runx1 ZFA:0009046 T cell BFO:0000050 part_of ZFA:0000669 head kidney PATO:0000470 increased amount abnormal ZDB-GENE-000605-1 58126 861 runx1 ZFA:0009142 B cell BFO:0000050 part_of ZFA:0000669 head kidney PATO:0001997 decreased amount abnormal ZDB-GENE-000605-1 58126 861 runx1 ZFA:0000737 cranium PATO:0000052 shape abnormal ZDB-GENE-000605-1 58126 861 runx1 ZFA:0001094 whole organism PATO:0000051 morphology abnormal ZDB-GENE-000605-1 58126 861 runx1 ZFA:0001094 whole organism PATO:0001604 decreased life span abnormal ZDB-GENE-000605-1 58126 861 runx1 ZFA:0009014 hematopoietic stem cell BFO:0000050 part_of ZFA:0005028 ventral wall of dorsal aorta PATO:0001997 decreased amount abnormal ZDB-GENE-000605-1 58126 861 runx1 ZFA:0009065 endothelial cell BFO:0000050 part_of ZFA:0005028 ventral wall of dorsal aorta PATO:0000638 apoptotic abnormal ZDB-GENE-000605-1 58126 861 runx1 ZFA:0009324 myeloid cell BFO:0000050 part_of ZFA:0005028 ventral wall of dorsal aorta PATO:0000462 absent abnormal ZDB-GENE-000605-1 58126 861 runx1 ZFA:0009324 myeloid cell BFO:0000050 part_of ZFA:0005028 ventral wall of dorsal aorta PATO:0001997 decreased amount abnormal ZDB-GENE-000605-1 58126 861 runx1 ZFA:0009327 neutrophil BFO:0000050 part_of ZFA:0005028 ventral wall of dorsal aorta PATO:0001997 decreased amount abnormal ZDB-GENE-000605-1 58126 861 runx1 ZFA:0009354 hematopoietic multipotent progenitor cell BFO:0000050 part_of ZFA:0005028 ventral wall of dorsal aorta PATO:0000462 absent abnormal ZDB-GENE-000605-1 58126 861 runx1 ZFA:0009354 hematopoietic multipotent progenitor cell BFO:0000050 part_of ZFA:0005028 ventral wall of dorsal aorta PATO:0001997 decreased amount abnormal ZDB-GENE-000605-1 58126 861 runx1 ZFA:0005057 epicardium PATO:0000644 hyperplastic abnormal ZDB-GENE-000605-1 58126 861 runx1 ZFA:0005061 ventricular myocardium PATO:0000645 hypoplastic abnormal ZDB-GENE-000605-1 58126 861 runx1 ZFA:0009014 hematopoietic stem cell PATO:0001483 aplastic abnormal ZDB-GENE-000605-1 58126 861 runx1 ZFA:0009014 hematopoietic stem cell PATO:0001997 decreased amount abnormal ZDB-GENE-000605-1 58126 861 runx1 ZFA:0009015 erythroid progenitor cell PATO:0000462 absent abnormal ZDB-GENE-000605-1 58126 861 runx1 ZFA:0009049 mature neutrophil PATO:0001997 decreased amount abnormal ZDB-GENE-000605-1 58126 861 runx1 ZFA:0009141 macrophage PATO:0000470 increased amount abnormal ZDB-GENE-000605-1 58126 861 runx1 GO:0006915 apoptotic process BFO:0000066 occurs_in ZFA:0009142 B cell PATO:0002051 increased occurrence abnormal ZDB-GENE-000605-1 58126 861 runx1 ZFA:0009250 lymphocyte PATO:0001997 decreased amount abnormal ZDB-GENE-000605-1 58126 861 runx1 ZFA:0009265 monocyte PATO:0001997 decreased amount abnormal ZDB-GENE-000605-1 58126 861 runx1 ZFA:0009323 thrombocyte PATO:0001997 decreased amount abnormal ZDB-GENE-000605-1 58126 861 runx1 ZFA:0009327 neutrophil PATO:0001997 decreased amount abnormal ZDB-GENE-000605-1 58126 861 runx1 ZFA:0009352 neutrophil progenitor cell PATO:0001997 decreased amount abnormal ZDB-GENE-000605-2 58127 864 runx3 GO:0002062 chondrocyte differentiation PATO:0000502 delayed abnormal ZDB-GENE-000605-2 58127 864 runx3 GO:0042221 response to chemical PATO:0001530 behavioral quality of a process abnormal ZDB-GENE-000605-2 58127 864 runx3 ZFA:0000737 cranium PATO:0000587 decreased size abnormal ZDB-GENE-000605-2 58127 864 runx3 ZFA:0001205 Meckel's cartilage PATO:0001483 aplastic abnormal ZDB-GENE-000605-2 58127 864 runx3 ZFA:0001216 splanchnocranium PATO:0001483 aplastic abnormal ZDB-GENE-000605-2 58127 864 runx3 ZFA:0001399 palatoquadrate cartilage PATO:0001483 aplastic abnormal ZDB-GENE-000605-2 58127 864 runx3 ZFA:0001400 ceratohyal cartilage PATO:0001483 aplastic abnormal ZDB-GENE-000605-2 58127 864 runx3 ZFA:0001422 hyosymplectic cartilage PATO:0001483 aplastic abnormal ZDB-GENE-000605-2 58127 864 runx3 ZFA:0001458 cranial cartilage PATO:0001483 aplastic abnormal ZDB-GENE-000605-2 58127 864 runx3 ZFA:0001516 ceratobranchial cartilage PATO:0001483 aplastic abnormal ZDB-GENE-000605-2 58127 864 runx3 BSPO:0000071 anterior region BFO:0000050 part_of ZFA:0001580 neurocranium PATO:0001483 aplastic abnormal ZDB-GENE-000607-1 572532 54510 pcdh18a GO:0001756 somitogenesis PATO:0000502 delayed abnormal ZDB-GENE-000607-1 572532 54510 pcdh18a GO:0016339 calcium-dependent cell-cell adhesion via plasma membrane cell adhesion molecules PATO:0001507 disrupted abnormal ZDB-GENE-000607-1 572532 54510 pcdh18a GO:0055113 epiboly involved in gastrulation with mouth forming second PATO:0000502 delayed abnormal ZDB-GENE-000607-1 572532 54510 pcdh18a ZFA:0000092 axis PATO:0000574 decreased length abnormal ZDB-GENE-000607-1 572532 54510 pcdh18a ZFA:0000135 notochord PATO:0000574 decreased length abnormal ZDB-GENE-000607-1 572532 54510 pcdh18a ZFA:0000135 notochord PATO:0000600 increased width abnormal ZDB-GENE-000607-1 572532 54510 pcdh18a ZFA:0000155 somite PATO:0000600 increased width abnormal ZDB-GENE-000607-1 572532 54510 pcdh18a ZFA:0001094 whole organism PATO:0000574 decreased length abnormal ZDB-GENE-000607-1 572532 54510 pcdh18a ZFA:0005746 notochord inner cell PATO:0000411 circular abnormal ZDB-GENE-000607-13 567413 6660 sox5 ZFA:0001463 melanophore stripe PATO:0000600 increased width abnormal ZDB-GENE-000607-13 567413 6660 sox5 ZFA:0001463 melanophore stripe PATO:0001997 decreased amount abnormal ZDB-GENE-000607-13 567413 6660 sox5 ZFA:0009198 xanthophore PATO:0000470 increased amount ameliorated ZDB-GENE-000607-13 567413 6660 sox5 ZFA:0009198 xanthophore PATO:0001671 increased distribution abnormal ZDB-GENE-000607-49 57987 23266 adgrl2a GO:0035329 hippo signaling BFO:0000066 occurs_in ZFA:0001079 blood vasculature PATO:0002304 increased process quality abnormal ZDB-GENE-000607-49 57987 23266 adgrl2a ZFA:0009065 endothelial cell BFO:0000050 part_of ZFA:0001079 blood vasculature PATO:0000592 decreased thickness abnormal ZDB-GENE-000607-49 57987 23266 adgrl2a ZFA:0001285 intersegmental vessel PATO:0001577 increased permeability abnormal ZDB-GENE-000607-49 57987 23266 adgrl2a GO:0070160 tight junction BFO:0000050 part_of ZFA:0009065 endothelial cell PATO:0040026 structurally discontinuous abnormal ZDB-GENE-000607-49 57987 23266 adgrl2a GO:0070160 tight junction BFO:0000050 part_of ZFA:0009065 endothelial cell PATO:0040047 fragmented abnormal ZDB-GENE-000607-49 57987 23266 adgrl2a ZFA:0009065 endothelial cell PATO:0000587 decreased size abnormal ZDB-GENE-000607-70 58008 23462 hey1 GO:0030182 neuron differentiation BFO:0000066 occurs_in ZFA:0009292 radial glial cell PATO:0002051 increased occurrence abnormal ZDB-GENE-000607-70 58008 23462 hey1 ZFA:0009019 neuronal stem cell BFO:0000050 part_of ZFA:0009292 radial glial cell PATO:0001997 decreased amount abnormal ZDB-GENE-000607-75 58013 26155 noc2l ZFA:0000054 pericardium PATO:0001450 edematous abnormal ZDB-GENE-000607-75 58013 26155 noc2l ZFA:0000084 yolk PATO:0000001 quality abnormal ZDB-GENE-000607-75 58013 26155 noc2l ZFA:0000084 yolk PATO:0000411 circular abnormal ZDB-GENE-000607-75 58013 26155 noc2l ZFA:0000107 eye PATO:0000587 decreased size abnormal ZDB-GENE-000607-75 58013 26155 noc2l ZFA:0000112 gut PATO:0000001 quality abnormal ZDB-GENE-000607-75 58013 26155 noc2l ZFA:0000112 gut PATO:0000645 hypoplastic abnormal ZDB-GENE-000607-75 58013 26155 noc2l ZFA:0000123 liver PATO:0000001 quality abnormal ZDB-GENE-000607-75 58013 26155 noc2l ZFA:0000123 liver PATO:0000645 hypoplastic abnormal ZDB-GENE-000607-75 58013 26155 noc2l ZFA:0001114 head PATO:0000587 decreased size abnormal ZDB-GENE-000607-75 58013 26155 noc2l ZFA:0001439 anatomical system PATO:0000001 quality abnormal ZDB-GENE-000607-82 564527 11060 wwp2 ZFA:0005509 palate PATO:0000642 fused with abnormal ZFA:0005509 palate ZDB-GENE-000607-82 564527 11060 wwp2 ZFA:0005509 palate PATO:0000587 decreased size abnormal ZDB-GENE-000616-1 58100 572 badb GO:0001704 formation of primary germ layer PATO:0001236 process quality abnormal ZDB-GENE-000616-1 58100 572 badb GO:0006915 apoptotic process PATO:0002051 increased occurrence abnormal ZDB-GENE-000616-1 58100 572 badb GO:0007420 brain development PATO:0001236 process quality abnormal ZDB-GENE-000616-1 58100 572 badb GO:0036268 swimming PATO:0002302 decreased process quality abnormal ZDB-GENE-000616-1 58100 572 badb GO:1903409 reactive oxygen species biosynthetic process PATO:0002304 increased process quality abnormal ZDB-GENE-000616-1 58100 572 badb ZFA:0000008 brain PATO:0000051 morphology abnormal ZDB-GENE-000616-1 58100 572 badb ZFA:0000008 brain PATO:0000600 increased width abnormal ZDB-GENE-000616-1 58100 572 badb ZFA:0000008 brain PATO:0002364 shortened abnormal ZDB-GENE-000616-1 58100 572 badb ZFA:0000029 hindbrain PATO:0000051 morphology abnormal ZDB-GENE-000616-1 58100 572 badb ZFA:0000128 midbrain PATO:0000051 morphology abnormal ZDB-GENE-000616-13 58083 351 appa GO:0007417 central nervous system development PATO:0001507 disrupted abnormal ZDB-GENE-000616-13 58083 351 appa GO:0008219 cell death PATO:0002051 increased occurrence abnormal ZDB-GENE-000616-13 58083 351 appa ZFA:0000012 central nervous system PATO:0000051 morphology abnormal ZDB-GENE-000616-13 58083 351 appa ZFA:0000737 cranium PATO:0001450 edematous abnormal ZDB-GENE-000616-13 58083 351 appa ZFA:0001094 whole organism PATO:0000051 morphology abnormal ZDB-GENE-000616-13 58083 351 appa ZFA:0001094 whole organism PATO:0000574 decreased length abnormal ZDB-GENE-000616-13 58083 351 appa ZFA:0001094 whole organism PATO:0000587 decreased size abnormal ZDB-GENE-000616-14 58141 2618 gart GO:0003407 neural retina development PATO:0001507 disrupted abnormal ZDB-GENE-000616-14 58141 2618 gart GO:0008283 cell population proliferation PATO:0002051 increased occurrence abnormal ZDB-GENE-000616-14 58141 2618 gart GO:0009790 embryo development PATO:0000297 arrested abnormal ZDB-GENE-000616-14 58141 2618 gart GO:0009790 embryo development PATO:0000502 delayed abnormal ZDB-GENE-000616-14 58141 2618 gart GO:0010842 retina layer formation PATO:0001507 disrupted abnormal ZDB-GENE-000616-14 58141 2618 gart GO:0043473 pigmentation PATO:0001507 disrupted abnormal ZDB-GENE-000616-14 58141 2618 gart GO:0060322 head development PATO:0001507 disrupted abnormal ZDB-GENE-000616-14 58141 2618 gart ZFA:0000107 eye PATO:0000587 decreased size abnormal ZDB-GENE-000616-14 58141 2618 gart ZFA:0000144 retinal pigmented epithelium PATO:0000001 quality abnormal ZDB-GENE-000616-14 58141 2618 gart ZFA:0000144 retinal pigmented epithelium PATO:0002251 decreased pigmentation abnormal ZDB-GENE-000616-14 58141 2618 gart ZFA:0001094 whole organism PATO:0001422 dead abnormal ZDB-GENE-000616-14 58141 2618 gart ZFA:0001114 head PATO:0000001 quality abnormal ZDB-GENE-000616-14 58141 2618 gart GO:0048770 pigment granule BFO:0000050 part_of ZFA:0009091 melanocyte PATO:0001997 decreased amount abnormal ZDB-GENE-000616-14 58141 2618 gart GO:0048770 pigment granule BFO:0000050 part_of ZFA:0009198 xanthophore PATO:0001997 decreased amount abnormal ZDB-GENE-000616-14 58141 2618 gart GO:0048770 pigment granule BFO:0000050 part_of ZFA:0009199 iridophore PATO:0001997 decreased amount abnormal ZDB-GENE-000616-15 57930 8928 foxh1 GO:0003146 heart jogging PATO:0000297 arrested abnormal ZDB-GENE-000616-15 57930 8928 foxh1 GO:0007368 determination of left/right symmetry PATO:0001507 disrupted abnormal ZDB-GENE-000616-15 57930 8928 foxh1 GO:0021508 floor plate formation PATO:0000297 arrested abnormal ZDB-GENE-000616-15 57930 8928 foxh1 GO:0021508 floor plate formation PATO:0001507 disrupted abnormal ZDB-GENE-000616-15 57930 8928 foxh1 GO:0021999 neural plate anterior/posterior regionalization PATO:0001507 disrupted abnormal ZDB-GENE-000616-15 57930 8928 foxh1 GO:0032502 developmental process PATO:0000502 delayed abnormal ZDB-GENE-000616-15 57930 8928 foxh1 GO:0042074 cell migration involved in gastrulation PATO:0001507 disrupted abnormal ZDB-GENE-000616-15 57930 8928 foxh1 GO:0048327 axial mesodermal cell fate specification PATO:0001507 disrupted abnormal ZDB-GENE-000616-15 57930 8928 foxh1 GO:0060026 convergent extension PATO:0001507 disrupted abnormal ZDB-GENE-000616-15 57930 8928 foxh1 GO:0060971 embryonic heart tube left/right pattern formation PATO:0001236 process quality abnormal ZDB-GENE-000616-15 57930 8928 foxh1 ZFA:0000008 brain PATO:0000001 quality abnormal ZDB-GENE-000616-15 57930 8928 foxh1 ZFA:0000008 brain PATO:0000051 morphology abnormal ZDB-GENE-000616-15 57930 8928 foxh1 BSPO:0000084 ventral region BFO:0000050 part_of ZFA:0000012 central nervous system PATO:0000587 decreased size abnormal ZDB-GENE-000616-15 57930 8928 foxh1 BSPO:0000084 ventral region BFO:0000050 part_of ZFA:0000022 floor plate PATO:0000645 hypoplastic abnormal ZDB-GENE-000616-15 57930 8928 foxh1 ZFA:0000022 floor plate PATO:0000001 quality abnormal ZDB-GENE-000616-15 57930 8928 foxh1 ZFA:0000022 floor plate PATO:0000462 absent abnormal ZDB-GENE-000616-15 57930 8928 foxh1 ZFA:0000022 floor plate PATO:0000587 decreased size abnormal ZDB-GENE-000616-15 57930 8928 foxh1 ZFA:0000022 floor plate PATO:0001483 aplastic abnormal ZDB-GENE-000616-15 57930 8928 foxh1 ZFA:0000023 forerunner cell group PATO:0000587 decreased size abnormal ZDB-GENE-000616-15 57930 8928 foxh1 ZFA:0000032 hypothalamus PATO:0000587 decreased size abnormal ZDB-GENE-000616-15 57930 8928 foxh1 ZFA:0000054 pericardium PATO:0001450 edematous abnormal ZDB-GENE-000616-15 57930 8928 foxh1 ZFA:0000060 prechordal plate PATO:0000051 morphology abnormal ZDB-GENE-000616-15 57930 8928 foxh1 ZFA:0000071 shield PATO:0002106 poorly differentiated abnormal ZDB-GENE-000616-15 57930 8928 foxh1 ZFA:0000075 spinal cord PATO:0000051 morphology abnormal ZDB-GENE-000616-15 57930 8928 foxh1 ZFA:0000091 axial chorda mesoderm PATO:0000051 morphology abnormal ZDB-GENE-000616-15 57930 8928 foxh1 ZFA:0000091 axial chorda mesoderm PATO:0001483 aplastic abnormal ZDB-GENE-000616-15 57930 8928 foxh1 ZFA:0000106 extension PATO:0000574 decreased length abnormal ZDB-GENE-000616-15 57930 8928 foxh1 ZFA:0000106 extension PATO:0000591 increased thickness abnormal ZDB-GENE-000616-15 57930 8928 foxh1 ZFA:0000107 eye PATO:0000375 decreased distance abnormal ZFA:0000107 eye ZDB-GENE-000616-15 57930 8928 foxh1 ZFA:0000107 eye PATO:0000642 fused with abnormal ZFA:0000107 eye ZDB-GENE-000616-15 57930 8928 foxh1 ZFA:0000107 eye PATO:0000001 quality abnormal ZDB-GENE-000616-15 57930 8928 foxh1 ZFA:0000107 eye PATO:0001924 mislocalised medially abnormal ZDB-GENE-000616-15 57930 8928 foxh1 BSPO:0000071 anterior region BFO:0000050 part_of ZFA:0000110 fourth ventricle PATO:0000462 absent abnormal ZDB-GENE-000616-15 57930 8928 foxh1 ZFA:0000111 germ ring PATO:0002106 poorly differentiated abnormal ZDB-GENE-000616-15 57930 8928 foxh1 GO:0003259 cardioblast anterior-lateral migration BFO:0000066 occurs_in ZFA:0000115 heart rudiment PATO:0001236 process quality abnormal ZDB-GENE-000616-15 57930 8928 foxh1 GO:0005634 nucleus BFO:0000050 part_of ZFA:0000135 notochord PATO:0001997 decreased amount abnormal ZDB-GENE-000616-15 57930 8928 foxh1 ZFA:0009000 cell BFO:0000050 part_of ZFA:0000135 notochord PATO:0000051 morphology abnormal ZDB-GENE-000616-15 57930 8928 foxh1 ZFA:0000135 notochord PATO:0000051 morphology abnormal ZDB-GENE-000616-15 57930 8928 foxh1 ZFA:0000135 notochord PATO:0000141 structure abnormal ZDB-GENE-000616-15 57930 8928 foxh1 ZFA:0000135 notochord PATO:0000587 decreased size abnormal ZDB-GENE-000616-15 57930 8928 foxh1 ZFA:0000135 notochord PATO:0000599 decreased width abnormal ZDB-GENE-000616-15 57930 8928 foxh1 ZFA:0000135 notochord PATO:0000617 bent abnormal ZDB-GENE-000616-15 57930 8928 foxh1 ZFA:0000135 notochord PATO:0001469 curved ventral abnormal ZDB-GENE-000616-15 57930 8928 foxh1 ZFA:0000135 notochord PATO:0001483 aplastic abnormal ZDB-GENE-000616-15 57930 8928 foxh1 ZFA:0000155 somite PATO:0000642 fused with abnormal ZFA:0000155 somite ZDB-GENE-000616-15 57930 8928 foxh1 ZFA:0000360 heart tube PATO:0002268 centered abnormal ZDB-GENE-000616-15 57930 8928 foxh1 ZFA:0000396 nervous system PATO:0000001 quality abnormal ZDB-GENE-000616-15 57930 8928 foxh1 GO:0030424 axon BFO:0000050 part_of ZFA:0000543 medial longitudinal fasciculus PATO:0000937 disorganized abnormal ZDB-GENE-000616-15 57930 8928 foxh1 ZFA:0000543 medial longitudinal fasciculus PATO:0000642 fused with abnormal ZFA:0000543 medial longitudinal fasciculus ZDB-GENE-000616-15 57930 8928 foxh1 ZFA:0000600 cranial nerve IV PATO:0000642 fused with abnormal ZFA:0000600 cranial nerve IV ZDB-GENE-000616-15 57930 8928 foxh1 ZFA:0000938 central canal PATO:0000462 absent abnormal ZDB-GENE-000616-15 57930 8928 foxh1 BSPO:0000013 anterior-posterior axis BFO:0000050 part_of ZFA:0001094 whole organism PATO:0001469 curved ventral abnormal ZDB-GENE-000616-15 57930 8928 foxh1 ZFA:0001094 whole organism PATO:0000052 shape abnormal ZDB-GENE-000616-15 57930 8928 foxh1 ZFA:0001094 whole organism PATO:0000718 lethal (sensu genetics) abnormal ZDB-GENE-000616-15 57930 8928 foxh1 ZFA:0001094 whole organism PATO:0001422 dead abnormal ZDB-GENE-000616-15 57930 8928 foxh1 ZFA:0001115 trunk PATO:0001469 curved ventral abnormal ZDB-GENE-000616-15 57930 8928 foxh1 ZFA:0001117 post-vent region PATO:0000406 curved abnormal ZDB-GENE-000616-15 57930 8928 foxh1 ZFA:0001117 post-vent region PATO:0001469 curved ventral abnormal ZDB-GENE-000616-15 57930 8928 foxh1 ZFA:0001120 neuroectoderm PATO:0000051 morphology abnormal ZDB-GENE-000616-15 57930 8928 foxh1 ZFA:0001135 neural tube PATO:0000001 quality abnormal ZDB-GENE-000616-15 57930 8928 foxh1 ZFA:0009000 cell BFO:0000050 part_of ZFA:0001218 presumptive floor plate PATO:0001997 decreased amount abnormal ZDB-GENE-000616-15 57930 8928 foxh1 ZFA:0009000 cell BFO:0000050 part_of ZFA:0001218 presumptive floor plate PATO:0002100 undifferentiated abnormal ZDB-GENE-000616-15 57930 8928 foxh1 ZFA:0001258 floor plate rhombomere region PATO:0001483 aplastic abnormal ZDB-GENE-000616-15 57930 8928 foxh1 ZFA:0001423 parachordal cartilage PATO:0000642 fused with abnormal ZFA:0001423 parachordal cartilage ZDB-GENE-000616-15 57930 8928 foxh1 ZFA:0001424 chondrocranium PATO:0000051 morphology abnormal ZDB-GENE-000616-15 57930 8928 foxh1 ZFA:0001507 trabecula cranii PATO:0000642 fused with abnormal ZFA:0001507 trabecula cranii ZDB-GENE-000616-15 57930 8928 foxh1 GO:0007507 heart development BFO:0000066 occurs_in ZFA:0001724 presumptive endocardium PATO:0002302 decreased process quality abnormal ZDB-GENE-000616-15 57930 8928 foxh1 ZFA:0007016 anterior neural plate PATO:0000051 morphology abnormal ZDB-GENE-000616-15 57930 8928 foxh1 ZFA:0009003 cranial neural crest cell PATO:0001920 mislocalised ventrally abnormal ZDB-GENE-000616-15 57930 8928 foxh1 GO:0030424 axon BFO:0000050 part_of ZFA:0009247 secondary motor neuron PATO:0001997 decreased amount abnormal ZDB-GENE-000616-16 58123 3297 hsf1 ZFA:0000035 lens PATO:0000141 structure abnormal ZDB-GENE-000616-16 58123 3297 hsf1 ZFA:0000035 lens PATO:0000587 decreased size abnormal ZDB-GENE-000616-16 58123 3297 hsf1 ZFA:0000035 lens PATO:0001501 immature abnormal ZDB-GENE-000616-16 58123 3297 hsf1 ZFA:0000107 eye PATO:0000587 decreased size abnormal ZDB-GENE-000616-16 58123 3297 hsf1 ZFA:0000107 eye PATO:0001715 decreased diameter abnormal ZDB-GENE-000616-16 58123 3297 hsf1 ZFA:0000107 eye PATO:0001899 decreased circumference abnormal ZDB-GENE-000616-16 58123 3297 hsf1 ZFA:0000152 retina PATO:0000141 structure abnormal ZDB-GENE-000616-16 58123 3297 hsf1 ZFA:0000152 retina PATO:0000587 decreased size abnormal ZDB-GENE-000616-16 58123 3297 hsf1 ZFA:0000152 retina PATO:0000937 disorganized abnormal ZDB-GENE-000616-16 58123 3297 hsf1 ZFA:0001283 pupil PATO:0001715 decreased diameter abnormal ZDB-GENE-000616-16 58123 3297 hsf1 ZFA:0009310 retinal ganglion cell PATO:0001997 decreased amount abnormal ZDB-GENE-000616-5 58119 103 adar ZFA:0000135 notochord PATO:0000052 shape abnormal ZDB-GENE-000616-5 58119 103 adar ZFA:0001094 whole organism PATO:0001422 dead abnormal ZDB-GENE-000616-5 58119 103 adar ZFA:0001094 whole organism PATO:0001604 decreased life span abnormal ZDB-GENE-000616-5 58119 103 adar ZFA:0001114 head PATO:0001617 deformed abnormal ZDB-GENE-000616-5 58119 103 adar ZFA:0001117 post-vent region PATO:0001617 deformed abnormal ZDB-GENE-000616-6 58097 4617 myf5 ZFA:0000071 shield PATO:0000600 increased width abnormal ZDB-GENE-000616-6 58097 4617 myf5 ZFA:0000095 pharyngeal arch 3-7 skeleton PATO:0000462 absent abnormal ZDB-GENE-000616-6 58097 4617 myf5 ZFA:0000328 cephalic musculature PATO:0001997 decreased amount abnormal ZDB-GENE-000616-6 58097 4617 myf5 GO:0010467 gene expression BFO:0000066 occurs_in ZFA:0000414 presumptive cephalic mesoderm PATO:0001507 disrupted abnormal ZDB-GENE-000616-6 58097 4617 myf5 ZFA:0001094 whole organism PATO:0000718 lethal (sensu genetics) abnormal ZDB-GENE-000616-6 58097 4617 myf5 ZFA:0001114 head PATO:0001999 lacks parts or has fewer parts of type abnormal ZFA:0000328 cephalic musculature ZDB-GENE-000616-6 58097 4617 myf5 ZFA:0001114 head PATO:0000587 decreased size abnormal ZDB-GENE-000616-6 58097 4617 myf5 ZFA:0009165 neural crest cell BFO:0000050 part_of ZFA:0001120 neuroectoderm PATO:0001997 decreased amount abnormal ZDB-GENE-000616-6 58097 4617 myf5 ZFA:0009027 chondroblast BFO:0000050 part_of ZFA:0001194 cranial neural crest PATO:0001997 decreased amount abnormal ZDB-GENE-000616-6 58097 4617 myf5 ZFA:0001194 cranial neural crest PATO:0001997 decreased amount abnormal ZDB-GENE-000616-6 58097 4617 myf5 ZFA:0001205 Meckel's cartilage PATO:0000646 malformed abnormal ZDB-GENE-000616-6 58097 4617 myf5 ZFA:0001220 copula PATO:0000462 absent abnormal ZDB-GENE-000616-6 58097 4617 myf5 ZFA:0001399 palatoquadrate cartilage PATO:0000646 malformed abnormal ZDB-GENE-000616-6 58097 4617 myf5 ZFA:0001400 ceratohyal cartilage PATO:0000646 malformed abnormal ZDB-GENE-000616-6 58097 4617 myf5 ZFA:0001516 ceratobranchial cartilage PATO:0000462 absent abnormal ZDB-GENE-000616-6 58097 4617 myf5 ZFA:0001522 hypobranchial cartilage PATO:0000462 absent abnormal ZDB-GENE-000616-6 58097 4617 myf5 ZFA:0001606 pharyngeal arch 3 PATO:0002001 has fewer parts of type abnormal ZFA:0001194 cranial neural crest ZDB-GENE-000616-6 58097 4617 myf5 ZFA:0001606 pharyngeal arch 3 PATO:0002001 has fewer parts of type abnormal ZFA:0009027 chondroblast ZDB-GENE-000616-6 58097 4617 myf5 ZFA:0001607 pharyngeal arch 4 PATO:0002001 has fewer parts of type abnormal ZFA:0001194 cranial neural crest ZDB-GENE-000616-6 58097 4617 myf5 ZFA:0001608 pharyngeal arch 5 PATO:0002001 has fewer parts of type abnormal ZFA:0001194 cranial neural crest ZDB-GENE-000616-6 58097 4617 myf5 ZFA:0001608 pharyngeal arch 5 PATO:0002001 has fewer parts of type abnormal ZFA:0009027 chondroblast ZDB-GENE-000616-6 58097 4617 myf5 ZFA:0001608 pharyngeal arch 5 PATO:0000462 absent abnormal ZDB-GENE-000616-6 58097 4617 myf5 ZFA:0001609 pharyngeal arch 6 PATO:0002001 has fewer parts of type abnormal ZFA:0001194 cranial neural crest ZDB-GENE-000616-6 58097 4617 myf5 ZFA:0001609 pharyngeal arch 6 PATO:0002001 has fewer parts of type abnormal ZFA:0009027 chondroblast ZDB-GENE-000616-6 58097 4617 myf5 ZFA:0001609 pharyngeal arch 6 PATO:0000462 absent abnormal ZDB-GENE-000622-1 58076 2627 gata6 GO:0003007 heart morphogenesis PATO:0001236 process quality abnormal ZDB-GENE-000622-1 58076 2627 gata6 GO:0003007 heart morphogenesis PATO:0001507 disrupted abnormal ZDB-GENE-000622-1 58076 2627 gata6 GO:0003007 heart morphogenesis PATO:0002302 decreased process quality abnormal ZDB-GENE-000622-1 58076 2627 gata6 GO:0007507 heart development PATO:0001507 disrupted abnormal ZDB-GENE-000622-1 58076 2627 gata6 GO:0008283 cell population proliferation PATO:0000912 increased rate abnormal ZDB-GENE-000622-1 58076 2627 gata6 GO:0035050 embryonic heart tube development PATO:0001507 disrupted abnormal ZDB-GENE-000622-1 58076 2627 gata6 GO:0055011 atrial cardiac muscle cell differentiation PATO:0002302 decreased process quality abnormal ZDB-GENE-000622-1 58076 2627 gata6 GO:0055012 ventricular cardiac muscle cell differentiation PATO:0002302 decreased process quality abnormal ZDB-GENE-000622-1 58076 2627 gata6 ZFA:0000009 cardiac ventricle PATO:0002001 has fewer parts of type abnormal ZFA:0009316 cardiac muscle cell ZDB-GENE-000622-1 58076 2627 gata6 ZFA:0000009 cardiac ventricle PATO:0000587 decreased size abnormal ZDB-GENE-000622-1 58076 2627 gata6 ZFA:0000054 pericardium PATO:0001450 edematous abnormal ZDB-GENE-000622-1 58076 2627 gata6 ZFA:0000076 swim bladder PATO:0001511 non-functional abnormal ZDB-GENE-000622-1 58076 2627 gata6 ZFA:0000112 gut PATO:0001501 immature abnormal ZDB-GENE-000622-1 58076 2627 gata6 ZFA:0000112 gut PATO:0001617 deformed abnormal ZDB-GENE-000622-1 58076 2627 gata6 ZFA:0000114 heart PATO:0000645 hypoplastic abnormal ZDB-GENE-000622-1 58076 2627 gata6 ZFA:0000360 heart tube PATO:0000646 malformed abnormal ZDB-GENE-000622-1 58076 2627 gata6 ZFA:0000471 atrium PATO:0000586 increased size abnormal ZDB-GENE-000622-1 58076 2627 gata6 ZFA:0000471 atrium PATO:0002057 increased area abnormal ZDB-GENE-000622-1 58076 2627 gata6 ZFA:0001094 whole organism PATO:0001422 dead abnormal ZDB-GENE-000626-1 58071 7139 tnnt2a GO:0001947 heart looping PATO:0001507 disrupted abnormal ZDB-GENE-000626-1 58071 7139 tnnt2a GO:0001974 blood vessel remodeling PATO:0001507 disrupted abnormal ZDB-GENE-000626-1 58071 7139 tnnt2a GO:0002040 sprouting angiogenesis PATO:0001236 process quality abnormal ZDB-GENE-000626-1 58071 7139 tnnt2a GO:0005179 hormone activity PATO:0002052 decreased occurrence abnormal ZDB-GENE-000626-1 58071 7139 tnnt2a GO:0006809 nitric oxide biosynthetic process PATO:0001507 disrupted abnormal ZDB-GENE-000626-1 58071 7139 tnnt2a GO:0008015 blood circulation PATO:0000297 arrested abnormal ZDB-GENE-000626-1 58071 7139 tnnt2a GO:0008015 blood circulation PATO:0000462 absent abnormal ZDB-GENE-000626-1 58071 7139 tnnt2a GO:0008015 blood circulation PATO:0000911 decreased rate abnormal ZDB-GENE-000626-1 58071 7139 tnnt2a GO:0008015 blood circulation PATO:0001507 disrupted abnormal ZDB-GENE-000626-1 58071 7139 tnnt2a GO:0008015 blood circulation PATO:0002052 decreased occurrence abnormal ZDB-GENE-000626-1 58071 7139 tnnt2a GO:0008015 blood circulation PATO:0002302 decreased process quality abnormal ZDB-GENE-000626-1 58071 7139 tnnt2a GO:0010882 regulation of cardiac muscle contraction by calcium ion signaling PATO:0001507 disrupted abnormal ZDB-GENE-000626-1 58071 7139 tnnt2a GO:0019722 calcium-mediated signaling PATO:0001507 disrupted abnormal ZDB-GENE-000626-1 58071 7139 tnnt2a GO:0030325 adrenal gland development PATO:0001558 lacking processual parts abnormal GO:0016477 cell migration ZDB-GENE-000626-1 58071 7139 tnnt2a GO:0030325 adrenal gland development PATO:0001236 process quality abnormal ZDB-GENE-000626-1 58071 7139 tnnt2a GO:0035775 pronephric glomerulus morphogenesis PATO:0001236 process quality abnormal ZDB-GENE-000626-1 58071 7139 tnnt2a GO:0036269 swimming behavior PATO:0001236 process quality abnormal ZDB-GENE-000626-1 58071 7139 tnnt2a GO:0048514 blood vessel morphogenesis PATO:0002302 decreased process quality abnormal ZDB-GENE-000626-1 58071 7139 tnnt2a GO:0048793 pronephros development PATO:0001236 process quality abnormal ZDB-GENE-000626-1 58071 7139 tnnt2a GO:0048823 nucleate erythrocyte development PATO:0001507 disrupted abnormal ZDB-GENE-000626-1 58071 7139 tnnt2a GO:0048844 artery morphogenesis PATO:0000502 delayed abnormal ZDB-GENE-000626-1 58071 7139 tnnt2a GO:0048845 venous blood vessel morphogenesis PATO:0001507 disrupted abnormal ZDB-GENE-000626-1 58071 7139 tnnt2a GO:0055117 regulation of cardiac muscle contraction PATO:0001507 disrupted abnormal ZDB-GENE-000626-1 58071 7139 tnnt2a GO:0060047 heart contraction PATO:0000297 arrested abnormal ZDB-GENE-000626-1 58071 7139 tnnt2a GO:0060047 heart contraction PATO:0000381 decreased frequency abnormal ZDB-GENE-000626-1 58071 7139 tnnt2a GO:0060047 heart contraction PATO:0000462 absent abnormal ZDB-GENE-000626-1 58071 7139 tnnt2a GO:0060047 heart contraction PATO:0000911 decreased rate abnormal ZDB-GENE-000626-1 58071 7139 tnnt2a GO:0060047 heart contraction PATO:0002052 decreased occurrence abnormal ZDB-GENE-000626-1 58071 7139 tnnt2a GO:0060047 heart contraction PATO:0002302 decreased process quality abnormal ZDB-GENE-000626-1 58071 7139 tnnt2a GO:0060047 heart contraction PATO:0040059 absent process abnormal ZDB-GENE-000626-1 58071 7139 tnnt2a GO:0060973 cell migration involved in heart development PATO:0002052 decreased occurrence abnormal ZDB-GENE-000626-1 58071 7139 tnnt2a GO:0061314 Notch signaling involved in heart development PATO:0002052 decreased occurrence abnormal ZDB-GENE-000626-1 58071 7139 tnnt2a GO:0072017 distal tubule development PATO:0000297 arrested abnormal ZDB-GENE-000626-1 58071 7139 tnnt2a GO:0072019 proximal convoluted tubule development PATO:0000297 arrested abnormal ZDB-GENE-000626-1 58071 7139 tnnt2a GO:0072554 blood vessel lumenization PATO:0001236 process quality abnormal ZDB-GENE-000626-1 58071 7139 tnnt2a GO:0072554 blood vessel lumenization PATO:0001507 disrupted abnormal ZDB-GENE-000626-1 58071 7139 tnnt2a ZFA:0000007 blood PATO:0002270 increased accumulation abnormal ZFA:0000180 caudal vein ZDB-GENE-000626-1 58071 7139 tnnt2a ZFA:0000007 blood PATO:0002269 accumulation abnormal ZFA:0001079 blood vasculature ZDB-GENE-000626-1 58071 7139 tnnt2a ZFA:0000007 blood PATO:0002269 accumulation abnormal ZFA:0001115 trunk ZDB-GENE-000626-1 58071 7139 tnnt2a ZFA:0000007 blood PATO:0001574 flow rate abnormal ZDB-GENE-000626-1 58071 7139 tnnt2a ZFA:0000008 brain PATO:0000001 quality abnormal ZDB-GENE-000626-1 58071 7139 tnnt2a ZFA:0000008 brain PATO:0000587 decreased size abnormal ZDB-GENE-000626-1 58071 7139 tnnt2a GO:0060048 cardiac muscle contraction BFO:0000066 occurs_in ZFA:0000009 cardiac ventricle PATO:0000297 arrested abnormal ZDB-GENE-000626-1 58071 7139 tnnt2a ZFA:0005059 trabecular layer BFO:0000050 part_of ZFA:0000009 cardiac ventricle PATO:0000462 absent abnormal ZDB-GENE-000626-1 58071 7139 tnnt2a ZFA:0000009 cardiac ventricle PATO:0000587 decreased size abnormal ZDB-GENE-000626-1 58071 7139 tnnt2a ZFA:0000009 cardiac ventricle PATO:0001602 distended abnormal ZDB-GENE-000626-1 58071 7139 tnnt2a ZFA:0000009 cardiac ventricle PATO:0001624 decreased functionality abnormal ZDB-GENE-000626-1 58071 7139 tnnt2a ZFA:0000009 cardiac ventricle PATO:0001715 decreased diameter abnormal ZDB-GENE-000626-1 58071 7139 tnnt2a ZFA:0009181 vascular associated smooth muscle cell BFO:0000050 part_of ZFA:0000014 dorsal aorta PATO:0001997 decreased amount abnormal ZDB-GENE-000626-1 58071 7139 tnnt2a ZFA:0000014 dorsal aorta PATO:0000141 structure abnormal ZDB-GENE-000626-1 58071 7139 tnnt2a ZFA:0000014 dorsal aorta PATO:0001571 dilated abnormal ZDB-GENE-000626-1 58071 7139 tnnt2a ZFA:0000014 dorsal aorta PATO:0001896 unlumenized abnormal ZDB-GENE-000626-1 58071 7139 tnnt2a ZFA:0000054 pericardium PATO:0001450 edematous abnormal ZDB-GENE-000626-1 58071 7139 tnnt2a ZFA:0000099 brain vasculature PATO:0002105 hemorrhagic abnormal ZDB-GENE-000626-1 58071 7139 tnnt2a ZFA:0000110 fourth ventricle PATO:0001715 decreased diameter abnormal ZDB-GENE-000626-1 58071 7139 tnnt2a GO:0006874 intracellular calcium ion homeostasis BFO:0000066 occurs_in ZFA:0000114 heart PATO:0001236 process quality abnormal ZDB-GENE-000626-1 58071 7139 tnnt2a GO:0006936 muscle contraction BFO:0000066 occurs_in ZFA:0000114 heart PATO:0000297 arrested abnormal ZDB-GENE-000626-1 58071 7139 tnnt2a GO:0007219 Notch signaling pathway BFO:0000066 occurs_in ZFA:0000114 heart PATO:0002302 decreased process quality abnormal ZDB-GENE-000626-1 58071 7139 tnnt2a ZFA:0000114 heart PATO:0000001 quality abnormal ZDB-GENE-000626-1 58071 7139 tnnt2a ZFA:0000114 heart PATO:0000051 morphology abnormal ZDB-GENE-000626-1 58071 7139 tnnt2a ZFA:0000114 heart PATO:0000586 increased size abnormal ZDB-GENE-000626-1 58071 7139 tnnt2a ZFA:0000114 heart PATO:0000587 decreased size abnormal ZDB-GENE-000626-1 58071 7139 tnnt2a ZFA:0000114 heart PATO:0001511 non-functional abnormal ZDB-GENE-000626-1 58071 7139 tnnt2a ZFA:0000114 heart PATO:0001598 protruding abnormal ZDB-GENE-000626-1 58071 7139 tnnt2a ZFA:0000114 heart PATO:0001691 non-contractile abnormal ZDB-GENE-000626-1 58071 7139 tnnt2a ZFA:0000123 liver PATO:0000587 decreased size abnormal ZDB-GENE-000626-1 58071 7139 tnnt2a ZFA:0001079 blood vasculature BFO:0000050 part_of ZFA:0000128 midbrain PATO:0002001 has fewer parts of type abnormal ZFA:0005314 blood vessel ZDB-GENE-000626-1 58071 7139 tnnt2a ZFA:0001079 blood vasculature BFO:0000050 part_of ZFA:0000128 midbrain PATO:0000051 morphology abnormal ZDB-GENE-000626-1 58071 7139 tnnt2a ZFA:0000170 basibranchial PATO:0001485 condensed abnormal ZDB-GENE-000626-1 58071 7139 tnnt2a GO:0048745 smooth muscle tissue development BFO:0000066 occurs_in ZFA:0000173 bulbus arteriosus PATO:0002302 decreased process quality abnormal ZDB-GENE-000626-1 58071 7139 tnnt2a ZFA:0000173 bulbus arteriosus PATO:0002000 lacks all parts of type abnormal ZFA:0001375 ventriculo bulbo valve ZDB-GENE-000626-1 58071 7139 tnnt2a ZFA:0000173 bulbus arteriosus PATO:0001715 decreased diameter abnormal ZDB-GENE-000626-1 58071 7139 tnnt2a ZFA:0009036 blood vessel endothelial cell BFO:0000050 part_of ZFA:0000186 common cardinal vein PATO:0001997 decreased amount abnormal ZDB-GENE-000626-1 58071 7139 tnnt2a GO:0048599 oocyte development BFO:0000066 occurs_in ZFA:0000303 female organism PATO:0002302 decreased process quality abnormal ZDB-GENE-000626-1 58071 7139 tnnt2a ZFA:0000423 anterior cardinal vein PATO:0001896 unlumenized abnormal ZDB-GENE-000626-1 58071 7139 tnnt2a GO:1904124 microglial cell migration BFO:0000066 occurs_in ZFA:0000445 optic tectum PATO:0001236 process quality abnormal ZDB-GENE-000626-1 58071 7139 tnnt2a ZFA:0009077 microglial cell BFO:0000050 part_of ZFA:0000445 optic tectum PATO:0001997 decreased amount abnormal ZDB-GENE-000626-1 58071 7139 tnnt2a ZFA:0000445 optic tectum PATO:0000599 decreased width abnormal ZDB-GENE-000626-1 58071 7139 tnnt2a CHEBI:3815 Collagen BFO:0000050 part_of ZFA:0000471 atrium PATO:0000470 increased amount abnormal ZDB-GENE-000626-1 58071 7139 tnnt2a CHEBI:5054 Fibrin BFO:0000050 part_of ZFA:0000471 atrium PATO:0000470 increased amount abnormal ZDB-GENE-000626-1 58071 7139 tnnt2a CHEBI:5054 Fibrin BFO:0000050 part_of ZFA:0000471 atrium PATO:0001671 increased distribution abnormal ZDB-GENE-000626-1 58071 7139 tnnt2a GO:0060048 cardiac muscle contraction BFO:0000066 occurs_in ZFA:0000471 atrium PATO:0000297 arrested abnormal ZDB-GENE-000626-1 58071 7139 tnnt2a ZFA:0001319 myocardium BFO:0000050 part_of ZFA:0000471 atrium PATO:0000591 increased thickness abnormal ZDB-GENE-000626-1 58071 7139 tnnt2a ZFA:0000471 atrium PATO:0000586 increased size abnormal ZDB-GENE-000626-1 58071 7139 tnnt2a ZFA:0000471 atrium PATO:0000644 hyperplastic abnormal ZDB-GENE-000626-1 58071 7139 tnnt2a ZFA:0000471 atrium PATO:0001571 dilated abnormal ZDB-GENE-000626-1 58071 7139 tnnt2a ZFA:0000471 atrium PATO:0001602 distended abnormal ZDB-GENE-000626-1 58071 7139 tnnt2a ZFA:0000477 posterior cardinal vein PATO:0001896 unlumenized abnormal ZDB-GENE-000626-1 58071 7139 tnnt2a GO:0043534 blood vessel endothelial cell migration BFO:0000066 occurs_in ZFA:0001051 caudal division of the internal carotid artery PATO:0001236 process quality abnormal ZDB-GENE-000626-1 58071 7139 tnnt2a ZFA:0001054 lateral dorsal aorta PATO:0000051 morphology abnormal ZDB-GENE-000626-1 58071 7139 tnnt2a ZFA:0009354 hematopoietic multipotent progenitor cell BFO:0000050 part_of ZFA:0001078 thymus PATO:0001997 decreased amount abnormal ZDB-GENE-000626-1 58071 7139 tnnt2a ZFA:0001078 thymus PATO:0000587 decreased size abnormal ZDB-GENE-000626-1 58071 7139 tnnt2a ZFA:0001094 whole organism PATO:0000169 viability abnormal ZDB-GENE-000626-1 58071 7139 tnnt2a ZFA:0001094 whole organism PATO:0000574 decreased length abnormal ZDB-GENE-000626-1 58071 7139 tnnt2a ZFA:0001094 whole organism PATO:0000718 lethal (sensu genetics) abnormal ZDB-GENE-000626-1 58071 7139 tnnt2a ZFA:0001094 whole organism PATO:0001422 dead abnormal ZDB-GENE-000626-1 58071 7139 tnnt2a ZFA:0001094 whole organism PATO:0001604 decreased life span abnormal ZDB-GENE-000626-1 58071 7139 tnnt2a BSPO:0000055 anterior side BFO:0000050 part_of ZFA:0001115 trunk PATO:0002270 increased accumulation abnormal ZFA:0009256 nucleate erythrocyte ZDB-GENE-000626-1 58071 7139 tnnt2a ZFA:0009354 hematopoietic multipotent progenitor cell BFO:0000050 part_of ZFA:0001115 trunk PATO:0001997 decreased amount abnormal ZDB-GENE-000626-1 58071 7139 tnnt2a ZFA:0001261 ventricular system PATO:0000587 decreased size abnormal ZDB-GENE-000626-1 58071 7139 tnnt2a ZFA:0001267 cranial vasculature PATO:0001896 unlumenized abnormal ZDB-GENE-000626-1 58071 7139 tnnt2a ZFA:0001272 palatoquadrate arch PATO:0000574 decreased length abnormal ZDB-GENE-000626-1 58071 7139 tnnt2a GO:0072554 blood vessel lumenization BFO:0000066 occurs_in ZFA:0001285 intersegmental vessel PATO:0001236 process quality abnormal ZDB-GENE-000626-1 58071 7139 tnnt2a ZFA:0001285 intersegmental vessel PATO:0000051 morphology abnormal ZDB-GENE-000626-1 58071 7139 tnnt2a ZFA:0001285 intersegmental vessel PATO:0000141 structure abnormal ZDB-GENE-000626-1 58071 7139 tnnt2a ZFA:0001285 intersegmental vessel PATO:0000587 decreased size abnormal ZDB-GENE-000626-1 58071 7139 tnnt2a ZFA:0001285 intersegmental vessel PATO:0001478 collapsed abnormal ZDB-GENE-000626-1 58071 7139 tnnt2a ZFA:0001285 intersegmental vessel PATO:0001896 unlumenized abnormal ZDB-GENE-000626-1 58071 7139 tnnt2a ZFA:0001285 intersegmental vessel PATO:0002014 structure, cavities abnormal ZDB-GENE-000626-1 58071 7139 tnnt2a GO:0002040 sprouting angiogenesis BFO:0000066 occurs_in ZFA:0001286 caudal vein plexus PATO:0002051 increased occurrence abnormal ZDB-GENE-000626-1 58071 7139 tnnt2a GO:0002040 sprouting angiogenesis BFO:0000066 occurs_in ZFA:0001286 caudal vein plexus PATO:0002052 decreased occurrence abnormal ZDB-GENE-000626-1 58071 7139 tnnt2a ZFA:0005604 angiogenic sprout BFO:0000050 part_of ZFA:0001286 caudal vein plexus PATO:0000470 increased amount abnormal ZDB-GENE-000626-1 58071 7139 tnnt2a ZFA:0001286 caudal vein plexus PATO:0000642 fused with abnormal ZFA:0001286 caudal vein plexus ZDB-GENE-000626-1 58071 7139 tnnt2a ZFA:0001286 caudal vein plexus PATO:0000051 morphology abnormal ZDB-GENE-000626-1 58071 7139 tnnt2a ZFA:0001286 caudal vein plexus PATO:0000587 decreased size abnormal ZDB-GENE-000626-1 58071 7139 tnnt2a ZFA:0001286 caudal vein plexus PATO:0000646 malformed abnormal ZDB-GENE-000626-1 58071 7139 tnnt2a ZFA:0001320 endocardium PATO:0000585 hypotrophic abnormal ZDB-GENE-000626-1 58071 7139 tnnt2a GO:0001837 epithelial to mesenchymal transition BFO:0000066 occurs_in ZFA:0001345 interrenal gland PATO:0002052 decreased occurrence abnormal ZDB-GENE-000626-1 58071 7139 tnnt2a GO:0009887 animal organ morphogenesis BFO:0000066 occurs_in ZFA:0001345 interrenal gland PATO:0001236 process quality abnormal ZDB-GENE-000626-1 58071 7139 tnnt2a ZFA:0001345 interrenal gland PATO:0000140 position abnormal ZDB-GENE-000626-1 58071 7139 tnnt2a ZFA:0001346 interrenal primordium PATO:0000140 position abnormal ZDB-GENE-000626-1 58071 7139 tnnt2a ZFA:0001400 ceratohyal cartilage PATO:0000133 orientation abnormal ZFA:0001400 ceratohyal cartilage ZDB-GENE-000626-1 58071 7139 tnnt2a ZFA:0001439 anatomical system PATO:0000001 quality abnormal ZDB-GENE-000626-1 58071 7139 tnnt2a ZFA:0001496 simple columnar epithelium PATO:0002181 displaced abnormal ZDB-GENE-000626-1 58071 7139 tnnt2a ZFA:0001497 simple cuboidal epithelium PATO:0002181 displaced abnormal ZDB-GENE-000626-1 58071 7139 tnnt2a ZFA:0001516 ceratobranchial cartilage PATO:0000133 orientation abnormal ZFA:0001516 ceratobranchial cartilage ZDB-GENE-000626-1 58071 7139 tnnt2a BSPO:0000007 right side BFO:0000050 part_of ZFA:0001557 pronephric glomerulus PATO:0000651 unfused from abnormal BSPO:0000000 left side BFO:0000050 part_of ZFA:0001557 pronephric glomerulus ZDB-GENE-000626-1 58071 7139 tnnt2a ZFA:0001557 pronephric glomerulus PATO:0000651 unfused from abnormal ZFA:0001557 pronephric glomerulus ZDB-GENE-000626-1 58071 7139 tnnt2a ZFA:0001557 pronephric glomerulus PATO:0001505 separated from abnormal ZFA:0001557 pronephric glomerulus ZDB-GENE-000626-1 58071 7139 tnnt2a ZFA:0001557 pronephric glomerulus PATO:0002000 lacks all parts of type abnormal ZFA:0005309 pronephric glomerular capillary ZDB-GENE-000626-1 58071 7139 tnnt2a ZFA:0001557 pronephric glomerulus PATO:0000051 morphology abnormal ZDB-GENE-000626-1 58071 7139 tnnt2a ZFA:0001557 pronephric glomerulus PATO:0000645 hypoplastic abnormal ZDB-GENE-000626-1 58071 7139 tnnt2a ZFA:0001557 pronephric glomerulus PATO:0000937 disorganized abnormal ZDB-GENE-000626-1 58071 7139 tnnt2a ZFA:0001639 vascular endothelium PATO:0000586 increased size abnormal ZDB-GENE-000626-1 58071 7139 tnnt2a ZFA:0001639 vascular endothelium PATO:0000628 mislocalised abnormal ZDB-GENE-000626-1 58071 7139 tnnt2a ZFA:0005002 basilar artery PATO:0001715 decreased diameter abnormal ZDB-GENE-000626-1 58071 7139 tnnt2a GO:0043534 blood vessel endothelial cell migration BFO:0000066 occurs_in ZFA:0005005 aortic arch 1 PATO:0001236 process quality abnormal ZDB-GENE-000626-1 58071 7139 tnnt2a GO:0060973 cell migration involved in heart development BFO:0000066 occurs_in ZFA:0005005 aortic arch 1 PATO:0002052 decreased occurrence abnormal ZDB-GENE-000626-1 58071 7139 tnnt2a ZFA:0005604 angiogenic sprout BFO:0000050 part_of ZFA:0005020 central artery PATO:0000470 increased amount abnormal ZDB-GENE-000626-1 58071 7139 tnnt2a ZFA:0005020 central artery PATO:0001241 physical object quality abnormal ZDB-GENE-000626-1 58071 7139 tnnt2a ZFA:0005020 central artery PATO:0001715 decreased diameter abnormal ZDB-GENE-000626-1 58071 7139 tnnt2a ZFA:0005023 hematopoietic system PATO:0001624 decreased functionality abnormal ZDB-GENE-000626-1 58071 7139 tnnt2a GO:0072554 blood vessel lumenization BFO:0000066 occurs_in ZFA:0005024 trunk vasculature PATO:0002302 decreased process quality abnormal ZDB-GENE-000626-1 58071 7139 tnnt2a ZFA:0005024 trunk vasculature PATO:0000051 morphology abnormal ZDB-GENE-000626-1 58071 7139 tnnt2a ZFA:0005028 ventral wall of dorsal aorta PATO:0002001 has fewer parts of type abnormal ZFA:0009014 hematopoietic stem cell ZDB-GENE-000626-1 58071 7139 tnnt2a GO:0048514 blood vessel morphogenesis BFO:0000066 occurs_in ZFA:0005035 subintestinal vein PATO:0001507 disrupted abnormal ZDB-GENE-000626-1 58071 7139 tnnt2a ZFA:0005035 subintestinal vein PATO:0000051 morphology abnormal ZDB-GENE-000626-1 58071 7139 tnnt2a ZFA:0005037 post-vent vasculature PATO:0000051 morphology abnormal ZDB-GENE-000626-1 58071 7139 tnnt2a ZFA:0005059 trabecular layer PATO:0000462 absent abnormal ZDB-GENE-000626-1 58071 7139 tnnt2a ZFA:0005059 trabecular layer PATO:0001483 aplastic abnormal ZDB-GENE-000626-1 58071 7139 tnnt2a GO:0030017 sarcomere BFO:0000050 part_of ZFA:0005061 ventricular myocardium PATO:0000937 disorganized abnormal ZDB-GENE-000626-1 58071 7139 tnnt2a ZFA:0005063 cardiac conduction system PATO:0000628 mislocalised abnormal ZDB-GENE-000626-1 58071 7139 tnnt2a ZFA:0005069 sinoatrial node PATO:0002057 increased area abnormal ZDB-GENE-000626-1 58071 7139 tnnt2a GO:0043534 blood vessel endothelial cell migration BFO:0000066 occurs_in ZFA:0005081 internal carotid artery PATO:0001236 process quality abnormal ZDB-GENE-000626-1 58071 7139 tnnt2a ZFA:0005091 hepatic sinusoid PATO:0001483 aplastic abnormal ZDB-GENE-000626-1 58071 7139 tnnt2a ZFA:0005309 pronephric glomerular capillary PATO:0000586 increased size abnormal ZDB-GENE-000626-1 58071 7139 tnnt2a ZFA:0005314 blood vessel PATO:0001478 collapsed abnormal ZDB-GENE-000626-1 58071 7139 tnnt2a ZFA:0005802 interrenal angiogenic sprout PATO:0001923 mislocalised laterally abnormal ZDB-GENE-000626-1 58071 7139 tnnt2a ZFA:0009014 hematopoietic stem cell PATO:0001997 decreased amount abnormal ZDB-GENE-000626-1 58071 7139 tnnt2a GO:0006915 apoptotic process BFO:0000066 occurs_in ZFA:0009065 endothelial cell PATO:0002051 increased occurrence abnormal ZDB-GENE-000626-1 58071 7139 tnnt2a GO:0006915 apoptotic process BFO:0000066 occurs_in ZFA:0009065 endothelial cell PATO:0002051 increased occurrence ameliorated ZDB-GENE-000626-1 58071 7139 tnnt2a ZFA:0009099 chromaffin cell PATO:0000628 mislocalised abnormal ZDB-GENE-000626-1 58071 7139 tnnt2a GO:0007219 Notch signaling pathway BFO:0000066 occurs_in ZFA:0009316 cardiac muscle cell PATO:0002302 decreased process quality abnormal ZDB-GENE-000626-1 58071 7139 tnnt2a GO:0030017 sarcomere BFO:0000050 part_of ZFA:0009316 cardiac muscle cell PATO:0000937 disorganized abnormal ZDB-GENE-000626-1 58071 7139 tnnt2a GO:0042995 cell projection BFO:0000050 part_of ZFA:0009316 cardiac muscle cell PATO:0002292 transient abnormal ZDB-GENE-000626-1 58071 7139 tnnt2a ZFA:0009316 cardiac muscle cell PATO:0000470 increased amount abnormal ZDB-GENE-000626-1 58071 7139 tnnt2a ZFA:0009316 cardiac muscle cell PATO:0001464 electric potential abnormal ZDB-GENE-000626-1 58071 7139 tnnt2a ZFA:0009316 cardiac muscle cell PATO:0002058 decreased area abnormal ZDB-GENE-000626-1 58071 7139 tnnt2a ZFA:0009354 hematopoietic multipotent progenitor cell PATO:0001997 decreased amount abnormal ZDB-GENE-000627-2 58134 104 adarb1a GO:0001755 neural crest cell migration PATO:0001236 process quality abnormal ZDB-GENE-000627-2 58134 104 adarb1a GO:0006915 apoptotic process PATO:0002304 increased process quality abnormal ZDB-GENE-000627-2 58134 104 adarb1a GO:0006915 apoptotic process BFO:0000066 occurs_in ZFA:0000029 hindbrain PATO:0002304 increased process quality abnormal ZDB-GENE-000627-2 58134 104 adarb1a ZFA:0000075 spinal cord PATO:0002001 has fewer parts of type abnormal ZFA:0009052 motor neuron ZDB-GENE-000627-2 58134 104 adarb1a GO:0006915 apoptotic process BFO:0000066 occurs_in ZFA:0000107 eye PATO:0002304 increased process quality abnormal ZDB-GENE-000627-2 58134 104 adarb1a ZFA:0000110 fourth ventricle PATO:0000586 increased size abnormal ZDB-GENE-000627-2 58134 104 adarb1a GO:0006915 apoptotic process BFO:0000066 occurs_in ZFA:0000128 midbrain PATO:0002304 increased process quality abnormal ZDB-GENE-000627-2 58134 104 adarb1a ZFA:0000161 third ventricle PATO:0000586 increased size abnormal ZDB-GENE-000627-2 58134 104 adarb1a GO:0006915 apoptotic process BFO:0000066 occurs_in ZFA:0000671 horizontal myoseptum PATO:0002304 increased process quality abnormal ZDB-GENE-000627-2 58134 104 adarb1a ZFA:0000940 posterior lateral line neuromast PATO:0001997 decreased amount abnormal ZDB-GENE-000627-2 58134 104 adarb1a GO:0006915 apoptotic process BFO:0000066 occurs_in ZFA:0001114 head PATO:0002304 increased process quality abnormal ZDB-GENE-000627-2 58134 104 adarb1a ZFA:0001114 head PATO:0000587 decreased size abnormal ZDB-GENE-000627-2 58134 104 adarb1a GO:0006915 apoptotic process BFO:0000066 occurs_in ZFA:0001115 trunk PATO:0002304 increased process quality abnormal ZDB-GENE-000627-2 58134 104 adarb1a ZFA:0001306 pharyngeal arch PATO:0000462 absent abnormal ZDB-GENE-000627-2 58134 104 adarb1a ZFA:0001306 pharyngeal arch PATO:0000587 decreased size abnormal ZDB-GENE-000627-2 58134 104 adarb1a ZFA:0001321 neurocranial trabecula PATO:0000587 decreased size abnormal ZDB-GENE-000627-2 58134 104 adarb1a ZFA:0001405 ethmoid cartilage PATO:0000462 absent abnormal ZDB-GENE-000627-2 58134 104 adarb1a ZFA:0001423 parachordal cartilage PATO:0000587 decreased size abnormal ZDB-GENE-000627-2 58134 104 adarb1a ZFA:0001458 cranial cartilage PATO:0000646 malformed abnormal ZDB-GENE-000627-2 58134 104 adarb1a ZFA:0001472 anterior lateral line neuromast PATO:0001997 decreased amount abnormal ZDB-GENE-000629-1 58101 6175 rplp0 ZFA:0000035 lens PATO:0000587 decreased size abnormal ZDB-GENE-000629-1 58101 6175 rplp0 ZFA:0000042 midbrain hindbrain boundary PATO:0001483 aplastic abnormal ZDB-GENE-000629-1 58101 6175 rplp0 ZFA:0000100 cerebellum PATO:0000592 decreased thickness abnormal ZDB-GENE-000629-1 58101 6175 rplp0 ZFA:0000106 extension PATO:0000592 decreased thickness abnormal ZDB-GENE-000629-1 58101 6175 rplp0 ZFA:0000108 fin PATO:0001483 aplastic abnormal ZDB-GENE-000629-1 58101 6175 rplp0 ZFA:0000110 fourth ventricle PATO:0000963 opaque abnormal ZDB-GENE-000629-1 58101 6175 rplp0 ZFA:0000138 otic placode PATO:0000587 decreased size abnormal ZDB-GENE-000629-1 58101 6175 rplp0 ZFA:0000152 retina PATO:0000587 decreased size abnormal ZDB-GENE-000629-1 58101 6175 rplp0 ZFA:0000445 optic tectum PATO:0000586 increased size abnormal ZDB-GENE-000629-1 58101 6175 rplp0 ZFA:0001117 post-vent region PATO:0000617 bent abnormal ZDB-GENE-000629-3 795398 4904 ybx1 GO:0001556 oocyte maturation PATO:0002052 decreased occurrence abnormal ZDB-GENE-000629-3 795398 4904 ybx1 GO:0001756 somitogenesis PATO:0000502 delayed abnormal ZDB-GENE-000629-3 795398 4904 ybx1 GO:0006396 RNA processing PATO:0000694 premature abnormal ZDB-GENE-000629-3 795398 4904 ybx1 GO:0006412 translation PATO:0002051 increased occurrence abnormal ZDB-GENE-000629-3 795398 4904 ybx1 GO:0006413 translational initiation PATO:0000694 premature abnormal ZDB-GENE-000629-3 795398 4904 ybx1 GO:0007021 tubulin complex assembly PATO:0002052 decreased occurrence abnormal ZDB-GENE-000629-3 795398 4904 ybx1 GO:0007049 cell cycle PATO:0000297 arrested abnormal ZDB-GENE-000629-3 795398 4904 ybx1 GO:0007343 egg activation PATO:0001236 process quality abnormal ZDB-GENE-000629-3 795398 4904 ybx1 GO:0007369 gastrulation PATO:0000297 arrested abnormal ZDB-GENE-000629-3 795398 4904 ybx1 GO:0007369 gastrulation PATO:0000498 increased duration abnormal ZDB-GENE-000629-3 795398 4904 ybx1 GO:0007369 gastrulation PATO:0000502 delayed abnormal ZDB-GENE-000629-3 795398 4904 ybx1 GO:0008283 cell population proliferation PATO:0001236 process quality abnormal ZDB-GENE-000629-3 795398 4904 ybx1 GO:0030968 endoplasmic reticulum unfolded protein response PATO:0002051 increased occurrence abnormal ZDB-GENE-000629-3 795398 4904 ybx1 GO:0036089 cleavage furrow formation PATO:0002052 decreased occurrence abnormal ZDB-GENE-000629-3 795398 4904 ybx1 GO:0038092 nodal signaling pathway PATO:0000694 premature abnormal ZDB-GENE-000629-3 795398 4904 ybx1 GO:0040016 embryonic cleavage PATO:0001236 process quality abnormal ZDB-GENE-000629-3 795398 4904 ybx1 GO:0055113 epiboly involved in gastrulation with mouth forming second PATO:0000297 arrested abnormal ZDB-GENE-000629-3 795398 4904 ybx1 GO:0055113 epiboly involved in gastrulation with mouth forming second PATO:0002325 onset quality abnormal ZDB-GENE-000629-3 795398 4904 ybx1 GO:0060471 cortical granule exocytosis PATO:0002052 decreased occurrence abnormal ZDB-GENE-000629-3 795398 4904 ybx1 GO:0090504 epiboly PATO:0000297 arrested abnormal ZDB-GENE-000629-3 795398 4904 ybx1 GO:1900107 regulation of nodal signaling pathway PATO:0001236 process quality abnormal ZDB-GENE-000629-3 795398 4904 ybx1 GO:0005634 nucleus BFO:0000050 part_of ZFA:0000088 yolk syncytial layer PATO:0000470 increased amount abnormal ZDB-GENE-000629-3 795398 4904 ybx1 GO:0005634 nucleus BFO:0000050 part_of ZFA:0000093 blastomere PATO:0001444 broken abnormal ZDB-GENE-000629-3 795398 4904 ybx1 GO:0005643 nuclear pore BFO:0000050 part_of ZFA:0000093 blastomere PATO:0000462 absent abnormal ZDB-GENE-000629-3 795398 4904 ybx1 GO:0005886 plasma membrane BFO:0000050 part_of ZFA:0000093 blastomere PATO:0000141 structure abnormal ZDB-GENE-000629-3 795398 4904 ybx1 GO:0006403 RNA localization BFO:0000066 occurs_in ZFA:0000093 blastomere PATO:0000502 delayed abnormal ZDB-GENE-000629-3 795398 4904 ybx1 ZFA:0000093 blastomere PATO:0000052 shape abnormal ZDB-GENE-000629-3 795398 4904 ybx1 ZFA:0000093 blastomere PATO:0000140 position abnormal ZDB-GENE-000629-3 795398 4904 ybx1 ZFA:0000329 chorion PATO:0001689 decreased elevation abnormal ZDB-GENE-000629-3 795398 4904 ybx1 ZFA:0000329 chorion PATO:0001715 decreased diameter abnormal ZDB-GENE-000629-3 795398 4904 ybx1 CHEBI:75909 double-stranded DNA fragment BFO:0000050 part_of ZFA:0001094 whole organism PATO:0001997 decreased amount abnormal ZDB-GENE-000629-3 795398 4904 ybx1 ZFA:0001094 whole organism PATO:0000169 viability abnormal ZDB-GENE-000629-3 795398 4904 ybx1 ZFA:0001094 whole organism PATO:0001604 decreased life span abnormal ZDB-GENE-000629-3 795398 4904 ybx1 GO:0006508 proteolysis BFO:0000066 occurs_in ZFA:0001569 oocyte stage V PATO:0002052 decreased occurrence abnormal ZDB-GENE-000629-3 795398 4904 ybx1 ZFA:0001569 oocyte stage V PATO:0000963 opaque abnormal ZDB-GENE-000629-3 795398 4904 ybx1 ZFA:0001569 oocyte stage V PATO:0001501 immature abnormal ZDB-GENE-000629-3 795398 4904 ybx1 GO:0060473 cortical granule BFO:0000050 part_of ZFA:0005772 fertilized egg PATO:0000470 increased amount abnormal ZDB-GENE-000710-4 58077 7546 zic2a GO:0001755 neural crest cell migration PATO:0002302 decreased process quality abnormal ZDB-GENE-000710-4 58077 7546 zic2a GO:0008589 regulation of smoothened signaling pathway PATO:0001507 disrupted abnormal ZDB-GENE-000710-4 58077 7546 zic2a GO:0021536 diencephalon development PATO:0001507 disrupted abnormal ZDB-GENE-000710-4 58077 7546 zic2a GO:0022008 neurogenesis PATO:0001507 disrupted abnormal ZDB-GENE-000710-4 58077 7546 zic2a GO:0030900 forebrain development PATO:0002302 decreased process quality abnormal ZDB-GENE-000710-4 58077 7546 zic2a GO:0045892 negative regulation of DNA-templated transcription PATO:0001507 disrupted abnormal ZDB-GENE-000710-4 58077 7546 zic2a GO:0048702 embryonic neurocranium morphogenesis PATO:0002302 decreased process quality abnormal ZDB-GENE-000710-4 58077 7546 zic2a GO:0048703 embryonic viscerocranium morphogenesis PATO:0002302 decreased process quality abnormal ZDB-GENE-000710-4 58077 7546 zic2a GO:0050936 xanthophore differentiation PATO:0002302 decreased process quality abnormal ZDB-GENE-000710-4 58077 7546 zic2a ZFA:0000029 hindbrain PATO:0000646 malformed abnormal ZDB-GENE-000710-4 58077 7546 zic2a ZFA:0000032 hypothalamus PATO:0001396 cellular quality abnormal ZDB-GENE-000710-4 58077 7546 zic2a ZFA:0000046 retinal neural layer PATO:0000587 decreased size abnormal ZDB-GENE-000710-4 58077 7546 zic2a ZFA:0000110 fourth ventricle PATO:0000646 malformed abnormal ZDB-GENE-000710-4 58077 7546 zic2a ZFA:0000128 midbrain PATO:0000646 malformed abnormal ZDB-GENE-000710-4 58077 7546 zic2a ZFA:0000159 tectal ventricle PATO:0000646 malformed abnormal ZDB-GENE-000710-4 58077 7546 zic2a ZFA:0000458 ventral thalamus PATO:0000587 decreased size abnormal ZDB-GENE-000710-4 58077 7546 zic2a ZFA:0000458 ventral thalamus PATO:0001396 cellular quality abnormal ZDB-GENE-000710-4 58077 7546 zic2a ZFA:0001114 head PATO:0002001 has fewer parts of type abnormal ZFA:0005245 xanthoblast ZDB-GENE-000710-4 58077 7546 zic2a ZFA:0001115 trunk PATO:0002001 has fewer parts of type abnormal ZFA:0005245 xanthoblast ZDB-GENE-000710-4 58077 7546 zic2a ZFA:0001135 neural tube PATO:0000646 malformed abnormal ZDB-GENE-000710-4 58077 7546 zic2a ZFA:0001194 cranial neural crest PATO:0001919 mislocalised dorsally abnormal ZDB-GENE-000710-4 58077 7546 zic2a ZFA:0001273 ventral mandibular arch PATO:0000646 malformed abnormal ZDB-GENE-000710-4 58077 7546 zic2a ZFA:0001284 optic fissure PATO:0000609 closure incomplete abnormal ZDB-GENE-000710-4 58077 7546 zic2a ZFA:0001284 optic fissure PATO:0000646 malformed abnormal ZDB-GENE-000710-4 58077 7546 zic2a ZFA:0001290 stomodeum PATO:0000587 decreased size abnormal ZDB-GENE-000710-4 58077 7546 zic2a ZFA:0001306 pharyngeal arch PATO:0001396 cellular quality abnormal ZDB-GENE-000710-4 58077 7546 zic2a ZFA:0001321 neurocranial trabecula PATO:0002364 shortened abnormal ZDB-GENE-000710-4 58077 7546 zic2a BSPO:0000083 medial region BFO:0000050 part_of ZFA:0001405 ethmoid cartilage PATO:0000462 absent abnormal ZDB-GENE-000710-4 58077 7546 zic2a ZFA:0001460 pharyngeal arch cartilage PATO:0000645 hypoplastic abnormal ZDB-GENE-000710-4 58077 7546 zic2a ZFA:0001611 pharyngeal arch 2 PATO:0000587 decreased size abnormal ZDB-GENE-000710-4 58077 7546 zic2a ZFA:0001611 pharyngeal arch 2 PATO:0000646 malformed abnormal ZDB-GENE-000710-4 58077 7546 zic2a ZFA:0001612 pharyngeal arch 1 PATO:0000587 decreased size abnormal ZDB-GENE-000804-1 58107 8863 per3 GO:0032922 circadian regulation of gene expression PATO:0001236 process quality abnormal ZDB-GENE-000816-1 58129 2261 fgfr3 GO:0033687 osteoblast proliferation PATO:0002052 decreased occurrence abnormal ZDB-GENE-000816-1 58129 2261 fgfr3 GO:0035988 chondrocyte proliferation PATO:0002051 increased occurrence abnormal ZDB-GENE-000816-1 58129 2261 fgfr3 GO:0060218 hematopoietic stem cell differentiation PATO:0002052 decreased occurrence abnormal ZDB-GENE-000816-1 58129 2261 fgfr3 BSPO:0000087 anterior compartment BFO:0000050 part_of ZFA:0000076 swim bladder PATO:0001667 attached to abnormal ZFA:0001188 Weberian apparatus ZDB-GENE-000816-1 58129 2261 fgfr3 ZFA:0000076 swim bladder PATO:0000411 circular abnormal ZDB-GENE-000816-1 58129 2261 fgfr3 ZFA:0000076 swim bladder PATO:0000462 absent abnormal ZDB-GENE-000816-1 58129 2261 fgfr3 GO:0001957 intramembranous ossification BFO:0000066 occurs_in ZFA:0000191 dentary PATO:0000502 delayed abnormal ZDB-GENE-000816-1 58129 2261 fgfr3 ZFA:0000191 dentary PATO:0002480 poorly ossified abnormal ZDB-GENE-000816-1 58129 2261 fgfr3 GO:0001957 intramembranous ossification BFO:0000066 occurs_in ZFA:0000250 opercle PATO:0000502 delayed abnormal ZDB-GENE-000816-1 58129 2261 fgfr3 ZFA:0000250 opercle PATO:0002480 poorly ossified abnormal ZDB-GENE-000816-1 58129 2261 fgfr3 ZFA:0000263 precaudal vertebra PATO:0002259 adjacent to abnormal ZFA:0000538 rib ZDB-GENE-000816-1 58129 2261 fgfr3 ZFA:0000277 scale PATO:0001997 decreased amount abnormal ZDB-GENE-000816-1 58129 2261 fgfr3 ZFA:0000277 scale PATO:0002444 mineralized abnormal ZDB-GENE-000816-1 58129 2261 fgfr3 ZFA:0009084 chondrocyte BFO:0000050 part_of ZFA:0000316 basihyal bone PATO:0000117 size abnormal ZDB-GENE-000816-1 58129 2261 fgfr3 ZFA:0009084 chondrocyte BFO:0000050 part_of ZFA:0000316 basihyal bone PATO:0000937 disorganized abnormal ZDB-GENE-000816-1 58129 2261 fgfr3 ZFA:0009084 chondrocyte BFO:0000050 part_of ZFA:0000316 basihyal bone PATO:0002186 polarity abnormal ZDB-GENE-000816-1 58129 2261 fgfr3 ZFA:0000316 basihyal bone PATO:0002480 poorly ossified abnormal ZDB-GENE-000816-1 58129 2261 fgfr3 ZFA:0000354 gill PATO:0002425 exposed abnormal ZDB-GENE-000816-1 58129 2261 fgfr3 ZFA:0000363 hypobranchial bone PATO:0002480 poorly ossified abnormal ZDB-GENE-000816-1 58129 2261 fgfr3 GO:0001958 endochondral ossification BFO:0000066 occurs_in ZFA:0000422 retroarticular PATO:0000502 delayed abnormal ZDB-GENE-000816-1 58129 2261 fgfr3 ZFA:0000422 retroarticular PATO:0002480 poorly ossified abnormal ZDB-GENE-000816-1 58129 2261 fgfr3 GO:0001503 ossification BFO:0000066 occurs_in ZFA:0000429 scaphium PATO:0000502 delayed abnormal ZDB-GENE-000816-1 58129 2261 fgfr3 ZFA:0000429 scaphium PATO:0000051 morphology abnormal ZDB-GENE-000816-1 58129 2261 fgfr3 ZFA:0000429 scaphium PATO:0002480 poorly ossified abnormal ZDB-GENE-000816-1 58129 2261 fgfr3 ZFA:0000444 suspensorium PATO:0000574 decreased length abnormal ZDB-GENE-000816-1 58129 2261 fgfr3 GO:0001503 ossification BFO:0000066 occurs_in ZFA:0000476 branchiostegal ray PATO:0000502 delayed abnormal ZDB-GENE-000816-1 58129 2261 fgfr3 GO:0001957 intramembranous ossification BFO:0000066 occurs_in ZFA:0000476 branchiostegal ray PATO:0000502 delayed abnormal ZDB-GENE-000816-1 58129 2261 fgfr3 GO:0048856 anatomical structure development BFO:0000066 occurs_in ZFA:0000476 branchiostegal ray PATO:0000502 delayed abnormal ZDB-GENE-000816-1 58129 2261 fgfr3 ZFA:0000476 branchiostegal ray PATO:0002480 poorly ossified abnormal ZDB-GENE-000816-1 58129 2261 fgfr3 GO:0001503 ossification BFO:0000066 occurs_in ZFA:0000486 parietal bone PATO:0000502 delayed abnormal ZDB-GENE-000816-1 58129 2261 fgfr3 GO:0001503 ossification BFO:0000066 occurs_in ZFA:0000514 frontal bone PATO:0000502 delayed abnormal ZDB-GENE-000816-1 58129 2261 fgfr3 GO:0001503 ossification BFO:0000066 occurs_in ZFA:0000525 intercalarium PATO:0000502 delayed abnormal ZDB-GENE-000816-1 58129 2261 fgfr3 ZFA:0000525 intercalarium PATO:0000051 morphology abnormal ZDB-GENE-000816-1 58129 2261 fgfr3 ZFA:0000525 intercalarium PATO:0002480 poorly ossified abnormal ZDB-GENE-000816-1 58129 2261 fgfr3 GO:0001503 ossification BFO:0000066 occurs_in ZFA:0000578 ceratohyal bone PATO:0000502 delayed abnormal ZDB-GENE-000816-1 58129 2261 fgfr3 ZFA:0009084 chondrocyte BFO:0000050 part_of ZFA:0000578 ceratohyal bone PATO:0000117 size abnormal ZDB-GENE-000816-1 58129 2261 fgfr3 ZFA:0009084 chondrocyte BFO:0000050 part_of ZFA:0000578 ceratohyal bone PATO:0000937 disorganized abnormal ZDB-GENE-000816-1 58129 2261 fgfr3 ZFA:0009084 chondrocyte BFO:0000050 part_of ZFA:0000578 ceratohyal bone PATO:0002186 polarity abnormal ZDB-GENE-000816-1 58129 2261 fgfr3 ZFA:0000578 ceratohyal bone PATO:0002480 poorly ossified abnormal ZDB-GENE-000816-1 58129 2261 fgfr3 GO:0001503 ossification BFO:0000066 occurs_in ZFA:0000637 claustrum cartilage PATO:0000502 delayed abnormal ZDB-GENE-000816-1 58129 2261 fgfr3 GO:0001503 ossification BFO:0000066 occurs_in ZFA:0000698 tripus PATO:0000502 delayed abnormal ZDB-GENE-000816-1 58129 2261 fgfr3 ZFA:0000698 tripus PATO:0000051 morphology abnormal ZDB-GENE-000816-1 58129 2261 fgfr3 ZFA:0000698 tripus PATO:0000574 decreased length abnormal ZDB-GENE-000816-1 58129 2261 fgfr3 ZFA:0000698 tripus PATO:0002480 poorly ossified abnormal ZDB-GENE-000816-1 58129 2261 fgfr3 ZFA:0000737 cranium PATO:0000609 closure incomplete abnormal ZDB-GENE-000816-1 58129 2261 fgfr3 ZFA:0001094 whole organism PATO:0000574 decreased length abnormal ZDB-GENE-000816-1 58129 2261 fgfr3 ZFA:0001114 head PATO:0000587 decreased size abnormal ZDB-GENE-000816-1 58129 2261 fgfr3 ZFA:0001115 trunk PATO:0001798 kinked abnormal ZDB-GENE-000816-1 58129 2261 fgfr3 ZFA:0001188 Weberian apparatus PATO:0000051 morphology abnormal ZDB-GENE-000816-1 58129 2261 fgfr3 ZFA:0009084 chondrocyte BFO:0000050 part_of ZFA:0001205 Meckel's cartilage PATO:0000330 irregular spatial pattern abnormal ZDB-GENE-000816-1 58129 2261 fgfr3 ZFA:0009084 chondrocyte BFO:0000050 part_of ZFA:0001205 Meckel's cartilage PATO:0000584 hypertrophic abnormal ZDB-GENE-000816-1 58129 2261 fgfr3 ZFA:0009314 columnar chondrocyte BFO:0000050 part_of ZFA:0001205 Meckel's cartilage PATO:0000937 disorganized abnormal ZDB-GENE-000816-1 58129 2261 fgfr3 ZFA:0001227 mandibular arch skeleton PATO:0000616 asymmetrical abnormal ZDB-GENE-000816-1 58129 2261 fgfr3 ZFA:0001227 mandibular arch skeleton PATO:0000646 malformed abnormal ZDB-GENE-000816-1 58129 2261 fgfr3 GO:0001958 endochondral ossification BFO:0000066 occurs_in ZFA:0001399 palatoquadrate cartilage PATO:0000502 delayed abnormal ZDB-GENE-000816-1 58129 2261 fgfr3 ZFA:0009084 chondrocyte BFO:0000050 part_of ZFA:0001399 palatoquadrate cartilage PATO:0000584 hypertrophic abnormal ZDB-GENE-000816-1 58129 2261 fgfr3 GO:0001503 ossification BFO:0000066 occurs_in ZFA:0001400 ceratohyal cartilage PATO:0000502 delayed abnormal ZDB-GENE-000816-1 58129 2261 fgfr3 GO:0036073 perichondral ossification BFO:0000066 occurs_in ZFA:0001400 ceratohyal cartilage PATO:0000502 delayed abnormal ZDB-GENE-000816-1 58129 2261 fgfr3 ZFA:0009084 chondrocyte BFO:0000050 part_of ZFA:0001400 ceratohyal cartilage PATO:0000052 shape abnormal ZDB-GENE-000816-1 58129 2261 fgfr3 ZFA:0009084 chondrocyte BFO:0000050 part_of ZFA:0001400 ceratohyal cartilage PATO:0000117 size abnormal ZDB-GENE-000816-1 58129 2261 fgfr3 ZFA:0009084 chondrocyte BFO:0000050 part_of ZFA:0001400 ceratohyal cartilage PATO:0000628 mislocalised abnormal ZDB-GENE-000816-1 58129 2261 fgfr3 ZFA:0001400 ceratohyal cartilage PATO:0000573 increased length abnormal ZDB-GENE-000816-1 58129 2261 fgfr3 GO:0001503 ossification BFO:0000066 occurs_in ZFA:0001510 basihyal cartilage PATO:0000502 delayed abnormal ZDB-GENE-000816-1 58129 2261 fgfr3 ZFA:0009084 chondrocyte BFO:0000050 part_of ZFA:0001510 basihyal cartilage PATO:0000330 irregular spatial pattern abnormal ZDB-GENE-000816-1 58129 2261 fgfr3 ZFA:0009084 chondrocyte BFO:0000050 part_of ZFA:0001510 basihyal cartilage PATO:0000584 hypertrophic abnormal ZDB-GENE-000816-1 58129 2261 fgfr3 ZFA:0009314 columnar chondrocyte BFO:0000050 part_of ZFA:0001510 basihyal cartilage PATO:0000937 disorganized abnormal ZDB-GENE-000816-1 58129 2261 fgfr3 GO:0001958 endochondral ossification BFO:0000066 occurs_in ZFA:0001516 ceratobranchial cartilage PATO:0000502 delayed abnormal ZDB-GENE-000816-1 58129 2261 fgfr3 GO:0001958 endochondral ossification BFO:0000066 occurs_in ZFA:0001522 hypobranchial cartilage PATO:0000502 delayed abnormal ZDB-GENE-000816-1 58129 2261 fgfr3 ZFA:0001592 claustrum bone PATO:0000051 morphology abnormal ZDB-GENE-000816-1 58129 2261 fgfr3 ZFA:0001592 claustrum bone PATO:0002480 poorly ossified abnormal ZDB-GENE-000816-1 58129 2261 fgfr3 ZFA:0001611 pharyngeal arch 2 PATO:0000051 morphology abnormal ZDB-GENE-000816-1 58129 2261 fgfr3 ZFA:0001611 pharyngeal arch 2 PATO:0000616 asymmetrical abnormal ZDB-GENE-000816-1 58129 2261 fgfr3 ZFA:0001611 pharyngeal arch 2 PATO:0002165 drooping abnormal ZDB-GENE-000816-1 58129 2261 fgfr3 ZFA:0001612 pharyngeal arch 1 PATO:0000051 morphology abnormal ZDB-GENE-000816-1 58129 2261 fgfr3 GO:0001503 ossification BFO:0000066 occurs_in ZFA:0001635 intramembranous bone PATO:0002018 decreased magnitude abnormal ZDB-GENE-000816-1 58129 2261 fgfr3 ZFA:0005606 cranial vault PATO:0001617 deformed abnormal ZDB-GENE-000816-1 58129 2261 fgfr3 ZFA:0005606 cranial vault PATO:0001789 domed abnormal ZDB-GENE-000816-1 58129 2261 fgfr3 GO:0098645 collagen network BFO:0000050 part_of ZFA:0009084 chondrocyte PATO:0000937 disorganized abnormal ZDB-GENE-000823-6 58052 3215 hoxb5b ZFA:0000008 brain PATO:0000645 hypoplastic abnormal ZDB-GENE-000823-6 58052 3215 hoxb5b GO:0030424 axon BFO:0000050 part_of ZFA:0000012 central nervous system PATO:0000574 decreased length abnormal ZDB-GENE-000823-6 58052 3215 hoxb5b ZFA:0000054 pericardium PATO:0001450 edematous abnormal ZDB-GENE-000823-6 58052 3215 hoxb5b ZFA:0000107 eye PATO:0000645 hypoplastic abnormal ZDB-GENE-000823-6 58052 3215 hoxb5b ZFA:0000114 heart PATO:0000586 increased size abnormal ZDB-GENE-000823-6 58052 3215 hoxb5b ZFA:0009316 cardiac muscle cell BFO:0000050 part_of ZFA:0000471 atrium PATO:0000470 increased amount abnormal ZDB-GENE-000823-6 58052 3215 hoxb5b ZFA:0001094 whole organism PATO:0000587 decreased size abnormal ZDB-GENE-000823-6 58052 3215 hoxb5b ZFA:0001115 trunk PATO:0000051 morphology abnormal ZDB-GENE-000823-6 58052 3215 hoxb5b ZFA:0009234 cardiac muscle myoblast BFO:0000050 part_of ZFA:0001721 presumptive atrium primitive heart tube PATO:0000470 increased amount abnormal ZDB-GENE-000828-1 58152 6334 scn8aa GO:0001764 neuron migration PATO:0001236 process quality abnormal ZDB-GENE-000828-1 58152 6334 scn8aa GO:0001966 thigmotaxis PATO:0002052 decreased occurrence abnormal ZDB-GENE-000828-1 58152 6334 scn8aa GO:0005248 voltage-gated sodium channel activity PATO:0000080 amplitude abnormal ZDB-GENE-000828-1 58152 6334 scn8aa GO:0005248 voltage-gated sodium channel activity PATO:0002052 decreased occurrence abnormal ZDB-GENE-000828-1 58152 6334 scn8aa GO:0007638 mechanosensory behavior PATO:0001507 disrupted abnormal ZDB-GENE-000828-1 58152 6334 scn8aa GO:0008345 larval locomotory behavior PATO:0002052 decreased occurrence abnormal ZDB-GENE-000828-1 58152 6334 scn8aa GO:0030182 neuron differentiation PATO:0001236 process quality abnormal ZDB-GENE-000828-1 58152 6334 scn8aa GO:0050975 sensory perception of touch PATO:0002018 decreased magnitude abnormal ZDB-GENE-000828-1 58152 6334 scn8aa GO:0044303 axon collateral BFO:0000050 part_of ZFA:0000200 dorsal root ganglion PATO:0001923 mislocalised laterally abnormal ZDB-GENE-000828-1 58152 6334 scn8aa ZFA:0009009 neuron neural crest derived BFO:0000050 part_of ZFA:0000200 dorsal root ganglion PATO:0001920 mislocalised ventrally abnormal ZDB-GENE-000828-1 58152 6334 scn8aa ZFA:0009248 neuron BFO:0000050 part_of ZFA:0000200 dorsal root ganglion PATO:0000299 mobile abnormal ZDB-GENE-000828-1 58152 6334 scn8aa ZFA:0009248 neuron BFO:0000050 part_of ZFA:0000200 dorsal root ganglion PATO:0001920 mislocalised ventrally abnormal ZDB-GENE-000828-1 58152 6334 scn8aa ZFA:0001094 whole organism PATO:0001422 dead abnormal ZDB-GENE-000828-1 58152 6334 scn8aa ZFA:0001094 whole organism PATO:0002076 movement behavioral quality abnormal ZDB-GENE-000828-1 58152 6334 scn8aa GO:0001518 voltage-gated sodium channel complex BFO:0000050 part_of ZFA:0009120 mechanoreceptor cell PATO:0001624 decreased functionality abnormal ZDB-GENE-000828-1 58152 6334 scn8aa ZFA:0009150 Rohon-Beard neuron PATO:0000467 present abnormal ZDB-GENE-000828-1 58152 6334 scn8aa ZFA:0009150 Rohon-Beard neuron PATO:0001462 membrane potential abnormal ZDB-GENE-000828-1 58152 6334 scn8aa ZFA:0009150 Rohon-Beard neuron PATO:0001603 increased life span abnormal ZDB-GENE-000828-1 58152 6334 scn8aa ZFA:0009150 Rohon-Beard neuron PATO:0001624 decreased functionality abnormal ZDB-GENE-000828-1 58152 6334 scn8aa ZFA:0009244 primary motor neuron PATO:0001624 decreased functionality abnormal ZDB-GENE-000828-1 58152 6334 scn8aa GO:0030424 axon BFO:0000050 part_of ZFA:0009247 secondary motor neuron PATO:0000629 misrouted abnormal ZDB-GENE-000830-1 58112 644524 nkx2.4b ZFA:0000368 integument PATO:0040048 erythematous abnormal ZDB-GENE-000830-1 58112 644524 nkx2.4b ZFA:0009091 melanocyte PATO:0000470 increased amount abnormal ZDB-GENE-000831-1 58068 5091 pcxb GO:0048565 digestive tract development PATO:0001236 process quality abnormal ZDB-GENE-000831-1 58068 5091 pcxb ZFA:0000054 pericardium PATO:0001450 edematous abnormal ZDB-GENE-000831-1 58068 5091 pcxb ZFA:0001161 pectoral fin PATO:0000462 absent abnormal ZDB-GENE-000831-1 58068 5091 pcxb GO:0051216 cartilage development BFO:0000066 occurs_in ZFA:0001227 mandibular arch skeleton PATO:0002052 decreased occurrence abnormal ZDB-GENE-000831-3 796322 6520 slc3a2a ZFA:0001117 post-vent region PATO:0001469 curved ventral abnormal ZDB-GENE-000906-1 58040 6710 sptb ZFA:0000007 blood PATO:0000001 quality abnormal ZDB-GENE-000906-1 58040 6710 sptb ZFA:0000009 cardiac ventricle PATO:0001571 dilated abnormal ZDB-GENE-000906-1 58040 6710 sptb ZFA:0000471 atrium PATO:0001571 dilated abnormal ZDB-GENE-000906-1 58040 6710 sptb ZFA:0000529 kidney PATO:0002002 has extra parts of type abnormal ZFA:0009015 erythroid progenitor cell ZDB-GENE-000906-1 58040 6710 sptb ZFA:0000529 kidney PATO:0000586 increased size abnormal ZDB-GENE-000906-1 58040 6710 sptb ZFA:0000529 kidney PATO:0000644 hyperplastic abnormal ZDB-GENE-000906-1 58040 6710 sptb ZFA:0001439 anatomical system PATO:0000001 quality abnormal ZDB-GENE-000906-1 58040 6710 sptb GO:0005634 nucleus BFO:0000050 part_of ZFA:0009256 nucleate erythrocyte PATO:0000141 structure abnormal ZDB-GENE-000906-1 58040 6710 sptb ZFA:0009256 nucleate erythrocyte PATO:0000052 shape abnormal ZDB-GENE-000906-1 58040 6710 sptb ZFA:0009256 nucleate erythrocyte PATO:0000462 absent abnormal ZDB-GENE-000906-1 58040 6710 sptb ZFA:0009256 nucleate erythrocyte PATO:0001406 binucleate abnormal ZDB-GENE-000906-1 58040 6710 sptb ZFA:0009256 nucleate erythrocyte PATO:0001499 spherical abnormal ZDB-GENE-000906-1 58040 6710 sptb ZFA:0009256 nucleate erythrocyte PATO:0001997 decreased amount abnormal ZDB-GENE-000906-1 58040 6710 sptb ZFA:0009256 nucleate erythrocyte PATO:0002240 teardrop-shaped abnormal ZDB-GENE-000906-2 58041 3336 hspe1 ZFA:0000076 swim bladder PATO:0001958 increased variability of size abnormal ZDB-GENE-000906-2 58041 3336 hspe1 ZFA:0000076 swim bladder PATO:0002377 uninflated abnormal ZDB-GENE-000906-2 58041 3336 hspe1 ZFA:0001094 whole organism PATO:0000574 decreased length abnormal ZDB-GENE-000920-1 58032 1906 edn1 GO:0001503 ossification PATO:0001507 disrupted abnormal ZDB-GENE-000920-1 58032 1906 edn1 GO:0014707 branchiomeric skeletal muscle development PATO:0002302 decreased process quality abnormal ZDB-GENE-000920-1 58032 1906 edn1 GO:0048703 embryonic viscerocranium morphogenesis PATO:0001507 disrupted abnormal ZDB-GENE-000920-1 58032 1906 edn1 GO:0048703 embryonic viscerocranium morphogenesis PATO:0002302 decreased process quality abnormal ZDB-GENE-000920-1 58032 1906 edn1 GO:0060037 pharyngeal system development PATO:0001507 disrupted abnormal ZDB-GENE-000920-1 58032 1906 edn1 GO:0060536 cartilage morphogenesis PATO:0001507 disrupted abnormal ZDB-GENE-000920-1 58032 1906 edn1 ZFA:0000095 pharyngeal arch 3-7 skeleton PATO:0000001 quality abnormal ZDB-GENE-000920-1 58032 1906 edn1 ZFA:0000136 otic lateral line neuromast PATO:0001997 decreased amount abnormal ZDB-GENE-000920-1 58032 1906 edn1 ZFA:0000184 cleithrum PATO:0000574 decreased length abnormal ZDB-GENE-000920-1 58032 1906 edn1 ZFA:0000184 cleithrum PATO:0000646 malformed abnormal ZDB-GENE-000920-1 58032 1906 edn1 ZFA:0000191 dentary PATO:0000642 fused with abnormal ZFA:0000270 maxilla ZDB-GENE-000920-1 58032 1906 edn1 ZFA:0000191 dentary PATO:0000646 malformed abnormal ZDB-GENE-000920-1 58032 1906 edn1 ZFA:0000191 dentary PATO:0001467 curved caudal abnormal ZDB-GENE-000920-1 58032 1906 edn1 ZFA:0000236 mandibular muscle PATO:0000620 wholly dorsalized abnormal ZDB-GENE-000920-1 58032 1906 edn1 ZFA:0005155 cartilaginous joint BFO:0000050 part_of ZFA:0000250 opercle PATO:0000591 increased thickness abnormal ZDB-GENE-000920-1 58032 1906 edn1 ZFA:0005155 cartilaginous joint BFO:0000050 part_of ZFA:0000250 opercle PATO:0001602 distended abnormal ZDB-GENE-000920-1 58032 1906 edn1 ZFA:0000250 opercle PATO:0000052 shape abnormal ZDB-GENE-000920-1 58032 1906 edn1 ZFA:0000250 opercle PATO:0000117 size abnormal ZDB-GENE-000920-1 58032 1906 edn1 ZFA:0000250 opercle PATO:0000586 increased size abnormal ZDB-GENE-000920-1 58032 1906 edn1 ZFA:0000250 opercle PATO:0000587 decreased size abnormal ZDB-GENE-000920-1 58032 1906 edn1 ZFA:0000250 opercle PATO:0000600 increased width abnormal ZDB-GENE-000920-1 58032 1906 edn1 ZFA:0000250 opercle PATO:0001483 aplastic abnormal ZDB-GENE-000920-1 58032 1906 edn1 ZFA:0000250 opercle PATO:0001958 increased variability of size abnormal ZDB-GENE-000920-1 58032 1906 edn1 ZFA:0000270 maxilla PATO:0000646 malformed abnormal ZDB-GENE-000920-1 58032 1906 edn1 ZFA:0000270 maxilla PATO:0001467 curved caudal abnormal ZDB-GENE-000920-1 58032 1906 edn1 ZFA:0000422 retroarticular PATO:0000462 absent abnormal ZDB-GENE-000920-1 58032 1906 edn1 ZFA:0000476 branchiostegal ray PATO:0000140 position abnormal ZDB-GENE-000920-1 58032 1906 edn1 ZFA:0000476 branchiostegal ray PATO:0000587 decreased size abnormal ZDB-GENE-000920-1 58032 1906 edn1 ZFA:0000476 branchiostegal ray PATO:0000646 malformed abnormal ZDB-GENE-000920-1 58032 1906 edn1 ZFA:0000476 branchiostegal ray PATO:0002215 falciform abnormal ZDB-GENE-000920-1 58032 1906 edn1 ZFA:0000547 mouth PATO:0000001 quality abnormal ZDB-GENE-000920-1 58032 1906 edn1 ZFA:0000547 mouth PATO:0002008 concave 3-D shape abnormal ZDB-GENE-000920-1 58032 1906 edn1 ZFA:0000692 symplectic PATO:0000462 absent abnormal ZDB-GENE-000920-1 58032 1906 edn1 ZFA:0000692 symplectic PATO:0000587 decreased size abnormal ZDB-GENE-000920-1 58032 1906 edn1 ZFA:0000813 infraorbital lateral line neuromast PATO:0001997 decreased amount abnormal ZDB-GENE-000920-1 58032 1906 edn1 ZFA:0000814 opercular lateral line neuromast PATO:0000462 absent abnormal ZDB-GENE-000920-1 58032 1906 edn1 ZFA:0000814 opercular lateral line neuromast PATO:0001919 mislocalised dorsally abnormal ZDB-GENE-000920-1 58032 1906 edn1 ZFA:0000814 opercular lateral line neuromast PATO:0001997 decreased amount abnormal ZDB-GENE-000920-1 58032 1906 edn1 ZFA:0000939 middle lateral line neuromast PATO:0001997 decreased amount abnormal ZDB-GENE-000920-1 58032 1906 edn1 ZFA:0001094 whole organism PATO:0000718 lethal (sensu genetics) abnormal ZDB-GENE-000920-1 58032 1906 edn1 ZFA:0001114 head PATO:0002000 lacks all parts of type abnormal ZFA:0007008 ventral intermandibularis anterior ZDB-GENE-000920-1 58032 1906 edn1 ZFA:0001114 head PATO:0002000 lacks all parts of type abnormal ZFA:0007048 ventral intermandibularis posterior ZDB-GENE-000920-1 58032 1906 edn1 ZFA:0001128 pharyngeal pouch 1 PATO:0001241 physical object quality abnormal ZDB-GENE-000920-1 58032 1906 edn1 ZFA:0001205 Meckel's cartilage PATO:0000642 fused with abnormal ZFA:0001272 palatoquadrate arch ZDB-GENE-000920-1 58032 1906 edn1 ZFA:0001205 Meckel's cartilage PATO:0000642 fused with abnormal ZFA:0001399 palatoquadrate cartilage ZDB-GENE-000920-1 58032 1906 edn1 ZFA:0001205 Meckel's cartilage PATO:0000051 morphology abnormal ZDB-GENE-000920-1 58032 1906 edn1 ZFA:0001205 Meckel's cartilage PATO:0000462 absent abnormal ZDB-GENE-000920-1 58032 1906 edn1 ZFA:0001205 Meckel's cartilage PATO:0000587 decreased size abnormal ZDB-GENE-000920-1 58032 1906 edn1 ZFA:0001205 Meckel's cartilage PATO:0000617 bent abnormal ZDB-GENE-000920-1 58032 1906 edn1 ZFA:0001205 Meckel's cartilage PATO:0000645 hypoplastic abnormal ZDB-GENE-000920-1 58032 1906 edn1 ZFA:0001205 Meckel's cartilage PATO:0001469 curved ventral abnormal ZDB-GENE-000920-1 58032 1906 edn1 ZFA:0001205 Meckel's cartilage PATO:0001483 aplastic abnormal ZDB-GENE-000920-1 58032 1906 edn1 ZFA:0001205 Meckel's cartilage PATO:0001598 protruding abnormal ZDB-GENE-000920-1 58032 1906 edn1 ZFA:0001205 Meckel's cartilage PATO:0001922 mislocalised posteriorly abnormal ZDB-GENE-000920-1 58032 1906 edn1 ZFA:0001216 splanchnocranium PATO:0000001 quality abnormal ZDB-GENE-000920-1 58032 1906 edn1 ZFA:0001596 joint BFO:0000050 part_of ZFA:0001227 mandibular arch skeleton PATO:0000462 absent abnormal ZDB-GENE-000920-1 58032 1906 edn1 ZFA:0001228 pharyngeal arch 3 skeleton PATO:0000574 decreased length abnormal ZDB-GENE-000920-1 58032 1906 edn1 ZFA:0001231 pharyngeal arch 4 skeleton PATO:0000574 decreased length abnormal ZDB-GENE-000920-1 58032 1906 edn1 ZFA:0001239 ceratobranchial 5 bone PATO:0000574 decreased length abnormal ZDB-GENE-000920-1 58032 1906 edn1 ZFA:0001239 ceratobranchial 5 bone PATO:0000646 malformed abnormal ZDB-GENE-000920-1 58032 1906 edn1 ZFA:0001273 ventral mandibular arch PATO:0000133 orientation abnormal ZFA:0000107 eye ZDB-GENE-000920-1 58032 1906 edn1 ZFA:0001273 ventral mandibular arch PATO:0000587 decreased size abnormal ZDB-GENE-000920-1 58032 1906 edn1 ZFA:0001273 ventral mandibular arch PATO:0001483 aplastic abnormal ZDB-GENE-000920-1 58032 1906 edn1 ZFA:0001276 pharyngeal arch 2 skeleton PATO:0000587 decreased size abnormal ZDB-GENE-000920-1 58032 1906 edn1 ZFA:0001290 stomodeum PATO:0001920 mislocalised ventrally abnormal ZDB-GENE-000920-1 58032 1906 edn1 ZFA:0001399 palatoquadrate cartilage PATO:0000642 fused with abnormal ZFA:0001205 Meckel's cartilage ZDB-GENE-000920-1 58032 1906 edn1 ZFA:0001399 palatoquadrate cartilage PATO:0000642 fused with abnormal ZFA:0001422 hyosymplectic cartilage ZDB-GENE-000920-1 58032 1906 edn1 ZFA:0001399 palatoquadrate cartilage PATO:0000573 increased length abnormal ZDB-GENE-000920-1 58032 1906 edn1 ZFA:0001399 palatoquadrate cartilage PATO:0000587 decreased size abnormal ZDB-GENE-000920-1 58032 1906 edn1 ZFA:0001400 ceratohyal cartilage PATO:0000051 morphology abnormal ZDB-GENE-000920-1 58032 1906 edn1 ZFA:0001400 ceratohyal cartilage PATO:0000141 structure abnormal ZDB-GENE-000920-1 58032 1906 edn1 ZFA:0001400 ceratohyal cartilage PATO:0000462 absent abnormal ZDB-GENE-000920-1 58032 1906 edn1 ZFA:0001400 ceratohyal cartilage PATO:0000587 decreased size abnormal ZDB-GENE-000920-1 58032 1906 edn1 ZFA:0001400 ceratohyal cartilage PATO:0000625 inverted abnormal ZDB-GENE-000920-1 58032 1906 edn1 ZFA:0001400 ceratohyal cartilage PATO:0000645 hypoplastic abnormal ZDB-GENE-000920-1 58032 1906 edn1 ZFA:0001400 ceratohyal cartilage PATO:0001469 curved ventral abnormal ZDB-GENE-000920-1 58032 1906 edn1 ZFA:0001400 ceratohyal cartilage PATO:0001483 aplastic abnormal ZDB-GENE-000920-1 58032 1906 edn1 ZFA:0001400 ceratohyal cartilage PATO:0001617 deformed abnormal ZDB-GENE-000920-1 58032 1906 edn1 ZFA:0001402 ventral hyoid arch PATO:0000051 morphology abnormal ZDB-GENE-000920-1 58032 1906 edn1 ZFA:0001422 hyosymplectic cartilage PATO:0000642 fused with abnormal ZFA:0001400 ceratohyal cartilage ZDB-GENE-000920-1 58032 1906 edn1 ZFA:0001422 hyosymplectic cartilage PATO:0000600 increased width abnormal ZDB-GENE-000920-1 58032 1906 edn1 ZFA:0001422 hyosymplectic cartilage PATO:0001483 aplastic abnormal ZDB-GENE-000920-1 58032 1906 edn1 BSPO:0000084 ventral region BFO:0000050 part_of ZFA:0001460 pharyngeal arch cartilage PATO:0000051 morphology abnormal ZDB-GENE-000920-1 58032 1906 edn1 BSPO:0000084 ventral region BFO:0000050 part_of ZFA:0001460 pharyngeal arch cartilage PATO:0001997 decreased amount abnormal ZDB-GENE-000920-1 58032 1906 edn1 ZFA:0001472 anterior lateral line neuromast PATO:0000470 increased amount abnormal ZDB-GENE-000920-1 58032 1906 edn1 ZFA:0001472 anterior lateral line neuromast PATO:0000628 mislocalised abnormal ZDB-GENE-000920-1 58032 1906 edn1 ZFA:0001510 basihyal cartilage PATO:0001617 deformed abnormal ZDB-GENE-000920-1 58032 1906 edn1 ZFA:0001511 interhyal cartilage PATO:0000462 absent abnormal ZDB-GENE-000920-1 58032 1906 edn1 ZFA:0001517 ceratobranchial 2 cartilage PATO:0000462 absent abnormal ZDB-GENE-000920-1 58032 1906 edn1 ZFA:0001518 ceratobranchial 3 cartilage PATO:0000462 absent abnormal ZDB-GENE-000920-1 58032 1906 edn1 ZFA:0001519 ceratobranchial 4 cartilage PATO:0000462 absent abnormal ZDB-GENE-000920-1 58032 1906 edn1 ZFA:0001520 ceratobranchial 1 cartilage PATO:0000462 absent abnormal ZDB-GENE-000920-1 58032 1906 edn1 BSPO:0000084 ventral region BFO:0000050 part_of ZFA:0001606 pharyngeal arch 3 PATO:0001241 physical object quality abnormal ZDB-GENE-000920-1 58032 1906 edn1 ZFA:0009081 mesenchymal cell BFO:0000050 part_of ZFA:0001606 pharyngeal arch 3 PATO:0001241 physical object quality abnormal ZDB-GENE-000920-1 58032 1906 edn1 BSPO:0000084 ventral region BFO:0000050 part_of ZFA:0001607 pharyngeal arch 4 PATO:0001241 physical object quality abnormal ZDB-GENE-000920-1 58032 1906 edn1 ZFA:0009081 mesenchymal cell BFO:0000050 part_of ZFA:0001607 pharyngeal arch 4 PATO:0001241 physical object quality abnormal ZDB-GENE-000920-1 58032 1906 edn1 BSPO:0000084 ventral region BFO:0000050 part_of ZFA:0001611 pharyngeal arch 2 PATO:0000587 decreased size abnormal ZDB-GENE-000920-1 58032 1906 edn1 BSPO:0000084 ventral region BFO:0000050 part_of ZFA:0001611 pharyngeal arch 2 PATO:0001241 physical object quality abnormal ZDB-GENE-000920-1 58032 1906 edn1 BSPO:0000084 ventral region BFO:0000050 part_of ZFA:0001611 pharyngeal arch 2 PATO:0001997 decreased amount abnormal ZDB-GENE-000920-1 58032 1906 edn1 ZFA:0009081 mesenchymal cell BFO:0000050 part_of ZFA:0001611 pharyngeal arch 2 PATO:0001241 physical object quality abnormal ZDB-GENE-000920-1 58032 1906 edn1 ZFA:0001611 pharyngeal arch 2 PATO:0000140 position abnormal ZDB-GENE-000920-1 58032 1906 edn1 ZFA:0001611 pharyngeal arch 2 PATO:0000646 malformed abnormal ZDB-GENE-000920-1 58032 1906 edn1 BSPO:0000084 ventral region BFO:0000050 part_of ZFA:0001612 pharyngeal arch 1 PATO:0000587 decreased size abnormal ZDB-GENE-000920-1 58032 1906 edn1 BSPO:0000084 ventral region BFO:0000050 part_of ZFA:0001612 pharyngeal arch 1 PATO:0001241 physical object quality abnormal ZDB-GENE-000920-1 58032 1906 edn1 BSPO:0000084 ventral region BFO:0000050 part_of ZFA:0001612 pharyngeal arch 1 PATO:0001997 decreased amount abnormal ZDB-GENE-000920-1 58032 1906 edn1 ZFA:0000393 mesenchyme BFO:0000050 part_of ZFA:0001612 pharyngeal arch 1 PATO:0002058 decreased area abnormal ZDB-GENE-000920-1 58032 1906 edn1 ZFA:0001596 joint BFO:0000050 part_of ZFA:0001612 pharyngeal arch 1 PATO:0001241 physical object quality abnormal ZDB-GENE-000920-1 58032 1906 edn1 ZFA:0009081 mesenchymal cell BFO:0000050 part_of ZFA:0001612 pharyngeal arch 1 PATO:0001241 physical object quality abnormal ZDB-GENE-000920-1 58032 1906 edn1 ZFA:0001612 pharyngeal arch 1 PATO:0000140 position abnormal ZDB-GENE-000920-1 58032 1906 edn1 ZFA:0001612 pharyngeal arch 1 PATO:0000574 decreased length abnormal ZDB-GENE-000920-1 58032 1906 edn1 ZFA:0001612 pharyngeal arch 1 PATO:0000646 malformed abnormal ZDB-GENE-000920-1 58032 1906 edn1 ZFA:0005465 ceratohyal-branchiostegal ray joint PATO:0000051 morphology abnormal ZDB-GENE-000920-1 58032 1906 edn1 ZFA:0005473 interhyal-epihyal joint PATO:0000462 absent abnormal ZDB-GENE-000920-1 58032 1906 edn1 ZFA:0005484 quadrate-anguloarticular joint PATO:0000462 absent abnormal ZDB-GENE-000920-1 58032 1906 edn1 ZFA:0007008 ventral intermandibularis anterior PATO:0001241 physical object quality abnormal ZDB-GENE-000920-1 58032 1906 edn1 ZFA:0007048 ventral intermandibularis posterior PATO:0001241 physical object quality abnormal ZDB-GENE-000920-1 58032 1906 edn1 ZFA:0007051 interhyoideus PATO:0000574 decreased length abnormal ZDB-GENE-000920-1 58032 1906 edn1 ZFA:0007051 interhyoideus PATO:0001241 physical object quality abnormal ZDB-GENE-000920-1 58032 1906 edn1 ZFA:0007052 hyohyoideus PATO:0000574 decreased length abnormal ZDB-GENE-000926-1 58216 220202 atoh7 GO:0007610 behavior PATO:0001236 process quality abnormal ZDB-GENE-000926-1 58216 220202 atoh7 GO:0031290 retinal ganglion cell axon guidance PATO:0001507 disrupted abnormal ZDB-GENE-000926-1 58216 220202 atoh7 GO:0032400 melanosome localization PATO:0001507 disrupted abnormal ZDB-GENE-000926-1 58216 220202 atoh7 GO:0036269 swimming behavior PATO:0000499 decreased duration abnormal ZDB-GENE-000926-1 58216 220202 atoh7 GO:0036269 swimming behavior PATO:0001507 disrupted abnormal ZDB-GENE-000926-1 58216 220202 atoh7 GO:0043482 cellular pigment accumulation PATO:0000297 arrested abnormal ZDB-GENE-000926-1 58216 220202 atoh7 GO:0060041 retina development in camera-type eye PATO:0001507 disrupted abnormal ZDB-GENE-000926-1 58216 220202 atoh7 GO:0071632 optomotor response PATO:0002302 decreased process quality abnormal ZDB-GENE-000926-1 58216 220202 atoh7 ZFA:0000107 eye PATO:0000001 quality abnormal ZDB-GENE-000926-1 58216 220202 atoh7 ZFA:0000107 eye PATO:0000051 morphology abnormal ZDB-GENE-000926-1 58216 220202 atoh7 ZFA:0000107 eye PATO:0000587 decreased size abnormal ZDB-GENE-000926-1 58216 220202 atoh7 ZFA:0009127 photoreceptor cell BFO:0000050 part_of ZFA:0000143 retinal photoreceptor layer PATO:0000462 absent abnormal ZDB-GENE-000926-1 58216 220202 atoh7 ZFA:0000282 sensory system PATO:0000001 quality abnormal ZDB-GENE-000926-1 58216 220202 atoh7 ZFA:0000396 nervous system PATO:0000001 quality abnormal ZDB-GENE-000926-1 58216 220202 atoh7 ZFA:0001329 retinal inner plexiform layer PATO:0000591 increased thickness abnormal ZDB-GENE-000926-1 58216 220202 atoh7 ZFA:0009090 pigment cell PATO:0000001 quality abnormal ZDB-GENE-000926-1 58216 220202 atoh7 GO:0042470 melanosome BFO:0000050 part_of ZFA:0009091 melanocyte PATO:0000060 spatial pattern abnormal ZDB-GENE-000926-1 58216 220202 atoh7 GO:0042470 melanosome BFO:0000050 part_of ZFA:0009091 melanocyte PATO:0001630 dispersed abnormal ZDB-GENE-000926-1 58216 220202 atoh7 ZFA:0009091 melanocyte PATO:0001323 area abnormal ZDB-GENE-000926-1 58216 220202 atoh7 ZFA:0009310 retinal ganglion cell PATO:0000462 absent abnormal ZDB-GENE-000926-1 58216 220202 atoh7 ZFA:0009310 retinal ganglion cell PATO:0001997 decreased amount abnormal ZDB-GENE-000926-1 58216 220202 atoh7 ZFA:0009318 retinal bipolar neuron PATO:0000470 increased amount abnormal ZDB-GENE-000928-1 58215 2235 fech GO:0006783 heme biosynthetic process PATO:0001507 disrupted abnormal ZDB-GENE-000928-1 58215 2235 fech ZFA:0000007 blood PATO:0000001 quality abnormal ZDB-GENE-000928-1 58215 2235 fech ZFA:0000112 gut PATO:0000001 quality abnormal ZDB-GENE-000928-1 58215 2235 fech ZFA:0000123 liver PATO:0002002 has extra parts of type abnormal ZFA:0009325 erythroid lineage cell ZDB-GENE-000928-1 58215 2235 fech ZFA:0000123 liver PATO:0000001 quality abnormal ZDB-GENE-000928-1 58215 2235 fech ZFA:0000529 kidney PATO:0002002 has extra parts of type abnormal ZFA:0009325 erythroid lineage cell ZDB-GENE-000928-1 58215 2235 fech ZFA:0001094 whole organism PATO:0000718 lethal (sensu genetics) abnormal ZDB-GENE-000928-1 58215 2235 fech ZFA:0001439 anatomical system PATO:0000001 quality abnormal ZDB-GENE-000928-1 58215 2235 fech GO:0005833 hemoglobin complex BFO:0000050 part_of ZFA:0009256 nucleate erythrocyte PATO:0000025 composition abnormal ZDB-GENE-000928-1 58215 2235 fech ZFA:0009256 nucleate erythrocyte PATO:0001868 autofluorescence abnormal ZDB-GENE-000928-1 58215 2235 fech ZFA:0009256 nucleate erythrocyte PATO:0001926 increased fluorescence abnormal ZDB-GENE-001006-1 570435 2249 fgf4 GO:0007507 heart development PATO:0001507 disrupted abnormal ZDB-GENE-001006-1 570435 2249 fgf4 GO:0035469 determination of pancreatic left/right asymmetry PATO:0001507 disrupted abnormal ZDB-GENE-001006-1 570435 2249 fgf4 GO:0061371 determination of heart left/right asymmetry PATO:0001507 disrupted abnormal ZDB-GENE-001006-1 570435 2249 fgf4 GO:0071910 determination of liver left/right asymmetry PATO:0001507 disrupted abnormal ZDB-GENE-001006-1 570435 2249 fgf4 GO:0005929 cilium BFO:0000050 part_of ZFA:0000001 Kupffer's vesicle PATO:0000574 decreased length abnormal ZDB-GENE-001006-1 570435 2249 fgf4 GO:0031514 motile cilium BFO:0000050 part_of ZFA:0000001 Kupffer's vesicle PATO:0000574 decreased length abnormal ZDB-GENE-001006-1 570435 2249 fgf4 ZFA:0000008 brain PATO:0000587 decreased size abnormal ZDB-GENE-001006-1 570435 2249 fgf4 ZFA:0000054 pericardium PATO:0001450 edematous abnormal ZDB-GENE-001006-1 570435 2249 fgf4 ZFA:0000114 heart PATO:0000628 mislocalised abnormal ZDB-GENE-001006-1 570435 2249 fgf4 ZFA:0000123 liver PATO:0000628 mislocalised abnormal ZDB-GENE-001006-1 570435 2249 fgf4 ZFA:0000140 pancreas PATO:0000628 mislocalised abnormal ZDB-GENE-001006-1 570435 2249 fgf4 ZFA:0001115 trunk PATO:0000617 bent abnormal ZDB-GENE-001019-1 60309 6092 robo2 GO:0007413 axonal fasciculation PATO:0001507 disrupted abnormal ZDB-GENE-001019-1 60309 6092 robo2 GO:0007416 synapse assembly PATO:0002051 increased occurrence abnormal ZDB-GENE-001019-1 60309 6092 robo2 GO:0016199 axon midline choice point recognition PATO:0001507 disrupted abnormal ZDB-GENE-001019-1 60309 6092 robo2 GO:0021960 anterior commissure morphogenesis PATO:0001236 process quality abnormal ZDB-GENE-001019-1 60309 6092 robo2 GO:0031290 retinal ganglion cell axon guidance PATO:0000001 quality abnormal ZDB-GENE-001019-1 60309 6092 robo2 GO:0031290 retinal ganglion cell axon guidance PATO:0001236 process quality abnormal ZDB-GENE-001019-1 60309 6092 robo2 GO:0031290 retinal ganglion cell axon guidance PATO:0001507 disrupted abnormal ZDB-GENE-001019-1 60309 6092 robo2 GO:0033564 anterior/posterior axon guidance PATO:0001236 process quality abnormal ZDB-GENE-001019-1 60309 6092 robo2 GO:0033564 anterior/posterior axon guidance PATO:0001507 disrupted abnormal ZDB-GENE-001019-1 60309 6092 robo2 GO:0048669 collateral sprouting in absence of injury PATO:0002051 increased occurrence abnormal ZDB-GENE-001019-1 60309 6092 robo2 ZFA:0000059 postoptic commissure PATO:0000599 decreased width abnormal ZDB-GENE-001019-1 60309 6092 robo2 GO:0007411 axon guidance BFO:0000066 occurs_in ZFA:0000247 cranial nerve VIII PATO:0001236 process quality abnormal ZDB-GENE-001019-1 60309 6092 robo2 GO:0030424 axon BFO:0000050 part_of ZFA:0000247 cranial nerve VIII PATO:0000628 mislocalised abnormal ZDB-GENE-001019-1 60309 6092 robo2 ZFA:0000247 cranial nerve VIII PATO:0001959 defasciculated abnormal ZDB-GENE-001019-1 60309 6092 robo2 GO:0030424 axon BFO:0000050 part_of ZFA:0000295 trigeminal ganglion PATO:0002285 increased branchiness abnormal ZDB-GENE-001019-1 60309 6092 robo2 GO:0044303 axon collateral BFO:0000050 part_of ZFA:0000295 trigeminal ganglion PATO:0000573 increased length abnormal ZDB-GENE-001019-1 60309 6092 robo2 ZFA:0009053 sensory neuron BFO:0000050 part_of ZFA:0000295 trigeminal ganglion PATO:0002002 has extra parts of type abnormal GO:0048786 presynaptic active zone BFO:0000050 part_of ZFA:0009053 sensory neuron ZDB-GENE-001019-1 60309 6092 robo2 ZFA:0000396 nervous system PATO:0000001 quality abnormal ZDB-GENE-001019-1 60309 6092 robo2 ZFA:0000405 cranial nerve III PATO:0000628 mislocalised abnormal ZDB-GENE-001019-1 60309 6092 robo2 GO:0030424 axon BFO:0000050 part_of ZFA:0000556 optic chiasm PATO:0000051 morphology abnormal ZDB-GENE-001019-1 60309 6092 robo2 GO:0005884 actin filament BFO:0000050 part_of ZFA:0001271 neurohypophysis PATO:0015027 increased stability abnormal ZDB-GENE-001019-1 60309 6092 robo2 GO:0048675 axon extension BFO:0000066 occurs_in ZFA:0001657 supraoptic tract PATO:0001236 process quality abnormal ZDB-GENE-001019-1 60309 6092 robo2 ZFA:0001657 supraoptic tract PATO:0000629 misrouted abnormal ZDB-GENE-001019-1 60309 6092 robo2 GO:0030424 axon BFO:0000050 part_of ZFA:0001659 diencephalic nucleus PATO:0002168 displaced to abnormal BSPO:0000083 medial region BFO:0000050 part_of ZFA:0000029 hindbrain ZDB-GENE-001019-1 60309 6092 robo2 ZFA:0005715 maG1 PATO:0002002 has extra parts of type abnormal GO:0043005 neuron projection BFO:0000050 part_of ZFA:0009125 olfactory receptor cell ZDB-GENE-001019-1 60309 6092 robo2 GO:0030424 axon BFO:0000050 part_of ZFA:0005778 hypocretin-secreting neuron PATO:0002168 displaced to abnormal BSPO:0000083 medial region BFO:0000050 part_of ZFA:0000029 hindbrain ZDB-GENE-001019-1 60309 6092 robo2 GO:0043005 neuron projection BFO:0000050 part_of ZFA:0007001 dorso-rostral cluster PATO:0000628 mislocalised abnormal ZDB-GENE-001019-1 60309 6092 robo2 GO:0043005 neuron projection BFO:0000050 part_of ZFA:0007001 dorso-rostral cluster PATO:0000629 misrouted abnormal ZDB-GENE-001019-1 60309 6092 robo2 GO:0048675 axon extension BFO:0000066 occurs_in ZFA:0007001 dorso-rostral cluster PATO:0001236 process quality abnormal ZDB-GENE-001019-1 60309 6092 robo2 GO:0007411 axon guidance BFO:0000066 occurs_in ZFA:0009125 olfactory receptor cell PATO:0001236 process quality abnormal ZDB-GENE-001019-1 60309 6092 robo2 GO:0030424 axon BFO:0000050 part_of ZFA:0009301 dopaminergic neuron PATO:0002259 adjacent to abnormal BSPO:0000013 anterior-posterior axis BFO:0000050 part_of ZFA:0000029 hindbrain ZDB-GENE-001019-1 60309 6092 robo2 GO:0030424 axon BFO:0000050 part_of ZFA:0009301 dopaminergic neuron PATO:0002259 adjacent to abnormal BSPO:0000013 anterior-posterior axis BFO:0000050 part_of ZFA:0000075 spinal cord ZDB-GENE-001019-1 60309 6092 robo2 GO:0030424 axon BFO:0000050 part_of ZFA:0009301 dopaminergic neuron PATO:0002259 adjacent to abnormal ZFA:0000092 axis BFO:0000050 part_of ZFA:0000075 spinal cord ZDB-GENE-001019-1 60309 6092 robo2 GO:0030424 axon BFO:0000050 part_of ZFA:0009301 dopaminergic neuron PATO:0001924 mislocalised medially abnormal ZDB-GENE-001019-1 60309 6092 robo2 GO:0004197 cysteine-type endopeptidase activity BFO:0000050 part_of ZFA:0009310 retinal ganglion cell PATO:0002052 decreased occurrence abnormal ZDB-GENE-001019-1 60309 6092 robo2 GO:0016322 neuron remodeling BFO:0000066 occurs_in ZFA:0009310 retinal ganglion cell PATO:0002302 decreased process quality abnormal ZDB-GENE-001019-1 60309 6092 robo2 GO:0030424 axon BFO:0000050 part_of ZFA:0009310 retinal ganglion cell PATO:0002168 displaced to abnormal ZFA:0000029 hindbrain ZDB-GENE-001019-1 60309 6092 robo2 GO:0030424 axon BFO:0000050 part_of ZFA:0009310 retinal ganglion cell PATO:0002168 displaced to abnormal ZFA:0000079 telencephalon ZDB-GENE-001019-1 60309 6092 robo2 GO:0030424 axon BFO:0000050 part_of ZFA:0009310 retinal ganglion cell PATO:0002168 displaced to abnormal BSPO:0000084 ventral region BFO:0000050 part_of ZFA:0000101 diencephalon ZDB-GENE-001019-1 60309 6092 robo2 GO:0030424 axon BFO:0000050 part_of ZFA:0009310 retinal ganglion cell PATO:0002168 displaced to abnormal BSPO:0000060 contralateral side BFO:0000050 part_of ZFA:0000107 eye ZDB-GENE-001019-1 60309 6092 robo2 GO:0030424 axon BFO:0000050 part_of ZFA:0009310 retinal ganglion cell PATO:0002002 has extra parts of type abnormal GO:0048786 presynaptic active zone BFO:0000050 part_of ZFA:0009310 retinal ganglion cell ZDB-GENE-001019-1 60309 6092 robo2 GO:0030424 axon BFO:0000050 part_of ZFA:0009310 retinal ganglion cell PATO:0000628 mislocalised abnormal ZDB-GENE-001019-1 60309 6092 robo2 GO:0030424 axon BFO:0000050 part_of ZFA:0009310 retinal ganglion cell PATO:0000629 misrouted abnormal ZDB-GENE-001019-1 60309 6092 robo2 GO:0030424 axon BFO:0000050 part_of ZFA:0009310 retinal ganglion cell PATO:0001241 physical object quality abnormal ZDB-GENE-001019-1 60309 6092 robo2 GO:0030424 axon BFO:0000050 part_of ZFA:0009310 retinal ganglion cell PATO:0002285 increased branchiness abnormal ZDB-GENE-001019-1 60309 6092 robo2 GO:0044303 axon collateral BFO:0000050 part_of ZFA:0009310 retinal ganglion cell PATO:0000573 increased length abnormal ZDB-GENE-001019-1 60309 6092 robo2 GO:0044303 axon collateral BFO:0000050 part_of ZFA:0009310 retinal ganglion cell PATO:0001241 physical object quality abnormal ZDB-GENE-001019-1 60309 6092 robo2 GO:0048669 collateral sprouting in absence of injury BFO:0000066 occurs_in ZFA:0009310 retinal ganglion cell PATO:0000057 occurrence abnormal ZDB-GENE-001019-1 60309 6092 robo2 GO:0048669 collateral sprouting in absence of injury BFO:0000066 occurs_in ZFA:0009310 retinal ganglion cell PATO:0002051 increased occurrence abnormal ZDB-GENE-001020-1 60310 340784 hmx3a GO:0042472 inner ear morphogenesis PATO:0002302 decreased process quality abnormal ZDB-GENE-001020-1 60310 340784 hmx3a GO:0048883 neuromast primordium migration PATO:0001507 disrupted abnormal ZDB-GENE-001020-1 60310 340784 hmx3a ZFA:0009225 inhibitory interneuron BFO:0000050 part_of ZFA:0000075 spinal cord PATO:0000470 increased amount abnormal ZDB-GENE-001020-1 60310 340784 hmx3a ZFA:0009276 GABAergic neuron BFO:0000050 part_of ZFA:0000075 spinal cord PATO:0000470 increased amount abnormal ZDB-GENE-001020-1 60310 340784 hmx3a ZFA:0009290 glutamatergic neuron BFO:0000050 part_of ZFA:0000075 spinal cord PATO:0001997 decreased amount abnormal ZDB-GENE-001020-1 60310 340784 hmx3a ZFA:0000168 anterior macula PATO:0000642 fused with abnormal ZFA:0000558 posterior macula ZDB-GENE-001020-1 60310 340784 hmx3a ZFA:0000530 lapillus PATO:0000642 fused with abnormal ZFA:0000676 sagitta ZDB-GENE-001020-1 60310 340784 hmx3a ZFA:0000558 posterior macula PATO:0000642 fused with abnormal ZFA:0000168 anterior macula ZDB-GENE-001020-1 60310 340784 hmx3a ZFA:0000940 posterior lateral line neuromast PATO:0001997 decreased amount abnormal ZDB-GENE-001020-1 60310 340784 hmx3a ZFA:0001094 whole organism PATO:0000185 balance abnormal ZDB-GENE-001020-1 60310 340784 hmx3a ZFA:0001094 whole organism PATO:0001860 decreased coordination abnormal ZDB-GENE-001020-1 60310 340784 hmx3a ZFA:0001617 otolith PATO:0000642 fused with abnormal ZFA:0001617 otolith ZDB-GENE-001030-2 60636 5079 pax5 GO:0006915 apoptotic process PATO:0002051 increased occurrence abnormal ZDB-GENE-001030-2 60636 5079 pax5 GO:0060005 vestibular reflex PATO:0000502 delayed abnormal ZDB-GENE-001030-2 60636 5079 pax5 GO:0060005 vestibular reflex PATO:0001507 disrupted abnormal ZDB-GENE-001030-2 60636 5079 pax5 ZFA:0009366 hair cell BFO:0000050 part_of ZFA:0000030 macula utricle PATO:0000330 irregular spatial pattern abnormal ZDB-GENE-001030-2 60636 5079 pax5 ZFA:0009366 hair cell BFO:0000050 part_of ZFA:0000700 utricle PATO:0000051 morphology abnormal ZDB-GENE-001030-2 60636 5079 pax5 ZFA:0000700 utricle PATO:0001999 lacks parts or has fewer parts of type abnormal ZFA:0009366 hair cell ZDB-GENE-001030-2 60636 5079 pax5 ZFA:0009366 hair cell PATO:0000628 mislocalised abnormal ZDB-GENE-001030-2 60636 5079 pax5 ZFA:0009366 hair cell PATO:0000638 apoptotic abnormal ZDB-GENE-001030-3 60637 7849 pax8 GO:0071600 otic vesicle morphogenesis PATO:0001236 process quality abnormal ZDB-GENE-001030-3 60637 7849 pax8 ZFA:0000042 midbrain hindbrain boundary PATO:0000599 decreased width abnormal ZDB-GENE-001030-3 60637 7849 pax8 ZFA:0000051 otic vesicle PATO:0002001 has fewer parts of type abnormal ZFA:0009366 hair cell ZDB-GENE-001030-3 60637 7849 pax8 ZFA:0000051 otic vesicle PATO:0000587 decreased size abnormal ZDB-GENE-001030-3 60637 7849 pax8 ZFA:0000138 otic placode PATO:0001241 physical object quality abnormal ZDB-GENE-001030-3 60637 7849 pax8 ZFA:0000166 lateral crista PATO:0001241 physical object quality abnormal ZDB-GENE-001031-1 60639 5080 pax6b GO:0001654 eye development PATO:0001507 disrupted abnormal ZDB-GENE-001031-1 60639 5080 pax6b GO:0002088 lens development in camera-type eye PATO:0001507 disrupted abnormal ZDB-GENE-001031-1 60639 5080 pax6b GO:0002089 lens morphogenesis in camera-type eye PATO:0000297 arrested abnormal ZDB-GENE-001031-1 60639 5080 pax6b GO:0002089 lens morphogenesis in camera-type eye PATO:0001507 disrupted abnormal ZDB-GENE-001031-1 60639 5080 pax6b GO:0003309 type B pancreatic cell differentiation PATO:0001507 disrupted abnormal ZDB-GENE-001031-1 60639 5080 pax6b GO:0009790 embryo development PATO:0001507 disrupted abnormal ZDB-GENE-001031-1 60639 5080 pax6b GO:0009790 embryo development PATO:0001749 paedomorphic growth abnormal ZDB-GENE-001031-1 60639 5080 pax6b GO:0009952 anterior/posterior pattern specification PATO:0001507 disrupted abnormal ZDB-GENE-001031-1 60639 5080 pax6b GO:0030902 hindbrain development PATO:0001507 disrupted abnormal ZDB-GENE-001031-1 60639 5080 pax6b ZFA:0000035 lens PATO:0000001 quality abnormal ZDB-GENE-001031-1 60639 5080 pax6b ZFA:0000035 lens PATO:0000051 morphology abnormal ZDB-GENE-001031-1 60639 5080 pax6b ZFA:0000035 lens PATO:0000140 position abnormal ZDB-GENE-001031-1 60639 5080 pax6b ZFA:0000035 lens PATO:0000587 decreased size abnormal ZDB-GENE-001031-1 60639 5080 pax6b ZFA:0000035 lens PATO:0000941 vacuolated abnormal ZDB-GENE-001031-1 60639 5080 pax6b ZFA:0000035 lens PATO:0000947 elliptic abnormal ZDB-GENE-001031-1 60639 5080 pax6b ZFA:0000035 lens PATO:0001483 aplastic abnormal ZDB-GENE-001031-1 60639 5080 pax6b ZFA:0000035 lens PATO:0001598 protruding abnormal ZDB-GENE-001031-1 60639 5080 pax6b ZFA:0000107 eye PATO:0000587 decreased size abnormal ZDB-GENE-001031-1 60639 5080 pax6b ZFA:0000152 retina PATO:0000646 malformed abnormal ZDB-GENE-001031-1 60639 5080 pax6b ZFA:0000640 cornea PATO:0000628 mislocalised abnormal ZDB-GENE-001031-1 60639 5080 pax6b ZFA:0000640 cornea PATO:0000646 malformed abnormal ZDB-GENE-001031-1 60639 5080 pax6b ZFA:0000640 cornea PATO:0001478 collapsed abnormal ZDB-GENE-001031-1 60639 5080 pax6b ZFA:0001064 rhombomere PATO:0001485 condensed abnormal ZDB-GENE-001031-1 60639 5080 pax6b ZFA:0009100 peptide hormone secreting cell BFO:0000050 part_of ZFA:0001260 endocrine pancreas PATO:0000470 increased amount abnormal ZDB-GENE-001031-1 60639 5080 pax6b ZFA:0001439 anatomical system PATO:0000001 quality abnormal ZDB-GENE-001031-1 60639 5080 pax6b ZFA:0001687 corneal endothelium PATO:0000646 malformed abnormal ZDB-GENE-001031-1 60639 5080 pax6b ZFA:0009081 mesenchymal cell BFO:0000050 part_of ZFA:0005566 anterior segment eye PATO:0000051 morphology abnormal ZDB-GENE-001031-1 60639 5080 pax6b ZFA:0005566 anterior segment eye PATO:0000051 morphology abnormal ZDB-GENE-001031-1 60639 5080 pax6b ZFA:0005566 anterior segment eye PATO:0000645 hypoplastic abnormal ZDB-GENE-001031-1 60639 5080 pax6b ZFA:0005598 pancreatic epsilon cell PATO:0000470 increased amount abnormal ZDB-GENE-001031-1 60639 5080 pax6b ZFA:0005743 pancreatic D cell PATO:0001997 decreased amount abnormal ZDB-GENE-001031-1 60639 5080 pax6b ZFA:0009102 pancreatic B cell PATO:0000462 absent abnormal ZDB-GENE-001031-1 60639 5080 pax6b ZFA:0009102 pancreatic B cell PATO:0001997 decreased amount abnormal ZDB-GENE-001031-1 60639 5080 pax6b ZFA:0009104 pancreatic A cell PATO:0000470 increased amount abnormal ZDB-GENE-001031-1 60639 5080 pax6b ZFA:0009104 pancreatic A cell PATO:0001241 physical object quality abnormal ZDB-GENE-001031-1 60639 5080 pax6b ZFA:0009104 pancreatic A cell PATO:0001997 decreased amount abnormal ZDB-GENE-001031-1 60639 5080 pax6b ZFA:0009228 D cell PATO:0001997 decreased amount abnormal ZDB-GENE-001101-1 60658 4842 nos1 GO:0001889 liver development PATO:0002302 decreased process quality abnormal ZDB-GENE-001101-1 60658 4842 nos1 GO:0001966 thigmotaxis PATO:0002052 decreased occurrence abnormal ZDB-GENE-001101-1 60658 4842 nos1 GO:0002118 aggressive behavior PATO:0002052 decreased occurrence abnormal ZDB-GENE-001101-1 60658 4842 nos1 GO:0008345 larval locomotory behavior PATO:0000080 amplitude abnormal ZDB-GENE-001101-1 60658 4842 nos1 GO:0008345 larval locomotory behavior PATO:0000380 increased frequency abnormal ZDB-GENE-001101-1 60658 4842 nos1 GO:0036269 swimming behavior PATO:0002052 decreased occurrence abnormal ZDB-GENE-001101-1 60658 4842 nos1 GO:0048668 collateral sprouting PATO:0002051 increased occurrence abnormal ZDB-GENE-001101-1 60658 4842 nos1 GO:0090648 response to environmental enrichment PATO:0000057 occurrence abnormal ZDB-GENE-001101-1 60658 4842 nos1 GO:0007263 nitric oxide mediated signal transduction BFO:0000066 occurs_in ZFA:0000008 brain PATO:0002052 decreased occurrence abnormal ZDB-GENE-001101-1 60658 4842 nos1 GO:0097621 monoamine oxidase activity BFO:0000050 part_of ZFA:0000008 brain PATO:0002052 decreased occurrence abnormal ZDB-GENE-001101-1 60658 4842 nos1 CHEBI:28790 serotonin BFO:0000050 part_of ZFA:0000029 hindbrain PATO:0000470 increased amount abnormal ZDB-GENE-001101-1 60658 4842 nos1 CHEBI:33569 noradrenaline BFO:0000050 part_of ZFA:0000029 hindbrain PATO:0001997 decreased amount abnormal ZDB-GENE-001101-1 60658 4842 nos1 CHEBI:41941 (3,4-dihydroxyphenyl)acetic acid BFO:0000050 part_of ZFA:0000029 hindbrain PATO:0001997 decreased amount abnormal ZDB-GENE-001101-1 60658 4842 nos1 CHEBI:41941 (3,4-dihydroxyphenyl)acetic acid BFO:0000050 part_of ZFA:0000079 telencephalon PATO:0001997 decreased amount abnormal ZDB-GENE-001101-1 60658 4842 nos1 CHEBI:41941 (3,4-dihydroxyphenyl)acetic acid BFO:0000050 part_of ZFA:0000101 diencephalon PATO:0001997 decreased amount abnormal ZDB-GENE-001101-1 60658 4842 nos1 ZFA:0000123 liver PATO:0000587 decreased size abnormal ZDB-GENE-001101-1 60658 4842 nos1 CHEBI:41941 (3,4-dihydroxyphenyl)acetic acid BFO:0000050 part_of ZFA:0000445 optic tectum PATO:0001997 decreased amount abnormal ZDB-GENE-001101-1 60658 4842 nos1 ZFA:0001094 whole organism PATO:0000303 increased speed abnormal ZDB-GENE-001101-1 60658 4842 nos1 ZFA:0009014 hematopoietic stem cell PATO:0001997 decreased amount abnormal ZDB-GENE-001101-1 60658 4842 nos1 GO:0044303 axon collateral BFO:0000050 part_of ZFA:0009052 motor neuron PATO:0000470 increased amount abnormal ZDB-GENE-001101-1 60658 4842 nos1 ZFA:0009052 motor neuron PATO:0001997 decreased amount abnormal ZDB-GENE-001103-1 60641 6662 sox9a GO:0048703 embryonic viscerocranium morphogenesis PATO:0002052 decreased occurrence abnormal ZDB-GENE-001103-1 60641 6662 sox9a GO:0051216 cartilage development PATO:0001507 disrupted abnormal ZDB-GENE-001103-1 60641 6662 sox9a GO:1904888 cranial skeletal system development PATO:0002052 decreased occurrence abnormal ZDB-GENE-001103-1 60641 6662 sox9a ZFA:0000051 otic vesicle PATO:0000587 decreased size abnormal ZDB-GENE-001103-1 60641 6662 sox9a ZFA:0000095 pharyngeal arch 3-7 skeleton PATO:0000001 quality abnormal ZDB-GENE-001103-1 60641 6662 sox9a ZFA:0000112 gut PATO:0000001 quality abnormal ZDB-GENE-001103-1 60641 6662 sox9a ZFA:0000123 liver PATO:0000001 quality abnormal ZDB-GENE-001103-1 60641 6662 sox9a ZFA:0000123 liver PATO:0000586 increased size abnormal ZDB-GENE-001103-1 60641 6662 sox9a ZFA:0000191 dentary PATO:0000587 decreased size abnormal ZDB-GENE-001103-1 60641 6662 sox9a ZFA:0000250 opercle PATO:0000587 decreased size abnormal ZDB-GENE-001103-1 60641 6662 sox9a ZFA:0000270 maxilla PATO:0000587 decreased size abnormal ZDB-GENE-001103-1 60641 6662 sox9a ZFA:0000332 coracoid PATO:0000462 absent abnormal ZDB-GENE-001103-1 60641 6662 sox9a ZFA:0000422 retroarticular PATO:0001483 aplastic abnormal ZDB-GENE-001103-1 60641 6662 sox9a ZFA:0000488 ceratobranchial bone PATO:0000587 decreased size abnormal ZDB-GENE-001103-1 60641 6662 sox9a ZFA:0000488 ceratobranchial bone PATO:0001483 aplastic abnormal ZDB-GENE-001103-1 60641 6662 sox9a ZFA:0000578 ceratohyal bone PATO:0001483 aplastic abnormal ZDB-GENE-001103-1 60641 6662 sox9a BSPO:0000070 anatomical region BFO:0000050 part_of ZFA:0000588 statoacoustic (VIII) ganglion PATO:0000587 decreased size abnormal ZDB-GENE-001103-1 60641 6662 sox9a ZFA:0000657 entopterygoid PATO:0001483 aplastic abnormal ZDB-GENE-001103-1 60641 6662 sox9a ZFA:0000672 hyomandibula PATO:0001483 aplastic abnormal ZDB-GENE-001103-1 60641 6662 sox9a ZFA:0001094 whole organism PATO:0000574 decreased length abnormal ZDB-GENE-001103-1 60641 6662 sox9a ZFA:0001094 whole organism PATO:0000718 lethal (sensu genetics) abnormal ZDB-GENE-001103-1 60641 6662 sox9a ZFA:0001114 head PATO:0000411 circular abnormal ZDB-GENE-001103-1 60641 6662 sox9a ZFA:0001161 pectoral fin PATO:0000574 decreased length abnormal ZDB-GENE-001103-1 60641 6662 sox9a ZFA:0001161 pectoral fin PATO:0000587 decreased size abnormal ZDB-GENE-001103-1 60641 6662 sox9a ZFA:0001205 Meckel's cartilage PATO:0000587 decreased size abnormal ZDB-GENE-001103-1 60641 6662 sox9a ZFA:0001205 Meckel's cartilage PATO:0001483 aplastic abnormal ZDB-GENE-001103-1 60641 6662 sox9a ZFA:0001216 splanchnocranium PATO:0000462 absent abnormal ZDB-GENE-001103-1 60641 6662 sox9a ZFA:0001227 mandibular arch skeleton PATO:0000051 morphology abnormal ZDB-GENE-001103-1 60641 6662 sox9a ZFA:0001239 ceratobranchial 5 bone PATO:0000587 decreased size abnormal ZDB-GENE-001103-1 60641 6662 sox9a ZFA:0001272 palatoquadrate arch PATO:0000001 quality abnormal ZDB-GENE-001103-1 60641 6662 sox9a ZFA:0001321 neurocranial trabecula PATO:0001483 aplastic abnormal ZDB-GENE-001103-1 60641 6662 sox9a ZFA:0001399 palatoquadrate cartilage PATO:0000587 decreased size abnormal ZDB-GENE-001103-1 60641 6662 sox9a ZFA:0001399 palatoquadrate cartilage PATO:0001483 aplastic abnormal ZDB-GENE-001103-1 60641 6662 sox9a ZFA:0001400 ceratohyal cartilage PATO:0000587 decreased size abnormal ZDB-GENE-001103-1 60641 6662 sox9a ZFA:0001405 ethmoid cartilage PATO:0001483 aplastic abnormal ZDB-GENE-001103-1 60641 6662 sox9a ZFA:0001422 hyosymplectic cartilage PATO:0000587 decreased size abnormal ZDB-GENE-001103-1 60641 6662 sox9a ZFA:0001422 hyosymplectic cartilage PATO:0001483 aplastic abnormal ZDB-GENE-001103-1 60641 6662 sox9a ZFA:0001423 parachordal cartilage PATO:0001483 aplastic abnormal ZDB-GENE-001103-1 60641 6662 sox9a ZFA:0001425 basal plate cartilage PATO:0001483 aplastic abnormal ZDB-GENE-001103-1 60641 6662 sox9a ZFA:0001455 scapulocoracoid PATO:0000587 decreased size abnormal ZDB-GENE-001103-1 60641 6662 sox9a ZFA:0001455 scapulocoracoid PATO:0001483 aplastic abnormal ZDB-GENE-001103-1 60641 6662 sox9a ZFA:0001458 cranial cartilage PATO:0001483 aplastic abnormal ZDB-GENE-001103-1 60641 6662 sox9a ZFA:0001458 cranial cartilage PATO:0001997 decreased amount abnormal ZDB-GENE-001103-1 60641 6662 sox9a ZFA:0001460 pharyngeal arch cartilage PATO:0000462 absent abnormal ZDB-GENE-001103-1 60641 6662 sox9a ZFA:0001510 basihyal cartilage PATO:0001483 aplastic abnormal ZDB-GENE-001103-1 60641 6662 sox9a ZFA:0001516 ceratobranchial cartilage PATO:0001483 aplastic abnormal ZDB-GENE-001103-1 60641 6662 sox9a ZFA:0001580 neurocranium PATO:0000462 absent abnormal ZDB-GENE-001103-1 60641 6662 sox9a ZFA:0001612 pharyngeal arch 1 PATO:0000587 decreased size abnormal ZDB-GENE-001103-1 60641 6662 sox9a ZFA:0001613 pharyngeal arch 3-7 PATO:0000587 decreased size abnormal ZDB-GENE-001103-1 60641 6662 sox9a ZFA:0009084 chondrocyte PATO:0000937 disorganized abnormal ZDB-GENE-001103-2 60642 6662 sox9b GO:0001947 heart looping PATO:0002302 decreased process quality abnormal ZDB-GENE-001103-2 60642 6662 sox9b GO:0003190 atrioventricular valve formation PATO:0002302 decreased process quality abnormal ZDB-GENE-001103-2 60642 6662 sox9b GO:0003309 type B pancreatic cell differentiation PATO:0002302 decreased process quality abnormal ZDB-GENE-001103-2 60642 6662 sox9b GO:0007219 Notch signaling pathway PATO:0001507 disrupted abnormal ZDB-GENE-001103-2 60642 6662 sox9b GO:0031017 exocrine pancreas development PATO:0002302 decreased process quality abnormal ZDB-GENE-001103-2 60642 6662 sox9b GO:0035622 intrahepatic bile duct development PATO:0001507 disrupted abnormal ZDB-GENE-001103-2 60642 6662 sox9b GO:0035622 intrahepatic bile duct development PATO:0002302 decreased process quality abnormal ZDB-GENE-001103-2 60642 6662 sox9b GO:0061008 hepaticobiliary system development PATO:0001507 disrupted abnormal ZDB-GENE-001103-2 60642 6662 sox9b GO:0061010 gallbladder development PATO:0001507 disrupted abnormal ZDB-GENE-001103-2 60642 6662 sox9b ZFA:0000051 otic vesicle PATO:0000587 decreased size abnormal ZDB-GENE-001103-2 60642 6662 sox9b ZFA:0000054 pericardium PATO:0001450 edematous abnormal ZDB-GENE-001103-2 60642 6662 sox9b ZFA:0000089 fin fold actinotrichium PATO:0001997 decreased amount abnormal ZDB-GENE-001103-2 60642 6662 sox9b ZFA:0000114 heart PATO:0002000 lacks all parts of type abnormal ZFA:0009000 cell BFO:0000050 part_of ZFA:0005058 ventricular epicardium ZDB-GENE-001103-2 60642 6662 sox9b ZFA:0000114 heart PATO:0000646 malformed abnormal ZDB-GENE-001103-2 60642 6662 sox9b ZFA:0000114 heart PATO:0001154 elongated abnormal ZDB-GENE-001103-2 60642 6662 sox9b ZFA:0000123 liver PATO:0000320 green abnormal ZDB-GENE-001103-2 60642 6662 sox9b ZFA:0009277 acinar cell BFO:0000050 part_of ZFA:0000140 pancreas PATO:0001997 decreased amount abnormal ZDB-GENE-001103-2 60642 6662 sox9b ZFA:0000140 pancreas PATO:0000320 green abnormal ZDB-GENE-001103-2 60642 6662 sox9b ZFA:0000184 cleithrum PATO:0000587 decreased size abnormal ZDB-GENE-001103-2 60642 6662 sox9b ZFA:0000191 dentary PATO:0001483 aplastic abnormal ZDB-GENE-001103-2 60642 6662 sox9b ZFA:0000200 dorsal root ganglion PATO:0000330 irregular spatial pattern abnormal ZDB-GENE-001103-2 60642 6662 sox9b ZFA:0000200 dorsal root ganglion PATO:0001997 decreased amount abnormal ZDB-GENE-001103-2 60642 6662 sox9b ZFA:0000208 gall bladder PATO:0000587 decreased size abnormal ZDB-GENE-001103-2 60642 6662 sox9b ZFA:0000250 opercle PATO:0000587 decreased size abnormal ZDB-GENE-001103-2 60642 6662 sox9b ZFA:0000270 maxilla PATO:0001483 aplastic abnormal ZDB-GENE-001103-2 60642 6662 sox9b ZFA:0000422 retroarticular PATO:0001483 aplastic abnormal ZDB-GENE-001103-2 60642 6662 sox9b ZFA:0000476 branchiostegal ray PATO:0001483 aplastic abnormal ZDB-GENE-001103-2 60642 6662 sox9b ZFA:0000561 parasphenoid PATO:0000587 decreased size abnormal ZDB-GENE-001103-2 60642 6662 sox9b ZFA:0000578 ceratohyal bone PATO:0001483 aplastic abnormal ZDB-GENE-001103-2 60642 6662 sox9b ZFA:0000657 entopterygoid PATO:0001483 aplastic abnormal ZDB-GENE-001103-2 60642 6662 sox9b ZFA:0000672 hyomandibula PATO:0001483 aplastic abnormal ZDB-GENE-001103-2 60642 6662 sox9b ZFA:0001094 whole organism PATO:0000587 decreased size abnormal ZDB-GENE-001103-2 60642 6662 sox9b ZFA:0001094 whole organism PATO:0000592 decreased thickness abnormal ZDB-GENE-001103-2 60642 6662 sox9b ZFA:0001094 whole organism PATO:0001604 decreased life span abnormal ZDB-GENE-001103-2 60642 6662 sox9b ZFA:0001114 head PATO:0000587 decreased size abnormal ZDB-GENE-001103-2 60642 6662 sox9b ZFA:0001117 post-vent region PATO:0001592 increased curvature abnormal ZDB-GENE-001103-2 60642 6662 sox9b ZFA:0001205 Meckel's cartilage PATO:0000587 decreased size abnormal ZDB-GENE-001103-2 60642 6662 sox9b ZFA:0001239 ceratobranchial 5 bone PATO:0001483 aplastic abnormal ZDB-GENE-001103-2 60642 6662 sox9b ZFA:0001260 endocrine pancreas PATO:0002000 lacks all parts of type abnormal ZFA:0005756 secondary islet ZDB-GENE-001103-2 60642 6662 sox9b ZFA:0001260 endocrine pancreas PATO:0000628 mislocalised abnormal ZDB-GENE-001103-2 60642 6662 sox9b ZFA:0001321 neurocranial trabecula PATO:0000587 decreased size abnormal ZDB-GENE-001103-2 60642 6662 sox9b ZFA:0001372 pancreatic duct PATO:0002001 has fewer parts of type abnormal ZFA:0009000 cell ZDB-GENE-001103-2 60642 6662 sox9b ZFA:0001372 pancreatic duct PATO:0000051 morphology abnormal ZDB-GENE-001103-2 60642 6662 sox9b ZFA:0001372 pancreatic duct PATO:0000646 malformed abnormal ZDB-GENE-001103-2 60642 6662 sox9b ZFA:0001372 pancreatic duct PATO:0001571 dilated abnormal ZDB-GENE-001103-2 60642 6662 sox9b ZFA:0001372 pancreatic duct PATO:0002286 decreased branchiness abnormal ZDB-GENE-001103-2 60642 6662 sox9b ZFA:0001399 palatoquadrate cartilage PATO:0000587 decreased size abnormal ZDB-GENE-001103-2 60642 6662 sox9b ZFA:0001400 ceratohyal cartilage PATO:0000587 decreased size abnormal ZDB-GENE-001103-2 60642 6662 sox9b ZFA:0001405 ethmoid cartilage PATO:0000587 decreased size abnormal ZDB-GENE-001103-2 60642 6662 sox9b ZFA:0001422 hyosymplectic cartilage PATO:0000587 decreased size abnormal ZDB-GENE-001103-2 60642 6662 sox9b ZFA:0001425 basal plate cartilage PATO:0000587 decreased size abnormal ZDB-GENE-001103-2 60642 6662 sox9b ZFA:0001456 pectoral fin endoskeletal disc PATO:0000587 decreased size abnormal ZDB-GENE-001103-2 60642 6662 sox9b ZFA:0001504 occipital arch cartilage PATO:0000587 decreased size abnormal ZDB-GENE-001103-2 60642 6662 sox9b ZFA:0001516 ceratobranchial cartilage PATO:0000587 decreased size abnormal ZDB-GENE-001103-2 60642 6662 sox9b ZFA:0005162 digestive system duct PATO:0001332 amorphous abnormal ZDB-GENE-001103-2 60642 6662 sox9b ZFA:0005163 bile canaliculus PATO:0000574 decreased length abnormal ZDB-GENE-001103-2 60642 6662 sox9b ZFA:0005163 bile canaliculus PATO:0000600 increased width abnormal ZDB-GENE-001103-2 60642 6662 sox9b ZFA:0005169 intrahepatic bile duct PATO:0000051 morphology abnormal ZDB-GENE-001103-2 60642 6662 sox9b ZFA:0005169 intrahepatic bile duct PATO:0000646 malformed abnormal ZDB-GENE-001103-2 60642 6662 sox9b ZFA:0005754 primary islet PATO:0000587 decreased size abnormal ZDB-GENE-001103-2 60642 6662 sox9b ZFA:0005808 proepicardial cluster PATO:0000462 absent abnormal ZDB-GENE-001103-2 60642 6662 sox9b ZFA:0009091 melanocyte PATO:0000586 increased size abnormal ZDB-GENE-001103-2 60642 6662 sox9b ZFA:0009111 hepatocyte PATO:0002264 organization quality abnormal ZDB-GENE-001103-2 60642 6662 sox9b ZFA:0009199 iridophore PATO:0001997 decreased amount abnormal ZDB-GENE-001103-3 60634 55079 fezf2 GO:0008015 blood circulation PATO:0001507 disrupted abnormal ZDB-GENE-001103-3 60634 55079 fezf2 GO:0021537 telencephalon development PATO:0002302 decreased process quality abnormal ZDB-GENE-001103-3 60634 55079 fezf2 GO:0071679 commissural neuron axon guidance PATO:0001507 disrupted abnormal ZDB-GENE-001103-3 60634 55079 fezf2 ZFA:0009301 dopaminergic neuron BFO:0000050 part_of ZFA:0000032 hypothalamus PATO:0001997 decreased amount abnormal ZDB-GENE-001103-3 60634 55079 fezf2 ZFA:0000032 hypothalamus PATO:0002001 has fewer parts of type abnormal ZFA:0009186 neurosecretory neuron ZDB-GENE-001103-3 60634 55079 fezf2 ZFA:0000032 hypothalamus PATO:0002001 has fewer parts of type abnormal ZFA:0009301 dopaminergic neuron ZDB-GENE-001103-3 60634 55079 fezf2 ZFA:0000032 hypothalamus PATO:0001241 physical object quality abnormal ZDB-GENE-001103-3 60634 55079 fezf2 ZFA:0000054 pericardium PATO:0001450 edematous abnormal ZDB-GENE-001103-3 60634 55079 fezf2 ZFA:0000079 telencephalon PATO:0001999 lacks parts or has fewer parts of type abnormal ZFA:0009301 dopaminergic neuron ZDB-GENE-001103-3 60634 55079 fezf2 ZFA:0000079 telencephalon PATO:0000587 decreased size abnormal ZDB-GENE-001103-3 60634 55079 fezf2 ZFA:0009301 dopaminergic neuron BFO:0000050 part_of ZFA:0000101 diencephalon PATO:0001997 decreased amount abnormal ZDB-GENE-001103-3 60634 55079 fezf2 ZFA:0009301 dopaminergic neuron BFO:0000050 part_of ZFA:0000109 forebrain PATO:0001997 decreased amount abnormal ZDB-GENE-001103-3 60634 55079 fezf2 ZFA:0009361 serotonergic neuron BFO:0000050 part_of ZFA:0000109 forebrain PATO:0001997 decreased amount abnormal ZDB-GENE-001103-3 60634 55079 fezf2 ZFA:0000152 retina PATO:0001999 lacks parts or has fewer parts of type abnormal ZFA:0009301 dopaminergic neuron ZDB-GENE-001103-3 60634 55079 fezf2 ZFA:0000396 nervous system PATO:0000001 quality abnormal ZDB-GENE-001103-3 60634 55079 fezf2 ZFA:0000458 ventral thalamus PATO:0000587 decreased size abnormal ZDB-GENE-001103-3 60634 55079 fezf2 ZFA:0000470 preoptic area PATO:0001241 physical object quality abnormal ZDB-GENE-001103-3 60634 55079 fezf2 GO:0007219 Notch signaling pathway BFO:0000066 occurs_in ZFA:0000505 dorsal telencephalon PATO:0002302 decreased process quality abnormal ZDB-GENE-001103-3 60634 55079 fezf2 GO:0022008 neurogenesis BFO:0000066 occurs_in ZFA:0000505 dorsal telencephalon PATO:0002051 increased occurrence abnormal ZDB-GENE-001103-3 60634 55079 fezf2 GO:0043005 neuron projection BFO:0000050 part_of ZFA:0000505 dorsal telencephalon PATO:0002286 decreased branchiness abnormal ZDB-GENE-001103-3 60634 55079 fezf2 GO:0048812 neuron projection morphogenesis BFO:0000066 occurs_in ZFA:0000505 dorsal telencephalon PATO:0002052 decreased occurrence abnormal ZDB-GENE-001103-3 60634 55079 fezf2 ZFA:0009019 neuronal stem cell BFO:0000050 part_of ZFA:0000505 dorsal telencephalon PATO:0002102 proliferative abnormal ZDB-GENE-001103-3 60634 55079 fezf2 ZFA:0009248 neuron BFO:0000050 part_of ZFA:0000505 dorsal telencephalon PATO:0001501 immature abnormal ZDB-GENE-001103-3 60634 55079 fezf2 ZFA:0000505 dorsal telencephalon PATO:0002002 has extra parts of type abnormal ZFA:0009248 neuron ZDB-GENE-001103-3 60634 55079 fezf2 ZFA:0000539 locus coeruleus PATO:0001999 lacks parts or has fewer parts of type abnormal ZFA:0009248 neuron ZDB-GENE-001103-3 60634 55079 fezf2 ZFA:0000633 caudal tuberculum PATO:0001241 physical object quality abnormal ZDB-GENE-001103-3 60634 55079 fezf2 GO:0007219 Notch signaling pathway BFO:0000066 occurs_in ZFA:0001083 ventricular zone PATO:0002302 decreased process quality abnormal ZDB-GENE-001103-3 60634 55079 fezf2 ZFA:0001094 whole organism PATO:0001422 dead abnormal ZDB-GENE-001103-4 60640 1588 cyp19a1b GO:0035188 hatching PATO:0002052 decreased occurrence abnormal ZDB-GENE-001103-4 60640 1588 cyp19a1b CHEBI:23965 estradiol BFO:0000050 part_of ZFA:0000007 blood PATO:0001997 decreased amount abnormal ZDB-GENE-001103-4 60640 1588 cyp19a1b ZFA:0000009 cardiac ventricle PATO:0000574 decreased length abnormal ZDB-GENE-001103-4 60640 1588 cyp19a1b ZFA:0000054 pericardium PATO:0001450 edematous abnormal ZDB-GENE-001103-4 60640 1588 cyp19a1b ZFA:0000076 swim bladder PATO:0002377 uninflated abnormal ZDB-GENE-001103-4 60640 1588 cyp19a1b ZFA:0000084 yolk PATO:0001450 edematous abnormal ZDB-GENE-001103-4 60640 1588 cyp19a1b ZFA:0000107 eye PATO:0000587 decreased size abnormal ZDB-GENE-001103-4 60640 1588 cyp19a1b ZFA:0000007 blood BFO:0000050 part_of ZFA:0000114 heart PATO:0000596 decreased volume abnormal ZDB-GENE-001103-4 60640 1588 cyp19a1b ZFA:0001058 caudal fin PATO:0000051 morphology abnormal ZDB-GENE-001103-4 60640 1588 cyp19a1b CHEBI:23965 estradiol BFO:0000050 part_of ZFA:0001094 whole organism PATO:0001997 decreased amount abnormal ZDB-GENE-001103-4 60640 1588 cyp19a1b ZFA:0001094 whole organism PATO:0000574 decreased length abnormal ZDB-GENE-001103-4 60640 1588 cyp19a1b ZFA:0001094 whole organism PATO:0001604 decreased life span abnormal ZDB-GENE-001103-5 60635 1366 cldn7b GO:0007605 sensory perception of sound PATO:0001507 disrupted abnormal ZDB-GENE-001103-5 60635 1366 cldn7b GO:0060872 semicircular canal development PATO:0000502 delayed abnormal ZDB-GENE-001103-5 60635 1366 cldn7b ZFA:0000051 otic vesicle PATO:0002057 increased area abnormal ZDB-GENE-001103-5 60635 1366 cldn7b GO:0031514 motile cilium BFO:0000050 part_of ZFA:0000151 pronephros PATO:0000406 curved abnormal ZDB-GENE-001103-5 60635 1366 cldn7b GO:0045198 establishment of epithelial cell apical/basal polarity BFO:0000066 occurs_in ZFA:0000151 pronephros PATO:0002302 decreased process quality abnormal ZDB-GENE-001103-5 60635 1366 cldn7b ZFA:0000151 pronephros PATO:0001624 decreased functionality abnormal ZDB-GENE-001103-5 60635 1366 cldn7b ZFA:0000151 pronephros PATO:0001673 cystic abnormal ZDB-GENE-001103-5 60635 1366 cldn7b ZFA:0000431 semicircular canal PATO:0001483 aplastic abnormal ZDB-GENE-001103-5 60635 1366 cldn7b ZFA:0000530 lapillus PATO:0000587 decreased size abnormal ZDB-GENE-001103-5 60635 1366 cldn7b ZFA:0000676 sagitta PATO:0000587 decreased size abnormal ZDB-GENE-001103-5 60635 1366 cldn7b ZFA:0001094 whole organism PATO:0001592 increased curvature abnormal ZDB-GENE-001103-5 60635 1366 cldn7b ZFA:0001617 otolith PATO:0000462 absent abnormal ZDB-GENE-001103-5 60635 1366 cldn7b ZFA:0005242 multi-ciliated epithelial cell PATO:0001999 lacks parts or has fewer parts of type abnormal GO:0005929 cilium BFO:0000050 part_of ZFA:0005242 multi-ciliated epithelial cell ZDB-GENE-001103-5 60635 1366 cldn7b GO:0043296 apical junction complex BFO:0000050 part_of ZFA:0007068 otic epithelium PATO:0000574 decreased length abnormal ZDB-GENE-001103-5 60635 1366 cldn7b ZFA:0007068 otic epithelium PATO:0000592 decreased thickness abnormal ZDB-GENE-001106-1 60632 89780 wnt3a GO:0001947 heart looping PATO:0001507 disrupted abnormal ZDB-GENE-001106-1 60632 89780 wnt3a GO:0036342 post-anal tail morphogenesis PATO:0001507 disrupted abnormal ZDB-GENE-001106-1 60632 89780 wnt3a GO:0048703 embryonic viscerocranium morphogenesis PATO:0001507 disrupted abnormal ZDB-GENE-001106-1 60632 89780 wnt3a GO:0060037 pharyngeal system development PATO:0001507 disrupted abnormal ZDB-GENE-001106-1 60632 89780 wnt3a GO:0060047 heart contraction PATO:0000911 decreased rate abnormal ZDB-GENE-001106-1 60632 89780 wnt3a GO:0060971 embryonic heart tube left/right pattern formation PATO:0001507 disrupted abnormal ZDB-GENE-001106-1 60632 89780 wnt3a GO:0005929 cilium BFO:0000050 part_of ZFA:0000001 Kupffer's vesicle PATO:0000574 decreased length abnormal ZDB-GENE-001106-1 60632 89780 wnt3a ZFA:0000054 pericardium PATO:0001450 edematous abnormal ZDB-GENE-001106-1 60632 89780 wnt3a ZFA:0000077 tail bud PATO:0000051 morphology abnormal ZDB-GENE-001106-1 60632 89780 wnt3a ZFA:0000077 tail bud PATO:0000574 decreased length abnormal ZDB-GENE-001106-1 60632 89780 wnt3a ZFA:0000095 pharyngeal arch 3-7 skeleton PATO:0000587 decreased size abnormal ZDB-GENE-001106-1 60632 89780 wnt3a ZFA:0000114 heart PATO:0001624 decreased functionality abnormal ZDB-GENE-001106-1 60632 89780 wnt3a ZFA:0000135 notochord PATO:0000936 truncated abnormal ZDB-GENE-001106-1 60632 89780 wnt3a ZFA:0000155 somite PATO:0001997 decreased amount abnormal ZDB-GENE-001106-1 60632 89780 wnt3a ZFA:0001094 whole organism PATO:0000574 decreased length abnormal ZDB-GENE-001106-1 60632 89780 wnt3a ZFA:0001117 post-vent region PATO:0000574 decreased length abnormal ZDB-GENE-001106-1 60632 89780 wnt3a ZFA:0001117 post-vent region PATO:0001469 curved ventral abnormal ZDB-GENE-001106-1 60632 89780 wnt3a ZFA:0001227 mandibular arch skeleton PATO:0001483 aplastic abnormal ZDB-GENE-001106-1 60632 89780 wnt3a ZFA:0001321 neurocranial trabecula PATO:0001483 aplastic abnormal ZDB-GENE-001106-1 60632 89780 wnt3a ZFA:0001405 ethmoid cartilage PATO:0001483 aplastic abnormal ZDB-GENE-001106-1 60632 89780 wnt3a ZFA:0001516 ceratobranchial cartilage PATO:0002291 agenesis abnormal ZDB-GENE-001106-1 60632 89780 wnt3a ZFA:0001613 pharyngeal arch 3-7 PATO:0000051 morphology abnormal ZDB-GENE-001106-1 60632 89780 wnt3a ZFA:0005004 aortic arch PATO:0000051 morphology abnormal ZDB-GENE-001120-3 63999 6770 star GO:0001556 oocyte maturation PATO:0000297 arrested abnormal ZDB-GENE-001120-3 63999 6770 star GO:0008585 female gonad development PATO:0001236 process quality abnormal ZDB-GENE-001120-3 63999 6770 star ZFA:0000303 female organism PATO:0001696 decreased fecundity abnormal ZDB-GENE-001120-3 63999 6770 star ZFA:0001094 whole organism PATO:0000169 viability abnormal ZDB-GENE-001120-3 63999 6770 star ZFA:0001263 ovarian follicle stage I PATO:0000470 increased amount abnormal ZDB-GENE-001127-3 64267 481 atp1b1a GO:0008283 cell population proliferation PATO:0000498 increased duration abnormal ZDB-GENE-001127-3 64267 481 atp1b1a GO:0008544 epidermis development PATO:0001507 disrupted abnormal ZDB-GENE-001127-3 64267 481 atp1b1a GO:0030216 keratinocyte differentiation PATO:0001507 disrupted abnormal ZDB-GENE-001127-3 64267 481 atp1b1a GO:0060047 heart contraction PATO:0000911 decreased rate abnormal ZDB-GENE-001127-3 64267 481 atp1b1a ZFA:0000054 pericardium PATO:0001450 edematous abnormal ZDB-GENE-001127-3 64267 481 atp1b1a ZFA:0000089 fin fold actinotrichium PATO:0001445 disassembled abnormal ZDB-GENE-001127-3 64267 481 atp1b1a GO:0005604 basement membrane BFO:0000050 part_of ZFA:0000105 epidermis PATO:0001444 broken abnormal ZDB-GENE-001127-3 64267 481 atp1b1a GO:0008219 cell death BFO:0000066 occurs_in ZFA:0000105 epidermis PATO:0002051 increased occurrence abnormal ZDB-GENE-001127-3 64267 481 atp1b1a ZFA:0000105 epidermis PATO:0000051 morphology abnormal ZDB-GENE-001127-3 64267 481 atp1b1a ZFA:0000105 epidermis PATO:0000141 structure abnormal ZDB-GENE-001127-3 64267 481 atp1b1a GO:0086001 cardiac muscle cell action potential BFO:0000066 occurs_in ZFA:0000114 heart PATO:0000499 decreased duration abnormal ZDB-GENE-001127-3 64267 481 atp1b1a ZFA:0000114 heart PATO:0001624 decreased functionality abnormal ZDB-GENE-001127-3 64267 481 atp1b1a ZFA:0000151 pronephros PATO:0001624 decreased functionality abnormal ZDB-GENE-001127-3 64267 481 atp1b1a ZFA:0001094 whole organism PATO:0000718 lethal (sensu genetics) abnormal ZDB-GENE-001127-3 64267 481 atp1b1a GO:0008283 cell population proliferation BFO:0000066 occurs_in ZFA:0001180 epidermal basal stratum PATO:0002051 increased occurrence abnormal ZDB-GENE-001127-3 64267 481 atp1b1a ZFA:0009158 keratinocyte BFO:0000050 part_of ZFA:0001180 epidermal basal stratum PATO:0000470 increased amount abnormal ZDB-GENE-001127-3 64267 481 atp1b1a ZFA:0009158 keratinocyte BFO:0000050 part_of ZFA:0001180 epidermal basal stratum PATO:0000628 mislocalised abnormal ZDB-GENE-001127-3 64267 481 atp1b1a ZFA:0009158 keratinocyte BFO:0000050 part_of ZFA:0001180 epidermal basal stratum PATO:0001629 aggregated abnormal ZDB-GENE-001127-3 64267 481 atp1b1a ZFA:0009041 peridermal cell PATO:0000411 circular abnormal ZDB-GENE-001127-3 64267 481 atp1b1a ZFA:0009041 peridermal cell PATO:0001629 aggregated abnormal ZDB-GENE-001127-3 64267 481 atp1b1a ZFA:0009183 epidermal cell PATO:0000470 increased amount abnormal ZDB-GENE-001127-3 64267 481 atp1b1a ZFA:0009183 epidermal cell PATO:0000628 mislocalised abnormal ZDB-GENE-001127-3 64267 481 atp1b1a ZFA:0009183 epidermal cell PATO:0001629 aggregated abnormal ZDB-GENE-001205-1 64274 1436 csf1ra GO:0001568 blood vessel development PATO:0001507 disrupted abnormal ZDB-GENE-001205-1 64274 1436 csf1ra GO:0003407 neural retina development PATO:0000502 delayed abnormal ZDB-GENE-001205-1 64274 1436 csf1ra GO:0003407 neural retina development PATO:0002302 decreased process quality abnormal ZDB-GENE-001205-1 64274 1436 csf1ra GO:0043473 pigmentation PATO:0001507 disrupted abnormal ZDB-GENE-001205-1 64274 1436 csf1ra GO:0045453 bone resorption PATO:0002302 decreased process quality abnormal ZDB-GENE-001205-1 64274 1436 csf1ra GO:0048246 macrophage chemotaxis PATO:0002302 decreased process quality abnormal ZDB-GENE-001205-1 64274 1436 csf1ra GO:0050936 xanthophore differentiation PATO:0001507 disrupted abnormal ZDB-GENE-001205-1 64274 1436 csf1ra GO:0070285 pigment cell development PATO:0002302 decreased process quality abnormal ZDB-GENE-001205-1 64274 1436 csf1ra ZFA:0009141 macrophage BFO:0000050 part_of ZFA:0000008 brain PATO:0001997 decreased amount abnormal ZDB-GENE-001205-1 64274 1436 csf1ra ZFA:0000008 brain PATO:0002000 lacks all parts of type abnormal ZFA:0009077 microglial cell ZDB-GENE-001205-1 64274 1436 csf1ra ZFA:0009141 macrophage BFO:0000050 part_of ZFA:0000054 pericardium PATO:0001997 decreased amount abnormal ZDB-GENE-001205-1 64274 1436 csf1ra ZFA:0000075 spinal cord PATO:0001645 protruding into abnormal ZFA:0000938 central canal ZDB-GENE-001205-1 64274 1436 csf1ra ZFA:0009141 macrophage BFO:0000050 part_of ZFA:0000094 blood island PATO:0001997 decreased amount abnormal ZDB-GENE-001205-1 64274 1436 csf1ra ZFA:0000107 eye PATO:0000587 decreased size abnormal ZDB-GENE-001205-1 64274 1436 csf1ra ZFA:0000108 fin PATO:0000019 color pattern abnormal ZDB-GENE-001205-1 64274 1436 csf1ra ZFA:0009111 hepatocyte BFO:0000050 part_of ZFA:0000123 liver PATO:0000937 disorganized abnormal ZDB-GENE-001205-1 64274 1436 csf1ra ZFA:0009141 macrophage BFO:0000050 part_of ZFA:0000123 liver PATO:0001997 decreased amount abnormal ZDB-GENE-001205-1 64274 1436 csf1ra GO:0030282 bone mineralization BFO:0000066 occurs_in ZFA:0000126 centrum PATO:0002304 increased process quality abnormal ZDB-GENE-001205-1 64274 1436 csf1ra ZFA:0000126 centrum PATO:0001714 increased diameter abnormal ZDB-GENE-001205-1 64274 1436 csf1ra ZFA:0000126 centrum PATO:0001788 increased mass density abnormal ZDB-GENE-001205-1 64274 1436 csf1ra ZFA:0009141 macrophage BFO:0000050 part_of ZFA:0000128 midbrain PATO:0001997 decreased amount abnormal ZDB-GENE-001205-1 64274 1436 csf1ra GO:0022008 neurogenesis BFO:0000066 occurs_in ZFA:0000152 retina PATO:0002302 decreased process quality abnormal ZDB-GENE-001205-1 64274 1436 csf1ra GO:0030182 neuron differentiation BFO:0000066 occurs_in ZFA:0000152 retina PATO:0000502 delayed abnormal ZDB-GENE-001205-1 64274 1436 csf1ra GO:0030182 neuron differentiation BFO:0000066 occurs_in ZFA:0000152 retina PATO:0002302 decreased process quality abnormal ZDB-GENE-001205-1 64274 1436 csf1ra ZFA:0000152 retina PATO:0002000 lacks all parts of type abnormal ZFA:0009077 microglial cell ZDB-GENE-001205-1 64274 1436 csf1ra ZFA:0000152 retina PATO:0002100 undifferentiated abnormal ZDB-GENE-001205-1 64274 1436 csf1ra ZFA:0000152 retina PATO:0002102 proliferative abnormal ZDB-GENE-001205-1 64274 1436 csf1ra ZFA:0000180 caudal vein PATO:0000628 mislocalised abnormal ZDB-GENE-001205-1 64274 1436 csf1ra GO:0045453 bone resorption BFO:0000066 occurs_in ZFA:0000277 scale PATO:0002052 decreased occurrence abnormal ZDB-GENE-001205-1 64274 1436 csf1ra ZFA:0001463 melanophore stripe BFO:0000050 part_of ZFA:0000368 integument PATO:0000060 spatial pattern abnormal ZDB-GENE-001205-1 64274 1436 csf1ra ZFA:0001463 melanophore stripe BFO:0000050 part_of ZFA:0000368 integument PATO:0040026 structurally discontinuous abnormal ZDB-GENE-001205-1 64274 1436 csf1ra ZFA:0009198 xanthophore BFO:0000050 part_of ZFA:0000368 integument PATO:0000462 absent abnormal ZDB-GENE-001205-1 64274 1436 csf1ra ZFA:0009198 xanthophore BFO:0000050 part_of ZFA:0000368 integument PATO:0001997 decreased amount abnormal ZDB-GENE-001205-1 64274 1436 csf1ra ZFA:0000368 integument PATO:0002001 has fewer parts of type abnormal ZFA:0009091 melanocyte ZDB-GENE-001205-1 64274 1436 csf1ra ZFA:0000368 integument PATO:0002000 lacks all parts of type abnormal ZFA:0009198 xanthophore ZDB-GENE-001205-1 64274 1436 csf1ra ZFA:0000368 integument PATO:0000019 color pattern abnormal ZDB-GENE-001205-1 64274 1436 csf1ra ZFA:0009141 macrophage BFO:0000050 part_of ZFA:0000436 spleen PATO:0001997 decreased amount abnormal ZDB-GENE-001205-1 64274 1436 csf1ra BSPO:0000080 dorso-lateral region BFO:0000050 part_of ZFA:0000445 optic tectum PATO:0002001 has fewer parts of type abnormal ZFA:0009077 microglial cell ZDB-GENE-001205-1 64274 1436 csf1ra ZFA:0009077 microglial cell BFO:0000050 part_of ZFA:0000445 optic tectum PATO:0001997 decreased amount abnormal ZDB-GENE-001205-1 64274 1436 csf1ra ZFA:0009047 osteoclast BFO:0000050 part_of ZFA:0000519 hemal arch PATO:0001997 decreased amount abnormal ZDB-GENE-001205-1 64274 1436 csf1ra BSPO:0000374 basal surface BFO:0000050 part_of ZFA:0000694 ceratobranchial 5 tooth PATO:0002126 osseous abnormal ZDB-GENE-001205-1 64274 1436 csf1ra ZFA:0000938 central canal PATO:0001715 decreased diameter abnormal ZDB-GENE-001205-1 64274 1436 csf1ra ZFA:0009141 macrophage BFO:0000050 part_of ZFA:0001058 caudal fin PATO:0001997 decreased amount abnormal ZDB-GENE-001205-1 64274 1436 csf1ra ZFA:0009047 osteoclast BFO:0000050 part_of ZFA:0001066 neural arch PATO:0001997 decreased amount abnormal ZDB-GENE-001205-1 64274 1436 csf1ra ZFA:0001066 neural arch PATO:0002328 decreased angle to abnormal ZFA:0001189 vertebra ZDB-GENE-001205-1 64274 1436 csf1ra ZFA:0001066 neural arch PATO:0002057 increased area abnormal ZDB-GENE-001205-1 64274 1436 csf1ra ZFA:0001066 neural arch PATO:0002495 dorsal orientation abnormal ZDB-GENE-001205-1 64274 1436 csf1ra GO:0007626 locomotory behavior BFO:0000066 occurs_in ZFA:0001094 whole organism PATO:0002304 increased process quality abnormal ZDB-GENE-001205-1 64274 1436 csf1ra ZFA:0001094 whole organism PATO:0002001 has fewer parts of type abnormal ZFA:0009091 melanocyte ZDB-GENE-001205-1 64274 1436 csf1ra ZFA:0001094 whole organism PATO:0002000 lacks all parts of type abnormal ZFA:0009198 xanthophore ZDB-GENE-001205-1 64274 1436 csf1ra ZFA:0001094 whole organism PATO:0002001 has fewer parts of type abnormal ZFA:0009198 xanthophore ZDB-GENE-001205-1 64274 1436 csf1ra ZFA:0001094 whole organism PATO:0000333 spotted abnormal ZDB-GENE-001205-1 64274 1436 csf1ra ZFA:0001094 whole organism PATO:0000587 decreased size abnormal ZDB-GENE-001205-1 64274 1436 csf1ra ZFA:0001094 whole organism PATO:0001286 desaturated yellow abnormal ZDB-GENE-001205-1 64274 1436 csf1ra ZFA:0001094 whole organism PATO:0002251 decreased pigmentation abnormal ZDB-GENE-001205-1 64274 1436 csf1ra ZFA:0009198 xanthophore BFO:0000050 part_of ZFA:0001114 head PATO:0000330 irregular spatial pattern abnormal ZDB-GENE-001205-1 64274 1436 csf1ra ZFA:0001114 head PATO:0002001 has fewer parts of type abnormal ZFA:0009198 xanthophore ZDB-GENE-001205-1 64274 1436 csf1ra BSPO:0000085 ventro-lateral region BFO:0000050 part_of ZFA:0001115 trunk PATO:0002001 has fewer parts of type abnormal ZFA:0009198 xanthophore ZDB-GENE-001205-1 64274 1436 csf1ra ZFA:0001119 dermis BFO:0000050 part_of ZFA:0001115 trunk PATO:0002001 has fewer parts of type abnormal ZFA:0009091 melanocyte ZDB-GENE-001205-1 64274 1436 csf1ra ZFA:0001119 dermis BFO:0000050 part_of ZFA:0001115 trunk PATO:0002000 lacks all parts of type abnormal ZFA:0009198 xanthophore ZDB-GENE-001205-1 64274 1436 csf1ra ZFA:0001463 melanophore stripe BFO:0000050 part_of ZFA:0001115 trunk PATO:0002001 has fewer parts of type abnormal ZFA:0009091 melanocyte ZDB-GENE-001205-1 64274 1436 csf1ra ZFA:0001463 melanophore stripe BFO:0000050 part_of ZFA:0001115 trunk PATO:0000646 malformed abnormal ZDB-GENE-001205-1 64274 1436 csf1ra ZFA:0001463 melanophore stripe BFO:0000050 part_of ZFA:0001115 trunk PATO:0000937 disorganized abnormal ZDB-GENE-001205-1 64274 1436 csf1ra ZFA:0009091 melanocyte BFO:0000050 part_of ZFA:0001115 trunk PATO:0000628 mislocalised abnormal ZDB-GENE-001205-1 64274 1436 csf1ra ZFA:0009199 iridophore BFO:0000050 part_of ZFA:0001115 trunk PATO:0000628 mislocalised abnormal ZDB-GENE-001205-1 64274 1436 csf1ra ZFA:0001115 trunk PATO:0002000 lacks all parts of type abnormal ZFA:0009198 xanthophore ZDB-GENE-001205-1 64274 1436 csf1ra ZFA:0009091 melanocyte BFO:0000050 part_of ZFA:0001136 hypodermis PATO:0001997 decreased amount abnormal ZDB-GENE-001205-1 64274 1436 csf1ra ZFA:0009198 xanthophore BFO:0000050 part_of ZFA:0001136 hypodermis PATO:0000462 absent abnormal ZDB-GENE-001205-1 64274 1436 csf1ra ZFA:0001463 melanophore stripe BFO:0000050 part_of ZFA:0001162 anal fin PATO:0001608 patchy abnormal ZDB-GENE-001205-1 64274 1436 csf1ra ZFA:0001162 anal fin PATO:0002001 has fewer parts of type abnormal ZFA:0001463 melanophore stripe ZDB-GENE-001205-1 64274 1436 csf1ra ZFA:0001162 anal fin PATO:0000333 spotted abnormal ZDB-GENE-001205-1 64274 1436 csf1ra ZFA:0001189 vertebra PATO:0000051 morphology abnormal ZDB-GENE-001205-1 64274 1436 csf1ra ZFA:0001189 vertebra PATO:0000587 decreased size abnormal ZDB-GENE-001205-1 64274 1436 csf1ra ZFA:0001189 vertebra PATO:0000595 increased volume abnormal ZDB-GENE-001205-1 64274 1436 csf1ra ZFA:0001463 melanophore stripe PATO:0000051 morphology abnormal ZDB-GENE-001205-1 64274 1436 csf1ra ZFA:0001463 melanophore stripe PATO:0000328 low saturation abnormal ZDB-GENE-001205-1 64274 1436 csf1ra ZFA:0001463 melanophore stripe PATO:0000330 irregular spatial pattern abnormal ZDB-GENE-001205-1 64274 1436 csf1ra ZFA:0001463 melanophore stripe PATO:0000333 spotted abnormal ZDB-GENE-001205-1 64274 1436 csf1ra ZFA:0001463 melanophore stripe PATO:0000462 absent abnormal ZDB-GENE-001205-1 64274 1436 csf1ra ZFA:0001463 melanophore stripe PATO:0000587 decreased size abnormal ZDB-GENE-001205-1 64274 1436 csf1ra ZFA:0001463 melanophore stripe PATO:0001608 patchy abnormal ZDB-GENE-001205-1 64274 1436 csf1ra ZFA:0005929 xantholeucophore PATO:0000462 absent abnormal ZDB-GENE-001205-1 64274 1436 csf1ra GO:0006915 apoptotic process BFO:0000066 occurs_in ZFA:0009047 osteoclast PATO:0002051 increased occurrence abnormal ZDB-GENE-001205-1 64274 1436 csf1ra GO:0006915 apoptotic process BFO:0000066 occurs_in ZFA:0009047 osteoclast PATO:0002052 decreased occurrence abnormal ZDB-GENE-001205-1 64274 1436 csf1ra ZFA:0009047 osteoclast PATO:0001997 decreased amount abnormal ZDB-GENE-001205-1 64274 1436 csf1ra ZFA:0009077 microglial cell PATO:0001790 decreased mass density abnormal ZDB-GENE-001205-1 64274 1436 csf1ra ZFA:0009077 microglial cell PATO:0001997 decreased amount abnormal ZDB-GENE-001205-1 64274 1436 csf1ra ZFA:0009090 pigment cell PATO:0000001 quality abnormal ZDB-GENE-001205-1 64274 1436 csf1ra ZFA:0009090 pigment cell PATO:0000330 irregular spatial pattern abnormal ZDB-GENE-001205-1 64274 1436 csf1ra ZFA:0009091 melanocyte PATO:0000001 quality abnormal ZDB-GENE-001205-1 64274 1436 csf1ra ZFA:0009091 melanocyte PATO:0000330 irregular spatial pattern abnormal ZDB-GENE-001205-1 64274 1436 csf1ra GO:0005811 lipid droplet BFO:0000050 part_of ZFA:0009111 hepatocyte PATO:0000470 increased amount abnormal ZDB-GENE-001205-1 64274 1436 csf1ra ZFA:0009141 macrophage PATO:0000304 decreased speed abnormal ZDB-GENE-001205-1 64274 1436 csf1ra ZFA:0009141 macrophage PATO:0001499 spherical abnormal ZDB-GENE-001205-1 64274 1436 csf1ra ZFA:0009141 macrophage PATO:0001997 decreased amount abnormal ZDB-GENE-001205-1 64274 1436 csf1ra ZFA:0009198 xanthophore PATO:0000001 quality abnormal ZDB-GENE-001205-1 64274 1436 csf1ra ZFA:0009198 xanthophore PATO:0000060 spatial pattern abnormal ZDB-GENE-001205-1 64274 1436 csf1ra ZFA:0009198 xanthophore PATO:0000462 absent abnormal ZDB-GENE-001205-1 64274 1436 csf1ra ZFA:0009198 xanthophore PATO:0001351 area density abnormal ZDB-GENE-001205-1 64274 1436 csf1ra ZFA:0009198 xanthophore PATO:0001997 decreased amount abnormal ZDB-GENE-001205-1 64274 1436 csf1ra ZFA:0009310 retinal ganglion cell PATO:0002100 undifferentiated abnormal ZDB-GENE-001205-3 64263 2643 gch2 ZFA:0009198 xanthophore BFO:0000050 part_of ZFA:0001058 caudal fin PATO:0001997 decreased amount abnormal ZDB-GENE-001205-3 64263 2643 gch2 ZFA:0009198 xanthophore BFO:0000050 part_of ZFA:0001114 head PATO:0000331 discolored abnormal ZDB-GENE-001205-3 64263 2643 gch2 ZFA:0009198 xanthophore BFO:0000050 part_of ZFA:0001115 trunk PATO:0000331 discolored abnormal ZDB-GENE-001205-4 550475 1513 ctsk GO:0030282 bone mineralization BFO:0000066 occurs_in ZFA:0001189 vertebra PATO:0002304 increased process quality abnormal ZDB-GENE-001205-4 550475 1513 ctsk ZFA:0001189 vertebra PATO:0001788 increased mass density abnormal ZDB-GENE-001205-4 550475 1513 ctsk ZFA:0005941 bone callus PATO:0001646 protruding out of abnormal ZFA:0001189 vertebra ZDB-GENE-001205-4 550475 1513 ctsk GO:0005581 collagen trimer BFO:0000050 part_of ZFA:0007118 vertebral body end plate PATO:0002264 organization quality abnormal ZDB-GENE-001205-4 550475 1513 ctsk GO:0030282 bone mineralization BFO:0000066 occurs_in ZFA:0007118 vertebral body end plate PATO:0002304 increased process quality abnormal ZDB-GENE-001205-4 550475 1513 ctsk ZFA:0007118 vertebral body end plate PATO:0000386 hard abnormal ZDB-GENE-001205-4 550475 1513 ctsk ZFA:0007118 vertebral body end plate PATO:0040019 fibrotic abnormal ZDB-GENE-001206-2 64276 85474 lbx2 GO:0003147 neural crest cell migration involved in heart formation PATO:0001507 disrupted abnormal ZDB-GENE-001206-2 64276 85474 lbx2 GO:0060070 canonical Wnt signaling pathway PATO:0002052 decreased occurrence abnormal ZDB-GENE-001206-2 64276 85474 lbx2 ZFA:0000003 adaxial cell PATO:0000051 morphology abnormal ZDB-GENE-001206-2 64276 85474 lbx2 ZFA:0000009 cardiac ventricle PATO:0000051 morphology abnormal ZDB-GENE-001206-2 64276 85474 lbx2 ZFA:0000009 cardiac ventricle PATO:0000586 increased size abnormal ZDB-GENE-001206-2 64276 85474 lbx2 ZFA:0000114 heart PATO:0000586 increased size abnormal ZDB-GENE-001206-2 64276 85474 lbx2 ZFA:0000471 atrium PATO:0000586 increased size abnormal ZDB-GENE-001206-2 64276 85474 lbx2 BSPO:0000072 posterior region BFO:0000050 part_of ZFA:0001058 caudal fin PATO:0000462 absent abnormal ZDB-GENE-001206-2 64276 85474 lbx2 BSPO:0000084 ventral region BFO:0000050 part_of ZFA:0001058 caudal fin PATO:0000462 absent abnormal ZDB-GENE-001206-2 64276 85474 lbx2 GO:0030016 myofibril BFO:0000050 part_of ZFA:0001086 muscle pioneer PATO:0000574 decreased length abnormal ZDB-GENE-001206-2 64276 85474 lbx2 GO:0030016 myofibril BFO:0000050 part_of ZFA:0001086 muscle pioneer PATO:0000592 decreased thickness abnormal ZDB-GENE-001206-2 64276 85474 lbx2 ZFA:0001094 whole organism PATO:0000620 wholly dorsalized abnormal ZDB-GENE-001206-2 64276 85474 lbx2 ZFA:0001094 whole organism PATO:0001154 elongated abnormal ZDB-GENE-001206-2 64276 85474 lbx2 BSPO:0000072 posterior region BFO:0000050 part_of ZFA:0001115 trunk PATO:0000462 absent abnormal ZDB-GENE-001206-2 64276 85474 lbx2 BSPO:0000084 ventral region BFO:0000050 part_of ZFA:0001115 trunk PATO:0000462 absent abnormal ZDB-GENE-001206-2 64276 85474 lbx2 GO:0030016 myofibril BFO:0000050 part_of ZFA:0009116 slow muscle cell PATO:0000574 decreased length abnormal ZDB-GENE-001206-2 64276 85474 lbx2 GO:0030016 myofibril BFO:0000050 part_of ZFA:0009116 slow muscle cell PATO:0000592 decreased thickness abnormal ZDB-GENE-001206-2 64276 85474 lbx2 ZFA:0009116 slow muscle cell PATO:0000646 malformed abnormal ZDB-GENE-001206-2 64276 85474 lbx2 GO:0030016 myofibril BFO:0000050 part_of ZFA:0009117 fast muscle cell PATO:0000574 decreased length abnormal ZDB-GENE-001206-2 64276 85474 lbx2 ZFA:0009117 fast muscle cell PATO:0000651 unfused from abnormal ZFA:0009117 fast muscle cell ZDB-GENE-001206-2 64276 85474 lbx2 ZFA:0009117 fast muscle cell PATO:0000646 malformed abnormal ZDB-GENE-001206-2 64276 85474 lbx2 ZFA:0009316 cardiac muscle cell PATO:0002452 decondensed abnormal ZDB-GENE-001207-1 64275 6829 supt5h GO:0002244 hematopoietic progenitor cell differentiation PATO:0002052 decreased occurrence abnormal ZDB-GENE-001207-1 64275 6829 supt5h GO:0009790 embryo development PATO:0000502 delayed abnormal ZDB-GENE-001207-1 64275 6829 supt5h GO:0030097 hemopoiesis PATO:0001507 disrupted abnormal ZDB-GENE-001207-1 64275 6829 supt5h GO:0043473 pigmentation PATO:0001507 disrupted abnormal ZDB-GENE-001207-1 64275 6829 supt5h GO:0060218 hematopoietic stem cell differentiation PATO:0002052 decreased occurrence abnormal ZDB-GENE-001207-1 64275 6829 supt5h ZFA:0000008 brain PATO:0000051 morphology abnormal ZDB-GENE-001207-1 64275 6829 supt5h ZFA:0009301 dopaminergic neuron BFO:0000050 part_of ZFA:0000032 hypothalamus PATO:0001997 decreased amount abnormal ZDB-GENE-001207-1 64275 6829 supt5h ZFA:0000054 pericardium PATO:0001450 edematous abnormal ZDB-GENE-001207-1 64275 6829 supt5h ZFA:0000106 extension PATO:0000574 decreased length abnormal ZDB-GENE-001207-1 64275 6829 supt5h ZFA:0000107 eye PATO:0000001 quality abnormal ZDB-GENE-001207-1 64275 6829 supt5h ZFA:0000114 heart PATO:0000001 quality abnormal ZDB-GENE-001207-1 64275 6829 supt5h ZFA:0000114 heart PATO:0001450 edematous abnormal ZDB-GENE-001207-1 64275 6829 supt5h ZFA:0000152 retina PATO:0001999 lacks parts or has fewer parts of type abnormal ZFA:0009301 dopaminergic neuron ZDB-GENE-001207-1 64275 6829 supt5h ZFA:0000155 somite PATO:0000639 degenerate abnormal ZDB-GENE-001207-1 64275 6829 supt5h ZFA:0000217 inner ear PATO:0000001 quality abnormal ZDB-GENE-001207-1 64275 6829 supt5h ZFA:0000282 sensory system PATO:0000001 quality abnormal ZDB-GENE-001207-1 64275 6829 supt5h ZFA:0000360 heart tube PATO:0002106 poorly differentiated abnormal ZDB-GENE-001207-1 64275 6829 supt5h ZFA:0000396 nervous system PATO:0000001 quality abnormal ZDB-GENE-001207-1 64275 6829 supt5h ZFA:0001094 whole organism PATO:0001422 dead abnormal ZDB-GENE-001207-1 64275 6829 supt5h ZFA:0001094 whole organism PATO:0002251 decreased pigmentation abnormal ZDB-GENE-001207-1 64275 6829 supt5h ZFA:0001117 post-vent region PATO:0000001 quality abnormal ZDB-GENE-001207-1 64275 6829 supt5h ZFA:0001117 post-vent region PATO:0000051 morphology abnormal ZDB-GENE-001207-1 64275 6829 supt5h ZFA:0001117 post-vent region PATO:0000574 decreased length abnormal ZDB-GENE-001207-1 64275 6829 supt5h ZFA:0001117 post-vent region PATO:0001469 curved ventral abnormal ZDB-GENE-001207-1 64275 6829 supt5h ZFA:0001202 optic cup PATO:0000051 morphology abnormal ZDB-GENE-001207-1 64275 6829 supt5h ZFA:0009014 hematopoietic stem cell BFO:0000050 part_of ZFA:0005028 ventral wall of dorsal aorta PATO:0001997 decreased amount abnormal ZDB-GENE-001207-1 64275 6829 supt5h ZFA:0009052 motor neuron PATO:0000001 quality abnormal ZDB-GENE-001207-1 64275 6829 supt5h ZFA:0009090 pigment cell PATO:0000001 quality abnormal ZDB-GENE-001207-1 64275 6829 supt5h ZFA:0009091 melanocyte PATO:0001997 decreased amount abnormal ZDB-GENE-001207-1 64275 6829 supt5h ZFA:0009248 neuron PATO:0000638 apoptotic abnormal ZDB-GENE-001207-1 64275 6829 supt5h GO:0048666 neuron development BFO:0000066 occurs_in ZFA:0009301 dopaminergic neuron PATO:0001507 disrupted abnormal ZDB-GENE-001207-1 64275 6829 supt5h GO:0008283 cell population proliferation BFO:0000066 occurs_in ZFA:0009354 hematopoietic multipotent progenitor cell PATO:0002052 decreased occurrence abnormal ZDB-GENE-001207-1 64275 6829 supt5h ZFA:0009354 hematopoietic multipotent progenitor cell PATO:0001997 decreased amount abnormal ZDB-GENE-001207-3 64277 9915 arnt2 GO:0001964 startle response PATO:0001507 disrupted abnormal ZDB-GENE-001207-3 64277 9915 arnt2 GO:0009605 response to external stimulus PATO:0000001 quality abnormal ZDB-GENE-001207-3 64277 9915 arnt2 GO:0021591 ventricular system development PATO:0001507 disrupted abnormal ZDB-GENE-001207-3 64277 9915 arnt2 GO:0021979 hypothalamus cell differentiation PATO:0001236 process quality abnormal ZDB-GENE-001207-3 64277 9915 arnt2 GO:0042417 dopamine metabolic process PATO:0000001 quality abnormal ZDB-GENE-001207-3 64277 9915 arnt2 GO:0048798 swim bladder inflation PATO:0001507 disrupted abnormal ZDB-GENE-001207-3 64277 9915 arnt2 GO:0050881 musculoskeletal movement PATO:0001507 disrupted abnormal ZDB-GENE-001207-3 64277 9915 arnt2 GO:0050975 sensory perception of touch PATO:0001507 disrupted abnormal ZDB-GENE-001207-3 64277 9915 arnt2 GO:0060047 heart contraction PATO:0000911 decreased rate abnormal ZDB-GENE-001207-3 64277 9915 arnt2 GO:0070586 cell-cell adhesion involved in gastrulation PATO:0001507 disrupted abnormal ZDB-GENE-001207-3 64277 9915 arnt2 GO:0071542 dopaminergic neuron differentiation PATO:0001236 process quality abnormal ZDB-GENE-001207-3 64277 9915 arnt2 ZFA:0000009 cardiac ventricle PATO:0000586 increased size abnormal ZDB-GENE-001207-3 64277 9915 arnt2 ZFA:0000009 cardiac ventricle PATO:0000592 decreased thickness abnormal ZDB-GENE-001207-3 64277 9915 arnt2 GO:0009952 anterior/posterior pattern specification BFO:0000066 occurs_in ZFA:0000029 hindbrain PATO:0001507 disrupted abnormal ZDB-GENE-001207-3 64277 9915 arnt2 GO:0030424 axon BFO:0000050 part_of ZFA:0000029 hindbrain PATO:0000051 morphology abnormal ZDB-GENE-001207-3 64277 9915 arnt2 GO:0030424 axon BFO:0000050 part_of ZFA:0000029 hindbrain PATO:0000628 mislocalised abnormal ZDB-GENE-001207-3 64277 9915 arnt2 ZFA:0009292 radial glial cell BFO:0000050 part_of ZFA:0000029 hindbrain PATO:0000051 morphology abnormal ZDB-GENE-001207-3 64277 9915 arnt2 ZFA:0009186 neurosecretory neuron BFO:0000050 part_of ZFA:0000032 hypothalamus PATO:0001997 decreased amount abnormal ZDB-GENE-001207-3 64277 9915 arnt2 ZFA:0009301 dopaminergic neuron BFO:0000050 part_of ZFA:0000032 hypothalamus PATO:0001997 decreased amount abnormal ZDB-GENE-001207-3 64277 9915 arnt2 ZFA:0000076 swim bladder PATO:0002377 uninflated abnormal ZDB-GENE-001207-3 64277 9915 arnt2 ZFA:0009301 dopaminergic neuron BFO:0000050 part_of ZFA:0000101 diencephalon PATO:0001997 decreased amount abnormal ZDB-GENE-001207-3 64277 9915 arnt2 ZFA:0000107 eye PATO:0000587 decreased size abnormal ZDB-GENE-001207-3 64277 9915 arnt2 ZFA:0009186 neurosecretory neuron BFO:0000050 part_of ZFA:0000470 preoptic area PATO:0001997 decreased amount abnormal ZDB-GENE-001207-3 64277 9915 arnt2 ZFA:0009186 neurosecretory neuron BFO:0000050 part_of ZFA:0000633 caudal tuberculum PATO:0001997 decreased amount abnormal ZDB-GENE-001207-3 64277 9915 arnt2 ZFA:0009301 dopaminergic neuron BFO:0000050 part_of ZFA:0000633 caudal tuberculum PATO:0001997 decreased amount abnormal ZDB-GENE-001207-3 64277 9915 arnt2 ZFA:0009147 glial cell (sensu Vertebrata) BFO:0000050 part_of ZFA:0000890 floor plate spinal cord region PATO:0000070 amount abnormal ZDB-GENE-001207-3 64277 9915 arnt2 ZFA:0009147 glial cell (sensu Vertebrata) BFO:0000050 part_of ZFA:0000890 floor plate spinal cord region PATO:0000586 increased size abnormal ZDB-GENE-001207-3 64277 9915 arnt2 GO:0043005 neuron projection BFO:0000050 part_of ZFA:0001083 ventricular zone PATO:0001997 decreased amount abnormal ZDB-GENE-001207-3 64277 9915 arnt2 ZFA:0001094 whole organism PATO:0002076 movement behavioral quality abnormal ZDB-GENE-001207-3 64277 9915 arnt2 ZFA:0001114 head PATO:0000587 decreased size abnormal ZDB-GENE-001207-3 64277 9915 arnt2 ZFA:0001114 head PATO:0001872 cuboid abnormal ZDB-GENE-001207-3 64277 9915 arnt2 ZFA:0009177 blastoderm cell BFO:0000050 part_of ZFA:0001176 blastoderm PATO:0000411 circular abnormal ZDB-GENE-001207-3 64277 9915 arnt2 ZFA:0001261 ventricular system PATO:0000595 increased volume abnormal ZDB-GENE-001207-3 64277 9915 arnt2 GO:0030424 axon BFO:0000050 part_of ZFA:0001659 diencephalic nucleus PATO:0002168 displaced to abnormal BSPO:0000083 medial region BFO:0000050 part_of ZFA:0000029 hindbrain ZDB-GENE-001207-3 64277 9915 arnt2 ZFA:0000007 blood BFO:0000050 part_of ZFA:0005091 hepatic sinusoid PATO:0000595 increased volume abnormal ZDB-GENE-001207-3 64277 9915 arnt2 ZFA:0005091 hepatic sinusoid PATO:0000051 morphology abnormal ZDB-GENE-001207-3 64277 9915 arnt2 ZFA:0005091 hepatic sinusoid PATO:0000586 increased size abnormal ZDB-GENE-001207-3 64277 9915 arnt2 GO:0043005 neuron projection BFO:0000050 part_of ZFA:0007024 anterior neural keel PATO:0001997 decreased amount abnormal ZDB-GENE-001207-3 64277 9915 arnt2 ZFA:0009301 dopaminergic neuron PATO:0001997 decreased amount abnormal ZDB-GENE-001212-1 64612 476 atp1a1a.1 GO:0003144 embryonic heart tube formation PATO:0001507 disrupted abnormal ZDB-GENE-001212-1 64612 476 atp1a1a.1 GO:0003161 cardiac conduction system development PATO:0001507 disrupted abnormal ZDB-GENE-001212-1 64612 476 atp1a1a.1 GO:0008015 blood circulation PATO:0000001 quality abnormal ZDB-GENE-001212-1 64612 476 atp1a1a.1 GO:0021555 midbrain-hindbrain boundary morphogenesis PATO:0001507 disrupted abnormal ZDB-GENE-001212-1 64612 476 atp1a1a.1 GO:0030198 extracellular matrix organization PATO:0001507 disrupted abnormal ZDB-GENE-001212-1 64612 476 atp1a1a.1 GO:0035050 embryonic heart tube development PATO:0001507 disrupted abnormal ZDB-GENE-001212-1 64612 476 atp1a1a.1 GO:0036306 embryonic heart tube elongation PATO:0000502 delayed abnormal ZDB-GENE-001212-1 64612 476 atp1a1a.1 GO:0036306 embryonic heart tube elongation PATO:0001507 disrupted abnormal ZDB-GENE-001212-1 64612 476 atp1a1a.1 GO:0060047 heart contraction PATO:0000297 arrested abnormal ZDB-GENE-001212-1 64612 476 atp1a1a.1 GO:0060047 heart contraction PATO:0000911 decreased rate abnormal ZDB-GENE-001212-1 64612 476 atp1a1a.1 GO:0060047 heart contraction PATO:0001783 decreased intensity abnormal ZDB-GENE-001212-1 64612 476 atp1a1a.1 GO:0060047 heart contraction PATO:0001845 irregular rhythm abnormal ZDB-GENE-001212-1 64612 476 atp1a1a.1 GO:0060974 cell migration involved in heart formation PATO:0001507 disrupted abnormal ZDB-GENE-001212-1 64612 476 atp1a1a.1 GO:0061337 cardiac conduction PATO:0002302 decreased process quality abnormal ZDB-GENE-001212-1 64612 476 atp1a1a.1 GO:0099622 cardiac muscle cell membrane repolarization PATO:0000911 decreased rate abnormal ZDB-GENE-001212-1 64612 476 atp1a1a.1 ZFA:0000008 brain PATO:0000001 quality abnormal ZDB-GENE-001212-1 64612 476 atp1a1a.1 ZFA:0000008 brain PATO:0000051 morphology abnormal ZDB-GENE-001212-1 64612 476 atp1a1a.1 ZFA:0000008 brain PATO:0000407 flat abnormal ZDB-GENE-001212-1 64612 476 atp1a1a.1 ZFA:0000008 brain PATO:0000587 decreased size abnormal ZDB-GENE-001212-1 64612 476 atp1a1a.1 ZFA:0000008 brain PATO:0000639 degenerate abnormal ZDB-GENE-001212-1 64612 476 atp1a1a.1 ZFA:0000008 brain PATO:0001412 unstructured abnormal ZDB-GENE-001212-1 64612 476 atp1a1a.1 ZFA:0000008 brain PATO:0001715 decreased diameter abnormal ZDB-GENE-001212-1 64612 476 atp1a1a.1 ZFA:0000008 brain PATO:0001925 surface feature shape abnormal ZDB-GENE-001212-1 64612 476 atp1a1a.1 ZFA:0000042 midbrain hindbrain boundary PATO:0000051 morphology abnormal ZDB-GENE-001212-1 64612 476 atp1a1a.1 ZFA:0001486 epithelium BFO:0000050 part_of ZFA:0000051 otic vesicle PATO:0000051 morphology abnormal ZDB-GENE-001212-1 64612 476 atp1a1a.1 ZFA:0000051 otic vesicle PATO:0000586 increased size abnormal ZDB-GENE-001212-1 64612 476 atp1a1a.1 ZFA:0000051 otic vesicle PATO:0000599 decreased width abnormal ZDB-GENE-001212-1 64612 476 atp1a1a.1 ZFA:0000051 otic vesicle PATO:0001154 elongated abnormal ZDB-GENE-001212-1 64612 476 atp1a1a.1 ZFA:0000054 pericardium PATO:0000586 increased size abnormal ZDB-GENE-001212-1 64612 476 atp1a1a.1 ZFA:0000054 pericardium PATO:0001450 edematous abnormal ZDB-GENE-001212-1 64612 476 atp1a1a.1 ZFA:0000084 yolk PATO:0000001 quality abnormal ZDB-GENE-001212-1 64612 476 atp1a1a.1 ZFA:0000084 yolk PATO:0001851 swollen abnormal ZDB-GENE-001212-1 64612 476 atp1a1a.1 ZFA:0000107 eye PATO:0000001 quality abnormal ZDB-GENE-001212-1 64612 476 atp1a1a.1 ZFA:0000107 eye PATO:0000587 decreased size abnormal ZDB-GENE-001212-1 64612 476 atp1a1a.1 ZFA:0000110 fourth ventricle PATO:0000587 decreased size abnormal ZDB-GENE-001212-1 64612 476 atp1a1a.1 ZFA:0000110 fourth ventricle PATO:0001715 decreased diameter abnormal ZDB-GENE-001212-1 64612 476 atp1a1a.1 ZFA:0000112 gut PATO:0000001 quality abnormal ZDB-GENE-001212-1 64612 476 atp1a1a.1 ZFA:0000114 heart PATO:0000001 quality abnormal ZDB-GENE-001212-1 64612 476 atp1a1a.1 ZFA:0000114 heart PATO:0000051 morphology abnormal ZDB-GENE-001212-1 64612 476 atp1a1a.1 ZFA:0000114 heart PATO:0001579 contractility abnormal ZDB-GENE-001212-1 64612 476 atp1a1a.1 ZFA:0000114 heart PATO:0001624 decreased functionality abnormal ZDB-GENE-001212-1 64612 476 atp1a1a.1 GO:0031012 extracellular matrix BFO:0000050 part_of ZFA:0000115 heart rudiment PATO:0000025 composition abnormal ZDB-GENE-001212-1 64612 476 atp1a1a.1 ZFA:0000115 heart rudiment PATO:0001999 lacks parts or has fewer parts of type abnormal GO:0031012 extracellular matrix BFO:0000050 part_of ZFA:0000115 heart rudiment ZDB-GENE-001212-1 64612 476 atp1a1a.1 ZFA:0000115 heart rudiment PATO:0002001 has fewer parts of type abnormal GO:0031012 extracellular matrix BFO:0000050 part_of ZFA:0000115 heart rudiment ZDB-GENE-001212-1 64612 476 atp1a1a.1 ZFA:0000159 tectal ventricle PATO:0000587 decreased size abnormal ZDB-GENE-001212-1 64612 476 atp1a1a.1 ZFA:0000217 inner ear PATO:0002000 lacks all parts of type abnormal ZFA:0001617 otolith ZDB-GENE-001212-1 64612 476 atp1a1a.1 ZFA:0000217 inner ear PATO:0000051 morphology abnormal ZDB-GENE-001212-1 64612 476 atp1a1a.1 ZFA:0000217 inner ear PATO:0000587 decreased size abnormal ZDB-GENE-001212-1 64612 476 atp1a1a.1 ZFA:0000282 sensory system PATO:0000001 quality abnormal ZDB-GENE-001212-1 64612 476 atp1a1a.1 ZFA:0000360 heart tube PATO:0000574 decreased length abnormal ZDB-GENE-001212-1 64612 476 atp1a1a.1 ZFA:0000396 nervous system PATO:0000001 quality abnormal ZDB-GENE-001212-1 64612 476 atp1a1a.1 ZFA:0000431 semicircular canal PATO:0001483 aplastic abnormal ZDB-GENE-001212-1 64612 476 atp1a1a.1 GO:0060047 heart contraction BFO:0000066 occurs_in ZFA:0000471 atrium PATO:0001845 irregular rhythm abnormal ZDB-GENE-001212-1 64612 476 atp1a1a.1 ZFA:0000938 central canal PATO:0000592 decreased thickness abnormal ZDB-GENE-001212-1 64612 476 atp1a1a.1 ZFA:0001094 whole organism PATO:0000169 viability abnormal ZDB-GENE-001212-1 64612 476 atp1a1a.1 ZFA:0001094 whole organism PATO:0000587 decreased size abnormal ZDB-GENE-001212-1 64612 476 atp1a1a.1 ZFA:0001094 whole organism PATO:0000639 degenerate abnormal ZDB-GENE-001212-1 64612 476 atp1a1a.1 ZFA:0001094 whole organism PATO:0000647 necrotic abnormal ZDB-GENE-001212-1 64612 476 atp1a1a.1 ZFA:0001094 whole organism PATO:0000718 lethal (sensu genetics) abnormal ZDB-GENE-001212-1 64612 476 atp1a1a.1 ZFA:0001105 embryonic structure PATO:0000625 inverted abnormal ZDB-GENE-001212-1 64612 476 atp1a1a.1 ZFA:0001114 head PATO:0000587 decreased size abnormal ZDB-GENE-001212-1 64612 476 atp1a1a.1 ZFA:0001114 head PATO:0001925 surface feature shape abnormal ZDB-GENE-001212-1 64612 476 atp1a1a.1 ZFA:0001115 trunk PATO:0001468 curved dorsal abnormal ZDB-GENE-001212-1 64612 476 atp1a1a.1 ZFA:0001117 post-vent region PATO:0000406 curved abnormal ZDB-GENE-001212-1 64612 476 atp1a1a.1 ZFA:0001117 post-vent region PATO:0001468 curved dorsal abnormal ZDB-GENE-001212-1 64612 476 atp1a1a.1 ZFA:0001227 mandibular arch skeleton PATO:0000051 morphology abnormal ZDB-GENE-001212-1 64612 476 atp1a1a.1 ZFA:0001259 forebrain ventricle PATO:0000587 decreased size abnormal ZDB-GENE-001212-1 64612 476 atp1a1a.1 ZFA:0001261 ventricular system PATO:0000587 decreased size abnormal ZDB-GENE-001212-1 64612 476 atp1a1a.1 ZFA:0001261 ventricular system PATO:0001478 collapsed abnormal ZDB-GENE-001212-1 64612 476 atp1a1a.1 ZFA:0001261 ventricular system PATO:0002014 structure, cavities abnormal ZDB-GENE-001212-1 64612 476 atp1a1a.1 ZFA:0001439 anatomical system PATO:0000001 quality abnormal ZDB-GENE-001212-1 64612 476 atp1a1a.1 ZFA:0001617 otolith PATO:0000375 decreased distance abnormal ZFA:0001617 otolith ZDB-GENE-001212-1 64612 476 atp1a1a.1 ZFA:0001617 otolith PATO:0000587 decreased size abnormal ZDB-GENE-001212-1 64612 476 atp1a1a.1 ZFA:0005070 atrioventricular node PATO:0000608 closed abnormal ZDB-GENE-001212-1 64612 476 atp1a1a.1 ZFA:0005070 atrioventricular node PATO:0001624 decreased functionality abnormal ZDB-GENE-001212-1 64612 476 atp1a1a.1 ZFA:0009090 pigment cell PATO:0000001 quality abnormal ZDB-GENE-001212-1 64612 476 atp1a1a.1 ZFA:0009091 melanocyte PATO:0000001 quality abnormal ZDB-GENE-001212-1 64612 476 atp1a1a.1 ZFA:0009091 melanocyte PATO:0000051 morphology abnormal ZDB-GENE-001212-1 64612 476 atp1a1a.1 GO:0045177 apical part of cell BFO:0000050 part_of ZFA:0009306 neuroepithelial cell PATO:0000599 decreased width abnormal ZDB-GENE-001212-6 64609 477 atp1a2a GO:0001889 liver development PATO:0001507 disrupted abnormal ZDB-GENE-001212-6 64609 477 atp1a2a GO:0001947 heart looping PATO:0001507 disrupted abnormal ZDB-GENE-001212-6 64609 477 atp1a2a GO:0001966 thigmotaxis PATO:0001507 disrupted abnormal ZDB-GENE-001212-6 64609 477 atp1a2a GO:0007368 determination of left/right symmetry PATO:0001507 disrupted abnormal ZDB-GENE-001212-6 64609 477 atp1a2a GO:0007638 mechanosensory behavior PATO:0001236 process quality abnormal ZDB-GENE-001212-6 64609 477 atp1a2a GO:0035050 embryonic heart tube development PATO:0001507 disrupted abnormal ZDB-GENE-001212-6 64609 477 atp1a2a GO:0048565 digestive tract development PATO:0001507 disrupted abnormal ZDB-GENE-001212-6 64609 477 atp1a2a GO:0051899 membrane depolarization PATO:0001236 process quality abnormal ZDB-GENE-001212-6 64609 477 atp1a2a GO:0060047 heart contraction PATO:0000911 decreased rate abnormal ZDB-GENE-001212-6 64609 477 atp1a2a GO:0060075 regulation of resting membrane potential PATO:0001507 disrupted abnormal ZDB-GENE-001212-6 64609 477 atp1a2a GO:0061371 determination of heart left/right asymmetry PATO:0001507 disrupted abnormal ZDB-GENE-001212-6 64609 477 atp1a2a GO:0005929 cilium BFO:0000050 part_of ZFA:0000001 Kupffer's vesicle PATO:0001906 movement quality abnormal ZDB-GENE-001212-6 64609 477 atp1a2a ZFA:0000054 pericardium PATO:0001450 edematous abnormal ZDB-GENE-001212-6 64609 477 atp1a2a ZFA:0000112 gut PATO:0000628 mislocalised abnormal ZDB-GENE-001212-6 64609 477 atp1a2a ZFA:0000114 heart PATO:0000628 mislocalised abnormal ZDB-GENE-001212-6 64609 477 atp1a2a ZFA:0000123 liver PATO:0000628 mislocalised abnormal ZDB-GENE-001212-6 64609 477 atp1a2a ZFA:0000155 somite PATO:0000051 morphology abnormal ZDB-GENE-001212-6 64609 477 atp1a2a ZFA:0001117 post-vent region PATO:0001468 curved dorsal abnormal ZDB-GENE-001212-7 64610 478 atp1a3a GO:0001966 thigmotaxis PATO:0001236 process quality abnormal ZDB-GENE-001212-7 64610 478 atp1a3a ZFA:0001261 ventricular system PATO:0001571 dilated abnormal ZDB-GENE-001212-7 64610 478 atp1a3a ZFA:0009150 Rohon-Beard neuron PATO:0001462 membrane potential abnormal ZDB-GENE-001212-8 64611 478 atp1a3b GO:0001966 thigmotaxis PATO:0001236 process quality abnormal ZDB-GENE-001212-8 64611 478 atp1a3b ZFA:0001261 ventricular system PATO:0001571 dilated abnormal ZDB-GENE-001221-1 64604 4899 nrf1 ZFA:0000107 eye PATO:0000001 quality abnormal ZDB-GENE-001221-1 64604 4899 nrf1 ZFA:0000107 eye PATO:0000587 decreased size abnormal ZDB-GENE-001221-1 64604 4899 nrf1 ZFA:0000119 retinal inner nuclear layer PATO:0000051 morphology abnormal ZDB-GENE-001221-1 64604 4899 nrf1 ZFA:0000143 retinal photoreceptor layer PATO:0001999 lacks parts or has fewer parts of type abnormal ZFA:0009127 photoreceptor cell ZDB-GENE-001221-1 64604 4899 nrf1 ZFA:0000143 retinal photoreceptor layer PATO:0000001 quality abnormal ZDB-GENE-001221-1 64604 4899 nrf1 ZFA:0000143 retinal photoreceptor layer PATO:0000592 decreased thickness abnormal ZDB-GENE-001221-1 64604 4899 nrf1 GO:0008219 cell death BFO:0000066 occurs_in ZFA:0000152 retina PATO:0002051 increased occurrence abnormal ZDB-GENE-001221-1 64604 4899 nrf1 ZFA:0009000 cell BFO:0000050 part_of ZFA:0000152 retina PATO:0000937 disorganized abnormal ZDB-GENE-001221-1 64604 4899 nrf1 ZFA:0000282 sensory system PATO:0000001 quality abnormal ZDB-GENE-001221-1 64604 4899 nrf1 ZFA:0000396 nervous system PATO:0000001 quality abnormal ZDB-GENE-001221-1 64604 4899 nrf1 GO:0001750 photoreceptor outer segment BFO:0000050 part_of ZFA:0009127 photoreceptor cell PATO:0001617 deformed abnormal ZDB-GENE-001221-1 64604 4899 nrf1 ZFA:0009127 photoreceptor cell PATO:0000411 circular abnormal ZDB-GENE-001221-1 64604 4899 nrf1 ZFA:0009127 photoreceptor cell PATO:0000638 apoptotic abnormal ZDB-GENE-001222-1 796163 338917 vsx2 GO:0003408 optic cup formation involved in camera-type eye development PATO:0001236 process quality abnormal ZDB-GENE-001222-1 796163 338917 vsx2 ZFA:0000107 eye PATO:0000587 decreased size abnormal ZDB-GENE-001222-1 796163 338917 vsx2 ZFA:0000107 eye PATO:0000609 closure incomplete abnormal ZDB-GENE-001222-1 796163 338917 vsx2 ZFA:0000107 eye PATO:0000610 open abnormal ZDB-GENE-001222-1 796163 338917 vsx2 GO:0035736 cell proliferation involved in compound eye morphogenesis BFO:0000066 occurs_in ZFA:0000152 retina PATO:0002052 decreased occurrence abnormal ZDB-GENE-001222-1 796163 338917 vsx2 ZFA:0001094 whole organism PATO:0001999 lacks parts or has fewer parts of type abnormal ZFA:0000107 eye ZDB-GENE-001222-1 796163 338917 vsx2 ZFA:0009280 Muller cell PATO:0001997 decreased amount abnormal ZDB-GENE-001222-1 796163 338917 vsx2 ZFA:0009318 retinal bipolar neuron PATO:0001997 decreased amount abnormal ZDB-GENE-001228-1 64603 8320 eomesa GO:0000226 microtubule cytoskeleton organization PATO:0002302 decreased process quality abnormal ZDB-GENE-001228-1 64603 8320 eomesa GO:0001714 endodermal cell fate specification PATO:0001236 process quality abnormal ZDB-GENE-001228-1 64603 8320 eomesa GO:0055109 invagination involved in gastrulation with mouth forming second PATO:0000502 delayed abnormal ZDB-GENE-001228-1 64603 8320 eomesa ZFA:0000023 forerunner cell group PATO:0001786 split abnormal ZDB-GENE-001228-1 64603 8320 eomesa GO:0005874 microtubule BFO:0000050 part_of ZFA:0000084 yolk PATO:0000060 spatial pattern abnormal ZDB-GENE-001228-1 64603 8320 eomesa ZFA:0000084 yolk PATO:0001154 elongated abnormal ZDB-GENE-001228-1 64603 8320 eomesa ZFA:0000084 yolk PATO:0002254 flattened abnormal ZDB-GENE-001228-1 64603 8320 eomesa GO:0005634 nucleus BFO:0000050 part_of ZFA:0000088 yolk syncytial layer PATO:0000051 morphology abnormal ZDB-GENE-001228-1 64603 8320 eomesa GO:0005634 nucleus BFO:0000050 part_of ZFA:0000088 yolk syncytial layer PATO:0001629 aggregated abnormal ZDB-GENE-001228-1 64603 8320 eomesa ZFA:0000106 extension PATO:0001602 distended abnormal ZDB-GENE-001228-1 64603 8320 eomesa ZFA:0001173 dorsal fin PATO:0000462 absent abnormal ZDB-GENE-001228-1 64603 8320 eomesa ZFA:0001473 deep blastomere BFO:0000050 part_of ZFA:0001175 blastodisc PATO:0000052 shape abnormal ZDB-GENE-001228-1 64603 8320 eomesa ZFA:0001473 deep blastomere BFO:0000050 part_of ZFA:0001175 blastodisc PATO:0000619 crowded abnormal ZDB-GENE-001228-2 64617 1901 s1pr1 GO:0001568 blood vessel development PATO:0001507 disrupted abnormal ZDB-GENE-001228-2 64617 1901 s1pr1 GO:0001947 heart looping PATO:0001507 disrupted abnormal ZDB-GENE-001228-2 64617 1901 s1pr1 GO:0001947 heart looping PATO:0002052 decreased occurrence abnormal ZDB-GENE-001228-2 64617 1901 s1pr1 GO:0002040 sprouting angiogenesis PATO:0001236 process quality abnormal ZDB-GENE-001228-2 64617 1901 s1pr1 GO:0002040 sprouting angiogenesis PATO:0002051 increased occurrence abnormal ZDB-GENE-001228-2 64617 1901 s1pr1 GO:0008078 mesodermal cell migration PATO:0000911 decreased rate abnormal ZDB-GENE-001228-2 64617 1901 s1pr1 GO:0042074 cell migration involved in gastrulation PATO:0001507 disrupted abnormal ZDB-GENE-001228-2 64617 1901 s1pr1 GO:0043542 endothelial cell migration PATO:0000502 delayed abnormal ZDB-GENE-001228-2 64617 1901 s1pr1 GO:0046847 filopodium assembly PATO:0002051 increased occurrence abnormal ZDB-GENE-001228-2 64617 1901 s1pr1 GO:0060312 regulation of blood vessel remodeling PATO:0001236 process quality abnormal ZDB-GENE-001228-2 64617 1901 s1pr1 ZFA:0009065 endothelial cell BFO:0000050 part_of ZFA:0000014 dorsal aorta PATO:0001997 decreased amount abnormal ZDB-GENE-001228-2 64617 1901 s1pr1 ZFA:0000029 hindbrain PATO:0000646 malformed abnormal ZDB-GENE-001228-2 64617 1901 s1pr1 ZFA:0000054 pericardium PATO:0001450 edematous abnormal ZDB-GENE-001228-2 64617 1901 s1pr1 ZFA:0000060 prechordal plate PATO:0000574 decreased length abnormal ZDB-GENE-001228-2 64617 1901 s1pr1 ZFA:0000114 heart PATO:0000051 morphology abnormal ZDB-GENE-001228-2 64617 1901 s1pr1 ZFA:0000114 heart PATO:0001241 physical object quality abnormal ZDB-GENE-001228-2 64617 1901 s1pr1 ZFA:0009138 mesodermal cell BFO:0000050 part_of ZFA:0000117 hypoblast PATO:0000304 decreased speed abnormal ZDB-GENE-001228-2 64617 1901 s1pr1 ZFA:0000131 neural keel PATO:0000574 decreased length abnormal ZDB-GENE-001228-2 64617 1901 s1pr1 GO:0030175 filopodium BFO:0000050 part_of ZFA:0000152 retina PATO:0000470 increased amount abnormal ZDB-GENE-001228-2 64617 1901 s1pr1 ZFA:0009065 endothelial cell BFO:0000050 part_of ZFA:0000477 posterior cardinal vein PATO:0001997 decreased amount abnormal ZDB-GENE-001228-2 64617 1901 s1pr1 ZFA:0009065 endothelial cell BFO:0000050 part_of ZFA:0001285 intersegmental vessel PATO:0001997 decreased amount abnormal ZDB-GENE-001228-2 64617 1901 s1pr1 ZFA:0001285 intersegmental vessel PATO:0000051 morphology abnormal ZDB-GENE-001228-2 64617 1901 s1pr1 ZFA:0001285 intersegmental vessel PATO:0000574 decreased length abnormal ZDB-GENE-001228-2 64617 1901 s1pr1 ZFA:0001285 intersegmental vessel PATO:0002364 shortened abnormal ZDB-GENE-001228-2 64617 1901 s1pr1 ZFA:0009065 endothelial cell BFO:0000050 part_of ZFA:0001286 caudal vein plexus PATO:0002002 has extra parts of type abnormal GO:0030175 filopodium BFO:0000050 part_of ZFA:0009065 endothelial cell ZDB-GENE-001228-2 64617 1901 s1pr1 ZFA:0001286 caudal vein plexus PATO:0000051 morphology abnormal ZDB-GENE-001228-2 64617 1901 s1pr1 ZFA:0001286 caudal vein plexus PATO:0000574 decreased length abnormal ZDB-GENE-001228-2 64617 1901 s1pr1 ZFA:0001286 caudal vein plexus PATO:0000599 decreased width abnormal ZDB-GENE-001228-2 64617 1901 s1pr1 ZFA:0001286 caudal vein plexus PATO:0002058 decreased area abnormal ZDB-GENE-001228-2 64617 1901 s1pr1 ZFA:0009065 endothelial cell BFO:0000050 part_of ZFA:0005025 dorsal longitudinal anastomotic vessel PATO:0001997 decreased amount abnormal ZDB-GENE-001228-2 64617 1901 s1pr1 ZFA:0005025 dorsal longitudinal anastomotic vessel PATO:0000937 disorganized abnormal ZDB-GENE-001228-2 64617 1901 s1pr1 ZFA:0005035 subintestinal vein PATO:0002002 has extra parts of type abnormal ZFA:0005604 angiogenic sprout ZDB-GENE-001228-2 64617 1901 s1pr1 ZFA:0005035 subintestinal vein PATO:0000051 morphology abnormal ZDB-GENE-001228-2 64617 1901 s1pr1 ZFA:0005035 subintestinal vein PATO:0001571 dilated abnormal ZDB-GENE-001228-2 64617 1901 s1pr1 ZFA:0005035 subintestinal vein PATO:0001617 deformed abnormal ZDB-GENE-001228-2 64617 1901 s1pr1 ZFA:0009256 nucleate erythrocyte PATO:0002270 increased accumulation abnormal ZFA:0000094 blood island ZDB-GENE-001229-1 64607 212 alas2 GO:0042541 hemoglobin biosynthetic process PATO:0001507 disrupted abnormal ZDB-GENE-001229-1 64607 212 alas2 ZFA:0000007 blood PATO:0000001 quality abnormal ZDB-GENE-001229-1 64607 212 alas2 ZFA:0000114 heart PATO:0000586 increased size abnormal ZDB-GENE-001229-1 64607 212 alas2 ZFA:0001094 whole organism PATO:0000169 viability abnormal ZDB-GENE-001229-1 64607 212 alas2 ZFA:0001439 anatomical system PATO:0000001 quality abnormal ZDB-GENE-001229-1 64607 212 alas2 ZFA:0005236 basophilic erythroblast PATO:0000586 increased size abnormal ZDB-GENE-001229-1 64607 212 alas2 ZFA:0005237 erythroblast PATO:0000470 increased amount abnormal ZDB-GENE-001229-1 64607 212 alas2 ZFA:0009256 nucleate erythrocyte PATO:0002000 lacks all parts of type abnormal GO:0005833 hemoglobin complex BFO:0000050 part_of ZFA:0009256 nucleate erythrocyte ZDB-GENE-001229-1 64607 212 alas2 ZFA:0009256 nucleate erythrocyte PATO:0000328 low saturation abnormal ZDB-GENE-001229-1 64607 212 alas2 ZFA:0009256 nucleate erythrocyte PATO:0001266 desaturated blue abnormal ZDB-GENE-001229-1 64607 212 alas2 ZFA:0009256 nucleate erythrocyte PATO:0001997 decreased amount abnormal ZDB-GENE-001229-2 64608 211 alas1 GO:0030223 neutrophil differentiation PATO:0001236 process quality abnormal ZDB-GENE-001229-2 64608 211 alas1 GO:0030851 granulocyte differentiation PATO:0001507 disrupted abnormal ZDB-GENE-001229-2 64608 211 alas1 CHEBI:30413 heme BFO:0000050 part_of ZFA:0001094 whole organism PATO:0000470 increased amount abnormal ZDB-GENE-001229-2 64608 211 alas1 CHEBI:30413 heme BFO:0000050 part_of ZFA:0009256 nucleate erythrocyte PATO:0000470 increased amount abnormal ZDB-GENE-001229-2 64608 211 alas1 CHEBI:30413 heme BFO:0000050 part_of ZFA:0009327 neutrophil PATO:0001997 decreased amount abnormal ZDB-GENE-001229-2 64608 211 alas1 GO:0004601 peroxidase activity BFO:0000050 part_of ZFA:0009327 neutrophil PATO:0000297 arrested abnormal ZDB-GENE-001229-2 64608 211 alas1 GO:0030141 secretory granule BFO:0000050 part_of ZFA:0009327 neutrophil PATO:0000462 absent abnormal ZDB-GENE-010102-1 64698 1634 dcn GO:0051216 cartilage development PATO:0001507 disrupted abnormal ZDB-GENE-010102-1 64698 1634 dcn GO:0060028 convergent extension involved in axis elongation PATO:0001507 disrupted abnormal ZDB-GENE-010102-1 64698 1634 dcn ZFA:0001094 whole organism PATO:0000574 decreased length abnormal ZDB-GENE-010102-1 64698 1634 dcn ZFA:0001115 trunk PATO:0000574 decreased length abnormal ZDB-GENE-010102-1 64698 1634 dcn ZFA:0001117 post-vent region PATO:0000574 decreased length abnormal ZDB-GENE-010102-1 64698 1634 dcn ZFA:0001205 Meckel's cartilage PATO:0000574 decreased length abnormal ZDB-GENE-010102-1 64698 1634 dcn ZFA:0001399 palatoquadrate cartilage PATO:0000574 decreased length abnormal ZDB-GENE-010102-1 64698 1634 dcn ZFA:0001400 ceratohyal cartilage PATO:0000574 decreased length abnormal ZDB-GENE-010102-1 64698 1634 dcn ZFA:0001460 pharyngeal arch cartilage PATO:0000617 bent abnormal ZDB-GENE-010102-1 64698 1634 dcn ZFA:0001460 pharyngeal arch cartilage PATO:0001485 condensed abnormal ZDB-GENE-010102-1 64698 1634 dcn ZFA:0001516 ceratobranchial cartilage PATO:0001997 decreased amount abnormal ZDB-GENE-010111-1 64812 6665 sox19b GO:0006338 chromatin remodeling PATO:0001507 disrupted abnormal ZDB-GENE-010111-1 64812 6665 sox19b GO:0007369 gastrulation PATO:0002052 decreased occurrence abnormal ZDB-GENE-010111-1 64812 6665 sox19b GO:0014032 neural crest cell development PATO:0002302 decreased process quality abnormal ZDB-GENE-010111-1 64812 6665 sox19b GO:0090504 epiboly PATO:0002052 decreased occurrence abnormal ZDB-GENE-010111-1 64812 6665 sox19b ZFA:0000079 telencephalon PATO:0000587 decreased size abnormal ZDB-GENE-010111-1 64812 6665 sox19b ZFA:0000092 axis PATO:0000574 decreased length abnormal ZDB-GENE-010111-1 64812 6665 sox19b ZFA:0000101 diencephalon PATO:0000587 decreased size abnormal ZDB-GENE-010111-1 64812 6665 sox19b ZFA:0000135 notochord PATO:0000051 morphology abnormal ZDB-GENE-010111-1 64812 6665 sox19b ZFA:0001058 caudal fin PATO:0001468 curved dorsal abnormal ZDB-GENE-010111-1 64812 6665 sox19b GO:0006915 apoptotic process BFO:0000066 occurs_in ZFA:0001094 whole organism PATO:0002051 increased occurrence abnormal ZDB-GENE-010111-1 64812 6665 sox19b GO:0010467 gene expression BFO:0000066 occurs_in ZFA:0001094 whole organism PATO:0000057 occurrence abnormal ZDB-GENE-010111-1 64812 6665 sox19b GO:0044770 cell cycle phase transition BFO:0000066 occurs_in ZFA:0001094 whole organism PATO:0002052 decreased occurrence abnormal ZDB-GENE-010111-1 64812 6665 sox19b GO:0097296 activation of cysteine-type endopeptidase activity involved in apoptotic signaling pathway BFO:0000066 occurs_in ZFA:0001094 whole organism PATO:0002051 increased occurrence abnormal ZDB-GENE-010111-1 64812 6665 sox19b ZFA:0009000 cell BFO:0000050 part_of ZFA:0001094 whole organism PATO:0000638 apoptotic abnormal ZDB-GENE-010111-1 64812 6665 sox19b ZFA:0001114 head PATO:0000051 morphology abnormal ZDB-GENE-010111-1 64812 6665 sox19b ZFA:0001114 head PATO:0000586 increased size abnormal ZDB-GENE-010111-1 64812 6665 sox19b ZFA:0001114 head PATO:0000587 decreased size abnormal ZDB-GENE-010111-1 64812 6665 sox19b ZFA:0001117 post-vent region PATO:0000462 absent abnormal ZDB-GENE-010111-1 64812 6665 sox19b ZFA:0001117 post-vent region PATO:0000574 decreased length abnormal ZDB-GENE-010111-1 64812 6665 sox19b ZFA:0001117 post-vent region PATO:0001798 kinked abnormal ZDB-GENE-010111-1 64812 6665 sox19b ZFA:0001215 thalamus PATO:0000587 decreased size abnormal ZDB-GENE-010111-1 64812 6665 sox19b ZFA:0001259 forebrain ventricle PATO:0001602 distended abnormal ZDB-GENE-010125-1 65088 4988 oprm1 GO:0000278 mitotic cell cycle BFO:0000066 occurs_in ZFA:0000008 brain PATO:0002304 increased process quality abnormal ZDB-GENE-010125-1 65088 4988 oprm1 BSPO:0000036 anterior-most region BFO:0000050 part_of ZFA:0000029 hindbrain PATO:0000638 apoptotic abnormal ZDB-GENE-010125-1 65088 4988 oprm1 ZFA:0000100 cerebellum PATO:0000638 apoptotic abnormal ZDB-GENE-010125-1 65088 4988 oprm1 ZFA:0000107 eye PATO:0000638 apoptotic abnormal ZDB-GENE-010125-1 65088 4988 oprm1 ZFA:0000109 forebrain PATO:0000638 apoptotic abnormal ZDB-GENE-010125-1 65088 4988 oprm1 GO:0000278 mitotic cell cycle BFO:0000066 occurs_in ZFA:0000110 fourth ventricle PATO:0002304 increased process quality abnormal ZDB-GENE-010125-1 65088 4988 oprm1 GO:0000278 mitotic cell cycle BFO:0000066 occurs_in ZFA:0000445 optic tectum PATO:0002304 increased process quality abnormal ZDB-GENE-010126-2 570240 4915 ntrk2b GO:0001964 startle response PATO:0002304 increased process quality abnormal ZDB-GENE-010126-2 570240 4915 ntrk2b GO:0042596 fear response PATO:0002304 increased process quality abnormal ZDB-GENE-010126-2 570240 4915 ntrk2b GO:0048920 posterior lateral line neuromast primordium migration PATO:0001236 process quality abnormal ZDB-GENE-010126-2 570240 4915 ntrk2b BSPO:0000084 ventral region BFO:0000050 part_of ZFA:0000101 diencephalon PATO:0002001 has fewer parts of type abnormal ZFA:0009301 dopaminergic neuron BFO:0000050 part_of ZFA:0000101 diencephalon ZDB-GENE-010126-2 570240 4915 ntrk2b ZFA:0000324 caudal periventricular hypothalamus PATO:0002001 has fewer parts of type abnormal ZFA:0009361 serotonergic neuron BFO:0000050 part_of ZFA:0000324 caudal periventricular hypothalamus ZDB-GENE-010126-2 570240 4915 ntrk2b ZFA:0000475 paraventricular organ PATO:0002001 has fewer parts of type abnormal ZFA:0009361 serotonergic neuron BFO:0000050 part_of ZFA:0000475 paraventricular organ ZDB-GENE-010126-2 570240 4915 ntrk2b ZFA:0000940 posterior lateral line neuromast PATO:0002001 has fewer parts of type abnormal ZFA:0009367 neuromast hair cell ZDB-GENE-010126-2 570240 4915 ntrk2b ZFA:0000940 posterior lateral line neuromast PATO:0001997 decreased amount abnormal ZDB-GENE-010126-2 570240 4915 ntrk2b GO:0030424 axon BFO:0000050 part_of ZFA:0000944 posterior lateral line PATO:0000574 decreased length abnormal ZDB-GENE-010126-2 570240 4915 ntrk2b ZFA:0000944 posterior lateral line PATO:0000051 morphology abnormal ZDB-GENE-010126-2 570240 4915 ntrk2b CHEBI:18243 dopamine BFO:0000050 part_of ZFA:0001094 whole organism PATO:0001997 decreased amount abnormal ZDB-GENE-010126-2 570240 4915 ntrk2b CHEBI:28790 serotonin BFO:0000050 part_of ZFA:0001094 whole organism PATO:0001997 decreased amount abnormal ZDB-GENE-010129-1 65238 128209 klf17 GO:0035188 hatching PATO:0002026 non-progressive abnormal ZDB-GENE-010129-1 65238 128209 klf17 GO:0042541 hemoglobin biosynthetic process PATO:0001507 disrupted abnormal ZDB-GENE-010129-1 65238 128209 klf17 GO:0060319 primitive erythrocyte differentiation PATO:0001507 disrupted abnormal ZDB-GENE-010129-1 65238 128209 klf17 ZFA:0000026 hatching gland PATO:0001483 aplastic abnormal ZDB-GENE-010129-1 65238 128209 klf17 ZFA:0000058 polster PATO:0001483 aplastic abnormal ZDB-GENE-010129-1 65238 128209 klf17 ZFA:0000086 EVL PATO:0001241 physical object quality abnormal ZDB-GENE-010129-1 65238 128209 klf17 ZFA:0000086 EVL PATO:0002106 poorly differentiated abnormal ZDB-GENE-010129-1 65238 128209 klf17 ZFA:0000114 heart PATO:0001450 edematous abnormal ZDB-GENE-010129-1 65238 128209 klf17 ZFA:0000940 posterior lateral line neuromast PATO:0001922 mislocalised posteriorly abnormal ZDB-GENE-010129-1 65238 128209 klf17 ZFA:0000940 posterior lateral line neuromast PATO:0001997 decreased amount abnormal ZDB-GENE-010129-1 65238 128209 klf17 ZFA:0001094 whole organism PATO:0000169 viability abnormal ZDB-GENE-010129-1 65238 128209 klf17 ZFA:0009151 hatching gland cell PATO:0000462 absent abnormal ZDB-GENE-010129-1 65238 128209 klf17 GO:0005634 nucleus BFO:0000050 part_of ZFA:0009256 nucleate erythrocyte PATO:0001501 immature abnormal ZDB-GENE-010129-1 65238 128209 klf17 GO:0005833 hemoglobin complex BFO:0000050 part_of ZFA:0009256 nucleate erythrocyte PATO:0000462 absent abnormal ZDB-GENE-010130-2 65230 1488 ctbp2a GO:0006915 apoptotic process PATO:0002051 increased occurrence abnormal ZDB-GENE-010130-2 65230 1488 ctbp2a GO:0007634 optokinetic behavior PATO:0001507 disrupted abnormal ZDB-GENE-010130-2 65230 1488 ctbp2a GO:0010996 response to auditory stimulus PATO:0002302 decreased process quality abnormal ZDB-GENE-010130-2 65230 1488 ctbp2a ZFA:0000107 eye PATO:0001906 movement quality abnormal ZDB-GENE-010130-2 65230 1488 ctbp2a ZFA:0000152 retina PATO:0000638 apoptotic abnormal ZDB-GENE-010130-2 65230 1488 ctbp2a ZFA:0009091 melanocyte BFO:0000050 part_of ZFA:0001114 head PATO:0000470 increased amount abnormal ZDB-GENE-010130-2 65230 1488 ctbp2a GO:0097386 glial cell projection BFO:0000050 part_of ZFA:0001115 trunk PATO:0000628 mislocalised abnormal ZDB-GENE-010130-2 65230 1488 ctbp2a ZFA:0009091 melanocyte PATO:0000470 increased amount abnormal ZDB-GENE-010130-2 65230 1488 ctbp2a GO:0048788 cytoskeleton of presynaptic active zone BFO:0000050 part_of ZFA:0009154 eye photoreceptor cell PATO:0000574 decreased length abnormal ZDB-GENE-010130-2 65230 1488 ctbp2a GO:0048788 cytoskeleton of presynaptic active zone BFO:0000050 part_of ZFA:0009318 retinal bipolar neuron PATO:0000051 morphology abnormal ZDB-GENE-010130-2 65230 1488 ctbp2a ZFA:0009321 rod bipolar cell PATO:0001997 decreased amount abnormal ZDB-GENE-010131-2 65234 1020 cdk5 GO:0004693 cyclin-dependent protein serine/threonine kinase activity PATO:0002052 decreased occurrence abnormal ZDB-GENE-010131-2 65234 1020 cdk5 GO:0010842 retina layer formation PATO:0001507 disrupted abnormal ZDB-GENE-010131-2 65234 1020 cdk5 GO:0060042 retina morphogenesis in camera-type eye PATO:0001507 disrupted abnormal ZDB-GENE-010131-2 65234 1020 cdk5 ZFA:0009052 motor neuron BFO:0000050 part_of ZFA:0000008 brain PATO:0000470 increased amount abnormal ZDB-GENE-010131-2 65234 1020 cdk5 ZFA:0000024 retinal ganglion cell layer PATO:0000051 morphology abnormal ZDB-GENE-010131-2 65234 1020 cdk5 ZFA:0009052 motor neuron BFO:0000050 part_of ZFA:0000075 spinal cord PATO:0000470 increased amount abnormal ZDB-GENE-010131-2 65234 1020 cdk5 ZFA:0000107 eye PATO:0000587 decreased size abnormal ZDB-GENE-010131-2 65234 1020 cdk5 ZFA:0000119 retinal inner nuclear layer PATO:0000051 morphology abnormal ZDB-GENE-010131-2 65234 1020 cdk5 ZFA:0000152 retina PATO:0000051 morphology abnormal ZDB-GENE-010131-2 65234 1020 cdk5 ZFA:0000435 cranial nerve II PATO:0001483 aplastic abnormal ZDB-GENE-010131-2 65234 1020 cdk5 ZFA:0001094 whole organism PATO:0000587 decreased size abnormal ZDB-GENE-010131-2 65234 1020 cdk5 ZFA:0009102 pancreatic B cell BFO:0000050 part_of ZFA:0001249 exocrine pancreas PATO:0000470 increased amount abnormal ZDB-GENE-010131-2 65234 1020 cdk5 ZFA:0001330 retinal outer plexiform layer PATO:0000051 morphology abnormal ZDB-GENE-010131-2 65234 1020 cdk5 ZFA:0001464 retinal outer nuclear layer PATO:0000051 morphology abnormal ZDB-GENE-010131-2 65234 1020 cdk5 ZFA:0009150 Rohon-Beard neuron PATO:0002168 displaced to abnormal ZFA:0000092 axis BFO:0000050 part_of ZFA:0000075 spinal cord ZDB-GENE-010131-6 65231 4192 mdkb ZFA:0000068 proneural cluster PATO:0000587 decreased size abnormal ZDB-GENE-010131-6 65231 4192 mdkb ZFA:0009053 sensory neuron PATO:0001997 decreased amount abnormal ZDB-GENE-010131-6 65231 4192 mdkb ZFA:0009150 Rohon-Beard neuron PATO:0001997 decreased amount abnormal ZDB-GENE-010131-8 65225 1509 ctsd GO:0014904 myotube cell development PATO:0001507 disrupted abnormal ZDB-GENE-010131-8 65225 1509 ctsd GO:0048798 swim bladder inflation PATO:0001507 disrupted abnormal ZDB-GENE-010131-8 65225 1509 ctsd ZFA:0000076 swim bladder PATO:0002377 uninflated abnormal ZDB-GENE-010131-8 65225 1509 ctsd ZFA:0000107 eye PATO:0000587 decreased size abnormal ZDB-GENE-010131-8 65225 1509 ctsd ZFA:0000152 retina PATO:0002000 lacks all parts of type abnormal GO:0005902 microvillus BFO:0000050 part_of ZFA:0000144 retinal pigmented epithelium ZDB-GENE-010131-8 65225 1509 ctsd ZFA:0000368 integument PATO:0002250 increased pigmentation abnormal ZDB-GENE-010131-8 65225 1509 ctsd ZFA:0000431 semicircular canal PATO:0000587 decreased size abnormal ZDB-GENE-010131-8 65225 1509 ctsd ZFA:0005145 muscle BFO:0000050 part_of ZFA:0000473 trunk musculature PATO:0000051 morphology abnormal ZDB-GENE-010131-8 65225 1509 ctsd ZFA:0009114 muscle cell BFO:0000050 part_of ZFA:0000473 trunk musculature PATO:0000937 disorganized abnormal ZDB-GENE-010131-8 65225 1509 ctsd ZFA:0001094 whole organism PATO:0000169 viability abnormal ZDB-GENE-010131-8 65225 1509 ctsd ZFA:0001094 whole organism PATO:0000574 decreased length abnormal ZDB-GENE-010131-8 65225 1509 ctsd ZFA:0001094 whole organism PATO:0000617 bent abnormal ZDB-GENE-010131-8 65225 1509 ctsd ZFA:0001094 whole organism PATO:0001422 dead abnormal ZDB-GENE-010131-8 65225 1509 ctsd ZFA:0001617 otolith PATO:0000587 decreased size abnormal ZDB-GENE-010131-8 65225 1509 ctsd ZFA:0001089 myoseptum BFO:0000050 part_of ZFA:0005145 muscle PATO:0000592 decreased thickness abnormal ZDB-GENE-010202-1 65236 5599 mapk8b GO:0009953 dorsal/ventral pattern formation PATO:0001507 disrupted abnormal ZDB-GENE-010202-1 65236 5599 mapk8b GO:0003351 epithelial cilium movement involved in extracellular fluid movement BFO:0000066 occurs_in ZFA:0000001 Kupffer's vesicle PATO:0002302 decreased process quality abnormal ZDB-GENE-010202-1 65236 5599 mapk8b GO:0005929 cilium BFO:0000050 part_of ZFA:0000001 Kupffer's vesicle PATO:0000574 decreased length abnormal ZDB-GENE-010202-1 65236 5599 mapk8b GO:0031514 motile cilium BFO:0000050 part_of ZFA:0000001 Kupffer's vesicle PATO:0000574 decreased length abnormal ZDB-GENE-010202-1 65236 5599 mapk8b GO:0060271 cilium assembly BFO:0000066 occurs_in ZFA:0000001 Kupffer's vesicle PATO:0002302 decreased process quality abnormal ZDB-GENE-010202-1 65236 5599 mapk8b GO:0070121 Kupffer's vesicle development BFO:0000066 occurs_in ZFA:0000001 Kupffer's vesicle PATO:0002302 decreased process quality abnormal ZDB-GENE-010202-1 65236 5599 mapk8b ZFA:0001094 whole organism PATO:0000636 wholly ventralized abnormal ZDB-GENE-010202-2 65237 1432 mapk14a GO:0001756 somitogenesis PATO:0001507 disrupted abnormal ZDB-GENE-010202-2 65237 1432 mapk14a ZFA:0001117 post-vent region PATO:0001468 curved dorsal abnormal ZDB-GENE-010202-2 65237 1432 mapk14a ZFA:0001462 somite border PATO:0001879 U-shaped abnormal ZDB-GENE-010202-2 65237 1432 mapk14a GO:0004197 cysteine-type endopeptidase activity BFO:0000050 part_of ZFA:0009310 retinal ganglion cell PATO:0002052 decreased occurrence abnormal ZDB-GENE-010202-2 65237 1432 mapk14a GO:0016322 neuron remodeling BFO:0000066 occurs_in ZFA:0009310 retinal ganglion cell PATO:0002302 decreased process quality abnormal ZDB-GENE-010202-2 65237 1432 mapk14a GO:0030424 axon BFO:0000050 part_of ZFA:0009310 retinal ganglion cell PATO:0001241 physical object quality abnormal ZDB-GENE-010202-2 65237 1432 mapk14a GO:0044303 axon collateral BFO:0000050 part_of ZFA:0009310 retinal ganglion cell PATO:0001241 physical object quality abnormal ZDB-GENE-010202-2 65237 1432 mapk14a GO:0048669 collateral sprouting in absence of injury BFO:0000066 occurs_in ZFA:0009310 retinal ganglion cell PATO:0000057 occurrence abnormal ZDB-GENE-010226-1 79379 2668 gdnfa GO:0007626 locomotory behavior PATO:0002302 decreased process quality abnormal ZDB-GENE-010226-1 79379 2668 gdnfa GO:0008283 cell population proliferation BFO:0000066 occurs_in ZFA:0000101 diencephalon PATO:0002302 decreased process quality abnormal ZDB-GENE-010226-1 79379 2668 gdnfa ZFA:0009301 dopaminergic neuron BFO:0000050 part_of ZFA:0000101 diencephalon PATO:0001997 decreased amount abnormal ZDB-GENE-010226-1 79379 2668 gdnfa ZFA:0009248 neuron BFO:0000050 part_of ZFA:0001155 enteric nervous system PATO:0001997 decreased amount abnormal ZDB-GENE-010226-1 79379 2668 gdnfa ZFA:0009238 afferent neuron PATO:0000936 truncated abnormal ZDB-GENE-010226-1 79379 2668 gdnfa GO:0008283 cell population proliferation BFO:0000066 occurs_in ZFA:0009301 dopaminergic neuron PATO:0002302 decreased process quality abnormal ZDB-GENE-010226-2 79376 2674 gfra1a ZFA:0005775 enteric neuron PATO:0001997 decreased amount abnormal ZDB-GENE-010302-1 100148408 2296 foxc1a GO:0001756 somitogenesis PATO:0001236 process quality abnormal ZDB-GENE-010302-1 100148408 2296 foxc1a GO:0001944 vasculature development PATO:0001507 disrupted abnormal ZDB-GENE-010302-1 100148408 2296 foxc1a GO:0008015 blood circulation PATO:0001507 disrupted abnormal ZDB-GENE-010302-1 100148408 2296 foxc1a GO:0048593 camera-type eye morphogenesis PATO:0002302 decreased process quality abnormal ZDB-GENE-010302-1 100148408 2296 foxc1a GO:0048821 erythrocyte development PATO:0001507 disrupted abnormal ZDB-GENE-010302-1 100148408 2296 foxc1a GO:0060047 heart contraction PATO:0001507 disrupted abnormal ZDB-GENE-010302-1 100148408 2296 foxc1a GO:0060047 heart contraction PATO:0002052 decreased occurrence abnormal ZDB-GENE-010302-1 100148408 2296 foxc1a GO:0061298 retina vasculature development in camera-type eye PATO:0002302 decreased process quality abnormal ZDB-GENE-010302-1 100148408 2296 foxc1a GO:0061371 determination of heart left/right asymmetry PATO:0001507 disrupted abnormal ZDB-GENE-010302-1 100148408 2296 foxc1a GO:0061386 closure of optic fissure PATO:0000297 arrested abnormal ZDB-GENE-010302-1 100148408 2296 foxc1a GO:0072015 podocyte development PATO:0002302 decreased process quality abnormal ZDB-GENE-010302-1 100148408 2296 foxc1a ZFA:0000008 brain PATO:0001853 hydrocephalic abnormal ZDB-GENE-010302-1 100148408 2296 foxc1a ZFA:0000008 brain PATO:0002105 hemorrhagic abnormal ZDB-GENE-010302-1 100148408 2296 foxc1a ZFA:0000009 cardiac ventricle PATO:0000587 decreased size abnormal ZDB-GENE-010302-1 100148408 2296 foxc1a ZFA:0000012 central nervous system PATO:0002105 hemorrhagic abnormal ZDB-GENE-010302-1 100148408 2296 foxc1a ZFA:0000054 pericardium PATO:0000592 decreased thickness abnormal ZDB-GENE-010302-1 100148408 2296 foxc1a ZFA:0000054 pericardium PATO:0001450 edematous abnormal ZDB-GENE-010302-1 100148408 2296 foxc1a ZFA:0000099 brain vasculature PATO:0002000 lacks all parts of type abnormal ZFA:0005020 central artery ZDB-GENE-010302-1 100148408 2296 foxc1a ZFA:0000107 eye PATO:0000587 decreased size abnormal ZDB-GENE-010302-1 100148408 2296 foxc1a ZFA:0000107 eye PATO:0000646 malformed abnormal ZDB-GENE-010302-1 100148408 2296 foxc1a ZFA:0000107 eye PATO:0002105 hemorrhagic abnormal ZDB-GENE-010302-1 100148408 2296 foxc1a ZFA:0000114 heart PATO:0001450 edematous abnormal ZDB-GENE-010302-1 100148408 2296 foxc1a ZFA:0000155 somite PATO:0000569 decreased height abnormal ZDB-GENE-010302-1 100148408 2296 foxc1a ZFA:0000155 somite PATO:0000587 decreased size abnormal ZDB-GENE-010302-1 100148408 2296 foxc1a ZFA:0000173 bulbus arteriosus PATO:0002364 shortened abnormal ZDB-GENE-010302-1 100148408 2296 foxc1a ZFA:0000180 caudal vein PATO:0001450 edematous abnormal ZDB-GENE-010302-1 100148408 2296 foxc1a GO:0007219 Notch signaling pathway BFO:0000066 occurs_in ZFA:0000255 paraxial mesoderm PATO:0002302 decreased process quality abnormal ZDB-GENE-010302-1 100148408 2296 foxc1a GO:0008543 fibroblast growth factor receptor signaling pathway BFO:0000066 occurs_in ZFA:0000255 paraxial mesoderm PATO:0002302 decreased process quality abnormal ZDB-GENE-010302-1 100148408 2296 foxc1a ZFA:0000471 atrium PATO:0000586 increased size abnormal ZDB-GENE-010302-1 100148408 2296 foxc1a GO:0001503 ossification BFO:0000066 occurs_in ZFA:0000555 opercular flap PATO:0002302 decreased process quality abnormal ZDB-GENE-010302-1 100148408 2296 foxc1a ZFA:0000604 ventral aorta PATO:0000574 decreased length abnormal ZDB-GENE-010302-1 100148408 2296 foxc1a ZFA:0000672 hyomandibula PATO:0000587 decreased size abnormal ZDB-GENE-010302-1 100148408 2296 foxc1a ZFA:0000692 symplectic PATO:0000587 decreased size abnormal ZDB-GENE-010302-1 100148408 2296 foxc1a ZFA:0001094 whole organism PATO:0000574 decreased length abnormal ZDB-GENE-010302-1 100148408 2296 foxc1a ZFA:0001094 whole organism PATO:0001422 dead abnormal ZDB-GENE-010302-1 100148408 2296 foxc1a ZFA:0001114 head PATO:0000587 decreased size abnormal ZDB-GENE-010302-1 100148408 2296 foxc1a ZFA:0001114 head PATO:0001617 deformed abnormal ZDB-GENE-010302-1 100148408 2296 foxc1a ZFA:0001161 pectoral fin PATO:0002283 decreased mobility abnormal ZDB-GENE-010302-1 100148408 2296 foxc1a GO:0001503 ossification BFO:0000066 occurs_in ZFA:0001189 vertebra PATO:0040059 absent process abnormal ZDB-GENE-010302-1 100148408 2296 foxc1a ZFA:0001284 optic fissure PATO:0000609 closure incomplete abnormal ZDB-GENE-010302-1 100148408 2296 foxc1a ZFA:0001285 intersegmental vessel PATO:0001997 decreased amount abnormal ZDB-GENE-010302-1 100148408 2296 foxc1a ZFA:0009065 endothelial cell BFO:0000050 part_of ZFA:0001315 atrioventricular canal PATO:0000628 mislocalised abnormal ZDB-GENE-010302-1 100148408 2296 foxc1a ZFA:0001319 myocardium PATO:0000592 decreased thickness abnormal ZDB-GENE-010302-1 100148408 2296 foxc1a ZFA:0001320 endocardium PATO:0000051 morphology abnormal ZDB-GENE-010302-1 100148408 2296 foxc1a ZFA:0001320 endocardium PATO:0000587 decreased size abnormal ZDB-GENE-010302-1 100148408 2296 foxc1a ZFA:0001399 palatoquadrate cartilage PATO:0000587 decreased size abnormal ZDB-GENE-010302-1 100148408 2296 foxc1a ZFA:0001557 pronephric glomerulus PATO:0002000 lacks all parts of type abnormal GO:0036057 slit diaphragm BFO:0000050 part_of ZFA:0001673 pronephric podocyte ZDB-GENE-010302-1 100148408 2296 foxc1a ZFA:0001557 pronephric glomerulus PATO:0002000 lacks all parts of type abnormal ZFA:0005309 pronephric glomerular capillary ZDB-GENE-010302-1 100148408 2296 foxc1a ZFA:0001557 pronephric glomerulus PATO:0001241 physical object quality abnormal ZDB-GENE-010302-1 100148408 2296 foxc1a GO:0001503 ossification BFO:0000066 occurs_in ZFA:0001611 pharyngeal arch 2 PATO:0002302 decreased process quality abnormal ZDB-GENE-010302-1 100148408 2296 foxc1a GO:0051216 cartilage development BFO:0000066 occurs_in ZFA:0001611 pharyngeal arch 2 PATO:0002052 decreased occurrence abnormal ZDB-GENE-010302-1 100148408 2296 foxc1a GO:0001503 ossification BFO:0000066 occurs_in ZFA:0001612 pharyngeal arch 1 PATO:0002302 decreased process quality abnormal ZDB-GENE-010302-1 100148408 2296 foxc1a GO:0051216 cartilage development BFO:0000066 occurs_in ZFA:0001612 pharyngeal arch 1 PATO:0002052 decreased occurrence abnormal ZDB-GENE-010302-1 100148408 2296 foxc1a GO:0042995 cell projection BFO:0000050 part_of ZFA:0001673 pronephric podocyte PATO:0000646 malformed abnormal ZDB-GENE-010302-1 100148408 2296 foxc1a ZFA:0001673 pronephric podocyte PATO:0001997 decreased amount abnormal ZDB-GENE-010302-1 100148408 2296 foxc1a ZFA:0001718 presumptive atrium heart tube PATO:0000586 increased size abnormal ZDB-GENE-010302-1 100148408 2296 foxc1a ZFA:0001719 presumptive cardiac ventricle heart tube PATO:0000587 decreased size abnormal ZDB-GENE-010302-1 100148408 2296 foxc1a ZFA:0005064 atrioventricular valve PATO:0000051 morphology abnormal ZDB-GENE-010302-1 100148408 2296 foxc1a GO:0031594 neuromuscular junction BFO:0000050 part_of ZFA:0005436 pectoral fin nerve PATO:0001997 decreased amount abnormal ZDB-GENE-010302-1 100148408 2296 foxc1a GO:0043679 axon terminus BFO:0000050 part_of ZFA:0005436 pectoral fin nerve PATO:0001997 decreased amount abnormal ZDB-GENE-010302-1 100148408 2296 foxc1a GO:0008045 motor neuron axon guidance BFO:0000066 occurs_in ZFA:0005439 pectoral fin motor nerve 1 PATO:0001236 process quality abnormal ZDB-GENE-010302-1 100148408 2296 foxc1a GO:0008045 motor neuron axon guidance BFO:0000066 occurs_in ZFA:0005440 pectoral fin motor nerve 2 PATO:0001236 process quality abnormal ZDB-GENE-010302-1 100148408 2296 foxc1a GO:0030424 axon BFO:0000050 part_of ZFA:0005440 pectoral fin motor nerve 2 PATO:0001959 defasciculated abnormal ZDB-GENE-010302-1 100148408 2296 foxc1a GO:0043679 axon terminus BFO:0000050 part_of ZFA:0005440 pectoral fin motor nerve 2 PATO:0000628 mislocalised abnormal ZDB-GENE-010302-1 100148408 2296 foxc1a GO:0008045 motor neuron axon guidance BFO:0000066 occurs_in ZFA:0005441 pectoral fin motor nerve 3 PATO:0001236 process quality abnormal ZDB-GENE-010302-1 100148408 2296 foxc1a GO:0030424 axon BFO:0000050 part_of ZFA:0005441 pectoral fin motor nerve 3 PATO:0001959 defasciculated abnormal ZDB-GENE-010302-1 100148408 2296 foxc1a GO:0043679 axon terminus BFO:0000050 part_of ZFA:0005441 pectoral fin motor nerve 3 PATO:0000628 mislocalised abnormal ZDB-GENE-010302-1 100148408 2296 foxc1a GO:0008045 motor neuron axon guidance BFO:0000066 occurs_in ZFA:0005450 pectoral fin motor nerve 4 PATO:0001236 process quality abnormal ZDB-GENE-010302-1 100148408 2296 foxc1a GO:0030424 axon BFO:0000050 part_of ZFA:0005450 pectoral fin motor nerve 4 PATO:0002286 decreased branchiness abnormal ZDB-GENE-010302-1 100148408 2296 foxc1a ZFA:0005566 anterior segment eye PATO:0002000 lacks all parts of type abnormal ZFA:0005876 anterior chamber eye ZDB-GENE-010302-1 100148408 2296 foxc1a ZFA:0007057 ocular blood vessel PATO:0000646 malformed abnormal ZDB-GENE-010302-1 100148408 2296 foxc1a GO:0007411 axon guidance BFO:0000066 occurs_in ZFA:0009244 primary motor neuron PATO:0001236 process quality abnormal ZDB-GENE-010302-2 79375 2296 foxc1b GO:0008015 blood circulation PATO:0001507 disrupted abnormal ZDB-GENE-010302-2 79375 2296 foxc1b GO:0048514 blood vessel morphogenesis PATO:0001507 disrupted abnormal ZDB-GENE-010302-2 79375 2296 foxc1b GO:0061371 determination of heart left/right asymmetry PATO:0001507 disrupted abnormal ZDB-GENE-010306-1 80374 1583 cyp11a1.1 GO:0055113 epiboly involved in gastrulation with mouth forming second PATO:0000502 delayed abnormal ZDB-GENE-010306-1 80374 1583 cyp11a1.1 GO:0055113 epiboly involved in gastrulation with mouth forming second PATO:0001507 disrupted abnormal ZDB-GENE-010306-1 80374 1583 cyp11a1.1 GO:0061371 determination of heart left/right asymmetry PATO:0001507 disrupted abnormal ZDB-GENE-010306-1 80374 1583 cyp11a1.1 GO:0090504 epiboly PATO:0000297 arrested abnormal ZDB-GENE-010306-1 80374 1583 cyp11a1.1 ZFA:0000009 cardiac ventricle PATO:0000625 inverted abnormal ZDB-GENE-010306-1 80374 1583 cyp11a1.1 GO:0005874 microtubule BFO:0000050 part_of ZFA:0000084 yolk PATO:0000592 decreased thickness abnormal ZDB-GENE-010306-1 80374 1583 cyp11a1.1 ZFA:0000092 axis PATO:0000574 decreased length abnormal ZDB-GENE-010306-1 80374 1583 cyp11a1.1 ZFA:0000106 extension PATO:0000574 decreased length abnormal ZDB-GENE-010306-1 80374 1583 cyp11a1.1 ZFA:0000114 heart PATO:0000051 morphology abnormal ZDB-GENE-010306-1 80374 1583 cyp11a1.1 ZFA:0000114 heart PATO:0001450 edematous abnormal ZDB-GENE-010306-1 80374 1583 cyp11a1.1 ZFA:0000471 atrium PATO:0000625 inverted abnormal ZDB-GENE-010306-1 80374 1583 cyp11a1.1 ZFA:0001094 whole organism PATO:0000574 decreased length abnormal ZDB-GENE-010306-1 80374 1583 cyp11a1.1 ZFA:0001094 whole organism PATO:0001422 dead abnormal ZDB-GENE-010306-1 80374 1583 cyp11a1.1 ZFA:0005024 trunk vasculature PATO:0000646 malformed abnormal ZDB-GENE-010306-3 80353 9353 slit2 GO:0003262 endocardial progenitor cell migration to the midline involved in heart field formation PATO:0002302 decreased process quality abnormal ZDB-GENE-010306-3 80353 9353 slit2 GO:0060214 endocardium formation PATO:0002302 decreased process quality abnormal ZDB-GENE-010306-3 80353 9353 slit2 GO:0061360 optic chiasma development PATO:0001507 disrupted abnormal ZDB-GENE-010306-3 80353 9353 slit2 GO:0030424 axon BFO:0000050 part_of ZFA:0000252 optic tract PATO:0000937 disorganized abnormal ZDB-GENE-010306-3 80353 9353 slit2 GO:0007411 axon guidance BFO:0000066 occurs_in ZFA:0000435 cranial nerve II PATO:0001507 disrupted abnormal ZDB-GENE-010306-3 80353 9353 slit2 GO:0030426 growth cone BFO:0000050 part_of ZFA:0000435 cranial nerve II PATO:0000586 increased size abnormal ZDB-GENE-010306-3 80353 9353 slit2 GO:0048675 axon extension BFO:0000066 occurs_in ZFA:0000435 cranial nerve II PATO:0000911 decreased rate abnormal ZDB-GENE-010306-3 80353 9353 slit2 ZFA:0000435 cranial nerve II PATO:0000591 increased thickness abnormal ZDB-GENE-010306-3 80353 9353 slit2 GO:0030424 axon BFO:0000050 part_of ZFA:0000556 optic chiasm PATO:0000937 disorganized abnormal ZDB-GENE-010306-3 80353 9353 slit2 ZFA:0000435 cranial nerve II BFO:0000050 part_of ZFA:0000556 optic chiasm PATO:0000937 disorganized abnormal ZDB-GENE-010306-3 80353 9353 slit2 ZFA:0000556 optic chiasm PATO:0000051 morphology abnormal ZDB-GENE-010306-3 80353 9353 slit2 ZFA:0009000 cell BFO:0000050 part_of ZFA:0001320 endocardium PATO:0000646 malformed abnormal ZDB-GENE-010306-3 80353 9353 slit2 ZFA:0001320 endocardium PATO:0000628 mislocalised abnormal ZDB-GENE-010306-3 80353 9353 slit2 GO:0048675 axon extension BFO:0000066 occurs_in ZFA:0001657 supraoptic tract PATO:0001236 process quality abnormal ZDB-GENE-010316-1 80787 6531 slc6a3 GO:0007610 behavior PATO:0001236 process quality abnormal ZDB-GENE-010316-1 80787 6531 slc6a3 GO:0007626 locomotory behavior PATO:0001236 process quality abnormal ZDB-GENE-010316-1 80787 6531 slc6a3 GO:0030534 adult behavior PATO:0001236 process quality abnormal ZDB-GENE-010316-1 80787 6531 slc6a3 GO:0036269 swimming behavior PATO:0001236 process quality abnormal ZDB-GENE-010316-1 80787 6531 slc6a3 CHEBI:18243 dopamine BFO:0000050 part_of ZFA:0000008 brain PATO:0001997 decreased amount abnormal ZDB-GENE-010316-1 80787 6531 slc6a3 GO:0140058 neuron projection arborization BFO:0000066 occurs_in ZFA:0000128 midbrain PATO:0002052 decreased occurrence abnormal ZDB-GENE-010316-1 80787 6531 slc6a3 ZFA:0009248 neuron BFO:0000050 part_of ZFA:0000128 midbrain PATO:0000051 morphology abnormal ZDB-GENE-010316-1 80787 6531 slc6a3 ZFA:0009248 neuron BFO:0000050 part_of ZFA:0000128 midbrain PATO:0001997 decreased amount abnormal ZDB-GENE-010316-1 80787 6531 slc6a3 ZFA:0001094 whole organism PATO:0000051 morphology abnormal ZDB-GENE-010319-1 80972 1857 dvl3a GO:0003401 axis elongation PATO:0000502 delayed abnormal ZDB-GENE-010319-1 80972 1857 dvl3a GO:0022007 convergent extension involved in neural plate elongation PATO:0000502 delayed abnormal ZDB-GENE-010319-1 80972 1857 dvl3a BSPO:0000013 anterior-posterior axis BFO:0000050 part_of ZFA:0001094 whole organism PATO:0000574 decreased length abnormal ZDB-GENE-010319-27 559345 57217 ttc7a GO:0030432 peristalsis BFO:0000066 occurs_in ZFA:0001076 intestinal bulb PATO:0001236 process quality abnormal ZDB-GENE-010319-27 559345 57217 ttc7a ZFA:0005930 lumen BFO:0000050 part_of ZFA:0001076 intestinal bulb PATO:0000599 decreased width abnormal ZDB-GENE-010319-27 559345 57217 ttc7a ZFA:0005125 intestinal villus PATO:0000051 morphology abnormal ZDB-GENE-010319-27 559345 57217 ttc7a GO:0006915 apoptotic process BFO:0000066 occurs_in ZFA:0005126 intestinal bulb epithelium PATO:0002304 increased process quality abnormal ZDB-GENE-010319-27 559345 57217 ttc7a ZFA:0005126 intestinal bulb epithelium PATO:0002068 stratified abnormal ZDB-GENE-010319-27 559345 57217 ttc7a GO:0031982 vesicle BFO:0000050 part_of ZFA:0009094 goblet cell PATO:0000470 increased amount abnormal ZDB-GENE-010319-35 80959 84552 pard6gb GO:0001841 neural tube formation PATO:0001507 disrupted abnormal ZDB-GENE-010319-35 80959 84552 pard6gb GO:0035050 embryonic heart tube development PATO:0001507 disrupted abnormal ZDB-GENE-010319-35 80959 84552 pard6gb GO:0035844 cloaca development PATO:0001507 disrupted abnormal ZDB-GENE-010319-35 80959 84552 pard6gb GO:0072157 epithelial cell migration involved in distal tubule morphogenesis PATO:0001507 disrupted abnormal ZDB-GENE-010319-35 80959 84552 pard6gb ZFA:0000054 pericardium PATO:0001450 edematous abnormal ZDB-GENE-010319-35 80959 84552 pard6gb ZFA:0000112 gut PATO:0000646 malformed abnormal ZDB-GENE-010319-35 80959 84552 pard6gb ZFA:0000121 lateral plate mesoderm PATO:0000646 malformed abnormal ZDB-GENE-010319-35 80959 84552 pard6gb ZFA:0000135 notochord PATO:0000967 undulate abnormal ZDB-GENE-010319-35 80959 84552 pard6gb ZFA:0000144 retinal pigmented epithelium PATO:0000051 morphology abnormal ZDB-GENE-010319-35 80959 84552 pard6gb GO:0005929 cilium BFO:0000050 part_of ZFA:0000150 pronephric duct PATO:0000613 disoriented abnormal ZDB-GENE-010319-35 80959 84552 pard6gb ZFA:0000150 pronephric duct PATO:0000574 decreased length abnormal ZDB-GENE-010319-35 80959 84552 pard6gb ZFA:0000150 pronephric duct PATO:0001571 dilated abnormal ZDB-GENE-010319-35 80959 84552 pard6gb ZFA:0000151 pronephros PATO:0001673 cystic abnormal ZDB-GENE-010319-35 80959 84552 pard6gb ZFA:0000330 cloacal chamber PATO:0001602 distended abnormal ZDB-GENE-010319-35 80959 84552 pard6gb ZFA:0000938 central canal PATO:0000646 malformed abnormal ZDB-GENE-010319-35 80959 84552 pard6gb ZFA:0001094 whole organism PATO:0000406 curved abnormal ZDB-GENE-010319-35 80959 84552 pard6gb ZFA:0001094 whole organism PATO:0001468 curved dorsal abnormal ZDB-GENE-010319-35 80959 84552 pard6gb ZFA:0001135 neural tube PATO:0000646 malformed abnormal ZDB-GENE-010319-35 80959 84552 pard6gb ZFA:0001261 ventricular system PATO:0001478 collapsed abnormal ZDB-GENE-010319-35 80959 84552 pard6gb ZFA:0001319 myocardium PATO:0000646 malformed abnormal ZDB-GENE-010319-35 80959 84552 pard6gb GO:0030424 axon BFO:0000050 part_of ZFA:0009310 retinal ganglion cell PATO:0002286 decreased branchiness abnormal ZDB-GENE-010319-35 80959 84552 pard6gb GO:0048669 collateral sprouting in absence of injury BFO:0000066 occurs_in ZFA:0009310 retinal ganglion cell PATO:0002302 decreased process quality abnormal ZDB-GENE-010320-1 80973 983 cdk1 ZFA:0000012 central nervous system PATO:0000647 necrotic abnormal ZDB-GENE-010320-1 80973 983 cdk1 ZFA:0000054 pericardium PATO:0001450 edematous abnormal ZDB-GENE-010320-1 80973 983 cdk1 ZFA:0000084 yolk PATO:0000001 quality abnormal ZDB-GENE-010320-1 80973 983 cdk1 ZFA:0000084 yolk PATO:0000411 circular abnormal ZDB-GENE-010320-1 80973 983 cdk1 ZFA:0000092 axis PATO:0001468 curved dorsal abnormal ZDB-GENE-010320-1 80973 983 cdk1 ZFA:0000107 eye PATO:0000587 decreased size abnormal ZDB-GENE-010320-1 80973 983 cdk1 BSPO:0000058 basal side BFO:0000050 part_of ZFA:0000152 retina PATO:0002102 proliferative abnormal ZDB-GENE-010320-1 80973 983 cdk1 GO:0000084 mitotic S phase BFO:0000066 occurs_in ZFA:0000152 retina PATO:0002052 decreased occurrence abnormal ZDB-GENE-010320-1 80973 983 cdk1 GO:0000087 mitotic M phase BFO:0000066 occurs_in ZFA:0000152 retina PATO:0000297 arrested abnormal ZDB-GENE-010320-1 80973 983 cdk1 GO:0035861 site of double-strand break BFO:0000050 part_of ZFA:0000152 retina PATO:0000470 increased amount abnormal ZDB-GENE-010320-1 80973 983 cdk1 GO:0051301 cell division BFO:0000066 occurs_in ZFA:0000152 retina PATO:0002052 decreased occurrence abnormal ZDB-GENE-010320-1 80973 983 cdk1 GO:0051301 cell division BFO:0000066 occurs_in ZFA:0000152 retina PATO:0055002 increased spatial extent of a process abnormal ZDB-GENE-010320-1 80973 983 cdk1 GO:0072686 mitotic spindle BFO:0000050 part_of ZFA:0000152 retina PATO:0000039 direction abnormal ZDB-GENE-010320-1 80973 983 cdk1 ZFA:0000152 retina PATO:0000638 apoptotic abnormal ZDB-GENE-010320-1 80973 983 cdk1 ZFA:0000396 nervous system PATO:0000001 quality abnormal ZDB-GENE-010320-1 80973 983 cdk1 ZFA:0001094 whole organism PATO:0000052 shape abnormal ZDB-GENE-010320-1 80973 983 cdk1 ZFA:0001094 whole organism PATO:0000169 viability abnormal ZDB-GENE-010320-1 80973 983 cdk1 ZFA:0001094 whole organism PATO:0000617 bent abnormal ZDB-GENE-010320-1 80973 983 cdk1 ZFA:0001114 head PATO:0000587 decreased size abnormal ZDB-GENE-010320-1 80973 983 cdk1 ZFA:0001114 head PATO:0001450 edematous abnormal ZDB-GENE-010320-1 80973 983 cdk1 ZFA:0001115 trunk PATO:0001450 edematous abnormal ZDB-GENE-010320-1 80973 983 cdk1 ZFA:0001115 trunk PATO:0001468 curved dorsal abnormal ZDB-GENE-010320-1 80973 983 cdk1 GO:0000084 mitotic S phase BFO:0000066 occurs_in ZFA:0001135 neural tube PATO:0002052 decreased occurrence abnormal ZDB-GENE-010320-1 80973 983 cdk1 ZFA:0009255 amacrine cell PATO:0001997 decreased amount abnormal ZDB-GENE-010320-1 80973 983 cdk1 ZFA:0009262 retinal cone cell PATO:0001997 decreased amount abnormal ZDB-GENE-010320-1 80973 983 cdk1 ZFA:0009275 retinal rod cell PATO:0001997 decreased amount abnormal ZDB-GENE-010320-1 80973 983 cdk1 ZFA:0009310 retinal ganglion cell PATO:0001997 decreased amount abnormal ZDB-GENE-010320-1 80973 983 cdk1 ZFA:0009315 horizontal cell PATO:0001997 decreased amount abnormal ZDB-GENE-010328-15 793823 3092 hip1 ZFA:0000106 extension PATO:0000587 decreased size abnormal ZDB-GENE-010328-15 793823 3092 hip1 ZFA:0000106 extension PATO:0001483 aplastic abnormal ZDB-GENE-010328-15 793823 3092 hip1 ZFA:0001115 trunk PATO:0000599 decreased width abnormal ZDB-GENE-010328-15 793823 3092 hip1 ZFA:0001273 ventral mandibular arch PATO:0001483 aplastic abnormal ZDB-GENE-010328-8 81587 1365 cldn3c GO:0010842 retina layer formation PATO:0002302 decreased process quality abnormal ZDB-GENE-010328-8 81587 1365 cldn3c ZFA:0000024 retinal ganglion cell layer PATO:0000592 decreased thickness abnormal ZDB-GENE-010328-8 81587 1365 cldn3c ZFA:0000046 retinal neural layer PATO:0000592 decreased thickness abnormal ZDB-GENE-010328-8 81587 1365 cldn3c ZFA:0000051 otic vesicle PATO:0002058 decreased area abnormal ZDB-GENE-010328-8 81587 1365 cldn3c ZFA:0000054 pericardium PATO:0001450 edematous abnormal ZDB-GENE-010328-8 81587 1365 cldn3c ZFA:0000076 swim bladder PATO:0000462 absent abnormal ZDB-GENE-010328-8 81587 1365 cldn3c ZFA:0000107 eye PATO:0000587 decreased size abnormal ZDB-GENE-010328-8 81587 1365 cldn3c ZFA:0000107 eye PATO:0002058 decreased area abnormal ZDB-GENE-010328-8 81587 1365 cldn3c GO:0031514 motile cilium BFO:0000050 part_of ZFA:0000151 pronephros PATO:0000406 curved abnormal ZDB-GENE-010328-8 81587 1365 cldn3c GO:0045198 establishment of epithelial cell apical/basal polarity BFO:0000066 occurs_in ZFA:0000151 pronephros PATO:0002302 decreased process quality abnormal ZDB-GENE-010328-8 81587 1365 cldn3c ZFA:0000151 pronephros PATO:0001624 decreased functionality abnormal ZDB-GENE-010328-8 81587 1365 cldn3c ZFA:0000151 pronephros PATO:0001673 cystic abnormal ZDB-GENE-010328-8 81587 1365 cldn3c GO:0006915 apoptotic process BFO:0000066 occurs_in ZFA:0000152 retina PATO:0002051 increased occurrence abnormal ZDB-GENE-010328-8 81587 1365 cldn3c GO:0008283 cell population proliferation BFO:0000066 occurs_in ZFA:0000152 retina PATO:0002302 decreased process quality abnormal ZDB-GENE-010328-8 81587 1365 cldn3c ZFA:0000152 retina PATO:0000587 decreased size abnormal ZDB-GENE-010328-8 81587 1365 cldn3c ZFA:0000152 retina PATO:0000592 decreased thickness abnormal ZDB-GENE-010328-8 81587 1365 cldn3c GO:0005929 cilium BFO:0000050 part_of ZFA:0000166 lateral crista PATO:0000574 decreased length abnormal ZDB-GENE-010328-8 81587 1365 cldn3c ZFA:0009366 hair cell BFO:0000050 part_of ZFA:0000166 lateral crista PATO:0001997 decreased amount abnormal ZDB-GENE-010328-8 81587 1365 cldn3c ZFA:0000530 lapillus PATO:0040060 absence of anatomical entity abnormal ZDB-GENE-010328-8 81587 1365 cldn3c GO:0005929 cilium BFO:0000050 part_of ZFA:0000566 posterior crista PATO:0000574 decreased length abnormal ZDB-GENE-010328-8 81587 1365 cldn3c ZFA:0009366 hair cell BFO:0000050 part_of ZFA:0000566 posterior crista PATO:0001997 decreased amount abnormal ZDB-GENE-010328-8 81587 1365 cldn3c GO:0005929 cilium BFO:0000050 part_of ZFA:0000619 anterior crista PATO:0000574 decreased length abnormal ZDB-GENE-010328-8 81587 1365 cldn3c ZFA:0009366 hair cell BFO:0000050 part_of ZFA:0000619 anterior crista PATO:0001997 decreased amount abnormal ZDB-GENE-010328-8 81587 1365 cldn3c ZFA:0000676 sagitta PATO:0000052 shape abnormal ZDB-GENE-010328-8 81587 1365 cldn3c ZFA:0009366 hair cell BFO:0000050 part_of ZFA:0000940 posterior lateral line neuromast PATO:0001997 decreased amount abnormal ZDB-GENE-010328-8 81587 1365 cldn3c ZFA:0000940 posterior lateral line neuromast PATO:0001997 decreased amount abnormal ZDB-GENE-010328-8 81587 1365 cldn3c GO:0036269 swimming behavior BFO:0000066 occurs_in ZFA:0001094 whole organism PATO:0002302 decreased process quality abnormal ZDB-GENE-010328-8 81587 1365 cldn3c GO:0050910 detection of mechanical stimulus involved in sensory perception of sound BFO:0000066 occurs_in ZFA:0001094 whole organism PATO:0002302 decreased process quality abnormal ZDB-GENE-010328-8 81587 1365 cldn3c ZFA:0001094 whole organism PATO:0001592 increased curvature abnormal ZDB-GENE-010328-8 81587 1365 cldn3c ZFA:0001329 retinal inner plexiform layer PATO:0000592 decreased thickness abnormal ZDB-GENE-010328-8 81587 1365 cldn3c ZFA:0001464 retinal outer nuclear layer PATO:0000592 decreased thickness abnormal ZDB-GENE-010328-8 81587 1365 cldn3c ZFA:0001617 otolith PATO:0000052 shape abnormal ZDB-GENE-010328-8 81587 1365 cldn3c ZFA:0001617 otolith PATO:0001997 decreased amount abnormal ZDB-GENE-010328-8 81587 1365 cldn3c ZFA:0005046 hyaloid vessel PATO:0000587 decreased size abnormal ZDB-GENE-010328-8 81587 1365 cldn3c ZFA:0005046 hyaloid vessel PATO:0001896 unlumenized abnormal ZDB-GENE-010328-8 81587 1365 cldn3c ZFA:0005046 hyaloid vessel PATO:0001997 decreased amount abnormal ZDB-GENE-010328-8 81587 1365 cldn3c ZFA:0005242 multi-ciliated epithelial cell PATO:0001999 lacks parts or has fewer parts of type abnormal GO:0005929 cilium BFO:0000050 part_of ZFA:0005242 multi-ciliated epithelial cell ZDB-GENE-010328-8 81587 1365 cldn3c GO:0006915 apoptotic process BFO:0000066 occurs_in ZFA:0009367 neuromast hair cell PATO:0002304 increased process quality abnormal ZDB-GENE-010403-1 81881 1406 crx GO:0007632 visual behavior PATO:0001236 process quality abnormal ZDB-GENE-010403-1 81881 1406 crx GO:0007632 visual behavior PATO:0001507 disrupted abnormal ZDB-GENE-010403-1 81881 1406 crx GO:0050962 detection of light stimulus involved in sensory perception PATO:0002052 decreased occurrence abnormal ZDB-GENE-010406-3 81884 10499 ncoa2 ZFA:0000033 intermediate cell mass of mesoderm PATO:0001483 aplastic abnormal ZDB-GENE-010406-3 81884 10499 ncoa2 ZFA:0000135 notochord PATO:0001617 deformed abnormal ZDB-GENE-010406-3 81884 10499 ncoa2 ZFA:0000155 somite PATO:0001879 U-shaped abnormal ZDB-GENE-010406-3 81884 10499 ncoa2 ZFA:0001117 post-vent region PATO:0000574 decreased length abnormal ZDB-GENE-010406-3 81884 10499 ncoa2 ZFA:0001285 intersegmental vessel PATO:0001483 aplastic abnormal ZDB-GENE-010406-5 81882 1719 dhfr GO:0001947 heart looping PATO:0000297 arrested abnormal ZDB-GENE-010406-5 81882 1719 dhfr GO:0001947 heart looping PATO:0001507 disrupted abnormal ZDB-GENE-010406-5 81882 1719 dhfr GO:0001966 thigmotaxis PATO:0001507 disrupted abnormal ZDB-GENE-010406-5 81882 1719 dhfr GO:0003401 axis elongation PATO:0000911 decreased rate abnormal ZDB-GENE-010406-5 81882 1719 dhfr GO:0006915 apoptotic process PATO:0002051 increased occurrence abnormal ZDB-GENE-010406-5 81882 1719 dhfr GO:0008283 cell population proliferation PATO:0002052 decreased occurrence abnormal ZDB-GENE-010406-5 81882 1719 dhfr GO:0009790 embryo development PATO:0000297 arrested abnormal ZDB-GENE-010406-5 81882 1719 dhfr GO:0055113 epiboly involved in gastrulation with mouth forming second PATO:0000297 arrested abnormal ZDB-GENE-010406-5 81882 1719 dhfr GO:0055113 epiboly involved in gastrulation with mouth forming second PATO:0000502 delayed abnormal ZDB-GENE-010406-5 81882 1719 dhfr GO:0060047 heart contraction PATO:0000911 decreased rate abnormal ZDB-GENE-010406-5 81882 1719 dhfr GO:0060047 heart contraction PATO:0001507 disrupted abnormal ZDB-GENE-010406-5 81882 1719 dhfr GO:0060047 heart contraction PATO:0001783 decreased intensity abnormal ZDB-GENE-010406-5 81882 1719 dhfr GO:0090504 epiboly PATO:0001507 disrupted abnormal ZDB-GENE-010406-5 81882 1719 dhfr ZFA:0000009 cardiac ventricle PATO:0000141 structure abnormal ZDB-GENE-010406-5 81882 1719 dhfr ZFA:0000054 pericardium PATO:0001450 edematous abnormal ZDB-GENE-010406-5 81882 1719 dhfr BSPO:0000071 anterior region BFO:0000050 part_of ZFA:0000092 axis PATO:0000592 decreased thickness abnormal ZDB-GENE-010406-5 81882 1719 dhfr ZFA:0000106 extension PATO:0000462 absent abnormal ZDB-GENE-010406-5 81882 1719 dhfr ZFA:0000106 extension PATO:0000574 decreased length abnormal ZDB-GENE-010406-5 81882 1719 dhfr ZFA:0000114 heart PATO:0000051 morphology abnormal ZDB-GENE-010406-5 81882 1719 dhfr ZFA:0000114 heart PATO:0000140 position abnormal ZDB-GENE-010406-5 81882 1719 dhfr ZFA:0000114 heart PATO:0000638 apoptotic abnormal ZDB-GENE-010406-5 81882 1719 dhfr ZFA:0000114 heart PATO:0000646 malformed abnormal ZDB-GENE-010406-5 81882 1719 dhfr ZFA:0000155 somite PATO:0000052 shape abnormal ZDB-GENE-010406-5 81882 1719 dhfr ZFA:0000155 somite PATO:0000574 decreased length abnormal ZDB-GENE-010406-5 81882 1719 dhfr ZFA:0000173 bulbus arteriosus PATO:0000051 morphology abnormal ZDB-GENE-010406-5 81882 1719 dhfr ZFA:0000471 atrium PATO:0000141 structure abnormal ZDB-GENE-010406-5 81882 1719 dhfr BSPO:0000013 anterior-posterior axis BFO:0000050 part_of ZFA:0001094 whole organism PATO:0000574 decreased length abnormal ZDB-GENE-010406-5 81882 1719 dhfr BSPO:0000084 ventral region BFO:0000050 part_of ZFA:0001094 whole organism PATO:0001450 edematous abnormal ZDB-GENE-010406-5 81882 1719 dhfr ZFA:0001094 whole organism PATO:0000169 viability abnormal ZDB-GENE-010406-5 81882 1719 dhfr ZFA:0001094 whole organism PATO:0000638 apoptotic abnormal ZDB-GENE-010406-5 81882 1719 dhfr ZFA:0001094 whole organism PATO:0000645 hypoplastic abnormal ZDB-GENE-010406-5 81882 1719 dhfr ZFA:0001094 whole organism PATO:0000963 opaque abnormal ZDB-GENE-010406-5 81882 1719 dhfr ZFA:0001094 whole organism PATO:0001468 curved dorsal abnormal ZDB-GENE-010406-5 81882 1719 dhfr ZFA:0001114 head PATO:0000638 apoptotic abnormal ZDB-GENE-010406-5 81882 1719 dhfr ZFA:0001115 trunk PATO:0000574 decreased length abnormal ZDB-GENE-010406-5 81882 1719 dhfr ZFA:0001117 post-vent region PATO:0001798 kinked abnormal ZDB-GENE-010406-5 81882 1719 dhfr ZFA:0001462 somite border PATO:0000639 degenerate abnormal ZDB-GENE-010410-3 83413 441509 glra4a GO:0001964 startle response PATO:0001507 disrupted abnormal ZDB-GENE-010410-3 83413 441509 glra4a GO:0001966 thigmotaxis PATO:0001236 process quality abnormal ZDB-GENE-010410-3 83413 441509 glra4a GO:0001966 thigmotaxis PATO:0001507 disrupted abnormal ZDB-GENE-010410-3 83413 441509 glra4a GO:0007638 mechanosensory behavior PATO:0001236 process quality abnormal ZDB-GENE-010410-3 83413 441509 glra4a GO:0021953 central nervous system neuron differentiation PATO:0001507 disrupted abnormal ZDB-GENE-010410-3 83413 441509 glra4a GO:0060012 synaptic transmission, glycinergic PATO:0000297 arrested abnormal ZDB-GENE-010410-3 83413 441509 glra4a GO:0071260 cellular response to mechanical stimulus PATO:0001507 disrupted abnormal ZDB-GENE-010410-3 83413 441509 glra4a GO:0006915 apoptotic process BFO:0000066 occurs_in ZFA:0000008 brain PATO:0000057 occurrence ameliorated ZDB-GENE-010410-3 83413 441509 glra4a GO:0006915 apoptotic process BFO:0000066 occurs_in ZFA:0000008 brain PATO:0002051 increased occurrence abnormal ZDB-GENE-010410-3 83413 441509 glra4a GO:0006915 apoptotic process BFO:0000066 occurs_in ZFA:0000075 spinal cord PATO:0000057 occurrence ameliorated ZDB-GENE-010410-3 83413 441509 glra4a GO:0006915 apoptotic process BFO:0000066 occurs_in ZFA:0000075 spinal cord PATO:0002051 increased occurrence abnormal ZDB-GENE-010410-3 83413 441509 glra4a ZFA:0009052 motor neuron BFO:0000050 part_of ZFA:0000075 spinal cord PATO:0001624 decreased functionality abnormal ZDB-GENE-010410-3 83413 441509 glra4a ZFA:0000107 eye PATO:0000587 decreased size abnormal ZDB-GENE-010410-3 83413 441509 glra4a ZFA:0009276 GABAergic neuron BFO:0000050 part_of ZFA:0000778 spinal cord interneuron PATO:0001997 decreased amount abnormal ZDB-GENE-010410-3 83413 441509 glra4a ZFA:0009290 glutamatergic neuron BFO:0000050 part_of ZFA:0000778 spinal cord interneuron PATO:0001997 decreased amount abnormal ZDB-GENE-010410-3 83413 441509 glra4a ZFA:0009396 glycinergic neuron BFO:0000050 part_of ZFA:0000778 spinal cord interneuron PATO:0001997 decreased amount abnormal ZDB-GENE-010410-3 83413 441509 glra4a ZFA:0000778 spinal cord interneuron PATO:0001997 decreased amount abnormal ZDB-GENE-010410-3 83413 441509 glra4a ZFA:0005247 CiA PATO:0001997 decreased amount abnormal ZDB-GENE-010410-3 83413 441509 glra4a ZFA:0009052 motor neuron PATO:0001624 decreased functionality abnormal ZDB-GENE-010412-1 83415 10736 six2a GO:0009951 polarity specification of dorsal/ventral axis PATO:0001507 disrupted abnormal ZDB-GENE-010412-1 83415 10736 six2a GO:0048793 pronephros development PATO:0001507 disrupted abnormal ZDB-GENE-010412-1 83415 10736 six2a ZFA:0000033 intermediate cell mass of mesoderm PATO:0000600 increased width abnormal ZDB-GENE-010412-1 83415 10736 six2a ZFA:0000135 notochord PATO:0001483 aplastic abnormal ZDB-GENE-010412-1 83415 10736 six2a ZFA:0001094 whole organism PATO:0000636 wholly ventralized abnormal ZDB-GENE-010412-1 83415 10736 six2a ZFA:0001094 whole organism PATO:0001409 spindle-shaped abnormal ZDB-GENE-010412-1 83415 10736 six2a ZFA:0001114 head PATO:0000587 decreased size abnormal ZDB-GENE-010412-1 83415 10736 six2a ZFA:0001114 head PATO:0001483 aplastic abnormal ZDB-GENE-010412-1 83415 10736 six2a ZFA:0001557 pronephric glomerulus PATO:0000051 morphology abnormal ZDB-GENE-010416-1 83496 25805 bambia GO:0070527 platelet aggregation PATO:0001507 disrupted abnormal ZDB-GENE-010416-1 83496 25805 bambia GO:0071892 thrombocyte activation PATO:0001507 disrupted abnormal ZDB-GENE-010416-1 83496 25805 bambia ZFA:0000011 caudal artery PATO:0002271 decreased accumulation abnormal ZFA:0009323 thrombocyte ZDB-GENE-010416-1 83496 25805 bambia ZFA:0009323 thrombocyte PATO:0001566 distributed abnormal ZDB-GENE-010426-1 83773 1756 dmd GO:0001964 startle response PATO:0001236 process quality abnormal ZDB-GENE-010426-1 83773 1756 dmd GO:0001966 thigmotaxis PATO:0000911 decreased rate abnormal ZDB-GENE-010426-1 83773 1756 dmd GO:0001966 thigmotaxis PATO:0001236 process quality abnormal ZDB-GENE-010426-1 83773 1756 dmd GO:0001966 thigmotaxis PATO:0002302 decreased process quality abnormal ZDB-GENE-010426-1 83773 1756 dmd GO:0003009 skeletal muscle contraction PATO:0002018 decreased magnitude abnormal ZDB-GENE-010426-1 83773 1756 dmd GO:0006874 intracellular calcium ion homeostasis PATO:0001236 process quality abnormal ZDB-GENE-010426-1 83773 1756 dmd GO:0006936 muscle contraction PATO:0001236 process quality abnormal ZDB-GENE-010426-1 83773 1756 dmd GO:0006936 muscle contraction PATO:0002018 decreased magnitude abnormal ZDB-GENE-010426-1 83773 1756 dmd GO:0007519 skeletal muscle tissue development PATO:0001507 disrupted abnormal ZDB-GENE-010426-1 83773 1756 dmd GO:0007626 locomotory behavior PATO:0001236 process quality abnormal ZDB-GENE-010426-1 83773 1756 dmd GO:0007626 locomotory behavior PATO:0002052 decreased occurrence abnormal ZDB-GENE-010426-1 83773 1756 dmd GO:0008345 larval locomotory behavior PATO:0000911 decreased rate abnormal ZDB-GENE-010426-1 83773 1756 dmd GO:0014720 tonic skeletal muscle contraction PATO:0001783 decreased intensity abnormal ZDB-GENE-010426-1 83773 1756 dmd GO:0014721 twitch skeletal muscle contraction PATO:0000498 increased duration abnormal ZDB-GENE-010426-1 83773 1756 dmd GO:0014721 twitch skeletal muscle contraction PATO:0001783 decreased intensity abnormal ZDB-GENE-010426-1 83773 1756 dmd GO:0014841 skeletal muscle satellite cell proliferation PATO:0002051 increased occurrence abnormal ZDB-GENE-010426-1 83773 1756 dmd GO:0014866 skeletal myofibril assembly PATO:0002302 decreased process quality abnormal ZDB-GENE-010426-1 83773 1756 dmd GO:0036268 swimming PATO:0002052 decreased occurrence abnormal ZDB-GENE-010426-1 83773 1756 dmd GO:0036269 swimming behavior PATO:0001236 process quality abnormal ZDB-GENE-010426-1 83773 1756 dmd GO:0043501 skeletal muscle adaptation PATO:0001507 disrupted abnormal ZDB-GENE-010426-1 83773 1756 dmd GO:0048741 skeletal muscle fiber development PATO:0001236 process quality abnormal ZDB-GENE-010426-1 83773 1756 dmd GO:0048741 skeletal muscle fiber development PATO:0001507 disrupted abnormal ZDB-GENE-010426-1 83773 1756 dmd GO:0050881 musculoskeletal movement PATO:0000001 quality abnormal ZDB-GENE-010426-1 83773 1756 dmd GO:0051881 regulation of mitochondrial membrane potential PATO:0001507 disrupted abnormal ZDB-GENE-010426-1 83773 1756 dmd GO:0060047 heart contraction PATO:0055004 decreased rate of occurrence abnormal ZDB-GENE-010426-1 83773 1756 dmd GO:0071929 alpha-tubulin acetylation PATO:0002052 decreased occurrence abnormal ZDB-GENE-010426-1 83773 1756 dmd GO:0030016 myofibril BFO:0000050 part_of ZFA:0000155 somite PATO:0001453 detached from abnormal ZFA:0000155 somite ZDB-GENE-010426-1 83773 1756 dmd GO:0030016 myofibril BFO:0000050 part_of ZFA:0000155 somite PATO:0000141 structure abnormal ZDB-GENE-010426-1 83773 1756 dmd GO:0030016 myofibril BFO:0000050 part_of ZFA:0000155 somite PATO:0000647 necrotic abnormal ZDB-GENE-010426-1 83773 1756 dmd GO:0030016 myofibril BFO:0000050 part_of ZFA:0000155 somite PATO:0000937 disorganized abnormal ZDB-GENE-010426-1 83773 1756 dmd GO:0030016 myofibril BFO:0000050 part_of ZFA:0000155 somite PATO:0001407 mononucleate abnormal ZDB-GENE-010426-1 83773 1756 dmd ZFA:0000155 somite PATO:0000639 degenerate abnormal ZDB-GENE-010426-1 83773 1756 dmd ZFA:0000155 somite PATO:0000937 disorganized abnormal ZDB-GENE-010426-1 83773 1756 dmd ZFA:0000155 somite PATO:0001987 saccular abnormal ZDB-GENE-010426-1 83773 1756 dmd GO:0016020 membrane BFO:0000050 part_of ZFA:0000473 trunk musculature PATO:0001020 damage abnormal ZDB-GENE-010426-1 83773 1756 dmd GO:0030017 sarcomere BFO:0000050 part_of ZFA:0000473 trunk musculature PATO:0000574 decreased length abnormal ZDB-GENE-010426-1 83773 1756 dmd GO:0030017 sarcomere BFO:0000050 part_of ZFA:0000473 trunk musculature PATO:0001714 increased diameter abnormal ZDB-GENE-010426-1 83773 1756 dmd GO:0030017 sarcomere BFO:0000050 part_of ZFA:0000473 trunk musculature PATO:0001715 decreased diameter abnormal ZDB-GENE-010426-1 83773 1756 dmd GO:0090075 relaxation of muscle BFO:0000066 occurs_in ZFA:0000473 trunk musculature PATO:0000498 increased duration abnormal ZDB-GENE-010426-1 83773 1756 dmd ZFA:0000473 trunk musculature PATO:0000001 quality abnormal ZDB-GENE-010426-1 83773 1756 dmd ZFA:0000473 trunk musculature PATO:0001297 reflectivity abnormal ZDB-GENE-010426-1 83773 1756 dmd ZFA:0000473 trunk musculature PATO:0001372 refractivity abnormal ZDB-GENE-010426-1 83773 1756 dmd ZFA:0000473 trunk musculature PATO:0001780 dystrophic abnormal ZDB-GENE-010426-1 83773 1756 dmd ZFA:0000473 trunk musculature PATO:0040025 lesioned abnormal ZDB-GENE-010426-1 83773 1756 dmd GO:0008015 blood circulation BFO:0000066 occurs_in ZFA:0000477 posterior cardinal vein PATO:0055004 decreased rate of occurrence abnormal ZDB-GENE-010426-1 83773 1756 dmd ZFA:0000610 vertical myoseptum PATO:0001241 physical object quality abnormal ZDB-GENE-010426-1 83773 1756 dmd ZFA:0000610 vertical myoseptum PATO:0001879 U-shaped abnormal ZDB-GENE-010426-1 83773 1756 dmd GO:0014866 skeletal myofibril assembly BFO:0000066 occurs_in ZFA:0001056 myotome PATO:0002302 decreased process quality abnormal ZDB-GENE-010426-1 83773 1756 dmd GO:0030017 sarcomere BFO:0000050 part_of ZFA:0001056 myotome PATO:0000646 malformed abnormal ZDB-GENE-010426-1 83773 1756 dmd GO:0042383 sarcolemma BFO:0000050 part_of ZFA:0001056 myotome PATO:0000937 disorganized abnormal ZDB-GENE-010426-1 83773 1756 dmd GO:0098723 skeletal muscle myofibril BFO:0000050 part_of ZFA:0001056 myotome PATO:0000646 malformed abnormal ZDB-GENE-010426-1 83773 1756 dmd GO:0098723 skeletal muscle myofibril BFO:0000050 part_of ZFA:0001056 myotome PATO:0000937 disorganized abnormal ZDB-GENE-010426-1 83773 1756 dmd GO:0098723 skeletal muscle myofibril BFO:0000050 part_of ZFA:0001056 myotome PATO:0002055 increased fragility abnormal ZDB-GENE-010426-1 83773 1756 dmd ZFA:0005277 skeletal muscle BFO:0000050 part_of ZFA:0001056 myotome PATO:0000639 degenerate abnormal ZDB-GENE-010426-1 83773 1756 dmd ZFA:0009114 muscle cell BFO:0000050 part_of ZFA:0001056 myotome PATO:0000639 degenerate abnormal ZDB-GENE-010426-1 83773 1756 dmd ZFA:0009114 muscle cell BFO:0000050 part_of ZFA:0001056 myotome PATO:0001444 broken abnormal ZDB-GENE-010426-1 83773 1756 dmd ZFA:0009115 skeletal muscle cell BFO:0000050 part_of ZFA:0001056 myotome PATO:0001997 decreased amount abnormal ZDB-GENE-010426-1 83773 1756 dmd ZFA:0009115 skeletal muscle cell BFO:0000050 part_of ZFA:0001056 myotome PATO:0002037 degeneration abnormal ZDB-GENE-010426-1 83773 1756 dmd ZFA:0009327 neutrophil BFO:0000050 part_of ZFA:0001056 myotome PATO:0000470 increased amount abnormal ZDB-GENE-010426-1 83773 1756 dmd ZFA:0001056 myotome PATO:0000639 degenerate abnormal ZDB-GENE-010426-1 83773 1756 dmd ZFA:0001056 myotome PATO:0001372 refractivity abnormal ZDB-GENE-010426-1 83773 1756 dmd ZFA:0001056 myotome PATO:0001444 broken abnormal ZDB-GENE-010426-1 83773 1756 dmd ZFA:0001056 myotome PATO:0040019 fibrotic abnormal ZDB-GENE-010426-1 83773 1756 dmd GO:0007585 respiratory gaseous exchange by respiratory system BFO:0000066 occurs_in ZFA:0001094 whole organism PATO:0001236 process quality abnormal ZDB-GENE-010426-1 83773 1756 dmd ZFA:0001094 whole organism PATO:0000169 viability abnormal ZDB-GENE-010426-1 83773 1756 dmd ZFA:0001094 whole organism PATO:0001372 refractivity abnormal ZDB-GENE-010426-1 83773 1756 dmd ZFA:0001094 whole organism PATO:0001422 dead abnormal ZDB-GENE-010426-1 83773 1756 dmd ZFA:0001094 whole organism PATO:0001604 decreased life span abnormal ZDB-GENE-010426-1 83773 1756 dmd ZFA:0001094 whole organism PATO:0001906 movement quality abnormal ZDB-GENE-010426-1 83773 1756 dmd CHEBI:26523 reactive oxygen species BFO:0000050 part_of ZFA:0001115 trunk PATO:0000470 increased amount abnormal ZDB-GENE-010426-1 83773 1756 dmd GO:0006915 apoptotic process BFO:0000066 occurs_in ZFA:0001115 trunk PATO:0002051 increased occurrence abnormal ZDB-GENE-010426-1 83773 1756 dmd ZFA:0001117 post-vent region PATO:0000574 decreased length abnormal ZDB-GENE-010426-1 83773 1756 dmd ZFA:0001117 post-vent region PATO:0001798 kinked abnormal ZDB-GENE-010426-1 83773 1756 dmd GO:0005739 mitochondrion BFO:0000050 part_of ZFA:0005145 muscle PATO:0000586 increased size abnormal ZDB-GENE-010426-1 83773 1756 dmd GO:0005759 mitochondrial matrix BFO:0000050 part_of ZFA:0005145 muscle PATO:0001790 decreased mass density abnormal ZDB-GENE-010426-1 83773 1756 dmd GO:0030016 myofibril BFO:0000050 part_of ZFA:0005145 muscle PATO:0001608 patchy abnormal ZDB-GENE-010426-1 83773 1756 dmd GO:0030017 sarcomere BFO:0000050 part_of ZFA:0005145 muscle PATO:0000937 disorganized abnormal ZDB-GENE-010426-1 83773 1756 dmd GO:0030061 mitochondrial crista BFO:0000050 part_of ZFA:0005145 muscle PATO:0001997 decreased amount abnormal ZDB-GENE-010426-1 83773 1756 dmd ZFA:0005145 muscle PATO:0000051 morphology abnormal ZDB-GENE-010426-1 83773 1756 dmd ZFA:0005145 muscle PATO:0000141 structure abnormal ZDB-GENE-010426-1 83773 1756 dmd ZFA:0005145 muscle PATO:0000937 disorganized abnormal ZDB-GENE-010426-1 83773 1756 dmd ZFA:0005145 muscle PATO:0001167 damaged abnormal ZDB-GENE-010426-1 83773 1756 dmd ZFA:0005145 muscle PATO:0001372 refractivity abnormal ZDB-GENE-010426-1 83773 1756 dmd ZFA:0005145 muscle PATO:0001444 broken abnormal ZDB-GENE-010426-1 83773 1756 dmd ZFA:0005145 muscle PATO:0001624 decreased functionality abnormal ZDB-GENE-010426-1 83773 1756 dmd ZFA:0005145 muscle PATO:0001779 decreased strength abnormal ZDB-GENE-010426-1 83773 1756 dmd ZFA:0005145 muscle PATO:0001780 dystrophic abnormal ZDB-GENE-010426-1 83773 1756 dmd ZFA:0005145 muscle PATO:0002037 degeneration abnormal ZDB-GENE-010426-1 83773 1756 dmd ZFA:0005145 muscle PATO:0002264 organization quality abnormal ZDB-GENE-010426-1 83773 1756 dmd GO:0030016 myofibril BFO:0000050 part_of ZFA:0005277 skeletal muscle PATO:0001453 detached from abnormal GO:0005927 muscle tendon junction BFO:0000050 part_of ZFA:0005277 skeletal muscle ZDB-GENE-010426-1 83773 1756 dmd ZFA:0009327 neutrophil BFO:0000050 part_of ZFA:0005277 skeletal muscle PATO:0000467 present abnormal ZDB-GENE-010426-1 83773 1756 dmd ZFA:0009327 neutrophil BFO:0000050 part_of ZFA:0005277 skeletal muscle PATO:0001629 aggregated abnormal ZDB-GENE-010426-1 83773 1756 dmd ZFA:0005277 skeletal muscle PATO:0002270 increased accumulation abnormal GO:0005583 fibrillar collagen trimer BFO:0000050 part_of ZFA:0009115 skeletal muscle cell ZDB-GENE-010426-1 83773 1756 dmd ZFA:0005277 skeletal muscle PATO:0000141 structure abnormal ZDB-GENE-010426-1 83773 1756 dmd ZFA:0005277 skeletal muscle PATO:0000937 disorganized abnormal ZDB-GENE-010426-1 83773 1756 dmd ZFA:0005277 skeletal muscle PATO:0001372 refractivity abnormal ZDB-GENE-010426-1 83773 1756 dmd ZFA:0005277 skeletal muscle PATO:0001444 broken abnormal ZDB-GENE-010426-1 83773 1756 dmd ZFA:0005277 skeletal muscle PATO:0001623 atrophied abnormal ZDB-GENE-010426-1 83773 1756 dmd ZFA:0005277 skeletal muscle PATO:0001779 decreased strength abnormal ZDB-GENE-010426-1 83773 1756 dmd ZFA:0005277 skeletal muscle PATO:0001780 dystrophic abnormal ZDB-GENE-010426-1 83773 1756 dmd ZFA:0005277 skeletal muscle PATO:0040025 lesioned abnormal ZDB-GENE-010426-1 83773 1756 dmd ZFA:0009114 muscle cell PATO:0000600 increased width abnormal ZDB-GENE-010426-1 83773 1756 dmd ZFA:0009114 muscle cell PATO:0000937 disorganized abnormal ZDB-GENE-010426-1 83773 1756 dmd ZFA:0009114 muscle cell PATO:0001422 dead abnormal ZDB-GENE-010426-1 83773 1756 dmd ZFA:0009114 muscle cell PATO:0001477 retracted abnormal ZDB-GENE-010426-1 83773 1756 dmd ZFA:0009114 muscle cell PATO:0001997 decreased amount abnormal ZDB-GENE-010426-1 83773 1756 dmd GO:0005634 nucleus BFO:0000050 part_of ZFA:0009115 skeletal muscle cell PATO:0000628 mislocalised abnormal ZDB-GENE-010426-1 83773 1756 dmd GO:0005739 mitochondrion BFO:0000050 part_of ZFA:0009115 skeletal muscle cell PATO:0000330 irregular spatial pattern abnormal ZDB-GENE-010426-1 83773 1756 dmd GO:0005739 mitochondrion BFO:0000050 part_of ZFA:0009115 skeletal muscle cell PATO:0001444 broken abnormal ZDB-GENE-010426-1 83773 1756 dmd GO:0030016 myofibril BFO:0000050 part_of ZFA:0009115 skeletal muscle cell PATO:0000937 disorganized abnormal ZDB-GENE-010426-1 83773 1756 dmd GO:0030016 myofibril BFO:0000050 part_of ZFA:0009115 skeletal muscle cell PATO:0001580 increased contractility abnormal ZDB-GENE-010426-1 83773 1756 dmd GO:0042383 sarcolemma BFO:0000050 part_of ZFA:0009115 skeletal muscle cell PATO:0001577 increased permeability abnormal ZDB-GENE-010426-1 83773 1756 dmd ZFA:0009115 skeletal muscle cell PATO:0001453 detached from abnormal ZFA:0001089 myoseptum ZDB-GENE-010426-1 83773 1756 dmd ZFA:0009115 skeletal muscle cell PATO:0001453 detached from abnormal ZFA:0001462 somite border ZDB-GENE-010426-1 83773 1756 dmd ZFA:0009115 skeletal muscle cell PATO:0000051 morphology abnormal ZDB-GENE-010426-1 83773 1756 dmd ZFA:0009115 skeletal muscle cell PATO:0000141 structure abnormal ZDB-GENE-010426-1 83773 1756 dmd ZFA:0009115 skeletal muscle cell PATO:0000639 degenerate abnormal ZDB-GENE-010426-1 83773 1756 dmd ZFA:0009115 skeletal muscle cell PATO:0000937 disorganized abnormal ZDB-GENE-010426-1 83773 1756 dmd ZFA:0009115 skeletal muscle cell PATO:0001167 damaged abnormal ZDB-GENE-010426-1 83773 1756 dmd ZFA:0009115 skeletal muscle cell PATO:0001444 broken abnormal ZDB-GENE-010426-1 83773 1756 dmd ZFA:0009115 skeletal muscle cell PATO:0001958 increased variability of size abnormal ZDB-GENE-010426-1 83773 1756 dmd GO:0005739 mitochondrion BFO:0000050 part_of ZFA:0009116 slow muscle cell PATO:0001509 functionality abnormal ZDB-GENE-010426-1 83773 1756 dmd GO:0005739 mitochondrion BFO:0000050 part_of ZFA:0009116 slow muscle cell PATO:0001624 decreased functionality abnormal ZDB-GENE-010426-1 83773 1756 dmd GO:0005746 mitochondrial respirasome BFO:0000050 part_of ZFA:0009116 slow muscle cell PATO:0001624 decreased functionality abnormal ZDB-GENE-010426-1 83773 1756 dmd ZFA:0009116 slow muscle cell PATO:0001453 detached from abnormal ZFA:0000610 vertical myoseptum ZDB-GENE-010426-1 83773 1756 dmd ZFA:0009116 slow muscle cell PATO:0001453 detached from abnormal ZFA:0001089 myoseptum ZDB-GENE-010426-1 83773 1756 dmd GO:0005739 mitochondrion BFO:0000050 part_of ZFA:0009117 fast muscle cell PATO:0001851 swollen abnormal ZDB-GENE-010426-1 83773 1756 dmd GO:0005741 mitochondrial outer membrane BFO:0000050 part_of ZFA:0009117 fast muscle cell PATO:0000374 increased distance abnormal GO:0005743 mitochondrial inner membrane BFO:0000050 part_of ZFA:0009117 fast muscle cell ZDB-GENE-010426-1 83773 1756 dmd GO:0005741 mitochondrial outer membrane BFO:0000050 part_of ZFA:0009117 fast muscle cell PATO:0001453 detached from abnormal GO:0005743 mitochondrial inner membrane BFO:0000050 part_of ZFA:0009117 fast muscle cell ZDB-GENE-010426-1 83773 1756 dmd GO:0005746 mitochondrial respirasome BFO:0000050 part_of ZFA:0009117 fast muscle cell PATO:0001624 decreased functionality abnormal ZDB-GENE-010426-1 83773 1756 dmd ZFA:0009117 fast muscle cell PATO:0001453 detached from abnormal ZFA:0001089 myoseptum ZDB-GENE-010426-1 83773 1756 dmd ZFA:0009117 fast muscle cell PATO:0040047 fragmented abnormal ZDB-GENE-010430-3 569581 4594 mmut GO:0009060 aerobic respiration PATO:0002302 decreased process quality abnormal ZDB-GENE-010430-3 569581 4594 mmut GO:0036269 swimming behavior PATO:0002302 decreased process quality abnormal ZDB-GENE-010430-3 569581 4594 mmut GO:0005739 mitochondrion BFO:0000050 part_of ZFA:0000123 liver PATO:0000051 morphology abnormal ZDB-GENE-010430-3 569581 4594 mmut GO:0005739 mitochondrion BFO:0000050 part_of ZFA:0000123 liver PATO:0000411 circular abnormal ZDB-GENE-010430-3 569581 4594 mmut GO:0030061 mitochondrial crista BFO:0000050 part_of ZFA:0000123 liver PATO:0000937 disorganized abnormal ZDB-GENE-010430-3 569581 4594 mmut GO:0005739 mitochondrion BFO:0000050 part_of ZFA:0000529 kidney PATO:0000051 morphology abnormal ZDB-GENE-010430-3 569581 4594 mmut GO:0005739 mitochondrion BFO:0000050 part_of ZFA:0000529 kidney PATO:0000411 circular abnormal ZDB-GENE-010430-3 569581 4594 mmut GO:0030061 mitochondrial crista BFO:0000050 part_of ZFA:0000529 kidney PATO:0000937 disorganized abnormal ZDB-GENE-010430-3 569581 4594 mmut CHEBI:30860 methylmalonic acid BFO:0000050 part_of ZFA:0001094 whole organism PATO:0000470 increased amount abnormal ZDB-GENE-010430-3 569581 4594 mmut ZFA:0001094 whole organism PATO:0000169 viability abnormal ZDB-GENE-010501-6 569250 10919 ehmt2 GO:0051567 histone H3-K9 methylation PATO:0002052 decreased occurrence abnormal ZDB-GENE-010501-6 569250 10919 ehmt2 ZFA:0000008 brain PATO:0000587 decreased size abnormal ZDB-GENE-010501-6 569250 10919 ehmt2 ZFA:0000054 pericardium PATO:0001450 edematous abnormal ZDB-GENE-010501-6 569250 10919 ehmt2 ZFA:0000107 eye PATO:0000587 decreased size abnormal ZDB-GENE-010501-6 569250 10919 ehmt2 GO:0006915 apoptotic process BFO:0000066 occurs_in ZFA:0000128 midbrain PATO:0002051 increased occurrence abnormal ZDB-GENE-010501-6 569250 10919 ehmt2 ZFA:0000128 midbrain PATO:0000051 morphology abnormal ZDB-GENE-010501-6 569250 10919 ehmt2 GO:0006915 apoptotic process BFO:0000066 occurs_in ZFA:0000152 retina PATO:0001236 process quality ameliorated ZDB-GENE-010501-6 569250 10919 ehmt2 GO:0006915 apoptotic process BFO:0000066 occurs_in ZFA:0000152 retina PATO:0002051 increased occurrence abnormal ZDB-GENE-010501-6 569250 10919 ehmt2 GO:0008283 cell population proliferation BFO:0000066 occurs_in ZFA:0000152 retina PATO:0002051 increased occurrence abnormal ZDB-GENE-010504-1 83916 2516 nr5a1a GO:0031018 endocrine pancreas development PATO:0001236 process quality abnormal ZDB-GENE-010504-1 83916 2516 nr5a1a GO:0048589 developmental growth PATO:0000911 decreased rate abnormal ZDB-GENE-010504-1 83916 2516 nr5a1a ZFA:0000076 swim bladder PATO:0000587 decreased size abnormal ZDB-GENE-010504-1 83916 2516 nr5a1a ZFA:0000084 yolk PATO:0001450 edematous abnormal ZDB-GENE-010504-1 83916 2516 nr5a1a ZFA:0001094 whole organism PATO:0000574 decreased length abnormal ZDB-GENE-010504-1 83916 2516 nr5a1a ZFA:0001260 endocrine pancreas PATO:0000646 malformed abnormal ZDB-GENE-010522-1 84702 1356 cp GO:0007368 determination of left/right symmetry PATO:0001507 disrupted abnormal ZDB-GENE-010522-1 84702 1356 cp BSPO:0000013 anterior-posterior axis BFO:0000050 part_of ZFA:0001094 whole organism PATO:0000406 curved abnormal ZDB-GENE-010522-1 84702 1356 cp ZFA:0001261 ventricular system PATO:0001853 hydrocephalic abnormal ZDB-GENE-010522-1 84702 1356 cp ZFA:0001617 otolith PATO:0000051 morphology abnormal ZDB-GENE-010525-1 84703 6521 slc4a1a GO:0008015 blood circulation PATO:0000911 decreased rate abnormal ZDB-GENE-010525-1 84703 6521 slc4a1a GO:0008015 blood circulation PATO:0000912 increased rate abnormal ZDB-GENE-010525-1 84703 6521 slc4a1a GO:0042541 hemoglobin biosynthetic process PATO:0001507 disrupted abnormal ZDB-GENE-010525-1 84703 6521 slc4a1a GO:0060038 cardiac muscle cell proliferation PATO:0002051 increased occurrence abnormal ZDB-GENE-010525-1 84703 6521 slc4a1a GO:0060047 heart contraction PATO:0000911 decreased rate abnormal ZDB-GENE-010525-1 84703 6521 slc4a1a GO:0060047 heart contraction PATO:0000912 increased rate abnormal ZDB-GENE-010525-1 84703 6521 slc4a1a ZFA:0000007 blood PATO:0000001 quality abnormal ZDB-GENE-010525-1 84703 6521 slc4a1a GO:0008219 cell death BFO:0000066 occurs_in ZFA:0000009 cardiac ventricle PATO:0002051 increased occurrence abnormal ZDB-GENE-010525-1 84703 6521 slc4a1a ZFA:0009316 cardiac muscle cell BFO:0000050 part_of ZFA:0000009 cardiac ventricle PATO:0000470 increased amount abnormal ZDB-GENE-010525-1 84703 6521 slc4a1a ZFA:0009316 cardiac muscle cell BFO:0000050 part_of ZFA:0000009 cardiac ventricle PATO:0001997 decreased amount abnormal ZDB-GENE-010525-1 84703 6521 slc4a1a ZFA:0000009 cardiac ventricle PATO:0000586 increased size abnormal ZDB-GENE-010525-1 84703 6521 slc4a1a ZFA:0000114 heart PATO:0000586 increased size abnormal ZDB-GENE-010525-1 84703 6521 slc4a1a ZFA:0000114 heart PATO:0001624 decreased functionality abnormal ZDB-GENE-010525-1 84703 6521 slc4a1a ZFA:0000173 bulbus arteriosus PATO:0000586 increased size abnormal ZDB-GENE-010525-1 84703 6521 slc4a1a ZFA:0000471 atrium PATO:0000586 increased size abnormal ZDB-GENE-010525-1 84703 6521 slc4a1a ZFA:0001094 whole organism PATO:0000169 viability abnormal ZDB-GENE-010525-1 84703 6521 slc4a1a ZFA:0001094 whole organism PATO:0001422 dead abnormal ZDB-GENE-010525-1 84703 6521 slc4a1a ZFA:0001094 whole organism PATO:0001604 decreased life span abnormal ZDB-GENE-010525-1 84703 6521 slc4a1a GO:0005833 hemoglobin complex BFO:0000050 part_of ZFA:0009256 nucleate erythrocyte PATO:0001997 decreased amount abnormal ZDB-GENE-010525-1 84703 6521 slc4a1a ZFA:0009256 nucleate erythrocyte PATO:0000586 increased size abnormal ZDB-GENE-010525-1 84703 6521 slc4a1a ZFA:0009256 nucleate erythrocyte PATO:0001997 decreased amount abnormal ZDB-GENE-010525-1 84703 6521 slc4a1a ZFA:0009256 nucleate erythrocyte PATO:0002094 basophilic abnormal ZDB-GENE-010525-1 84703 6521 slc4a1a GO:0030016 myofibril BFO:0000050 part_of ZFA:0009316 cardiac muscle cell PATO:0000937 disorganized abnormal ZDB-GENE-010525-1 84703 6521 slc4a1a ZFA:0009316 cardiac muscle cell PATO:0000584 hypertrophic abnormal ZDB-GENE-010525-1 84703 6521 slc4a1a ZFA:0009316 cardiac muscle cell PATO:0000586 increased size abnormal ZDB-GENE-010525-1 84703 6521 slc4a1a ZFA:0009316 cardiac muscle cell PATO:0000587 decreased size abnormal ZDB-GENE-010525-1 84703 6521 slc4a1a ZFA:0009316 cardiac muscle cell PATO:0000644 hyperplastic abnormal ZDB-GENE-010601-1 114427 7407 vars1 GO:0010842 retina layer formation PATO:0000502 delayed abnormal ZDB-GENE-010601-1 114427 7407 vars1 GO:0036269 swimming behavior PATO:0002052 decreased occurrence abnormal ZDB-GENE-010601-1 114427 7407 vars1 GO:0006915 apoptotic process BFO:0000066 occurs_in ZFA:0000008 brain PATO:0002051 increased occurrence abnormal ZDB-GENE-010601-1 114427 7407 vars1 ZFA:0000008 brain PATO:0000051 morphology abnormal ZDB-GENE-010601-1 114427 7407 vars1 ZFA:0000008 brain PATO:0000587 decreased size abnormal ZDB-GENE-010601-1 114427 7407 vars1 ZFA:0000035 lens PATO:0000587 decreased size abnormal ZDB-GENE-010601-1 114427 7407 vars1 ZFA:0000054 pericardium PATO:0001450 edematous abnormal ZDB-GENE-010601-1 114427 7407 vars1 ZFA:0000084 yolk PATO:0000950 grey abnormal ZDB-GENE-010601-1 114427 7407 vars1 ZFA:0000084 yolk PATO:0001851 swollen abnormal ZDB-GENE-010601-1 114427 7407 vars1 ZFA:0000107 eye PATO:0000587 decreased size abnormal ZDB-GENE-010601-1 114427 7407 vars1 ZFA:0000109 forebrain PATO:0000587 decreased size abnormal ZDB-GENE-010601-1 114427 7407 vars1 ZFA:0000112 gut PATO:0000645 hypoplastic abnormal ZDB-GENE-010601-1 114427 7407 vars1 ZFA:0000114 heart PATO:0000001 quality abnormal ZDB-GENE-010601-1 114427 7407 vars1 ZFA:0000123 liver PATO:0000645 hypoplastic abnormal ZDB-GENE-010601-1 114427 7407 vars1 ZFA:0000159 tectal ventricle PATO:0000051 morphology abnormal ZDB-GENE-010601-1 114427 7407 vars1 GO:0098908 regulation of neuronal action potential BFO:0000066 occurs_in ZFA:0000445 optic tectum PATO:0001507 disrupted abnormal ZDB-GENE-010601-1 114427 7407 vars1 ZFA:0000640 cornea PATO:0001450 edematous abnormal ZDB-GENE-010601-1 114427 7407 vars1 ZFA:0001094 whole organism PATO:0001422 dead abnormal ZDB-GENE-010601-1 114427 7407 vars1 ZFA:0001094 whole organism PATO:0001604 decreased life span abnormal ZDB-GENE-010601-1 114427 7407 vars1 ZFA:0001114 head PATO:0000587 decreased size abnormal ZDB-GENE-010601-1 114427 7407 vars1 ZFA:0001227 mandibular arch skeleton PATO:0000587 decreased size abnormal ZDB-GENE-010601-1 114427 7407 vars1 ZFA:0001259 forebrain ventricle PATO:0000051 morphology abnormal ZDB-GENE-010605-4 114463 9935 mafbb ZFA:0009077 microglial cell BFO:0000050 part_of ZFA:0000008 brain PATO:0001997 decreased amount abnormal ZDB-GENE-010605-4 114463 9935 mafbb ZFA:0009047 osteoclast BFO:0000050 part_of ZFA:0000277 scale PATO:0001671 increased distribution abnormal ZDB-GENE-010605-4 114463 9935 mafbb ZFA:0000364 hypural PATO:0000642 fused with abnormal ZFA:0000364 hypural ZDB-GENE-010605-4 114463 9935 mafbb ZFA:0000364 hypural PATO:0000596 decreased volume abnormal ZDB-GENE-010605-4 114463 9935 mafbb ZFA:0000519 hemal arch PATO:0005020 irregularly shaped abnormal ZDB-GENE-010605-4 114463 9935 mafbb ZFA:0009265 monocyte BFO:0000050 part_of ZFA:0000669 head kidney PATO:0000470 increased amount abnormal ZDB-GENE-010605-4 114463 9935 mafbb ZFA:0009324 myeloid cell BFO:0000050 part_of ZFA:0000669 head kidney PATO:0000470 increased amount abnormal ZDB-GENE-010605-4 114463 9935 mafbb GO:0030282 bone mineralization BFO:0000066 occurs_in ZFA:0000694 ceratobranchial 5 tooth PATO:0002302 decreased process quality abnormal ZDB-GENE-010605-4 114463 9935 mafbb ZFA:0000694 ceratobranchial 5 tooth PATO:0001997 decreased amount abnormal ZDB-GENE-010605-4 114463 9935 mafbb ZFA:0009047 osteoclast BFO:0000050 part_of ZFA:0001058 caudal fin PATO:0001671 increased distribution abnormal ZDB-GENE-010605-4 114463 9935 mafbb ZFA:0001058 caudal fin PATO:0000616 asymmetrical abnormal ZDB-GENE-010605-4 114463 9935 mafbb ZFA:0001066 neural arch PATO:0005020 irregularly shaped abnormal ZDB-GENE-010605-4 114463 9935 mafbb ZFA:0001094 whole organism PATO:0001770 semi-viable abnormal ZDB-GENE-010605-4 114463 9935 mafbb ZFA:0009256 nucleate erythrocyte BFO:0000050 part_of ZFA:0001114 head PATO:0001997 decreased amount abnormal ZDB-GENE-010605-4 114463 9935 mafbb ZFA:0009141 macrophage BFO:0000050 part_of ZFA:0001117 post-vent region PATO:0000470 increased amount abnormal ZDB-GENE-010605-4 114463 9935 mafbb ZFA:0009256 nucleate erythrocyte BFO:0000050 part_of ZFA:0001117 post-vent region PATO:0001997 decreased amount abnormal ZDB-GENE-010605-4 114463 9935 mafbb ZFA:0009327 neutrophil BFO:0000050 part_of ZFA:0001117 post-vent region PATO:0000470 increased amount abnormal ZDB-GENE-010605-4 114463 9935 mafbb ZFA:0009354 hematopoietic multipotent progenitor cell BFO:0000050 part_of ZFA:0001117 post-vent region PATO:0001997 decreased amount abnormal ZDB-GENE-010605-4 114463 9935 mafbb ZFA:0001117 post-vent region PATO:0000406 curved abnormal ZDB-GENE-010605-4 114463 9935 mafbb ZFA:0001205 Meckel's cartilage PATO:0000617 bent abnormal ZDB-GENE-010605-4 114463 9935 mafbb ZFA:0001273 ventral mandibular arch PATO:0001598 protruding abnormal ZDB-GENE-010605-4 114463 9935 mafbb ZFA:0001400 ceratohyal cartilage PATO:0002327 increased angle to abnormal ZFA:0001400 ceratohyal cartilage ZDB-GENE-010605-4 114463 9935 mafbb ZFA:0001400 ceratohyal cartilage PATO:0000617 bent abnormal ZDB-GENE-010605-4 114463 9935 mafbb ZFA:0001510 basihyal cartilage PATO:0000617 bent abnormal ZDB-GENE-010605-4 114463 9935 mafbb ZFA:0009047 osteoclast BFO:0000050 part_of ZFA:0001559 vertebral column PATO:0001671 increased distribution abnormal ZDB-GENE-010605-4 114463 9935 mafbb ZFA:0001559 vertebral column PATO:0000406 curved abnormal ZDB-GENE-010605-4 114463 9935 mafbb ZFA:0001560 hypural 1 PATO:0000051 morphology abnormal ZDB-GENE-010605-4 114463 9935 mafbb ZFA:0001561 hypural 2 PATO:0000051 morphology abnormal ZDB-GENE-010605-4 114463 9935 mafbb ZFA:0009141 macrophage PATO:0001997 decreased amount abnormal ZDB-GENE-010606-1 114424 999 cdh1 GO:0001947 heart looping PATO:0001236 process quality abnormal ZDB-GENE-010606-1 114424 999 cdh1 GO:0001947 heart looping PATO:0001507 disrupted abnormal ZDB-GENE-010606-1 114424 999 cdh1 GO:0003370 cell-cell adhesion involved in mesendodermal cell migration PATO:0001507 disrupted abnormal ZDB-GENE-010606-1 114424 999 cdh1 GO:0034109 homotypic cell-cell adhesion PATO:0000297 arrested abnormal ZDB-GENE-010606-1 114424 999 cdh1 GO:0042074 cell migration involved in gastrulation PATO:0000911 decreased rate abnormal ZDB-GENE-010606-1 114424 999 cdh1 GO:0042074 cell migration involved in gastrulation PATO:0001236 process quality abnormal ZDB-GENE-010606-1 114424 999 cdh1 GO:0043009 chordate embryonic development PATO:0000297 arrested abnormal ZDB-GENE-010606-1 114424 999 cdh1 GO:0055113 epiboly involved in gastrulation with mouth forming second PATO:0000297 arrested abnormal ZDB-GENE-010606-1 114424 999 cdh1 GO:0055113 epiboly involved in gastrulation with mouth forming second PATO:0001507 disrupted abnormal ZDB-GENE-010606-1 114424 999 cdh1 GO:0070586 cell-cell adhesion involved in gastrulation PATO:0002302 decreased process quality abnormal ZDB-GENE-010606-1 114424 999 cdh1 GO:0072659 protein localization to plasma membrane PATO:0001507 disrupted abnormal ZDB-GENE-010606-1 114424 999 cdh1 GO:0005884 actin filament BFO:0000050 part_of ZFA:0000023 forerunner cell group PATO:0000141 structure abnormal ZDB-GENE-010606-1 114424 999 cdh1 ZFA:0000026 hatching gland PATO:0000586 increased size abnormal ZDB-GENE-010606-1 114424 999 cdh1 ZFA:0000026 hatching gland PATO:0000628 mislocalised abnormal ZDB-GENE-010606-1 114424 999 cdh1 BSPO:0000072 posterior region BFO:0000050 part_of ZFA:0000029 hindbrain PATO:0000051 morphology abnormal ZDB-GENE-010606-1 114424 999 cdh1 ZFA:0000058 polster PATO:0000051 morphology abnormal ZDB-GENE-010606-1 114424 999 cdh1 ZFA:0000058 polster PATO:0000574 decreased length abnormal ZDB-GENE-010606-1 114424 999 cdh1 ZFA:0000058 polster PATO:0000628 mislocalised abnormal ZDB-GENE-010606-1 114424 999 cdh1 BSPO:0000071 anterior region BFO:0000050 part_of ZFA:0000075 spinal cord PATO:0000051 morphology abnormal ZDB-GENE-010606-1 114424 999 cdh1 ZFA:0000077 tail bud PATO:0000587 decreased size abnormal ZDB-GENE-010606-1 114424 999 cdh1 ZFA:0000084 yolk PATO:0000001 quality abnormal ZDB-GENE-010606-1 114424 999 cdh1 ZFA:0000135 notochord PATO:0001798 kinked abnormal ZDB-GENE-010606-1 114424 999 cdh1 ZFA:0000155 somite PATO:0000600 increased width abnormal ZDB-GENE-010606-1 114424 999 cdh1 ZFA:0009248 neuron BFO:0000050 part_of ZFA:0000295 trigeminal ganglion PATO:0000937 disorganized abnormal ZDB-GENE-010606-1 114424 999 cdh1 ZFA:0009248 neuron BFO:0000050 part_of ZFA:0000295 trigeminal ganglion PATO:0001566 distributed abnormal ZDB-GENE-010606-1 114424 999 cdh1 ZFA:0000295 trigeminal ganglion PATO:0001923 mislocalised laterally abnormal ZDB-GENE-010606-1 114424 999 cdh1 ZFA:0000360 heart tube PATO:0000140 position abnormal ZDB-GENE-010606-1 114424 999 cdh1 ZFA:0000396 nervous system PATO:0002254 flattened abnormal ZDB-GENE-010606-1 114424 999 cdh1 ZFA:0000711 DEL PATO:0001453 detached from abnormal ZFA:0000086 EVL ZDB-GENE-010606-1 114424 999 cdh1 ZFA:0000711 DEL PATO:0000140 position abnormal ZDB-GENE-010606-1 114424 999 cdh1 ZFA:0009138 mesodermal cell BFO:0000050 part_of ZFA:0001065 lateral mesoderm PATO:0000304 decreased speed abnormal ZDB-GENE-010606-1 114424 999 cdh1 ZFA:0009138 mesodermal cell BFO:0000050 part_of ZFA:0001065 lateral mesoderm PATO:0000629 misrouted abnormal ZDB-GENE-010606-1 114424 999 cdh1 BSPO:0000013 anterior-posterior axis BFO:0000050 part_of ZFA:0001094 whole organism PATO:0000574 decreased length abnormal ZDB-GENE-010606-1 114424 999 cdh1 ZFA:0001094 whole organism PATO:0000001 quality abnormal ZDB-GENE-010606-1 114424 999 cdh1 ZFA:0001094 whole organism PATO:0000647 necrotic abnormal ZDB-GENE-010606-1 114424 999 cdh1 ZFA:0001094 whole organism PATO:0000718 lethal (sensu genetics) abnormal ZDB-GENE-010606-1 114424 999 cdh1 ZFA:0001117 post-vent region PATO:0000001 quality abnormal ZDB-GENE-010606-1 114424 999 cdh1 ZFA:0009000 cell BFO:0000050 part_of ZFA:0001135 neural tube PATO:0000628 mislocalised abnormal ZDB-GENE-010606-1 114424 999 cdh1 GO:0030175 filopodium BFO:0000050 part_of ZFA:0001378 axial hypoblast PATO:0001997 decreased amount abnormal ZDB-GENE-010606-1 114424 999 cdh1 ZFA:0009150 Rohon-Beard neuron PATO:0000628 mislocalised abnormal ZDB-GENE-010607-2 114433 3479 igf1 ZFA:0001094 whole organism PATO:0000051 morphology abnormal ZDB-GENE-010614-1 114447 7852 cxcr4b GO:0001755 neural crest cell migration PATO:0002052 decreased occurrence abnormal ZDB-GENE-010614-1 114447 7852 cxcr4b GO:0001764 neuron migration PATO:0001507 disrupted abnormal ZDB-GENE-010614-1 114447 7852 cxcr4b GO:0007368 determination of left/right symmetry PATO:0002052 decreased occurrence abnormal ZDB-GENE-010614-1 114447 7852 cxcr4b GO:0007411 axon guidance PATO:0001236 process quality abnormal ZDB-GENE-010614-1 114447 7852 cxcr4b GO:0007411 axon guidance PATO:0001507 disrupted abnormal ZDB-GENE-010614-1 114447 7852 cxcr4b GO:0008354 germ cell migration PATO:0001236 process quality abnormal ZDB-GENE-010614-1 114447 7852 cxcr4b GO:0031290 retinal ganglion cell axon guidance PATO:0000001 quality abnormal ZDB-GENE-010614-1 114447 7852 cxcr4b GO:0048846 axon extension involved in axon guidance PATO:0001507 disrupted abnormal ZDB-GENE-010614-1 114447 7852 cxcr4b GO:0048883 neuromast primordium migration PATO:0000297 arrested abnormal ZDB-GENE-010614-1 114447 7852 cxcr4b GO:0048883 neuromast primordium migration PATO:0000502 delayed abnormal ZDB-GENE-010614-1 114447 7852 cxcr4b GO:0048920 posterior lateral line neuromast primordium migration PATO:0001236 process quality abnormal ZDB-GENE-010614-1 114447 7852 cxcr4b GO:0048920 posterior lateral line neuromast primordium migration PATO:0001507 disrupted abnormal ZDB-GENE-010614-1 114447 7852 cxcr4b ZFA:0009043 circulating cell BFO:0000050 part_of ZFA:0000014 dorsal aorta PATO:0002002 has extra parts of type abnormal ZFA:0009327 neutrophil ZDB-GENE-010614-1 114447 7852 cxcr4b ZFA:0000023 forerunner cell group PATO:0000330 irregular spatial pattern abnormal ZDB-GENE-010614-1 114447 7852 cxcr4b ZFA:0000023 forerunner cell group PATO:0001566 distributed abnormal ZDB-GENE-010614-1 114447 7852 cxcr4b ZFA:0000155 somite PATO:0001396 cellular quality abnormal ZDB-GENE-010614-1 114447 7852 cxcr4b GO:0030424 axon BFO:0000050 part_of ZFA:0000295 trigeminal ganglion PATO:0000140 position abnormal ZDB-GENE-010614-1 114447 7852 cxcr4b ZFA:0009327 neutrophil BFO:0000050 part_of ZFA:0000529 kidney PATO:0001997 decreased amount abnormal ZDB-GENE-010614-1 114447 7852 cxcr4b ZFA:0000940 posterior lateral line neuromast PATO:0001997 decreased amount abnormal ZDB-GENE-010614-1 114447 7852 cxcr4b GO:0061572 actin filament bundle organization BFO:0000066 occurs_in ZFA:0001157 posterior lateral line primordium PATO:0001236 process quality abnormal ZDB-GENE-010614-1 114447 7852 cxcr4b ZFA:0001157 posterior lateral line primordium PATO:0001241 physical object quality abnormal ZDB-GENE-010614-1 114447 7852 cxcr4b GO:0016477 cell migration BFO:0000066 occurs_in ZFA:0005768 trigeminal sensory neuron PATO:0001236 process quality abnormal ZDB-GENE-010614-1 114447 7852 cxcr4b ZFA:0005768 trigeminal sensory neuron PATO:0000628 mislocalised abnormal ZDB-GENE-010614-1 114447 7852 cxcr4b GO:0030424 axon BFO:0000050 part_of ZFA:0009125 olfactory receptor cell PATO:0000629 misrouted abnormal ZDB-GENE-010614-1 114447 7852 cxcr4b ZFA:0009125 olfactory receptor cell PATO:0000628 mislocalised abnormal ZDB-GENE-010614-1 114447 7852 cxcr4b ZFA:0009125 olfactory receptor cell PATO:0001920 mislocalised ventrally abnormal ZDB-GENE-010614-1 114447 7852 cxcr4b ZFA:0009125 olfactory receptor cell PATO:0001924 mislocalised medially abnormal ZDB-GENE-010614-1 114447 7852 cxcr4b GO:0030010 establishment of cell polarity BFO:0000066 occurs_in ZFA:0009288 primordial germ cell PATO:0002052 decreased occurrence abnormal ZDB-GENE-010614-1 114447 7852 cxcr4b GO:0051453 regulation of intracellular pH BFO:0000066 occurs_in ZFA:0009288 primordial germ cell PATO:0001236 process quality abnormal ZDB-GENE-010614-1 114447 7852 cxcr4b ZFA:0009288 primordial germ cell PATO:0000001 quality abnormal ZDB-GENE-010614-1 114447 7852 cxcr4b ZFA:0009288 primordial germ cell PATO:0000628 mislocalised abnormal ZDB-GENE-010618-1 114402 1948 efnb2b GO:0070121 Kupffer's vesicle development PATO:0002302 decreased process quality abnormal ZDB-GENE-010618-1 114402 1948 efnb2b ZFA:0000001 Kupffer's vesicle PATO:0000587 decreased size abnormal ZDB-GENE-010618-1 114402 1948 efnb2b ZFA:0000023 forerunner cell group PATO:0001630 dispersed abnormal ZDB-GENE-010618-1 114402 1948 efnb2b GO:0001947 heart looping BFO:0000066 occurs_in ZFA:0000114 heart PATO:0002052 decreased occurrence abnormal ZDB-GENE-010618-1 114402 1948 efnb2b ZFA:0001094 whole organism PATO:0002000 lacks all parts of type abnormal ZFA:0000001 Kupffer's vesicle ZDB-GENE-010618-2 114377 1947 efnb1 GO:0002194 hepatocyte cell migration PATO:0001236 process quality abnormal ZDB-GENE-010618-2 114377 1947 efnb1 GO:0002194 hepatocyte cell migration PATO:0002052 decreased occurrence abnormal ZDB-GENE-010618-2 114377 1947 efnb1 GO:0048566 embryonic digestive tract development PATO:0002302 decreased process quality abnormal ZDB-GENE-010618-2 114377 1947 efnb1 GO:1990402 embryonic liver development PATO:0001236 process quality abnormal ZDB-GENE-010618-2 114377 1947 efnb1 GO:0045198 establishment of epithelial cell apical/basal polarity BFO:0000066 occurs_in ZFA:0000121 lateral plate mesoderm PATO:0002302 decreased process quality abnormal ZDB-GENE-010618-2 114377 1947 efnb1 ZFA:0000124 liver primordium PATO:0000646 malformed abnormal ZDB-GENE-010618-2 114377 1947 efnb1 ZFA:0000208 gall bladder PATO:0000587 decreased size abnormal ZDB-GENE-010618-2 114377 1947 efnb1 ZFA:0005162 digestive system duct PATO:0000051 morphology abnormal ZDB-GENE-010618-2 114377 1947 efnb1 GO:0060562 epithelial tube morphogenesis BFO:0000066 occurs_in ZFA:0005165 common bile duct PATO:0001507 disrupted abnormal ZDB-GENE-010618-2 114377 1947 efnb1 ZFA:0005930 lumen BFO:0000050 part_of ZFA:0005165 common bile duct PATO:0000141 structure abnormal ZDB-GENE-010618-2 114377 1947 efnb1 ZFA:0009372 duct epithelial cell BFO:0000050 part_of ZFA:0005165 common bile duct PATO:0000051 morphology abnormal ZDB-GENE-010618-2 114377 1947 efnb1 ZFA:0005165 common bile duct PATO:0000051 morphology abnormal ZDB-GENE-010618-2 114377 1947 efnb1 ZFA:0005165 common bile duct PATO:0000402 branched abnormal ZDB-GENE-010618-2 114377 1947 efnb1 ZFA:0005165 common bile duct PATO:0000574 decreased length abnormal ZDB-GENE-010618-2 114377 1947 efnb1 ZFA:0005165 common bile duct PATO:0010001 disconnected abnormal ZDB-GENE-010618-2 114377 1947 efnb1 ZFA:0005166 cystic duct PATO:0000586 increased size abnormal ZDB-GENE-010618-2 114377 1947 efnb1 ZFA:0005170 extrahepatic duct PATO:0000462 absent abnormal ZDB-GENE-010618-2 114377 1947 efnb1 ZFA:0005170 extrahepatic duct PATO:0000600 increased width abnormal ZDB-GENE-010618-2 114377 1947 efnb1 ZFA:0005346 extrapancreatic duct PATO:0000051 morphology abnormal ZDB-GENE-010618-2 114377 1947 efnb1 ZFA:0005738 intestinal bulb primordium PATO:0001593 decreased curvature abnormal ZDB-GENE-010618-2 114377 1947 efnb1 GO:0030175 filopodium BFO:0000050 part_of ZFA:0009398 hepatoblast PATO:0000574 decreased length abnormal ZDB-GENE-010618-2 114377 1947 efnb1 GO:0051489 regulation of filopodium assembly BFO:0000066 occurs_in ZFA:0009398 hepatoblast PATO:0001236 process quality abnormal ZDB-GENE-010618-2 114377 1947 efnb1 ZFA:0009398 hepatoblast PATO:0002001 has fewer parts of type abnormal GO:0030175 filopodium BFO:0000050 part_of ZFA:0009398 hepatoblast ZDB-GENE-010618-2 114377 1947 efnb1 ZFA:0009398 hepatoblast PATO:0000052 shape abnormal ZDB-GENE-010618-2 114377 1947 efnb1 ZFA:0009398 hepatoblast PATO:0000628 mislocalised abnormal ZDB-GENE-010618-2 114377 1947 efnb1 ZFA:0009398 hepatoblast PATO:0001922 mislocalised posteriorly abnormal ZDB-GENE-010618-2 114377 1947 efnb1 ZFA:0009398 hepatoblast PATO:0001924 mislocalised medially abnormal ZDB-GENE-010618-2 114377 1947 efnb1 ZFA:0009398 hepatoblast PATO:0002490 anterior orientation abnormal ZDB-GENE-010619-3 81025 gja9a GO:0050953 sensory perception of light stimulus PATO:0001236 process quality abnormal ZDB-GENE-010619-3 81025 gja9a GO:0051966 regulation of synaptic transmission, glutamatergic PATO:0001236 process quality abnormal ZDB-GENE-010619-3 81025 gja9a GO:0055077 gap junction hemi-channel activity PATO:0001236 process quality abnormal ZDB-GENE-010619-3 81025 gja9a GO:0071632 optomotor response PATO:0002052 decreased occurrence abnormal ZDB-GENE-010619-3 81025 gja9a GO:0019226 transmission of nerve impulse BFO:0000066 occurs_in ZFA:0009262 retinal cone cell PATO:0001236 process quality abnormal ZDB-GENE-010619-3 81025 gja9a GO:0005921 gap junction BFO:0000050 part_of ZFA:0009315 horizontal cell PATO:0000470 increased amount abnormal ZDB-GENE-010619-3 81025 gja9a GO:0005921 gap junction BFO:0000050 part_of ZFA:0009315 horizontal cell PATO:0000587 decreased size abnormal ZDB-GENE-010619-3 81025 gja9a GO:0005922 connexin complex BFO:0000050 part_of ZFA:0009315 horizontal cell PATO:0001509 functionality abnormal ZDB-GENE-010621-1 114425 6935 zeb1b GO:0009790 embryo development PATO:0001507 disrupted abnormal ZDB-GENE-010621-1 114425 6935 zeb1b GO:0060030 dorsal convergence PATO:0001236 process quality abnormal ZDB-GENE-010621-1 114425 6935 zeb1b BSPO:0000013 anterior-posterior axis BFO:0000050 part_of ZFA:0001094 whole organism PATO:0002364 shortened abnormal ZDB-GENE-010621-1 114425 6935 zeb1b ZFA:0001094 whole organism PATO:0000051 morphology abnormal ZDB-GENE-010702-1 114412 8543 lmo4a GO:0008283 cell population proliferation PATO:0002051 increased occurrence abnormal ZDB-GENE-010702-1 114412 8543 lmo4a GO:0016477 cell migration PATO:0001507 disrupted abnormal ZDB-GENE-010702-1 114412 8543 lmo4a GO:0035162 embryonic hemopoiesis PATO:0001507 disrupted abnormal ZDB-GENE-010702-1 114412 8543 lmo4a GO:0060318 definitive erythrocyte differentiation PATO:0001507 disrupted abnormal ZDB-GENE-010702-1 114412 8543 lmo4a ZFA:0000008 brain PATO:0000051 morphology abnormal ZDB-GENE-010702-1 114412 8543 lmo4a ZFA:0000032 hypothalamus PATO:0000586 increased size abnormal ZDB-GENE-010702-1 114412 8543 lmo4a ZFA:0000050 optic vesicle PATO:0002002 has extra parts of type abnormal ZFA:0009080 neurectodermal cell ZDB-GENE-010702-1 114412 8543 lmo4a ZFA:0000050 optic vesicle PATO:0000586 increased size abnormal ZDB-GENE-010702-1 114412 8543 lmo4a ZFA:0000051 otic vesicle PATO:0000051 morphology abnormal ZDB-GENE-010702-1 114412 8543 lmo4a ZFA:0000079 telencephalon PATO:0000573 increased length abnormal ZDB-GENE-010702-1 114412 8543 lmo4a ZFA:0000101 diencephalon PATO:0000573 increased length abnormal ZDB-GENE-010702-1 114412 8543 lmo4a ZFA:0000101 diencephalon PATO:0000586 increased size abnormal ZDB-GENE-010702-1 114412 8543 lmo4a ZFA:0000107 eye PATO:0000586 increased size abnormal ZDB-GENE-010702-1 114412 8543 lmo4a ZFA:0000132 neural plate PATO:0000586 increased size abnormal ZDB-GENE-010702-1 114412 8543 lmo4a ZFA:0000137 optic stalk PATO:0000586 increased size abnormal ZDB-GENE-010702-1 114412 8543 lmo4a ZFA:0000152 retina PATO:0000586 increased size abnormal ZDB-GENE-010702-1 114412 8543 lmo4a ZFA:0001114 head PATO:0000051 morphology abnormal ZDB-GENE-010702-1 114412 8543 lmo4a ZFA:0001114 head PATO:0000586 increased size abnormal ZDB-GENE-010702-1 114412 8543 lmo4a ZFA:0001161 pectoral fin PATO:0000051 morphology abnormal ZDB-GENE-010702-1 114412 8543 lmo4a ZFA:0009256 nucleate erythrocyte PATO:0001997 decreased amount abnormal ZDB-GENE-010716-1 114430 79192 irx1b GO:0021794 thalamus development PATO:0001507 disrupted abnormal ZDB-GENE-010716-1 114430 79192 irx1b ZFA:0001344 zona limitans intrathalamica PATO:0000051 morphology abnormal ZDB-GENE-010717-1 114429 80139 znf703 GO:0007368 determination of left/right symmetry PATO:0001507 disrupted abnormal ZDB-GENE-010717-1 114429 80139 znf703 GO:0048596 embryonic camera-type eye morphogenesis PATO:0001507 disrupted abnormal ZDB-GENE-010717-1 114429 80139 znf703 GO:0061371 determination of heart left/right asymmetry PATO:0001507 disrupted abnormal ZDB-GENE-010717-1 114429 80139 znf703 GO:1904888 cranial skeletal system development PATO:0001507 disrupted abnormal ZDB-GENE-010717-1 114429 80139 znf703 GO:0031514 motile cilium BFO:0000050 part_of ZFA:0000001 Kupffer's vesicle PATO:0000462 absent abnormal ZDB-GENE-010717-1 114429 80139 znf703 GO:0031514 motile cilium BFO:0000050 part_of ZFA:0000001 Kupffer's vesicle PATO:0001997 decreased amount abnormal ZDB-GENE-010717-1 114429 80139 znf703 ZFA:0000001 Kupffer's vesicle PATO:0002000 lacks all parts of type abnormal GO:0031514 motile cilium BFO:0000050 part_of ZFA:0000001 Kupffer's vesicle ZDB-GENE-010717-1 114429 80139 znf703 ZFA:0000001 Kupffer's vesicle PATO:0000587 decreased size abnormal ZDB-GENE-010717-1 114429 80139 znf703 ZFA:0000008 brain PATO:0001853 hydrocephalic abnormal ZDB-GENE-010717-1 114429 80139 znf703 GO:0031514 motile cilium BFO:0000050 part_of ZFA:0000022 floor plate PATO:0001997 decreased amount abnormal ZDB-GENE-010717-1 114429 80139 znf703 ZFA:0000054 pericardium PATO:0001450 edematous abnormal ZDB-GENE-010717-1 114429 80139 znf703 ZFA:0000107 eye PATO:0000646 malformed abnormal ZDB-GENE-010717-1 114429 80139 znf703 ZFA:0000144 retinal pigmented epithelium PATO:0001786 split abnormal ZDB-GENE-010717-1 114429 80139 znf703 GO:0031514 motile cilium BFO:0000050 part_of ZFA:0000151 pronephros PATO:0001997 decreased amount abnormal ZDB-GENE-010717-1 114429 80139 znf703 ZFA:0000151 pronephros PATO:0001673 cystic abnormal ZDB-GENE-010717-1 114429 80139 znf703 ZFA:0000152 retina PATO:0000646 malformed abnormal ZDB-GENE-010717-1 114429 80139 znf703 ZFA:0000360 heart tube PATO:0000628 mislocalised abnormal ZDB-GENE-010717-1 114429 80139 znf703 BSPO:0000013 anterior-posterior axis BFO:0000050 part_of ZFA:0001094 whole organism PATO:0000574 decreased length abnormal ZDB-GENE-010717-1 114429 80139 znf703 ZFA:0001117 post-vent region PATO:0001592 increased curvature abnormal ZDB-GENE-010717-1 114429 80139 znf703 ZFA:0001284 optic fissure PATO:0000609 closure incomplete abnormal ZDB-GENE-010717-1 114429 80139 znf703 ZFA:0001617 otolith PATO:0000470 increased amount abnormal ZDB-GENE-010717-1 114429 80139 znf703 ZFA:0007057 ocular blood vessel PATO:0000646 malformed abnormal ZDB-GENE-010718-1 114457 482 atp1b2b GO:0001964 startle response PATO:0001507 disrupted abnormal ZDB-GENE-010718-1 114457 482 atp1b2b GO:0042472 inner ear morphogenesis PATO:0001507 disrupted abnormal ZDB-GENE-010718-1 114457 482 atp1b2b GO:0060047 heart contraction PATO:0000911 decreased rate abnormal ZDB-GENE-010718-1 114457 482 atp1b2b ZFA:0000009 cardiac ventricle PATO:0000587 decreased size abnormal ZDB-GENE-010718-1 114457 482 atp1b2b ZFA:0000051 otic vesicle PATO:0000052 shape abnormal ZDB-GENE-010718-1 114457 482 atp1b2b ZFA:0000051 otic vesicle PATO:0000587 decreased size abnormal ZDB-GENE-010718-1 114457 482 atp1b2b ZFA:0000054 pericardium PATO:0001450 edematous abnormal ZDB-GENE-010718-1 114457 482 atp1b2b ZFA:0000431 semicircular canal PATO:0000646 malformed abnormal ZDB-GENE-010718-1 114457 482 atp1b2b ZFA:0009367 neuromast hair cell BFO:0000050 part_of ZFA:0000940 posterior lateral line neuromast PATO:0001997 decreased amount abnormal ZDB-GENE-010718-1 114457 482 atp1b2b ZFA:0001617 otolith PATO:0001598 protruding abnormal ZDB-GENE-010718-1 114457 482 atp1b2b ZFA:0001617 otolith PATO:0001997 decreased amount abnormal ZDB-GENE-010718-1 114457 482 atp1b2b ZFA:0007054 pillar of the anterior semicircular canal PATO:0000646 malformed abnormal ZDB-GENE-010718-1 114457 482 atp1b2b ZFA:0007055 pillar of the lateral semicircular canal PATO:0000646 malformed abnormal ZDB-GENE-010718-1 114457 482 atp1b2b ZFA:0007056 pillar of the posterior semicircular canal PATO:0000646 malformed abnormal ZDB-GENE-010724-1 114452 8548 blzf1 GO:0030017 sarcomere BFO:0000050 part_of ZFA:0000155 somite PATO:0000462 absent abnormal ZDB-GENE-010724-1 114452 8548 blzf1 ZFA:0000155 somite PATO:0000937 disorganized abnormal ZDB-GENE-010724-1 114452 8548 blzf1 ZFA:0000610 vertical myoseptum PATO:0000051 morphology abnormal ZDB-GENE-010724-1 114452 8548 blzf1 ZFA:0000610 vertical myoseptum PATO:0000937 disorganized abnormal ZDB-GENE-010724-1 114452 8548 blzf1 BSPO:0000013 anterior-posterior axis BFO:0000050 part_of ZFA:0001094 whole organism PATO:0000574 decreased length abnormal ZDB-GENE-010724-1 114452 8548 blzf1 ZFA:0009114 muscle cell PATO:0000937 disorganized abnormal ZDB-GENE-010724-1 114452 8548 blzf1 ZFA:0009116 slow muscle cell PATO:0000937 disorganized abnormal ZDB-GENE-010724-1 114452 8548 blzf1 ZFA:0009117 fast muscle cell PATO:0000937 disorganized abnormal ZDB-GENE-010724-15 114420 6203 rps9 ZFA:0000029 hindbrain PATO:0000051 morphology abnormal ZDB-GENE-010724-15 114420 6203 rps9 ZFA:0000029 hindbrain PATO:0000586 increased size abnormal ZDB-GENE-010724-15 114420 6203 rps9 ZFA:0000054 pericardium PATO:0001450 edematous abnormal ZDB-GENE-010724-15 114420 6203 rps9 ZFA:0000107 eye PATO:0000587 decreased size abnormal ZDB-GENE-010724-15 114420 6203 rps9 ZFA:0009256 nucleate erythrocyte BFO:0000050 part_of ZFA:0000114 heart PATO:0001997 decreased amount abnormal ZDB-GENE-010724-15 114420 6203 rps9 ZFA:0009091 melanocyte BFO:0000050 part_of ZFA:0000368 integument PATO:0001997 decreased amount abnormal ZDB-GENE-010724-15 114420 6203 rps9 CHEBI:35143 hemoglobin BFO:0000050 part_of ZFA:0001094 whole organism PATO:0001997 decreased amount abnormal ZDB-GENE-010724-15 114420 6203 rps9 CHEBI:35143 hemoglobin BFO:0000050 part_of ZFA:0001115 trunk PATO:0001997 decreased amount abnormal ZDB-GENE-010724-15 114420 6203 rps9 ZFA:0009256 nucleate erythrocyte BFO:0000050 part_of ZFA:0001115 trunk PATO:0000462 absent abnormal ZDB-GENE-010724-15 114420 6203 rps9 ZFA:0001115 trunk PATO:0002364 shortened abnormal ZDB-GENE-010724-15 114420 6203 rps9 ZFA:0001460 pharyngeal arch cartilage PATO:0000462 absent abnormal ZDB-GENE-010724-15 114420 6203 rps9 GO:0021700 developmental maturation BFO:0000066 occurs_in ZFA:0009256 nucleate erythrocyte PATO:0001542 delayed phase abnormal ZDB-GENE-010724-15 114420 6203 rps9 ZFA:0009256 nucleate erythrocyte PATO:0001997 decreased amount abnormal ZDB-GENE-010724-18 553587 348 apoea ZFA:0001094 whole organism PATO:0000051 morphology abnormal ZDB-GENE-010724-5 114428 375 arf1 GO:0060872 semicircular canal development PATO:0001507 disrupted abnormal ZDB-GENE-010724-5 114428 375 arf1 ZFA:0000107 eye PATO:0000587 decreased size abnormal ZDB-GENE-010724-5 114428 375 arf1 ZFA:0000431 semicircular canal PATO:0000646 malformed abnormal ZDB-GENE-010724-5 114428 375 arf1 ZFA:0001094 whole organism PATO:0000574 decreased length abnormal ZDB-GENE-010724-5 114428 375 arf1 ZFA:0001117 post-vent region PATO:0001592 increased curvature abnormal ZDB-GENE-010724-6 393938 2271 fh ZFA:0001094 whole organism PATO:0000051 morphology abnormal ZDB-GENE-010724-6 393938 2271 fh ZFA:0001094 whole organism PATO:0001422 dead abnormal ZDB-GENE-010724-7 114454 9276 copb2 GO:0030903 notochord development PATO:0000001 quality abnormal ZDB-GENE-010724-7 114454 9276 copb2 GO:0048066 developmental pigmentation PATO:0001507 disrupted abnormal ZDB-GENE-010724-7 114454 9276 copb2 ZFA:0000042 midbrain hindbrain boundary PATO:0000574 decreased length abnormal ZDB-GENE-010724-7 114454 9276 copb2 GO:0005604 basement membrane BFO:0000050 part_of ZFA:0000135 notochord PATO:0000462 absent abnormal ZDB-GENE-010724-7 114454 9276 copb2 GO:0005604 basement membrane BFO:0000050 part_of ZFA:0000135 notochord PATO:0000592 decreased thickness abnormal ZDB-GENE-010724-7 114454 9276 copb2 GO:0005604 basement membrane BFO:0000050 part_of ZFA:0000135 notochord PATO:0000937 disorganized abnormal ZDB-GENE-010724-7 114454 9276 copb2 GO:0005783 endoplasmic reticulum BFO:0000050 part_of ZFA:0000135 notochord PATO:0001851 swollen abnormal ZDB-GENE-010724-7 114454 9276 copb2 GO:0005794 Golgi apparatus BFO:0000050 part_of ZFA:0000135 notochord PATO:0000141 structure abnormal ZDB-GENE-010724-7 114454 9276 copb2 ZFA:0009000 cell BFO:0000050 part_of ZFA:0000135 notochord PATO:0000141 structure abnormal ZDB-GENE-010724-7 114454 9276 copb2 ZFA:0000135 notochord PATO:0000001 quality abnormal ZDB-GENE-010724-7 114454 9276 copb2 ZFA:0000135 notochord PATO:0000141 structure abnormal ZDB-GENE-010724-7 114454 9276 copb2 ZFA:0000135 notochord PATO:0000574 decreased length abnormal ZDB-GENE-010724-7 114454 9276 copb2 ZFA:0000135 notochord PATO:0000638 apoptotic abnormal ZDB-GENE-010724-7 114454 9276 copb2 ZFA:0000135 notochord PATO:0001798 kinked abnormal ZDB-GENE-010724-7 114454 9276 copb2 ZFA:0000135 notochord PATO:0001848 asymmetrically curved abnormal ZDB-GENE-010724-7 114454 9276 copb2 ZFA:0000135 notochord PATO:0002100 undifferentiated abnormal ZDB-GENE-010724-7 114454 9276 copb2 ZFA:0000135 notochord PATO:0002106 poorly differentiated abnormal ZDB-GENE-010724-7 114454 9276 copb2 ZFA:0000155 somite PATO:0000051 morphology abnormal ZDB-GENE-010724-7 114454 9276 copb2 ZFA:0000155 somite PATO:0000117 size abnormal ZDB-GENE-010724-7 114454 9276 copb2 ZFA:0000155 somite PATO:0001485 condensed abnormal ZDB-GENE-010724-7 114454 9276 copb2 ZFA:0000368 integument PATO:0002251 decreased pigmentation abnormal ZDB-GENE-010724-7 114454 9276 copb2 ZFA:0001094 whole organism PATO:0000052 shape abnormal ZDB-GENE-010724-7 114454 9276 copb2 ZFA:0001094 whole organism PATO:0000169 viability abnormal ZDB-GENE-010724-7 114454 9276 copb2 ZFA:0001094 whole organism PATO:0000574 decreased length abnormal ZDB-GENE-010724-7 114454 9276 copb2 ZFA:0001094 whole organism PATO:0000639 degenerate abnormal ZDB-GENE-010724-7 114454 9276 copb2 ZFA:0001094 whole organism PATO:0000718 lethal (sensu genetics) abnormal ZDB-GENE-010724-7 114454 9276 copb2 ZFA:0001094 whole organism PATO:0001422 dead abnormal ZDB-GENE-010724-7 114454 9276 copb2 GO:0042470 melanosome BFO:0000050 part_of ZFA:0001115 trunk PATO:0000462 absent abnormal ZDB-GENE-010724-7 114454 9276 copb2 ZFA:0001261 ventricular system PATO:0000595 increased volume abnormal ZDB-GENE-010724-7 114454 9276 copb2 ZFA:0005746 notochord inner cell PATO:0000937 disorganized abnormal ZDB-GENE-010724-7 114454 9276 copb2 GO:0042470 melanosome BFO:0000050 part_of ZFA:0009091 melanocyte PATO:0000462 absent abnormal ZDB-GENE-010724-7 114454 9276 copb2 GO:0005783 endoplasmic reticulum BFO:0000050 part_of ZFA:0009114 muscle cell PATO:0001851 swollen abnormal ZDB-GENE-010724-7 114454 9276 copb2 GO:0005794 Golgi apparatus BFO:0000050 part_of ZFA:0009114 muscle cell PATO:0000141 structure abnormal ZDB-GENE-010727-1 114444 2120 etv6 ZFA:0001094 whole organism PATO:0002002 has extra parts of type abnormal ZFA:0005237 erythroblast ZDB-GENE-010727-1 114444 2120 etv6 ZFA:0001094 whole organism PATO:0002002 has extra parts of type abnormal ZFA:0009141 macrophage ZDB-GENE-010727-1 114444 2120 etv6 ZFA:0001094 whole organism PATO:0002002 has extra parts of type abnormal ZFA:0009265 monocyte ZDB-GENE-010727-1 114444 2120 etv6 ZFA:0001094 whole organism PATO:0002002 has extra parts of type abnormal ZFA:0009327 neutrophil ZDB-GENE-010730-1 114401 598 bcl2l1 GO:0006915 apoptotic process PATO:0002051 increased occurrence abnormal ZDB-GENE-010730-1 114401 598 bcl2l1 GO:0030878 thyroid gland development PATO:0001507 disrupted abnormal ZDB-GENE-010730-1 114401 598 bcl2l1 ZFA:0000012 central nervous system PATO:0000645 hypoplastic abnormal ZDB-GENE-010730-1 114401 598 bcl2l1 ZFA:0001072 thyroid follicle PATO:0000645 hypoplastic abnormal ZDB-GENE-010730-1 114401 598 bcl2l1 ZFA:0001094 whole organism PATO:0002000 lacks all parts of type abnormal ZFA:0000106 extension ZDB-GENE-010803-2 114437 81848 spry4 GO:0001974 blood vessel remodeling PATO:0001507 disrupted abnormal ZDB-GENE-010803-2 114437 81848 spry4 GO:0008015 blood circulation PATO:0001507 disrupted abnormal ZDB-GENE-010803-2 114437 81848 spry4 GO:0021594 rhombomere formation PATO:0002302 decreased process quality abnormal ZDB-GENE-010803-2 114437 81848 spry4 GO:0035162 embryonic hemopoiesis PATO:0001507 disrupted abnormal ZDB-GENE-010803-2 114437 81848 spry4 ZFA:0000132 neural plate PATO:0000574 decreased length abnormal ZDB-GENE-010803-2 114437 81848 spry4 ZFA:0000132 neural plate PATO:0000600 increased width abnormal ZDB-GENE-010803-2 114437 81848 spry4 ZFA:0000186 common cardinal vein PATO:0000051 morphology abnormal ZDB-GENE-010803-2 114437 81848 spry4 ZFA:0000823 rhombomere 5 PATO:0001241 physical object quality abnormal ZDB-GENE-010803-2 114437 81848 spry4 ZFA:0000823 rhombomere 5 PATO:0002057 increased area abnormal ZDB-GENE-010803-2 114437 81848 spry4 ZFA:0000948 rhombomere 3 PATO:0000642 fused with abnormal ZFA:0000823 rhombomere 5 ZDB-GENE-010803-2 114437 81848 spry4 ZFA:0000948 rhombomere 3 PATO:0002057 increased area abnormal ZDB-GENE-010803-2 114437 81848 spry4 ZFA:0001032 rhombomere 4 PATO:0002058 decreased area abnormal ZDB-GENE-010803-2 114437 81848 spry4 ZFA:0001086 muscle pioneer PATO:0001997 decreased amount abnormal ZDB-GENE-010803-2 114437 81848 spry4 ZFA:0001094 whole organism PATO:0000620 wholly dorsalized abnormal ZDB-GENE-010803-2 114437 81848 spry4 ZFA:0001114 head PATO:0000638 apoptotic abnormal ZDB-GENE-010803-2 114437 81848 spry4 ZFA:0009044 blood cell PATO:0001997 decreased amount abnormal ZDB-GENE-010814-1 114423 2155 f7 GO:0072378 blood coagulation, fibrin clot formation PATO:0000502 delayed abnormal ZDB-GENE-010816-1 114426 4953 odc1 ZFA:0000107 eye PATO:0000587 decreased size abnormal ZDB-GENE-010816-1 114426 4953 odc1 ZFA:0000112 gut PATO:0000645 hypoplastic abnormal ZDB-GENE-010816-1 114426 4953 odc1 ZFA:0000123 liver PATO:0000645 hypoplastic abnormal ZDB-GENE-010816-1 114426 4953 odc1 ZFA:0000143 retinal photoreceptor layer PATO:0000001 quality abnormal ZDB-GENE-010816-1 114426 4953 odc1 ZFA:0001114 head PATO:0000587 decreased size abnormal ZDB-GENE-010817-1 114407 284 angpt1 GO:0003007 heart morphogenesis PATO:0001236 process quality abnormal ZDB-GENE-010817-1 114407 284 angpt1 GO:0008015 blood circulation PATO:0000297 arrested abnormal ZDB-GENE-010817-1 114407 284 angpt1 GO:0048514 blood vessel morphogenesis PATO:0001507 disrupted abnormal ZDB-GENE-010817-1 114407 284 angpt1 ZFA:0000008 brain PATO:0000587 decreased size abnormal ZDB-GENE-010817-1 114407 284 angpt1 ZFA:0000114 heart PATO:0001450 edematous abnormal ZDB-GENE-010817-1 114407 284 angpt1 ZFA:0000186 common cardinal vein PATO:0000051 morphology abnormal ZDB-GENE-010817-1 114407 284 angpt1 ZFA:0005035 subintestinal vein PATO:0000051 morphology abnormal ZDB-GENE-010817-2 114408 285 angpt2b GO:0002040 sprouting angiogenesis PATO:0001507 disrupted abnormal ZDB-GENE-010817-2 114408 285 angpt2b GO:0003007 heart morphogenesis PATO:0001236 process quality abnormal ZDB-GENE-010817-2 114408 285 angpt2b GO:0008015 blood circulation PATO:0000297 arrested abnormal ZDB-GENE-010817-2 114408 285 angpt2b GO:0048514 blood vessel morphogenesis PATO:0001507 disrupted abnormal ZDB-GENE-010817-2 114408 285 angpt2b ZFA:0000114 heart PATO:0001450 edematous abnormal ZDB-GENE-010817-2 114408 285 angpt2b ZFA:0000180 caudal vein PATO:0000051 morphology abnormal ZDB-GENE-010817-2 114408 285 angpt2b ZFA:0001285 intersegmental vessel PATO:0000936 truncated abnormal ZDB-GENE-010817-2 114408 285 angpt2b ZFA:0001285 intersegmental vessel PATO:0001483 aplastic abnormal ZDB-GENE-010817-2 114408 285 angpt2b ZFA:0001285 intersegmental vessel PATO:0001997 decreased amount abnormal ZDB-GENE-010817-2 114408 285 angpt2b ZFA:0005034 parachordal vessel PATO:0001483 aplastic abnormal ZDB-GENE-010817-2 114408 285 angpt2b ZFA:0005035 subintestinal vein PATO:0000051 morphology abnormal ZDB-GENE-010817-2 114408 285 angpt2b ZFA:0005035 subintestinal vein PATO:0000574 decreased length abnormal ZDB-GENE-010817-3 114421 27329 angptl3 GO:0006869 lipid transport PATO:0001507 disrupted abnormal ZDB-GENE-010817-3 114421 27329 angptl3 GO:0005811 lipid droplet BFO:0000050 part_of ZFA:0000123 liver PATO:0001997 decreased amount abnormal ZDB-GENE-010817-3 114421 27329 angptl3 GO:0008283 cell population proliferation BFO:0000066 occurs_in ZFA:0000123 liver PATO:0002052 decreased occurrence abnormal ZDB-GENE-010817-3 114421 27329 angptl3 ZFA:0000123 liver PATO:0000587 decreased size abnormal ZDB-GENE-010817-3 114421 27329 angptl3 GO:0005811 lipid droplet BFO:0000050 part_of ZFA:0000208 gall bladder PATO:0001997 decreased amount abnormal ZDB-GENE-010817-3 114421 27329 angptl3 GO:0005811 lipid droplet BFO:0000050 part_of ZFA:0001338 intestine PATO:0001997 decreased amount abnormal ZDB-GENE-010822-2 114442 4684 ncam1b GO:0007411 axon guidance PATO:0001507 disrupted abnormal ZDB-GENE-010822-2 114442 4684 ncam1b GO:0048675 axon extension PATO:0001236 process quality abnormal ZDB-GENE-010822-2 114442 4684 ncam1b GO:0048675 axon extension PATO:0001507 disrupted abnormal ZDB-GENE-010822-2 114442 4684 ncam1b GO:0030424 axon BFO:0000050 part_of ZFA:0000320 caudal commissure PATO:0000574 decreased length abnormal ZDB-GENE-010822-2 114442 4684 ncam1b GO:0030424 axon BFO:0000050 part_of ZFA:0009052 motor neuron PATO:0002285 increased branchiness abnormal ZDB-GENE-010906-1 114549 43 ache GO:0001964 startle response PATO:0001507 disrupted abnormal ZDB-GENE-010906-1 114549 43 ache GO:0001966 thigmotaxis PATO:0000911 decreased rate abnormal ZDB-GENE-010906-1 114549 43 ache GO:0001966 thigmotaxis PATO:0001507 disrupted abnormal ZDB-GENE-010906-1 114549 43 ache GO:0003009 skeletal muscle contraction PATO:0001507 disrupted abnormal ZDB-GENE-010906-1 114549 43 ache GO:0003990 acetylcholinesterase activity PATO:0000297 arrested abnormal ZDB-GENE-010906-1 114549 43 ache GO:0003990 acetylcholinesterase activity PATO:0001507 disrupted abnormal ZDB-GENE-010906-1 114549 43 ache GO:0006915 apoptotic process PATO:0002051 increased occurrence abnormal ZDB-GENE-010906-1 114549 43 ache GO:0007271 synaptic transmission, cholinergic PATO:0000498 increased duration abnormal ZDB-GENE-010906-1 114549 43 ache GO:0007411 axon guidance PATO:0001507 disrupted abnormal ZDB-GENE-010906-1 114549 43 ache GO:0007528 neuromuscular junction development PATO:0001236 process quality abnormal ZDB-GENE-010906-1 114549 43 ache GO:0007528 neuromuscular junction development PATO:0001507 disrupted abnormal ZDB-GENE-010906-1 114549 43 ache GO:0007610 behavior PATO:0000001 quality abnormal ZDB-GENE-010906-1 114549 43 ache GO:0007626 locomotory behavior PATO:0000297 arrested abnormal ZDB-GENE-010906-1 114549 43 ache GO:0007626 locomotory behavior PATO:0001507 disrupted abnormal ZDB-GENE-010906-1 114549 43 ache GO:0008306 associative learning PATO:0000912 increased rate abnormal ZDB-GENE-010906-1 114549 43 ache GO:0008306 associative learning PATO:0002051 increased occurrence abnormal ZDB-GENE-010906-1 114549 43 ache GO:0009605 response to external stimulus PATO:0000001 quality abnormal ZDB-GENE-010906-1 114549 43 ache GO:0040011 locomotion PATO:0001530 behavioral quality of a process abnormal ZDB-GENE-010906-1 114549 43 ache GO:0050881 musculoskeletal movement PATO:0001507 disrupted abnormal ZDB-GENE-010906-1 114549 43 ache ZFA:0009150 Rohon-Beard neuron BFO:0000050 part_of ZFA:0000075 spinal cord PATO:0000638 apoptotic abnormal ZDB-GENE-010906-1 114549 43 ache ZFA:0000084 yolk PATO:0000586 increased size abnormal ZDB-GENE-010906-1 114549 43 ache ZFA:0000135 notochord PATO:0000001 quality abnormal ZDB-GENE-010906-1 114549 43 ache ZFA:0000135 notochord PATO:0001167 damaged abnormal ZDB-GENE-010906-1 114549 43 ache GO:0005635 nuclear envelope BFO:0000050 part_of ZFA:0000473 trunk musculature PATO:0000052 shape abnormal ZDB-GENE-010906-1 114549 43 ache GO:0005635 nuclear envelope BFO:0000050 part_of ZFA:0000473 trunk musculature PATO:0000941 vacuolated abnormal ZDB-GENE-010906-1 114549 43 ache GO:0005892 acetylcholine-gated channel complex BFO:0000050 part_of ZFA:0000473 trunk musculature PATO:0000140 position abnormal ZDB-GENE-010906-1 114549 43 ache GO:0016528 sarcoplasm BFO:0000050 part_of ZFA:0000473 trunk musculature PATO:0000941 vacuolated abnormal ZDB-GENE-010906-1 114549 43 ache GO:0030016 myofibril BFO:0000050 part_of ZFA:0000473 trunk musculature PATO:0000574 decreased length abnormal ZDB-GENE-010906-1 114549 43 ache GO:0030016 myofibril BFO:0000050 part_of ZFA:0000473 trunk musculature PATO:0000937 disorganized abnormal ZDB-GENE-010906-1 114549 43 ache ZFA:0000473 trunk musculature PATO:0000001 quality abnormal ZDB-GENE-010906-1 114549 43 ache ZFA:0000473 trunk musculature PATO:0001579 contractility abnormal ZDB-GENE-010906-1 114549 43 ache ZFA:0001094 whole organism PATO:0000169 viability abnormal ZDB-GENE-010906-1 114549 43 ache ZFA:0001094 whole organism PATO:0000300 immobile abnormal ZDB-GENE-010906-1 114549 43 ache ZFA:0001094 whole organism PATO:0000718 lethal (sensu genetics) abnormal ZDB-GENE-010906-1 114549 43 ache ZFA:0001094 whole organism PATO:0000763 paralysed abnormal ZDB-GENE-010906-1 114549 43 ache ZFA:0001094 whole organism PATO:0002076 movement behavioral quality abnormal ZDB-GENE-010906-1 114549 43 ache ZFA:0009150 Rohon-Beard neuron BFO:0000050 part_of ZFA:0001135 neural tube PATO:0000638 apoptotic abnormal ZDB-GENE-010906-1 114549 43 ache GO:0030424 axon BFO:0000050 part_of ZFA:0009052 motor neuron PATO:0000587 decreased size abnormal ZDB-GENE-010906-1 114549 43 ache GO:0030424 axon BFO:0000050 part_of ZFA:0009052 motor neuron PATO:0000592 decreased thickness abnormal ZDB-GENE-010906-1 114549 43 ache GO:0005892 acetylcholine-gated channel complex BFO:0000050 part_of ZFA:0009114 muscle cell PATO:0000587 decreased size abnormal ZDB-GENE-010906-1 114549 43 ache GO:0005892 acetylcholine-gated channel complex BFO:0000050 part_of ZFA:0009114 muscle cell PATO:0001997 decreased amount abnormal ZDB-GENE-010906-1 114549 43 ache GO:0032982 myosin filament BFO:0000050 part_of ZFA:0009116 slow muscle cell PATO:0001997 decreased amount abnormal ZDB-GENE-010906-1 114549 43 ache GO:0030425 dendrite BFO:0000050 part_of ZFA:0009150 Rohon-Beard neuron PATO:0000574 decreased length abnormal ZDB-GENE-010906-1 114549 43 ache GO:0030425 dendrite BFO:0000050 part_of ZFA:0009150 Rohon-Beard neuron PATO:0001997 decreased amount abnormal ZDB-GENE-010906-2 114550 1909 ednraa GO:0001966 thigmotaxis PATO:0001236 process quality abnormal ZDB-GENE-010906-2 114550 1909 ednraa GO:0002118 aggressive behavior PATO:0002051 increased occurrence abnormal ZDB-GENE-010906-2 114550 1909 ednraa GO:0007626 locomotory behavior PATO:0001236 process quality abnormal ZDB-GENE-010906-2 114550 1909 ednraa GO:0035176 social behavior PATO:0001236 process quality abnormal ZDB-GENE-010906-2 114550 1909 ednraa CHEBI:9937 vasopressin BFO:0000050 part_of ZFA:0000008 brain PATO:0001997 decreased amount abnormal ZDB-GENE-010906-2 114550 1909 ednraa CHEBI:28790 serotonin BFO:0000050 part_of ZFA:0000079 telencephalon PATO:0000470 increased amount abnormal ZDB-GENE-010906-2 114550 1909 ednraa CHEBI:28790 serotonin BFO:0000050 part_of ZFA:0000100 cerebellum PATO:0000470 increased amount abnormal ZDB-GENE-010906-2 114550 1909 ednraa CHEBI:18243 dopamine BFO:0000050 part_of ZFA:0000101 diencephalon PATO:0000470 increased amount abnormal ZDB-GENE-010906-2 114550 1909 ednraa CHEBI:27823 (5-hydroxyindol-3-yl)acetic acid BFO:0000050 part_of ZFA:0000101 diencephalon PATO:0000470 increased amount abnormal ZDB-GENE-010906-2 114550 1909 ednraa CHEBI:28790 serotonin BFO:0000050 part_of ZFA:0000101 diencephalon PATO:0000470 increased amount abnormal ZDB-GENE-010906-2 114550 1909 ednraa GO:0030424 axon BFO:0000050 part_of ZFA:0000248 magnocellular preoptic nucleus PATO:0000591 increased thickness abnormal ZDB-GENE-010906-2 114550 1909 ednraa GO:0044297 cell body BFO:0000050 part_of ZFA:0000248 magnocellular preoptic nucleus PATO:0000586 increased size abnormal ZDB-GENE-010906-2 114550 1909 ednraa CHEBI:18243 dopamine BFO:0000050 part_of ZFA:0000445 optic tectum PATO:0000470 increased amount abnormal ZDB-GENE-010906-2 114550 1909 ednraa CHEBI:28790 serotonin BFO:0000050 part_of ZFA:0000545 medulla oblongata PATO:0000470 increased amount abnormal ZDB-GENE-010906-2 114550 1909 ednraa CHEBI:9937 vasopressin BFO:0000050 part_of ZFA:0001094 whole organism PATO:0001997 decreased amount abnormal ZDB-GENE-010906-2 114550 1909 ednraa BSPO:0000084 ventral region BFO:0000050 part_of ZFA:0001115 trunk PATO:0002002 has extra parts of type abnormal ZFA:0009090 pigment cell ZDB-GENE-010906-2 114550 1909 ednraa BSPO:0000084 ventral region BFO:0000050 part_of ZFA:0001115 trunk PATO:0002002 has extra parts of type abnormal ZFA:0009091 melanocyte ZDB-GENE-010906-2 114550 1909 ednraa BSPO:0000084 ventral region BFO:0000050 part_of ZFA:0001115 trunk PATO:0002002 has extra parts of type abnormal ZFA:0009199 iridophore ZDB-GENE-010906-2 114550 1909 ednraa BSPO:0000085 ventro-lateral region BFO:0000050 part_of ZFA:0001115 trunk PATO:0002270 increased accumulation abnormal ZFA:0009091 melanocyte ZDB-GENE-010906-2 114550 1909 ednraa BSPO:0000085 ventro-lateral region BFO:0000050 part_of ZFA:0001115 trunk PATO:0002270 increased accumulation abnormal ZFA:0009199 iridophore ZDB-GENE-010906-2 114550 1909 ednraa BSPO:0000085 ventro-lateral region BFO:0000050 part_of ZFA:0001117 post-vent region PATO:0002270 increased accumulation abnormal ZFA:0009091 melanocyte ZDB-GENE-010906-2 114550 1909 ednraa BSPO:0000085 ventro-lateral region BFO:0000050 part_of ZFA:0001117 post-vent region PATO:0002270 increased accumulation abnormal ZFA:0009199 iridophore ZDB-GENE-010906-2 114550 1909 ednraa GO:0006885 regulation of pH BFO:0000066 occurs_in ZFA:0005327 vH ionocyte PATO:0001236 process quality abnormal ZDB-GENE-010906-2 114550 1909 ednraa GO:1902600 proton transmembrane transport BFO:0000066 occurs_in ZFA:0005327 vH ionocyte PATO:0000161 rate abnormal ZDB-GENE-010906-2 114550 1909 ednraa GO:1902600 proton transmembrane transport BFO:0000066 occurs_in ZFA:0005327 vH ionocyte PATO:0000911 decreased rate abnormal ZDB-GENE-010906-2 114550 1909 ednraa ZFA:0009090 pigment cell PATO:0000001 quality abnormal ZDB-GENE-010906-2 114550 1909 ednraa ZFA:0009090 pigment cell PATO:0000628 mislocalised abnormal ZDB-GENE-010906-2 114550 1909 ednraa ZFA:0009091 melanocyte PATO:0000628 mislocalised abnormal ZDB-GENE-010906-2 114550 1909 ednraa GO:0008283 cell population proliferation BFO:0000066 occurs_in ZFA:0009165 neural crest cell PATO:0002051 increased occurrence abnormal ZDB-GENE-010906-2 114550 1909 ednraa ZFA:0009199 iridophore PATO:0000060 spatial pattern abnormal ZDB-GENE-010906-2 114550 1909 ednraa ZFA:0009199 iridophore PATO:0000330 irregular spatial pattern abnormal ZDB-GENE-010906-2 114550 1909 ednraa ZFA:0009199 iridophore PATO:0000628 mislocalised abnormal ZDB-GENE-011003-1 116517 128 adh5 ZFA:0000123 liver PATO:0000586 increased size abnormal ZDB-GENE-011010-3 116713 8854 aldh1a2 GO:0021575 hindbrain morphogenesis PATO:0001236 process quality abnormal ZDB-GENE-011010-3 116713 8854 aldh1a2 GO:0033339 pectoral fin development PATO:0001507 disrupted abnormal ZDB-GENE-011010-3 116713 8854 aldh1a2 GO:0035118 embryonic pectoral fin morphogenesis PATO:0002302 decreased process quality abnormal ZDB-GENE-011010-3 116713 8854 aldh1a2 GO:0039022 pronephric duct development PATO:0000502 delayed abnormal ZDB-GENE-011010-3 116713 8854 aldh1a2 GO:0048318 axial mesoderm development PATO:0002302 decreased process quality abnormal ZDB-GENE-011010-3 116713 8854 aldh1a2 GO:0048339 paraxial mesoderm development PATO:0001236 process quality abnormal ZDB-GENE-011010-3 116713 8854 aldh1a2 GO:0048339 paraxial mesoderm development PATO:0002302 decreased process quality abnormal ZDB-GENE-011010-3 116713 8854 aldh1a2 GO:0048384 retinoic acid receptor signaling pathway PATO:0001236 process quality abnormal ZDB-GENE-011010-3 116713 8854 aldh1a2 GO:0048384 retinoic acid receptor signaling pathway PATO:0002302 decreased process quality abnormal ZDB-GENE-011010-3 116713 8854 aldh1a2 GO:0048565 digestive tract development PATO:0001507 disrupted abnormal ZDB-GENE-011010-3 116713 8854 aldh1a2 GO:0048918 posterior lateral line nerve development PATO:0001236 process quality abnormal ZDB-GENE-011010-3 116713 8854 aldh1a2 GO:0060385 axonogenesis involved in innervation PATO:0002302 decreased process quality abnormal ZDB-GENE-011010-3 116713 8854 aldh1a2 BSPO:0000072 posterior region BFO:0000050 part_of ZFA:0000029 hindbrain PATO:0001241 physical object quality abnormal ZDB-GENE-011010-3 116713 8854 aldh1a2 ZFA:0000029 hindbrain PATO:0002364 shortened abnormal ZDB-GENE-011010-3 116713 8854 aldh1a2 ZFA:0000035 lens PATO:0000051 morphology abnormal ZDB-GENE-011010-3 116713 8854 aldh1a2 ZFA:0000035 lens PATO:0000587 decreased size abnormal ZDB-GENE-011010-3 116713 8854 aldh1a2 ZFA:0000051 otic vesicle PATO:0000375 decreased distance abnormal ZFA:0000072 somite 1 ZDB-GENE-011010-3 116713 8854 aldh1a2 ZFA:0000054 pericardium PATO:0001450 edematous abnormal ZDB-GENE-011010-3 116713 8854 aldh1a2 ZFA:0000069 rhombomere 6 PATO:0000573 increased length abnormal ZDB-GENE-011010-3 116713 8854 aldh1a2 ZFA:0000072 somite 1 PATO:0000642 fused with abnormal ZFA:0000728 somite 2 ZDB-GENE-011010-3 116713 8854 aldh1a2 BSPO:0000071 anterior region BFO:0000050 part_of ZFA:0000075 spinal cord PATO:0002001 has fewer parts of type abnormal ZFA:0000778 spinal cord interneuron ZDB-GENE-011010-3 116713 8854 aldh1a2 BSPO:0000071 anterior region BFO:0000050 part_of ZFA:0000075 spinal cord PATO:0002001 has fewer parts of type abnormal ZFA:0009052 motor neuron ZDB-GENE-011010-3 116713 8854 aldh1a2 ZFA:0000076 swim bladder PATO:0000001 quality abnormal ZDB-GENE-011010-3 116713 8854 aldh1a2 ZFA:0000076 swim bladder PATO:0000462 absent abnormal ZDB-GENE-011010-3 116713 8854 aldh1a2 ZFA:0000084 yolk PATO:0001617 deformed abnormal ZDB-GENE-011010-3 116713 8854 aldh1a2 ZFA:0000095 pharyngeal arch 3-7 skeleton PATO:0000001 quality abnormal ZDB-GENE-011010-3 116713 8854 aldh1a2 GO:0006915 apoptotic process BFO:0000066 occurs_in ZFA:0000107 eye PATO:0002051 increased occurrence abnormal ZDB-GENE-011010-3 116713 8854 aldh1a2 ZFA:0009000 cell BFO:0000050 part_of ZFA:0000107 eye PATO:0000638 apoptotic abnormal ZDB-GENE-011010-3 116713 8854 aldh1a2 ZFA:0000107 eye PATO:0000051 morphology abnormal ZDB-GENE-011010-3 116713 8854 aldh1a2 ZFA:0000107 eye PATO:0000587 decreased size abnormal ZDB-GENE-011010-3 116713 8854 aldh1a2 ZFA:0000114 heart PATO:0000001 quality abnormal ZDB-GENE-011010-3 116713 8854 aldh1a2 ZFA:0000114 heart PATO:0001450 edematous abnormal ZDB-GENE-011010-3 116713 8854 aldh1a2 ZFA:0000121 lateral plate mesoderm PATO:0001241 physical object quality abnormal ZDB-GENE-011010-3 116713 8854 aldh1a2 ZFA:0000123 liver PATO:0000587 decreased size abnormal ZDB-GENE-011010-3 116713 8854 aldh1a2 BSPO:0000071 anterior region BFO:0000050 part_of ZFA:0000135 notochord PATO:0000638 apoptotic abnormal ZDB-GENE-011010-3 116713 8854 aldh1a2 ZFA:0000141 pectoral fin bud PATO:0000462 absent abnormal ZDB-GENE-011010-3 116713 8854 aldh1a2 ZFA:0000141 pectoral fin bud PATO:0001241 physical object quality abnormal ZDB-GENE-011010-3 116713 8854 aldh1a2 ZFA:0000141 pectoral fin bud PATO:0001483 aplastic abnormal ZDB-GENE-011010-3 116713 8854 aldh1a2 BSPO:0000077 proximal region BFO:0000050 part_of ZFA:0000150 pronephric duct PATO:0000574 decreased length abnormal ZDB-GENE-011010-3 116713 8854 aldh1a2 BSPO:0000078 distal region BFO:0000050 part_of ZFA:0000150 pronephric duct PATO:0000573 increased length abnormal ZDB-GENE-011010-3 116713 8854 aldh1a2 ZFA:0000155 somite PATO:0001997 decreased amount abnormal ZDB-GENE-011010-3 116713 8854 aldh1a2 ZFA:0000163 renal system PATO:0001999 lacks parts or has fewer parts of type abnormal ZFA:0009285 podocyte ZDB-GENE-011010-3 116713 8854 aldh1a2 GO:0030425 dendrite BFO:0000050 part_of ZFA:0000175 posterior lateral line nerve PATO:0000414 unbranched abnormal ZDB-GENE-011010-3 116713 8854 aldh1a2 ZFA:0009248 neuron BFO:0000050 part_of ZFA:0000215 inferior olive PATO:0001997 decreased amount abnormal ZDB-GENE-011010-3 116713 8854 aldh1a2 GO:0030016 myofibril BFO:0000050 part_of ZFA:0000301 medial rectus PATO:0000937 disorganized abnormal ZDB-GENE-011010-3 116713 8854 aldh1a2 ZFA:0000369 intermandibularis PATO:0000574 decreased length abnormal ZDB-GENE-011010-3 116713 8854 aldh1a2 BSPO:0000070 anatomical region BFO:0000050 part_of ZFA:0000387 motor nucleus of vagal nerve PATO:0000587 decreased size abnormal ZDB-GENE-011010-3 116713 8854 aldh1a2 ZFA:0000396 nervous system PATO:0000615 wholly anteriorized abnormal ZDB-GENE-011010-3 116713 8854 aldh1a2 ZFA:0000407 pectoral girdle PATO:0000462 absent abnormal ZDB-GENE-011010-3 116713 8854 aldh1a2 ZFA:0000640 cornea PATO:0000591 increased thickness abnormal ZDB-GENE-011010-3 116713 8854 aldh1a2 ZFA:0000823 rhombomere 5 PATO:0000375 decreased distance abnormal ZFA:0000072 somite 1 ZDB-GENE-011010-3 116713 8854 aldh1a2 ZFA:0000823 rhombomere 5 PATO:0000573 increased length abnormal ZDB-GENE-011010-3 116713 8854 aldh1a2 GO:0001756 somitogenesis BFO:0000066 occurs_in ZFA:0000857 somite 4 PATO:0000498 increased duration abnormal ZDB-GENE-011010-3 116713 8854 aldh1a2 ZFA:0000949 rhombomere 7 PATO:0000573 increased length abnormal ZDB-GENE-011010-3 116713 8854 aldh1a2 ZFA:0000949 rhombomere 7 PATO:0001241 physical object quality abnormal ZDB-GENE-011010-3 116713 8854 aldh1a2 ZFA:0001058 caudal fin PATO:0000406 curved abnormal ZDB-GENE-011010-3 116713 8854 aldh1a2 ZFA:0001076 intestinal bulb PATO:0000645 hypoplastic abnormal ZDB-GENE-011010-3 116713 8854 aldh1a2 ZFA:0001094 whole organism PATO:0002000 lacks all parts of type abnormal ZFA:0000257 pectoral fin cartilage ZDB-GENE-011010-3 116713 8854 aldh1a2 ZFA:0001094 whole organism PATO:0002000 lacks all parts of type abnormal ZFA:0001131 pharyngeal pouch 3 ZDB-GENE-011010-3 116713 8854 aldh1a2 ZFA:0001094 whole organism PATO:0002000 lacks all parts of type abnormal ZFA:0001134 pharyngeal pouch 4 ZDB-GENE-011010-3 116713 8854 aldh1a2 ZFA:0001094 whole organism PATO:0002000 lacks all parts of type abnormal ZFA:0001161 pectoral fin ZDB-GENE-011010-3 116713 8854 aldh1a2 ZFA:0001094 whole organism PATO:0002000 lacks all parts of type abnormal ZFA:0001517 ceratobranchial 2 cartilage ZDB-GENE-011010-3 116713 8854 aldh1a2 ZFA:0001094 whole organism PATO:0002000 lacks all parts of type abnormal ZFA:0001518 ceratobranchial 3 cartilage ZDB-GENE-011010-3 116713 8854 aldh1a2 ZFA:0001094 whole organism PATO:0002000 lacks all parts of type abnormal ZFA:0001519 ceratobranchial 4 cartilage ZDB-GENE-011010-3 116713 8854 aldh1a2 ZFA:0001094 whole organism PATO:0002000 lacks all parts of type abnormal ZFA:0001521 ceratobranchial 5 cartilage ZDB-GENE-011010-3 116713 8854 aldh1a2 ZFA:0001094 whole organism PATO:0000574 decreased length abnormal ZDB-GENE-011010-3 116713 8854 aldh1a2 ZFA:0001094 whole organism PATO:0000718 lethal (sensu genetics) abnormal ZDB-GENE-011010-3 116713 8854 aldh1a2 BSPO:0000013 anterior-posterior axis BFO:0000050 part_of ZFA:0001114 head PATO:0000574 decreased length abnormal ZDB-GENE-011010-3 116713 8854 aldh1a2 ZFA:0000135 notochord BFO:0000050 part_of ZFA:0001114 head PATO:0002001 has fewer parts of type abnormal ZFA:0009000 cell BFO:0000050 part_of ZFA:0000135 notochord ZDB-GENE-011010-3 116713 8854 aldh1a2 ZFA:0001114 head PATO:0001654 misaligned with abnormal ZFA:0001115 trunk ZDB-GENE-011010-3 116713 8854 aldh1a2 ZFA:0001114 head PATO:0000586 increased size abnormal ZDB-GENE-011010-3 116713 8854 aldh1a2 ZFA:0001117 post-vent region PATO:0001469 curved ventral abnormal ZDB-GENE-011010-3 116713 8854 aldh1a2 ZFA:0001161 pectoral fin PATO:0000001 quality abnormal ZDB-GENE-011010-3 116713 8854 aldh1a2 ZFA:0001161 pectoral fin PATO:0000462 absent abnormal ZDB-GENE-011010-3 116713 8854 aldh1a2 ZFA:0001161 pectoral fin PATO:0001483 aplastic abnormal ZDB-GENE-011010-3 116713 8854 aldh1a2 ZFA:0001168 vertebra 2 PATO:0000462 absent abnormal ZDB-GENE-011010-3 116713 8854 aldh1a2 ZFA:0001205 Meckel's cartilage PATO:0000462 absent abnormal ZDB-GENE-011010-3 116713 8854 aldh1a2 ZFA:0001205 Meckel's cartilage PATO:0000587 decreased size abnormal ZDB-GENE-011010-3 116713 8854 aldh1a2 ZFA:0001227 mandibular arch skeleton PATO:0000646 malformed abnormal ZDB-GENE-011010-3 116713 8854 aldh1a2 ZFA:0001306 pharyngeal arch PATO:0000462 absent abnormal ZDB-GENE-011010-3 116713 8854 aldh1a2 ZFA:0001330 retinal outer plexiform layer PATO:0000937 disorganized abnormal ZDB-GENE-011010-3 116713 8854 aldh1a2 ZFA:0001338 intestine PATO:0002000 lacks all parts of type abnormal ZFA:0005125 intestinal villus ZDB-GENE-011010-3 116713 8854 aldh1a2 ZFA:0001338 intestine PATO:0002000 lacks all parts of type abnormal ZFA:0009038 columnar/cuboidal epithelial cell ZDB-GENE-011010-3 116713 8854 aldh1a2 ZFA:0001338 intestine PATO:0000051 morphology abnormal ZDB-GENE-011010-3 116713 8854 aldh1a2 ZFA:0001399 palatoquadrate cartilage PATO:0000587 decreased size abnormal ZDB-GENE-011010-3 116713 8854 aldh1a2 ZFA:0001400 ceratohyal cartilage PATO:0000051 morphology abnormal ZDB-GENE-011010-3 116713 8854 aldh1a2 ZFA:0001422 hyosymplectic cartilage PATO:0000587 decreased size abnormal ZDB-GENE-011010-3 116713 8854 aldh1a2 ZFA:0001453 pectoral fin field PATO:0001241 physical object quality abnormal ZDB-GENE-011010-3 116713 8854 aldh1a2 ZFA:0001456 pectoral fin endoskeletal disc PATO:0000462 absent abnormal ZDB-GENE-011010-3 116713 8854 aldh1a2 ZFA:0001466 photoreceptor outer segment layer PATO:0000462 absent abnormal ZDB-GENE-011010-3 116713 8854 aldh1a2 BSPO:0000071 anterior region BFO:0000050 part_of ZFA:0001559 vertebral column PATO:0000574 decreased length abnormal ZDB-GENE-011010-3 116713 8854 aldh1a2 ZFA:0000045 neural crest BFO:0000050 part_of ZFA:0001613 pharyngeal arch 3-7 PATO:0000638 apoptotic abnormal ZDB-GENE-011010-3 116713 8854 aldh1a2 ZFA:0001613 pharyngeal arch 3-7 PATO:0000462 absent abnormal ZDB-GENE-011010-3 116713 8854 aldh1a2 ZFA:0001613 pharyngeal arch 3-7 PATO:0001241 physical object quality abnormal ZDB-GENE-011010-3 116713 8854 aldh1a2 ZFA:0001620 pronephric proximal convoluted tubule PATO:0000574 decreased length abnormal ZDB-GENE-011010-3 116713 8854 aldh1a2 ZFA:0001624 pronephric distal late tubule PATO:0000573 increased length abnormal ZDB-GENE-011010-3 116713 8854 aldh1a2 ZFA:0001651 sternohyoid PATO:0000574 decreased length abnormal ZDB-GENE-011010-3 116713 8854 aldh1a2 ZFA:0001651 sternohyoid PATO:0000587 decreased size abnormal ZDB-GENE-011010-3 116713 8854 aldh1a2 ZFA:0001673 pronephric podocyte PATO:0001997 decreased amount abnormal ZDB-GENE-011010-3 116713 8854 aldh1a2 ZFA:0001683 corneal epithelium PATO:0001889 scalloped abnormal ZDB-GENE-011010-3 116713 8854 aldh1a2 ZFA:0001687 corneal endothelium PATO:0000462 absent abnormal ZDB-GENE-011010-3 116713 8854 aldh1a2 ZFA:0005124 intestinal epithelium PATO:0001483 aplastic abnormal ZDB-GENE-011010-3 116713 8854 aldh1a2 ZFA:0005650 primitive pectoral fin adductor PATO:0000462 absent abnormal ZDB-GENE-011010-3 116713 8854 aldh1a2 ZFA:0005651 primitive pectoral fin abductor PATO:0000462 absent abnormal ZDB-GENE-011010-3 116713 8854 aldh1a2 GO:0016477 cell migration BFO:0000066 occurs_in ZFA:0005921 migratory muscle precursor PATO:0000502 delayed abnormal ZDB-GENE-011010-3 116713 8854 aldh1a2 ZFA:0005922 migratory muscle precursor stream PATO:0000645 hypoplastic abnormal ZDB-GENE-011010-3 116713 8854 aldh1a2 ZFA:0005923 anterior migratory muscle precursor stream PATO:0000645 hypoplastic abnormal ZDB-GENE-011010-3 116713 8854 aldh1a2 ZFA:0005925 posterior migratory muscle precursor stream PATO:0000645 hypoplastic abnormal ZDB-GENE-011010-3 116713 8854 aldh1a2 ZFA:0005926 posterior hypaxial muscle PATO:0000587 decreased size abnormal ZDB-GENE-011010-3 116713 8854 aldh1a2 ZFA:0007052 hyohyoideus PATO:0000574 decreased length abnormal ZDB-GENE-011022-1 116991 7358 ugdh GO:0003140 determination of left/right asymmetry in lateral mesoderm PATO:0001236 process quality abnormal ZDB-GENE-011022-1 116991 7358 ugdh GO:0003188 heart valve formation PATO:0001507 disrupted abnormal ZDB-GENE-011022-1 116991 7358 ugdh GO:0003190 atrioventricular valve formation PATO:0001236 process quality abnormal ZDB-GENE-011022-1 116991 7358 ugdh GO:0003190 atrioventricular valve formation PATO:0001507 disrupted abnormal ZDB-GENE-011022-1 116991 7358 ugdh GO:0007417 central nervous system development PATO:0001236 process quality abnormal ZDB-GENE-011022-1 116991 7358 ugdh GO:0007507 heart development PATO:0001236 process quality abnormal ZDB-GENE-011022-1 116991 7358 ugdh GO:0008015 blood circulation PATO:0001507 disrupted abnormal ZDB-GENE-011022-1 116991 7358 ugdh GO:0008543 fibroblast growth factor receptor signaling pathway PATO:0002302 decreased process quality abnormal ZDB-GENE-011022-1 116991 7358 ugdh GO:0030213 hyaluronan biosynthetic process PATO:0001507 disrupted abnormal ZDB-GENE-011022-1 116991 7358 ugdh GO:0036269 swimming behavior PATO:0002302 decreased process quality abnormal ZDB-GENE-011022-1 116991 7358 ugdh GO:0051216 cartilage development PATO:0001507 disrupted abnormal ZDB-GENE-011022-1 116991 7358 ugdh GO:0060026 convergent extension PATO:0001236 process quality abnormal ZDB-GENE-011022-1 116991 7358 ugdh GO:0060070 canonical Wnt signaling pathway PATO:0002304 increased process quality abnormal ZDB-GENE-011022-1 116991 7358 ugdh GO:0019722 calcium-mediated signaling BFO:0000066 occurs_in ZFA:0000001 Kupffer's vesicle PATO:0001236 process quality abnormal ZDB-GENE-011022-1 116991 7358 ugdh ZFA:0000001 Kupffer's vesicle PATO:0001714 increased diameter abnormal ZDB-GENE-011022-1 116991 7358 ugdh ZFA:0000007 blood PATO:0002269 accumulation abnormal ZFA:0000009 cardiac ventricle ZDB-GENE-011022-1 116991 7358 ugdh ZFA:0000007 blood PATO:0002269 accumulation abnormal ZFA:0000471 atrium ZDB-GENE-011022-1 116991 7358 ugdh ZFA:0000009 cardiac ventricle PATO:0000051 morphology abnormal ZDB-GENE-011022-1 116991 7358 ugdh ZFA:0000009 cardiac ventricle PATO:0000052 shape abnormal ZDB-GENE-011022-1 116991 7358 ugdh ZFA:0000012 central nervous system PATO:0000051 morphology abnormal ZDB-GENE-011022-1 116991 7358 ugdh ZFA:0000054 pericardium PATO:0001450 edematous abnormal ZDB-GENE-011022-1 116991 7358 ugdh ZFA:0000076 swim bladder PATO:0002377 uninflated abnormal ZDB-GENE-011022-1 116991 7358 ugdh ZFA:0000095 pharyngeal arch 3-7 skeleton PATO:0000001 quality abnormal ZDB-GENE-011022-1 116991 7358 ugdh ZFA:0000114 heart PATO:0002000 lacks all parts of type abnormal ZFA:0005064 atrioventricular valve ZDB-GENE-011022-1 116991 7358 ugdh ZFA:0000114 heart PATO:0000001 quality abnormal ZDB-GENE-011022-1 116991 7358 ugdh ZFA:0000114 heart PATO:0000586 increased size abnormal ZDB-GENE-011022-1 116991 7358 ugdh ZFA:0000114 heart PATO:0000646 malformed abnormal ZDB-GENE-011022-1 116991 7358 ugdh ZFA:0000114 heart PATO:0001450 edematous abnormal ZDB-GENE-011022-1 116991 7358 ugdh ZFA:0000431 semicircular canal PATO:0001483 aplastic abnormal ZDB-GENE-011022-1 116991 7358 ugdh ZFA:0000471 atrium PATO:0000052 shape abnormal ZDB-GENE-011022-1 116991 7358 ugdh ZFA:0001058 caudal fin PATO:0000587 decreased size abnormal ZDB-GENE-011022-1 116991 7358 ugdh ZFA:0001094 whole organism PATO:0000574 decreased length abnormal ZDB-GENE-011022-1 116991 7358 ugdh ZFA:0001094 whole organism PATO:0000600 increased width abnormal ZDB-GENE-011022-1 116991 7358 ugdh ZFA:0001094 whole organism PATO:0001422 dead abnormal ZDB-GENE-011022-1 116991 7358 ugdh ZFA:0001094 whole organism PATO:0001604 decreased life span abnormal ZDB-GENE-011022-1 116991 7358 ugdh ZFA:0001114 head PATO:0000574 decreased length abnormal ZDB-GENE-011022-1 116991 7358 ugdh ZFA:0001161 pectoral fin PATO:0000574 decreased length abnormal ZDB-GENE-011022-1 116991 7358 ugdh ZFA:0001161 pectoral fin PATO:0001798 kinked abnormal ZDB-GENE-011022-1 116991 7358 ugdh ZFA:0001306 pharyngeal arch PATO:0000051 morphology abnormal ZDB-GENE-011022-1 116991 7358 ugdh ZFA:0001460 pharyngeal arch cartilage PATO:0000587 decreased size abnormal ZDB-GENE-011022-1 116991 7358 ugdh ZFA:0001460 pharyngeal arch cartilage PATO:0001485 condensed abnormal ZDB-GENE-011022-1 116991 7358 ugdh ZFA:0001606 pharyngeal arch 3 PATO:0001714 increased diameter abnormal ZDB-GENE-011022-1 116991 7358 ugdh ZFA:0001613 pharyngeal arch 3-7 PATO:0000133 orientation abnormal BSPO:0000013 anterior-posterior axis BFO:0000050 part_of ZFA:0001094 whole organism ZDB-GENE-011022-1 116991 7358 ugdh ZFA:0005064 atrioventricular valve PATO:0000051 morphology abnormal ZDB-GENE-011022-1 116991 7358 ugdh ZFA:0005064 atrioventricular valve PATO:0001483 aplastic abnormal ZDB-GENE-011023-1 116993 1462 vcana CHEBI:36080 protein BFO:0000050 part_of ZFA:0000007 blood PATO:0001997 decreased amount abnormal ZDB-GENE-011023-1 116993 1462 vcana ZFA:0000054 pericardium PATO:0001450 edematous abnormal ZDB-GENE-011023-1 116993 1462 vcana ZFA:0001317 endocardial cushion PATO:0000051 morphology abnormal ZDB-GENE-011023-1 116993 1462 vcana ZFA:0001557 pronephric glomerulus PATO:0001999 lacks parts or has fewer parts of type abnormal GO:0036053 glomerular endothelium fenestra BFO:0000050 part_of ZFA:0005285 glomerular basement membrane ZDB-GENE-011023-1 116993 1462 vcana ZFA:0001673 pronephric podocyte PATO:0000574 decreased length abnormal ZDB-GENE-011023-1 116993 1462 vcana ZFA:0001673 pronephric podocyte PATO:0000600 increased width abnormal ZDB-GENE-011101-2 569360 1630 dcc GO:0001945 lymph vessel development PATO:0001236 process quality abnormal ZDB-GENE-011101-2 569360 1630 dcc GO:0001964 startle response PATO:0001236 process quality abnormal ZDB-GENE-011101-2 569360 1630 dcc GO:0008345 larval locomotory behavior PATO:0000078 rhythm quality abnormal ZDB-GENE-011101-2 569360 1630 dcc GO:0016358 dendrite development PATO:0001507 disrupted abnormal ZDB-GENE-011101-2 569360 1630 dcc GO:0031223 auditory behavior PATO:0001236 process quality abnormal ZDB-GENE-011101-2 569360 1630 dcc GO:0050881 musculoskeletal movement PATO:0000001 quality abnormal ZDB-GENE-011101-2 569360 1630 dcc GO:0050885 neuromuscular process controlling balance PATO:0000001 quality abnormal ZDB-GENE-011101-2 569360 1630 dcc GO:0050885 neuromuscular process controlling balance PATO:0001507 disrupted abnormal ZDB-GENE-011101-2 569360 1630 dcc GO:0060854 branching involved in lymph vessel morphogenesis PATO:0001236 process quality abnormal ZDB-GENE-011101-2 569360 1630 dcc GO:0071678 olfactory bulb axon guidance PATO:0001507 disrupted abnormal ZDB-GENE-011101-2 569360 1630 dcc GO:0071679 commissural neuron axon guidance PATO:0001236 process quality abnormal ZDB-GENE-011101-2 569360 1630 dcc ZFA:0000671 horizontal myoseptum PATO:0001999 lacks parts or has fewer parts of type abnormal GO:0030424 axon BFO:0000050 part_of ZFA:0005180 RoP motor neuron ZDB-GENE-011101-2 569360 1630 dcc ZFA:0000671 horizontal myoseptum PATO:0001999 lacks parts or has fewer parts of type abnormal GO:0030424 axon BFO:0000050 part_of ZFA:0009052 motor neuron ZDB-GENE-011101-2 569360 1630 dcc ZFA:0001094 whole organism PATO:0002076 movement behavioral quality abnormal ZDB-GENE-011101-2 569360 1630 dcc ZFA:0001117 post-vent region PATO:0001906 movement quality abnormal ZDB-GENE-011101-2 569360 1630 dcc GO:0060855 venous endothelial cell migration involved in lymph vessel development BFO:0000066 occurs_in ZFA:0005034 parachordal vessel PATO:0000297 arrested abnormal ZDB-GENE-011101-2 569360 1630 dcc ZFA:0005034 parachordal vessel PATO:0001501 immature abnormal ZDB-GENE-011101-2 569360 1630 dcc ZFA:0005110 thoracic duct PATO:0001483 aplastic abnormal ZDB-GENE-011101-2 569360 1630 dcc GO:0043005 neuron projection BFO:0000050 part_of ZFA:0005175 CoPA PATO:0000629 misrouted abnormal ZDB-GENE-011101-2 569360 1630 dcc GO:0048846 axon extension involved in axon guidance BFO:0000066 occurs_in ZFA:0005175 CoPA PATO:0002302 decreased process quality abnormal ZDB-GENE-011101-2 569360 1630 dcc GO:0030424 axon BFO:0000050 part_of ZFA:0005181 VaP motor neuron PATO:0001645 protruding into abnormal ZFA:0001086 muscle pioneer ZDB-GENE-011101-2 569360 1630 dcc GO:0071679 commissural neuron axon guidance BFO:0000066 occurs_in ZFA:0005185 MiD2cm PATO:0002052 decreased occurrence abnormal ZDB-GENE-011101-2 569360 1630 dcc GO:0044297 cell body BFO:0000050 part_of ZFA:0005195 MiD3cl PATO:0000140 position abnormal ZDB-GENE-011101-2 569360 1630 dcc GO:0071679 commissural neuron axon guidance BFO:0000066 occurs_in ZFA:0005195 MiD3cl PATO:0002052 decreased occurrence abnormal ZDB-GENE-011101-2 569360 1630 dcc GO:0071679 commissural neuron axon guidance BFO:0000066 occurs_in ZFA:0005196 MiD3cm PATO:0002052 decreased occurrence abnormal ZDB-GENE-011101-2 569360 1630 dcc GO:0071679 commissural neuron axon guidance BFO:0000066 occurs_in ZFA:0005198 RoL2 PATO:0002052 decreased occurrence abnormal ZDB-GENE-011101-2 569360 1630 dcc GO:0071679 commissural neuron axon guidance BFO:0000066 occurs_in ZFA:0005209 hindbrain interneuron PATO:0002052 decreased occurrence abnormal ZDB-GENE-011101-2 569360 1630 dcc GO:0043005 neuron projection BFO:0000050 part_of ZFA:0007001 dorso-rostral cluster PATO:0000628 mislocalised abnormal ZDB-GENE-011101-2 569360 1630 dcc GO:0043005 neuron projection BFO:0000050 part_of ZFA:0007001 dorso-rostral cluster PATO:0000629 misrouted abnormal ZDB-GENE-011101-2 569360 1630 dcc GO:0043005 neuron projection BFO:0000050 part_of ZFA:0007001 dorso-rostral cluster PATO:0001241 physical object quality abnormal ZDB-GENE-011101-2 569360 1630 dcc GO:0043005 neuron projection BFO:0000050 part_of ZFA:0007001 dorso-rostral cluster PATO:0001919 mislocalised dorsally abnormal ZDB-GENE-011101-2 569360 1630 dcc GO:0043005 neuron projection BFO:0000050 part_of ZFA:0007001 dorso-rostral cluster PATO:0002118 multiple abnormal ZDB-GENE-011101-2 569360 1630 dcc GO:0048675 axon extension BFO:0000066 occurs_in ZFA:0007001 dorso-rostral cluster PATO:0001236 process quality abnormal ZDB-GENE-011101-2 569360 1630 dcc GO:0030424 axon BFO:0000050 part_of ZFA:0009125 olfactory receptor cell PATO:0001667 attached to abnormal ZFA:0001108 anterior commissure ZDB-GENE-011101-2 569360 1630 dcc GO:0030424 axon BFO:0000050 part_of ZFA:0009125 olfactory receptor cell PATO:0001667 attached to abnormal ZFA:0005717 lateral protoglomerulus 1 ZDB-GENE-011101-2 569360 1630 dcc GO:0030424 axon BFO:0000050 part_of ZFA:0009125 olfactory receptor cell PATO:0001667 attached to abnormal ZFA:0005718 lateral protoglomerulus 2 ZDB-GENE-011101-2 569360 1630 dcc GO:0030424 axon BFO:0000050 part_of ZFA:0009125 olfactory receptor cell PATO:0000140 position abnormal ZDB-GENE-011101-2 569360 1630 dcc GO:0030425 dendrite BFO:0000050 part_of ZFA:0009239 efferent neuron PATO:0000628 mislocalised abnormal ZDB-GENE-011101-2 569360 1630 dcc GO:0030425 dendrite BFO:0000050 part_of ZFA:0009239 efferent neuron PATO:0001997 decreased amount abnormal ZDB-GENE-011101-3 117234 10586 mab21l2 GO:0001654 eye development PATO:0001236 process quality abnormal ZDB-GENE-011101-3 117234 10586 mab21l2 GO:0002089 lens morphogenesis in camera-type eye PATO:0000502 delayed abnormal ZDB-GENE-011101-3 117234 10586 mab21l2 GO:0010842 retina layer formation PATO:0001236 process quality abnormal ZDB-GENE-011101-3 117234 10586 mab21l2 GO:0035645 enteric smooth muscle cell differentiation PATO:0001236 process quality abnormal ZDB-GENE-011101-3 117234 10586 mab21l2 GO:0048703 embryonic viscerocranium morphogenesis PATO:0001507 disrupted abnormal ZDB-GENE-011101-3 117234 10586 mab21l2 GO:0060465 pharynx development PATO:0001236 process quality abnormal ZDB-GENE-011101-3 117234 10586 mab21l2 GO:0061386 closure of optic fissure PATO:0002052 decreased occurrence abnormal ZDB-GENE-011101-3 117234 10586 mab21l2 GO:0006915 apoptotic process BFO:0000066 occurs_in ZFA:0000035 lens PATO:0002051 increased occurrence abnormal ZDB-GENE-011101-3 117234 10586 mab21l2 GO:0008219 cell death BFO:0000066 occurs_in ZFA:0000035 lens PATO:0002051 increased occurrence abnormal ZDB-GENE-011101-3 117234 10586 mab21l2 GO:0008283 cell population proliferation BFO:0000066 occurs_in ZFA:0000035 lens PATO:0002052 decreased occurrence abnormal ZDB-GENE-011101-3 117234 10586 mab21l2 ZFA:0000035 lens PATO:0000051 morphology abnormal ZDB-GENE-011101-3 117234 10586 mab21l2 ZFA:0000035 lens PATO:0000462 absent abnormal ZDB-GENE-011101-3 117234 10586 mab21l2 ZFA:0000035 lens PATO:0000587 decreased size abnormal ZDB-GENE-011101-3 117234 10586 mab21l2 ZFA:0000035 lens PATO:0000639 degenerate abnormal ZDB-GENE-011101-3 117234 10586 mab21l2 ZFA:0000050 optic vesicle PATO:0000587 decreased size abnormal ZDB-GENE-011101-3 117234 10586 mab21l2 ZFA:0000050 optic vesicle PATO:0001847 constricted abnormal ZDB-GENE-011101-3 117234 10586 mab21l2 GO:0008283 cell population proliferation BFO:0000066 occurs_in ZFA:0000107 eye PATO:0002052 decreased occurrence abnormal ZDB-GENE-011101-3 117234 10586 mab21l2 ZFA:0000107 eye PATO:0000052 shape abnormal ZDB-GENE-011101-3 117234 10586 mab21l2 ZFA:0000107 eye PATO:0000462 absent abnormal ZDB-GENE-011101-3 117234 10586 mab21l2 ZFA:0000107 eye PATO:0000587 decreased size abnormal ZDB-GENE-011101-3 117234 10586 mab21l2 ZFA:0000107 eye PATO:0000596 decreased volume abnormal ZDB-GENE-011101-3 117234 10586 mab21l2 ZFA:0000107 eye PATO:0001617 deformed abnormal ZDB-GENE-011101-3 117234 10586 mab21l2 ZFA:0000107 eye PATO:0002053 dorso-ventrally flattened abnormal ZDB-GENE-011101-3 117234 10586 mab21l2 ZFA:0000107 eye PATO:0002112 perforate abnormal ZDB-GENE-011101-3 117234 10586 mab21l2 GO:0006915 apoptotic process BFO:0000066 occurs_in ZFA:0000128 midbrain PATO:0002051 increased occurrence abnormal ZDB-GENE-011101-3 117234 10586 mab21l2 GO:0008219 cell death BFO:0000066 occurs_in ZFA:0000137 optic stalk PATO:0002051 increased occurrence abnormal ZDB-GENE-011101-3 117234 10586 mab21l2 ZFA:0000144 retinal pigmented epithelium PATO:0000628 mislocalised abnormal ZDB-GENE-011101-3 117234 10586 mab21l2 ZFA:0000144 retinal pigmented epithelium PATO:0002251 decreased pigmentation abnormal ZDB-GENE-011101-3 117234 10586 mab21l2 ZFA:0000144 retinal pigmented epithelium PATO:0010001 disconnected abnormal ZDB-GENE-011101-3 117234 10586 mab21l2 BSPO:0000079 dorsal region BFO:0000050 part_of ZFA:0000152 retina PATO:0000051 morphology abnormal ZDB-GENE-011101-3 117234 10586 mab21l2 GO:0006915 apoptotic process BFO:0000066 occurs_in ZFA:0000152 retina PATO:0002051 increased occurrence abnormal ZDB-GENE-011101-3 117234 10586 mab21l2 GO:0008283 cell population proliferation BFO:0000066 occurs_in ZFA:0000152 retina PATO:0001507 disrupted abnormal ZDB-GENE-011101-3 117234 10586 mab21l2 GO:0022008 neurogenesis BFO:0000066 occurs_in ZFA:0000152 retina PATO:0000502 delayed abnormal ZDB-GENE-011101-3 117234 10586 mab21l2 ZFA:0000152 retina PATO:0000052 shape abnormal ZDB-GENE-011101-3 117234 10586 mab21l2 ZFA:0000152 retina PATO:0000628 mislocalised abnormal ZDB-GENE-011101-3 117234 10586 mab21l2 ZFA:0000152 retina PATO:0000937 disorganized abnormal ZDB-GENE-011101-3 117234 10586 mab21l2 ZFA:0000152 retina PATO:0001910 folded abnormal ZDB-GENE-011101-3 117234 10586 mab21l2 ZFA:0000152 retina PATO:0002254 flattened abnormal ZDB-GENE-011101-3 117234 10586 mab21l2 ZFA:0000640 cornea PATO:0000051 morphology abnormal ZDB-GENE-011101-3 117234 10586 mab21l2 ZFA:0000640 cornea PATO:0002248 pigmented abnormal ZDB-GENE-011101-3 117234 10586 mab21l2 BSPO:0000084 ventral region BFO:0000050 part_of ZFA:0001202 optic cup PATO:0001472 decreased depth abnormal ZDB-GENE-011101-3 117234 10586 mab21l2 ZFA:0001202 optic cup PATO:0001617 deformed abnormal ZDB-GENE-011101-3 117234 10586 mab21l2 ZFA:0001202 optic cup PATO:0002254 flattened abnormal ZDB-GENE-011101-3 117234 10586 mab21l2 ZFA:0001284 optic fissure PATO:0000609 closure incomplete abnormal ZDB-GENE-011101-3 117234 10586 mab21l2 ZFA:0001284 optic fissure PATO:0000610 open abnormal ZDB-GENE-011101-3 117234 10586 mab21l2 ZFA:0001289 ciliary marginal zone PATO:0002002 has extra parts of type abnormal ZFA:0009000 cell ZDB-GENE-011101-3 117234 10586 mab21l2 ZFA:0001289 ciliary marginal zone PATO:0000586 increased size abnormal ZDB-GENE-011101-3 117234 10586 mab21l2 GO:0008283 cell population proliferation BFO:0000066 occurs_in ZFA:0001326 lens epithelium PATO:0002052 decreased occurrence abnormal ZDB-GENE-011101-3 117234 10586 mab21l2 ZFA:0001400 ceratohyal cartilage BFO:0000050 part_of ZFA:0001611 pharyngeal arch 2 PATO:0000646 malformed abnormal ZDB-GENE-011101-3 117234 10586 mab21l2 ZFA:0001683 corneal epithelium PATO:0000051 morphology abnormal ZDB-GENE-011101-3 117234 10586 mab21l2 GO:0001944 vasculature development BFO:0000066 occurs_in ZFA:0005046 hyaloid vessel PATO:0000502 delayed abnormal ZDB-GENE-011101-3 117234 10586 mab21l2 GO:0001944 vasculature development BFO:0000066 occurs_in ZFA:0005046 hyaloid vessel PATO:0001236 process quality abnormal ZDB-GENE-011101-3 117234 10586 mab21l2 ZFA:0005046 hyaloid vessel PATO:0000330 irregular spatial pattern abnormal ZDB-GENE-011101-3 117234 10586 mab21l2 ZFA:0005046 hyaloid vessel PATO:0000591 increased thickness abnormal ZDB-GENE-011101-3 117234 10586 mab21l2 ZFA:0005775 enteric neuron PATO:0001997 decreased amount abnormal ZDB-GENE-011105-1 117507 5584 prkci GO:0000278 mitotic cell cycle PATO:0001236 process quality abnormal ZDB-GENE-011105-1 117507 5584 prkci GO:0003007 heart morphogenesis PATO:0001236 process quality abnormal ZDB-GENE-011105-1 117507 5584 prkci GO:0007097 nuclear migration PATO:0001507 disrupted abnormal ZDB-GENE-011105-1 117507 5584 prkci GO:0007420 brain development PATO:0001507 disrupted abnormal ZDB-GENE-011105-1 117507 5584 prkci GO:0008015 blood circulation PATO:0001507 disrupted abnormal ZDB-GENE-011105-1 117507 5584 prkci GO:0008594 photoreceptor cell morphogenesis PATO:0002302 decreased process quality abnormal ZDB-GENE-011105-1 117507 5584 prkci GO:0010842 retina layer formation PATO:0000297 arrested abnormal ZDB-GENE-011105-1 117507 5584 prkci GO:0014019 neuroblast development PATO:0001507 disrupted abnormal ZDB-GENE-011105-1 117507 5584 prkci GO:0021744 dorsal motor nucleus of vagus nerve development PATO:0001507 disrupted abnormal ZDB-GENE-011105-1 117507 5584 prkci GO:0030318 melanocyte differentiation PATO:0000502 delayed abnormal ZDB-GENE-011105-1 117507 5584 prkci GO:0035148 tube formation PATO:0001507 disrupted abnormal ZDB-GENE-011105-1 117507 5584 prkci GO:0039011 pronephric proximal tubule morphogenesis PATO:0002302 decreased process quality abnormal ZDB-GENE-011105-1 117507 5584 prkci GO:0045199 maintenance of epithelial cell apical/basal polarity PATO:0001507 disrupted abnormal ZDB-GENE-011105-1 117507 5584 prkci GO:0048069 eye pigmentation PATO:0001507 disrupted abnormal ZDB-GENE-011105-1 117507 5584 prkci GO:0060219 camera-type eye photoreceptor cell differentiation PATO:0002052 decreased occurrence abnormal ZDB-GENE-011105-1 117507 5584 prkci GO:0090521 podocyte cell migration PATO:0002302 decreased process quality abnormal ZDB-GENE-011105-1 117507 5584 prkci ZFA:0000008 brain PATO:0000001 quality abnormal ZDB-GENE-011105-1 117507 5584 prkci ZFA:0000008 brain PATO:0000051 morphology abnormal ZDB-GENE-011105-1 117507 5584 prkci ZFA:0000008 brain PATO:0000052 shape abnormal ZDB-GENE-011105-1 117507 5584 prkci ZFA:0000009 cardiac ventricle PATO:0001571 dilated abnormal ZDB-GENE-011105-1 117507 5584 prkci ZFA:0000024 retinal ganglion cell layer PATO:0000937 disorganized abnormal ZDB-GENE-011105-1 117507 5584 prkci ZFA:0000054 pericardium PATO:0001450 edematous abnormal ZDB-GENE-011105-1 117507 5584 prkci ZFA:0000075 spinal cord PATO:0002001 has fewer parts of type abnormal ZFA:0009076 oligodendrocyte ZDB-GENE-011105-1 117507 5584 prkci ZFA:0000075 spinal cord PATO:0002001 has fewer parts of type abnormal ZFA:0009292 radial glial cell ZDB-GENE-011105-1 117507 5584 prkci ZFA:0000084 yolk PATO:0000001 quality abnormal ZDB-GENE-011105-1 117507 5584 prkci ZFA:0000107 eye PATO:0000587 decreased size abnormal ZDB-GENE-011105-1 117507 5584 prkci ZFA:0000110 fourth ventricle PATO:0001715 decreased diameter abnormal ZDB-GENE-011105-1 117507 5584 prkci ZFA:0000114 heart PATO:0000001 quality abnormal ZDB-GENE-011105-1 117507 5584 prkci ZFA:0000114 heart PATO:0000051 morphology abnormal ZDB-GENE-011105-1 117507 5584 prkci ZFA:0000114 heart PATO:0000587 decreased size abnormal ZDB-GENE-011105-1 117507 5584 prkci ZFA:0000114 heart PATO:0000646 malformed abnormal ZDB-GENE-011105-1 117507 5584 prkci ZFA:0000114 heart PATO:0000937 disorganized abnormal ZDB-GENE-011105-1 117507 5584 prkci ZFA:0000114 heart PATO:0001164 dense abnormal ZDB-GENE-011105-1 117507 5584 prkci ZFA:0000123 liver PATO:0000051 morphology abnormal ZDB-GENE-011105-1 117507 5584 prkci ZFA:0000144 retinal pigmented epithelium PATO:0000001 quality abnormal ZDB-GENE-011105-1 117507 5584 prkci ZFA:0000144 retinal pigmented epithelium PATO:0000051 morphology abnormal ZDB-GENE-011105-1 117507 5584 prkci ZFA:0000144 retinal pigmented epithelium PATO:0000141 structure abnormal ZDB-GENE-011105-1 117507 5584 prkci ZFA:0000144 retinal pigmented epithelium PATO:0001608 patchy abnormal ZDB-GENE-011105-1 117507 5584 prkci ZFA:0000144 retinal pigmented epithelium PATO:0002106 poorly differentiated abnormal ZDB-GENE-011105-1 117507 5584 prkci ZFA:0000151 pronephros PATO:0000001 quality abnormal ZDB-GENE-011105-1 117507 5584 prkci ZFA:0009306 neuroepithelial cell BFO:0000050 part_of ZFA:0000152 retina PATO:0001769 positional polarity abnormal ZDB-GENE-011105-1 117507 5584 prkci ZFA:0000152 retina PATO:0002001 has fewer parts of type abnormal ZFA:0009275 retinal rod cell ZDB-GENE-011105-1 117507 5584 prkci ZFA:0000152 retina PATO:0000001 quality abnormal ZDB-GENE-011105-1 117507 5584 prkci ZFA:0000152 retina PATO:0000141 structure abnormal ZDB-GENE-011105-1 117507 5584 prkci ZFA:0000152 retina PATO:0000639 degenerate abnormal ZDB-GENE-011105-1 117507 5584 prkci ZFA:0000152 retina PATO:0002069 unstratified abnormal ZDB-GENE-011105-1 117507 5584 prkci ZFA:0000396 nervous system PATO:0000001 quality abnormal ZDB-GENE-011105-1 117507 5584 prkci ZFA:0000471 atrium PATO:0001483 aplastic abnormal ZDB-GENE-011105-1 117507 5584 prkci ZFA:0000471 atrium PATO:0001571 dilated abnormal ZDB-GENE-011105-1 117507 5584 prkci BSPO:0000005 anatomical surface BFO:0000050 part_of ZFA:0000640 cornea PATO:0000141 structure abnormal ZDB-GENE-011105-1 117507 5584 prkci ZFA:0000640 cornea PATO:0000141 structure abnormal ZDB-GENE-011105-1 117507 5584 prkci ZFA:0000938 central canal PATO:0000586 increased size abnormal ZDB-GENE-011105-1 117507 5584 prkci ZFA:0001094 whole organism PATO:0000052 shape abnormal ZDB-GENE-011105-1 117507 5584 prkci ZFA:0001114 head PATO:0000574 decreased length abnormal ZDB-GENE-011105-1 117507 5584 prkci ZFA:0001117 post-vent region PATO:0000406 curved abnormal ZDB-GENE-011105-1 117507 5584 prkci ZFA:0001117 post-vent region PATO:0001468 curved dorsal abnormal ZDB-GENE-011105-1 117507 5584 prkci ZFA:0001239 ceratobranchial 5 bone PATO:0002001 has fewer parts of type abnormal ZFA:0000694 ceratobranchial 5 tooth ZDB-GENE-011105-1 117507 5584 prkci ZFA:0001239 ceratobranchial 5 bone PATO:0000574 decreased length abnormal ZDB-GENE-011105-1 117507 5584 prkci ZFA:0001261 ventricular system PATO:0000587 decreased size abnormal ZDB-GENE-011105-1 117507 5584 prkci ZFA:0001261 ventricular system PATO:0002014 structure, cavities abnormal ZDB-GENE-011105-1 117507 5584 prkci ZFA:0001439 anatomical system PATO:0000001 quality abnormal ZDB-GENE-011105-1 117507 5584 prkci ZFA:0001620 pronephric proximal convoluted tubule PATO:0000646 malformed abnormal ZDB-GENE-011105-1 117507 5584 prkci ZFA:0001673 pronephric podocyte PATO:0001923 mislocalised laterally abnormal ZDB-GENE-011105-1 117507 5584 prkci GO:0030057 desmosome BFO:0000050 part_of ZFA:0001683 corneal epithelium PATO:0001997 decreased amount abnormal ZDB-GENE-011105-1 117507 5584 prkci ZFA:0001683 corneal epithelium PATO:0001987 saccular abnormal ZDB-GENE-011105-1 117507 5584 prkci ZFA:0001685 corneal stroma PATO:0000937 disorganized abnormal ZDB-GENE-011105-1 117507 5584 prkci ZFA:0001695 dorsolateral motor nucleus of vagal nerve PATO:0000646 malformed abnormal ZDB-GENE-011105-1 117507 5584 prkci GO:0005634 nucleus BFO:0000050 part_of ZFA:0009011 neuroblast PATO:0000140 position abnormal ZDB-GENE-011105-1 117507 5584 prkci GO:0098858 actin-based cell projection BFO:0000050 part_of ZFA:0009041 peridermal cell PATO:0000573 increased length abnormal ZDB-GENE-011105-1 117507 5584 prkci GO:0098858 actin-based cell projection BFO:0000050 part_of ZFA:0009041 peridermal cell PATO:0000574 decreased length abnormal ZDB-GENE-011105-1 117507 5584 prkci ZFA:0009091 melanocyte PATO:0000001 quality abnormal ZDB-GENE-011105-1 117507 5584 prkci BSPO:0000073 apical region BFO:0000050 part_of ZFA:0009154 eye photoreceptor cell PATO:0000574 decreased length abnormal ZDB-GENE-011105-1 117507 5584 prkci GO:0048770 pigment granule BFO:0000050 part_of ZFA:0009241 pigmented epithelial cell PATO:0000628 mislocalised abnormal ZDB-GENE-011105-1 117507 5584 prkci ZFA:0009241 pigmented epithelial cell PATO:0000052 shape abnormal ZDB-GENE-011105-1 117507 5584 prkci ZFA:0009255 amacrine cell PATO:0000060 spatial pattern abnormal ZDB-GENE-011105-1 117507 5584 prkci ZFA:0009264 corneal epithelial cell PATO:0001531 cellular adhesivity abnormal ZFA:0009264 corneal epithelial cell ZDB-GENE-011105-1 117507 5584 prkci GO:0005911 cell-cell junction BFO:0000050 part_of ZFA:0009306 neuroepithelial cell PATO:0001444 broken abnormal ZDB-GENE-011108-2 117510 6425 sfrp5 ZFA:0000017 endoderm PATO:0000587 decreased size abnormal ZDB-GENE-011108-2 117510 6425 sfrp5 ZFA:0000123 liver PATO:0000587 decreased size abnormal ZDB-GENE-011108-2 117510 6425 sfrp5 ZFA:0000123 liver PATO:0000937 disorganized abnormal ZDB-GENE-011108-2 117510 6425 sfrp5 ZFA:0000140 pancreas PATO:0000587 decreased size abnormal ZDB-GENE-011108-2 117510 6425 sfrp5 ZFA:0001338 intestine PATO:0000587 decreased size abnormal ZDB-GENE-011108-2 117510 6425 sfrp5 ZFA:0009398 hepatoblast PATO:0000587 decreased size abnormal ZDB-GENE-011109-1 117508 10365 klf2a GO:0003171 atrioventricular valve development PATO:0001236 process quality abnormal ZDB-GENE-011109-1 117508 10365 klf2a GO:0003181 atrioventricular valve morphogenesis PATO:0002302 decreased process quality abnormal ZDB-GENE-011109-1 117508 10365 klf2a GO:0003187 ventriculo bulbo valve morphogenesis PATO:0000502 delayed abnormal ZDB-GENE-011109-1 117508 10365 klf2a GO:0003190 atrioventricular valve formation PATO:0001507 disrupted abnormal ZDB-GENE-011109-1 117508 10365 klf2a GO:0006809 nitric oxide biosynthetic process PATO:0001507 disrupted abnormal ZDB-GENE-011109-1 117508 10365 klf2a GO:0007501 mesodermal cell fate specification PATO:0002304 increased process quality abnormal ZDB-GENE-011109-1 117508 10365 klf2a GO:0030325 adrenal gland development PATO:0001236 process quality abnormal ZDB-GENE-011109-1 117508 10365 klf2a GO:0036302 atrioventricular canal development PATO:0001507 disrupted abnormal ZDB-GENE-011109-1 117508 10365 klf2a ZFA:0001377 presumptive mesoderm BFO:0000050 part_of ZFA:0000038 margin PATO:0002099 differentiated abnormal ZDB-GENE-011109-1 117508 10365 klf2a ZFA:0009181 vascular associated smooth muscle cell BFO:0000050 part_of ZFA:0000186 common cardinal vein PATO:0000470 increased amount abnormal ZDB-GENE-011109-1 117508 10365 klf2a ZFA:0000186 common cardinal vein PATO:0000599 decreased width abnormal ZDB-GENE-011109-1 117508 10365 klf2a ZFA:0009354 hematopoietic multipotent progenitor cell BFO:0000050 part_of ZFA:0001078 thymus PATO:0001997 decreased amount abnormal ZDB-GENE-011109-1 117508 10365 klf2a GO:0002040 sprouting angiogenesis BFO:0000066 occurs_in ZFA:0001286 caudal vein plexus PATO:0002052 decreased occurrence abnormal ZDB-GENE-011109-1 117508 10365 klf2a ZFA:0001286 caudal vein plexus PATO:0000646 malformed abnormal ZDB-GENE-011109-1 117508 10365 klf2a ZFA:0001315 atrioventricular canal PATO:0000051 morphology abnormal ZDB-GENE-011109-1 117508 10365 klf2a ZFA:0009000 cell BFO:0000050 part_of ZFA:0001317 endocardial cushion PATO:0001997 decreased amount abnormal ZDB-GENE-011109-1 117508 10365 klf2a ZFA:0009000 cell BFO:0000050 part_of ZFA:0001318 cardiac jelly PATO:0000937 disorganized abnormal ZDB-GENE-011109-1 117508 10365 klf2a GO:0001837 epithelial to mesenchymal transition BFO:0000066 occurs_in ZFA:0001345 interrenal gland PATO:0002052 decreased occurrence abnormal ZDB-GENE-011109-1 117508 10365 klf2a GO:0009887 animal organ morphogenesis BFO:0000066 occurs_in ZFA:0001345 interrenal gland PATO:0001236 process quality abnormal ZDB-GENE-011109-1 117508 10365 klf2a ZFA:0001345 interrenal gland PATO:0000140 position abnormal ZDB-GENE-011109-1 117508 10365 klf2a GO:0061314 Notch signaling involved in heart development BFO:0000066 occurs_in ZFA:0001375 ventriculo bulbo valve PATO:0002302 decreased process quality abnormal ZDB-GENE-011109-1 117508 10365 klf2a ZFA:0005009 aortic arch 5 PATO:0000462 absent abnormal ZDB-GENE-011109-1 117508 10365 klf2a ZFA:0005064 atrioventricular valve PATO:0000051 morphology abnormal ZDB-GENE-011109-1 117508 10365 klf2a ZFA:0005802 interrenal angiogenic sprout PATO:0000574 decreased length abnormal ZDB-GENE-011109-1 117508 10365 klf2a ZFA:0009354 hematopoietic multipotent progenitor cell PATO:0001997 decreased amount abnormal ZDB-GENE-011109-2 117509 10365 klf2b GO:0007501 mesodermal cell fate specification PATO:0002304 increased process quality abnormal ZDB-GENE-011109-2 117509 10365 klf2b ZFA:0001377 presumptive mesoderm BFO:0000050 part_of ZFA:0000038 margin PATO:0002099 differentiated abnormal ZDB-GENE-011115-1 117604 7532 ywhag1 GO:0060047 heart contraction PATO:0000504 arrhythmic abnormal ZDB-GENE-011115-1 117604 7532 ywhag1 ZFA:0000008 brain PATO:0000646 malformed abnormal ZDB-GENE-011115-1 117604 7532 ywhag1 ZFA:0000009 cardiac ventricle PATO:0001714 increased diameter abnormal ZDB-GENE-011115-1 117604 7532 ywhag1 ZFA:0000360 heart tube PATO:0000586 increased size abnormal ZDB-GENE-011115-1 117604 7532 ywhag1 ZFA:0001114 head PATO:0000645 hypoplastic abnormal ZDB-GENE-011116-1 117603 51274 klf3 GO:0043249 erythrocyte maturation PATO:0000297 arrested abnormal ZDB-GENE-011116-1 117603 51274 klf3 GO:0043249 erythrocyte maturation PATO:0002302 decreased process quality abnormal ZDB-GENE-011116-1 117603 51274 klf3 GO:0060319 primitive erythrocyte differentiation PATO:0002302 decreased process quality abnormal ZDB-GENE-011116-1 117603 51274 klf3 ZFA:0009256 nucleate erythrocyte PATO:0001997 decreased amount abnormal ZDB-GENE-011119-1 118437 2239 gpc4 GO:0000902 cell morphogenesis PATO:0001507 disrupted abnormal ZDB-GENE-011119-1 118437 2239 gpc4 GO:0001503 ossification PATO:0001236 process quality abnormal ZDB-GENE-011119-1 118437 2239 gpc4 GO:0001958 endochondral ossification PATO:0001507 disrupted abnormal ZDB-GENE-011119-1 118437 2239 gpc4 GO:0003401 axis elongation PATO:0002302 decreased process quality abnormal ZDB-GENE-011119-1 118437 2239 gpc4 GO:0008078 mesodermal cell migration PATO:0000502 delayed abnormal ZDB-GENE-011119-1 118437 2239 gpc4 GO:0014028 notochord formation PATO:0001507 disrupted abnormal ZDB-GENE-011119-1 118437 2239 gpc4 GO:0014812 muscle cell migration PATO:0001507 disrupted abnormal ZDB-GENE-011119-1 118437 2239 gpc4 GO:0030203 glycosaminoglycan metabolic process PATO:0001507 disrupted abnormal ZDB-GENE-011119-1 118437 2239 gpc4 GO:0031016 pancreas development PATO:0002302 decreased process quality abnormal ZDB-GENE-011119-1 118437 2239 gpc4 GO:0036342 post-anal tail morphogenesis PATO:0001561 having extra processual parts abnormal GO:0036342 post-anal tail morphogenesis ZDB-GENE-011119-1 118437 2239 gpc4 GO:0036342 post-anal tail morphogenesis PATO:0001507 disrupted abnormal ZDB-GENE-011119-1 118437 2239 gpc4 GO:0042074 cell migration involved in gastrulation PATO:0000502 delayed abnormal ZDB-GENE-011119-1 118437 2239 gpc4 GO:0048570 notochord morphogenesis PATO:0001507 disrupted abnormal ZDB-GENE-011119-1 118437 2239 gpc4 GO:0048920 posterior lateral line neuromast primordium migration PATO:0001236 process quality abnormal ZDB-GENE-011119-1 118437 2239 gpc4 GO:0055002 striated muscle cell development PATO:0001507 disrupted abnormal ZDB-GENE-011119-1 118437 2239 gpc4 GO:0060026 convergent extension PATO:0001236 process quality abnormal ZDB-GENE-011119-1 118437 2239 gpc4 GO:0060026 convergent extension PATO:0001507 disrupted abnormal ZDB-GENE-011119-1 118437 2239 gpc4 GO:0060027 convergent extension involved in gastrulation PATO:0001507 disrupted abnormal ZDB-GENE-011119-1 118437 2239 gpc4 GO:0060028 convergent extension involved in axis elongation PATO:0001236 process quality abnormal ZDB-GENE-011119-1 118437 2239 gpc4 GO:0060028 convergent extension involved in axis elongation PATO:0001507 disrupted abnormal ZDB-GENE-011119-1 118437 2239 gpc4 GO:0060030 dorsal convergence PATO:0000502 delayed abnormal ZDB-GENE-011119-1 118437 2239 gpc4 ZFA:0009032 ciliated cell BFO:0000050 part_of ZFA:0000001 Kupffer's vesicle PATO:0002448 oriented towards abnormal BSPO:0000071 anterior region BFO:0000050 part_of ZFA:0000001 Kupffer's vesicle ZDB-GENE-011119-1 118437 2239 gpc4 ZFA:0000003 adaxial cell PATO:0000052 shape abnormal ZDB-GENE-011119-1 118437 2239 gpc4 GO:0042074 cell migration involved in gastrulation BFO:0000066 occurs_in ZFA:0000017 endoderm PATO:0001236 process quality abnormal ZDB-GENE-011119-1 118437 2239 gpc4 GO:0042074 cell migration involved in gastrulation BFO:0000066 occurs_in ZFA:0000017 endoderm PATO:0015003 decreased efficacy abnormal ZDB-GENE-011119-1 118437 2239 gpc4 GO:0060027 convergent extension involved in gastrulation BFO:0000066 occurs_in ZFA:0000017 endoderm PATO:0001236 process quality abnormal ZDB-GENE-011119-1 118437 2239 gpc4 GO:0060027 convergent extension involved in gastrulation BFO:0000066 occurs_in ZFA:0000017 endoderm PATO:0015003 decreased efficacy abnormal ZDB-GENE-011119-1 118437 2239 gpc4 ZFA:0000017 endoderm PATO:0000600 increased width abnormal ZDB-GENE-011119-1 118437 2239 gpc4 ZFA:0000017 endoderm PATO:0000628 mislocalised abnormal ZDB-GENE-011119-1 118437 2239 gpc4 ZFA:0009032 ciliated cell BFO:0000050 part_of ZFA:0000022 floor plate PATO:0002448 oriented towards abnormal BSPO:0000071 anterior region BFO:0000050 part_of ZFA:0000022 floor plate ZDB-GENE-011119-1 118437 2239 gpc4 ZFA:0000060 prechordal plate PATO:0001154 elongated abnormal ZDB-GENE-011119-1 118437 2239 gpc4 ZFA:0000092 axis PATO:0000574 decreased length abnormal ZDB-GENE-011119-1 118437 2239 gpc4 ZFA:0000092 axis PATO:0000600 increased width abnormal ZDB-GENE-011119-1 118437 2239 gpc4 ZFA:0000092 axis PATO:0002364 shortened abnormal ZDB-GENE-011119-1 118437 2239 gpc4 ZFA:0000095 pharyngeal arch 3-7 skeleton PATO:0000001 quality abnormal ZDB-GENE-011119-1 118437 2239 gpc4 ZFA:0000106 extension PATO:0000574 decreased length abnormal ZDB-GENE-011119-1 118437 2239 gpc4 ZFA:0000106 extension PATO:0001483 aplastic abnormal ZDB-GENE-011119-1 118437 2239 gpc4 ZFA:0000107 eye PATO:0000051 morphology abnormal ZDB-GENE-011119-1 118437 2239 gpc4 ZFA:0000107 eye PATO:0001924 mislocalised medially abnormal ZDB-GENE-011119-1 118437 2239 gpc4 ZFA:0000109 forebrain PATO:0000600 increased width abnormal ZDB-GENE-011119-1 118437 2239 gpc4 ZFA:0000131 neural keel PATO:0000574 decreased length abnormal ZDB-GENE-011119-1 118437 2239 gpc4 ZFA:0009000 cell BFO:0000050 part_of ZFA:0000135 notochord PATO:0000937 disorganized abnormal ZDB-GENE-011119-1 118437 2239 gpc4 ZFA:0000135 notochord PATO:0000001 quality abnormal ZDB-GENE-011119-1 118437 2239 gpc4 ZFA:0000135 notochord PATO:0000574 decreased length abnormal ZDB-GENE-011119-1 118437 2239 gpc4 ZFA:0000135 notochord PATO:0000600 increased width abnormal ZDB-GENE-011119-1 118437 2239 gpc4 ZFA:0000135 notochord PATO:0000967 undulate abnormal ZDB-GENE-011119-1 118437 2239 gpc4 ZFA:0009032 ciliated cell BFO:0000050 part_of ZFA:0000150 pronephric duct PATO:0002448 oriented towards abnormal BSPO:0000071 anterior region BFO:0000050 part_of ZFA:0000150 pronephric duct ZDB-GENE-011119-1 118437 2239 gpc4 ZFA:0000155 somite PATO:0000001 quality abnormal ZDB-GENE-011119-1 118437 2239 gpc4 ZFA:0000155 somite PATO:0000574 decreased length abnormal ZDB-GENE-011119-1 118437 2239 gpc4 ZFA:0000155 somite PATO:0000600 increased width abnormal ZDB-GENE-011119-1 118437 2239 gpc4 ZFA:0000155 somite PATO:0001879 U-shaped abnormal ZDB-GENE-011119-1 118437 2239 gpc4 ZFA:0000270 maxilla PATO:0000462 absent abnormal ZDB-GENE-011119-1 118437 2239 gpc4 ZFA:0000369 intermandibularis PATO:0000937 disorganized abnormal ZDB-GENE-011119-1 118437 2239 gpc4 ZFA:0000422 retroarticular PATO:0000462 absent abnormal ZDB-GENE-011119-1 118437 2239 gpc4 ZFA:0000422 retroarticular PATO:0000646 malformed abnormal ZDB-GENE-011119-1 118437 2239 gpc4 ZFA:0000422 retroarticular PATO:0002364 shortened abnormal ZDB-GENE-011119-1 118437 2239 gpc4 ZFA:0000621 quadrate PATO:0000462 absent abnormal ZDB-GENE-011119-1 118437 2239 gpc4 ZFA:0000692 symplectic PATO:0000574 decreased length abnormal ZDB-GENE-011119-1 118437 2239 gpc4 ZFA:0000692 symplectic PATO:0000591 increased thickness abnormal ZDB-GENE-011119-1 118437 2239 gpc4 ZFA:0000692 symplectic PATO:0000596 decreased volume abnormal ZDB-GENE-011119-1 118437 2239 gpc4 ZFA:0001056 myotome PATO:0000574 decreased length abnormal ZDB-GENE-011119-1 118437 2239 gpc4 ZFA:0001064 rhombomere PATO:0000600 increased width abnormal ZDB-GENE-011119-1 118437 2239 gpc4 ZFA:0009000 cell BFO:0000050 part_of ZFA:0001069 ventral fin fold PATO:0001852 dislocated abnormal ZFA:0000066 proctodeum ZDB-GENE-011119-1 118437 2239 gpc4 BSPO:0000013 anterior-posterior axis BFO:0000050 part_of ZFA:0001094 whole organism PATO:0000574 decreased length abnormal ZDB-GENE-011119-1 118437 2239 gpc4 BSPO:0000013 anterior-posterior axis BFO:0000050 part_of ZFA:0001094 whole organism PATO:0000969 dwarf-like abnormal ZDB-GENE-011119-1 118437 2239 gpc4 BSPO:0001001 medial-lateral axis BFO:0000050 part_of ZFA:0001094 whole organism PATO:0000573 increased length abnormal ZDB-GENE-011119-1 118437 2239 gpc4 ZFA:0001094 whole organism PATO:0002002 has extra parts of type abnormal ZFA:0001117 post-vent region ZDB-GENE-011119-1 118437 2239 gpc4 ZFA:0001094 whole organism PATO:0000051 morphology abnormal ZDB-GENE-011119-1 118437 2239 gpc4 ZFA:0001094 whole organism PATO:0000052 shape abnormal ZDB-GENE-011119-1 118437 2239 gpc4 ZFA:0001094 whole organism PATO:0000574 decreased length abnormal ZDB-GENE-011119-1 118437 2239 gpc4 ZFA:0001114 head PATO:0000587 decreased size abnormal ZDB-GENE-011119-1 118437 2239 gpc4 ZFA:0001115 trunk PATO:0000574 decreased length abnormal ZDB-GENE-011119-1 118437 2239 gpc4 ZFA:0000135 notochord BFO:0000050 part_of ZFA:0001117 post-vent region PATO:0001910 folded abnormal ZDB-GENE-011119-1 118437 2239 gpc4 ZFA:0001117 post-vent region PATO:0000001 quality abnormal ZDB-GENE-011119-1 118437 2239 gpc4 ZFA:0001117 post-vent region PATO:0000574 decreased length abnormal ZDB-GENE-011119-1 118437 2239 gpc4 ZFA:0001117 post-vent region PATO:0000646 malformed abnormal ZDB-GENE-011119-1 118437 2239 gpc4 ZFA:0001117 post-vent region PATO:0000936 truncated abnormal ZDB-GENE-011119-1 118437 2239 gpc4 ZFA:0001117 post-vent region PATO:0001617 deformed abnormal ZDB-GENE-011119-1 118437 2239 gpc4 ZFA:0001157 posterior lateral line primordium PATO:0000051 morphology abnormal ZDB-GENE-011119-1 118437 2239 gpc4 ZFA:0001157 posterior lateral line primordium PATO:0000411 circular abnormal ZDB-GENE-011119-1 118437 2239 gpc4 ZFA:0001157 posterior lateral line primordium PATO:0000591 increased thickness abnormal ZDB-GENE-011119-1 118437 2239 gpc4 ZFA:0001157 posterior lateral line primordium PATO:0000628 mislocalised abnormal ZDB-GENE-011119-1 118437 2239 gpc4 ZFA:0001157 posterior lateral line primordium PATO:0001919 mislocalised dorsally abnormal ZDB-GENE-011119-1 118437 2239 gpc4 ZFA:0001157 posterior lateral line primordium PATO:0001921 mislocalised anteriorly abnormal ZDB-GENE-011119-1 118437 2239 gpc4 GO:0060536 cartilage morphogenesis BFO:0000066 occurs_in ZFA:0001205 Meckel's cartilage PATO:0001236 process quality abnormal ZDB-GENE-011119-1 118437 2239 gpc4 ZFA:0009084 chondrocyte BFO:0000050 part_of ZFA:0001205 Meckel's cartilage PATO:0000051 morphology abnormal ZDB-GENE-011119-1 118437 2239 gpc4 ZFA:0009084 chondrocyte BFO:0000050 part_of ZFA:0001205 Meckel's cartilage PATO:0000411 circular abnormal ZDB-GENE-011119-1 118437 2239 gpc4 ZFA:0009084 chondrocyte BFO:0000050 part_of ZFA:0001205 Meckel's cartilage PATO:0000937 disorganized abnormal ZDB-GENE-011119-1 118437 2239 gpc4 ZFA:0009084 chondrocyte BFO:0000050 part_of ZFA:0001205 Meckel's cartilage PATO:0001769 positional polarity abnormal ZDB-GENE-011119-1 118437 2239 gpc4 ZFA:0001205 Meckel's cartilage PATO:0002434 perpendicular to abnormal BSPO:0000013 anterior-posterior axis BFO:0000050 part_of ZFA:0001094 whole organism ZDB-GENE-011119-1 118437 2239 gpc4 ZFA:0001205 Meckel's cartilage PATO:0000052 shape abnormal ZDB-GENE-011119-1 118437 2239 gpc4 ZFA:0001205 Meckel's cartilage PATO:0000141 structure abnormal ZDB-GENE-011119-1 118437 2239 gpc4 ZFA:0001205 Meckel's cartilage PATO:0001485 condensed abnormal ZDB-GENE-011119-1 118437 2239 gpc4 ZFA:0001205 Meckel's cartilage PATO:0001617 deformed abnormal ZDB-GENE-011119-1 118437 2239 gpc4 ZFA:0001205 Meckel's cartilage PATO:0002364 shortened abnormal ZDB-GENE-011119-1 118437 2239 gpc4 ZFA:0009084 chondrocyte BFO:0000050 part_of ZFA:0001227 mandibular arch skeleton PATO:0000051 morphology abnormal ZDB-GENE-011119-1 118437 2239 gpc4 ZFA:0009084 chondrocyte BFO:0000050 part_of ZFA:0001227 mandibular arch skeleton PATO:0000140 position abnormal ZDB-GENE-011119-1 118437 2239 gpc4 ZFA:0001239 ceratobranchial 5 bone PATO:0000462 absent abnormal ZDB-GENE-011119-1 118437 2239 gpc4 ZFA:0001321 neurocranial trabecula PATO:0000374 increased distance abnormal ZFA:0001321 neurocranial trabecula ZDB-GENE-011119-1 118437 2239 gpc4 ZFA:0001390 pancreatic bud PATO:0002169 split medially abnormal ZDB-GENE-011119-1 118437 2239 gpc4 ZFA:0001399 palatoquadrate cartilage PATO:0000574 decreased length abnormal ZDB-GENE-011119-1 118437 2239 gpc4 ZFA:0001399 palatoquadrate cartilage PATO:0000591 increased thickness abnormal ZDB-GENE-011119-1 118437 2239 gpc4 ZFA:0009084 chondrocyte BFO:0000050 part_of ZFA:0001400 ceratohyal cartilage PATO:0000411 circular abnormal ZDB-GENE-011119-1 118437 2239 gpc4 ZFA:0009084 chondrocyte BFO:0000050 part_of ZFA:0001400 ceratohyal cartilage PATO:0000587 decreased size abnormal ZDB-GENE-011119-1 118437 2239 gpc4 ZFA:0009084 chondrocyte BFO:0000050 part_of ZFA:0001400 ceratohyal cartilage PATO:0000937 disorganized abnormal ZDB-GENE-011119-1 118437 2239 gpc4 ZFA:0001400 ceratohyal cartilage PATO:0002434 perpendicular to abnormal BSPO:0000013 anterior-posterior axis BFO:0000050 part_of ZFA:0001094 whole organism ZDB-GENE-011119-1 118437 2239 gpc4 ZFA:0001400 ceratohyal cartilage PATO:0000141 structure abnormal ZDB-GENE-011119-1 118437 2239 gpc4 ZFA:0001400 ceratohyal cartilage PATO:0000574 decreased length abnormal ZDB-GENE-011119-1 118437 2239 gpc4 ZFA:0001400 ceratohyal cartilage PATO:0000591 increased thickness abnormal ZDB-GENE-011119-1 118437 2239 gpc4 ZFA:0001400 ceratohyal cartilage PATO:0000596 decreased volume abnormal ZDB-GENE-011119-1 118437 2239 gpc4 ZFA:0001400 ceratohyal cartilage PATO:0001485 condensed abnormal ZDB-GENE-011119-1 118437 2239 gpc4 ZFA:0001400 ceratohyal cartilage PATO:0001617 deformed abnormal ZDB-GENE-011119-1 118437 2239 gpc4 ZFA:0001405 ethmoid cartilage PATO:0000574 decreased length abnormal ZDB-GENE-011119-1 118437 2239 gpc4 GO:0031012 extracellular matrix BFO:0000050 part_of ZFA:0001458 cranial cartilage PATO:0000025 composition abnormal ZDB-GENE-011119-1 118437 2239 gpc4 ZFA:0001458 cranial cartilage PATO:0001617 deformed abnormal ZDB-GENE-011119-1 118437 2239 gpc4 ZFA:0001460 pharyngeal arch cartilage PATO:0001617 deformed abnormal ZDB-GENE-011119-1 118437 2239 gpc4 ZFA:0009084 chondrocyte BFO:0000050 part_of ZFA:0001511 interhyal cartilage PATO:0001997 decreased amount abnormal ZDB-GENE-011119-1 118437 2239 gpc4 ZFA:0001591 endochondral bone PATO:0000462 absent abnormal ZDB-GENE-011119-1 118437 2239 gpc4 ZFA:0001652 head muscle PATO:0000574 decreased length abnormal ZDB-GENE-011119-1 118437 2239 gpc4 ZFA:0009000 cell BFO:0000050 part_of ZFA:0001670 notochord posterior region PATO:0001505 separated from abnormal ZFA:0009000 cell BFO:0000050 part_of ZFA:0001670 notochord posterior region ZDB-GENE-011119-1 118437 2239 gpc4 ZFA:0001670 notochord posterior region PATO:0001910 folded abnormal ZDB-GENE-011119-1 118437 2239 gpc4 ZFA:0005113 dorsal lateral line neuromast PATO:0001769 positional polarity abnormal ZDB-GENE-011119-1 118437 2239 gpc4 ZFA:0005484 quadrate-anguloarticular joint PATO:0000051 morphology abnormal ZDB-GENE-011119-1 118437 2239 gpc4 ZFA:0009084 chondrocyte BFO:0000050 part_of ZFA:0005509 palate PATO:0000330 irregular spatial pattern abnormal ZDB-GENE-011119-1 118437 2239 gpc4 ZFA:0005509 palate PATO:0000574 decreased length abnormal ZDB-GENE-011119-1 118437 2239 gpc4 ZFA:0005509 palate PATO:0000600 increased width abnormal ZDB-GENE-011119-1 118437 2239 gpc4 ZFA:0005625 hypophyseal fenestra PATO:0000586 increased size abnormal ZDB-GENE-011119-1 118437 2239 gpc4 GO:0030010 establishment of cell polarity BFO:0000066 occurs_in ZFA:0005919 dorsal-ventral polarized posterior lateral line neuromast PATO:0001507 disrupted abnormal ZDB-GENE-011119-1 118437 2239 gpc4 ZFA:0009363 neuromast support cell BFO:0000050 part_of ZFA:0005919 dorsal-ventral polarized posterior lateral line neuromast PATO:0000140 position abnormal ZDB-GENE-011119-1 118437 2239 gpc4 ZFA:0009367 neuromast hair cell BFO:0000050 part_of ZFA:0005919 dorsal-ventral polarized posterior lateral line neuromast PATO:0000613 disoriented abnormal ZDB-GENE-011119-1 118437 2239 gpc4 ZFA:0009367 neuromast hair cell BFO:0000050 part_of ZFA:0005919 dorsal-ventral polarized posterior lateral line neuromast PATO:0001951 whorled abnormal ZDB-GENE-011119-1 118437 2239 gpc4 ZFA:0005919 dorsal-ventral polarized posterior lateral line neuromast PATO:0001769 positional polarity abnormal ZDB-GENE-011119-1 118437 2239 gpc4 ZFA:0009367 neuromast hair cell BFO:0000050 part_of ZFA:0005920 anterior-posterior polarized posterior lateral line neuromast PATO:0000613 disoriented abnormal ZDB-GENE-011119-1 118437 2239 gpc4 ZFA:0005920 anterior-posterior polarized posterior lateral line neuromast PATO:0001769 positional polarity abnormal ZDB-GENE-011119-1 118437 2239 gpc4 ZFA:0007016 anterior neural plate PATO:0000600 increased width abnormal ZDB-GENE-011119-1 118437 2239 gpc4 GO:0031012 extracellular matrix BFO:0000050 part_of ZFA:0009000 cell PATO:0000586 increased size abnormal ZDB-GENE-011119-1 118437 2239 gpc4 GO:0031012 extracellular matrix BFO:0000050 part_of ZFA:0009000 cell PATO:0002264 organization quality abnormal ZDB-GENE-011119-1 118437 2239 gpc4 ZFA:0009065 endothelial cell PATO:0000628 mislocalised abnormal ZDB-GENE-011119-1 118437 2239 gpc4 GO:0005815 microtubule organizing center BFO:0000050 part_of ZFA:0009084 chondrocyte PATO:0000937 disorganized abnormal ZDB-GENE-011119-1 118437 2239 gpc4 ZFA:0009116 slow muscle cell PATO:0000574 decreased length abnormal ZDB-GENE-011119-1 118437 2239 gpc4 ZFA:0009116 slow muscle cell PATO:0000937 disorganized abnormal ZDB-GENE-011128-10 140429 2780 gnat2 GO:0007601 visual perception PATO:0000001 quality abnormal ZDB-GENE-011128-10 140429 2780 gnat2 GO:0007632 visual behavior PATO:0000001 quality abnormal ZDB-GENE-011128-10 140429 2780 gnat2 ZFA:0000107 eye PATO:0000001 quality abnormal ZDB-GENE-011128-10 140429 2780 gnat2 ZFA:0000282 sensory system PATO:0000001 quality abnormal ZDB-GENE-011128-10 140429 2780 gnat2 ZFA:0009090 pigment cell PATO:0000001 quality abnormal ZDB-GENE-011128-10 140429 2780 gnat2 ZFA:0009091 melanocyte PATO:0000051 morphology abnormal ZDB-GENE-011128-2 140421 182 jag1a GO:0030878 thyroid gland development PATO:0002302 decreased process quality abnormal ZDB-GENE-011128-2 140421 182 jag1a GO:0048703 embryonic viscerocranium morphogenesis PATO:0002302 decreased process quality abnormal ZDB-GENE-011128-2 140421 182 jag1a ZFA:0009354 hematopoietic multipotent progenitor cell BFO:0000050 part_of ZFA:0000033 intermediate cell mass of mesoderm PATO:0001997 decreased amount abnormal ZDB-GENE-011128-2 140421 182 jag1a ZFA:0001158 endocrine system PATO:0002001 has fewer parts of type abnormal ZFA:0001072 thyroid follicle ZDB-GENE-011128-2 140421 182 jag1a ZFA:0001205 Meckel's cartilage PATO:0000587 decreased size abnormal ZDB-GENE-011128-2 140421 182 jag1a ZFA:0001399 palatoquadrate cartilage PATO:0000587 decreased size abnormal ZDB-GENE-011128-2 140421 182 jag1a ZFA:0001400 ceratohyal cartilage PATO:0000587 decreased size abnormal ZDB-GENE-011128-2 140421 182 jag1a ZFA:0009014 hematopoietic stem cell BFO:0000050 part_of ZFA:0005028 ventral wall of dorsal aorta PATO:0001997 decreased amount abnormal ZDB-GENE-011128-2 140421 182 jag1a ZFA:0009354 hematopoietic multipotent progenitor cell PATO:0001997 decreased amount abnormal ZDB-GENE-011128-3 140422 3714 jag2b GO:0039014 cell differentiation involved in pronephros development PATO:0001507 disrupted abnormal ZDB-GENE-011128-3 140422 3714 jag2b GO:0060218 hematopoietic stem cell differentiation PATO:0002302 decreased process quality abnormal ZDB-GENE-011128-3 140422 3714 jag2b GO:0060271 cilium assembly PATO:0002051 increased occurrence abnormal ZDB-GENE-011128-3 140422 3714 jag2b ZFA:0000014 dorsal aorta PATO:0002001 has fewer parts of type abnormal ZFA:0009014 hematopoietic stem cell ZDB-GENE-011128-3 140422 3714 jag2b ZFA:0009052 motor neuron BFO:0000050 part_of ZFA:0000075 spinal cord PATO:0000470 increased amount abnormal ZDB-GENE-011128-3 140422 3714 jag2b ZFA:0009052 motor neuron BFO:0000050 part_of ZFA:0000075 spinal cord PATO:0000628 mislocalised abnormal ZDB-GENE-011128-3 140422 3714 jag2b ZFA:0009276 GABAergic neuron BFO:0000050 part_of ZFA:0000075 spinal cord PATO:0000470 increased amount abnormal ZDB-GENE-011128-3 140422 3714 jag2b ZFA:0009276 GABAergic neuron BFO:0000050 part_of ZFA:0000075 spinal cord PATO:0000628 mislocalised abnormal ZDB-GENE-011128-3 140422 3714 jag2b GO:0060070 canonical Wnt signaling pathway BFO:0000066 occurs_in ZFA:0000123 liver PATO:0002052 decreased occurrence abnormal ZDB-GENE-011128-3 140422 3714 jag2b GO:0005929 cilium BFO:0000050 part_of ZFA:0000151 pronephros PATO:0000470 increased amount abnormal ZDB-GENE-011128-3 140422 3714 jag2b GO:1903251 multi-ciliated epithelial cell differentiation BFO:0000066 occurs_in ZFA:0000151 pronephros PATO:0002051 increased occurrence abnormal ZDB-GENE-011128-3 140422 3714 jag2b ZFA:0005242 multi-ciliated epithelial cell BFO:0000050 part_of ZFA:0000151 pronephros PATO:0000470 increased amount abnormal ZDB-GENE-011128-3 140422 3714 jag2b GO:0007219 Notch signaling pathway BFO:0000066 occurs_in ZFA:0000155 somite PATO:0002302 decreased process quality abnormal ZDB-GENE-011128-3 140422 3714 jag2b GO:0043292 contractile fiber BFO:0000050 part_of ZFA:0000563 pectoral fin musculature PATO:0000646 malformed abnormal ZDB-GENE-011128-3 140422 3714 jag2b GO:0005884 actin filament BFO:0000050 part_of ZFA:0001161 pectoral fin PATO:0000628 mislocalised abnormal ZDB-GENE-011128-3 140422 3714 jag2b GO:0060070 canonical Wnt signaling pathway BFO:0000066 occurs_in ZFA:0001249 exocrine pancreas PATO:0002052 decreased occurrence abnormal ZDB-GENE-011128-3 140422 3714 jag2b ZFA:0001456 pectoral fin endoskeletal disc PATO:0000937 disorganized abnormal ZDB-GENE-011128-3 140422 3714 jag2b ZFA:0001558 pronephric tubule PATO:0002002 has extra parts of type abnormal ZFA:0005242 multi-ciliated epithelial cell BFO:0000050 part_of ZFA:0001558 pronephric tubule ZDB-GENE-011128-3 140422 3714 jag2b GO:0060218 hematopoietic stem cell differentiation BFO:0000066 occurs_in ZFA:0005028 ventral wall of dorsal aorta PATO:0002302 decreased process quality abnormal ZDB-GENE-011128-3 140422 3714 jag2b ZFA:0005028 ventral wall of dorsal aorta PATO:0002001 has fewer parts of type abnormal ZFA:0009014 hematopoietic stem cell ZDB-GENE-011128-4 140423 182 jag1b GO:0030878 thyroid gland development PATO:0002302 decreased process quality abnormal ZDB-GENE-011128-4 140423 182 jag1b GO:0048703 embryonic viscerocranium morphogenesis PATO:0002302 decreased process quality abnormal ZDB-GENE-011128-4 140423 182 jag1b GO:0048839 inner ear development PATO:0001749 paedomorphic growth abnormal ZDB-GENE-011128-4 140423 182 jag1b BSPO:0000013 anterior-posterior axis BFO:0000050 part_of ZFA:0000051 otic vesicle PATO:0000574 decreased length abnormal ZDB-GENE-011128-4 140423 182 jag1b ZFA:0000566 posterior crista BFO:0000050 part_of ZFA:0000051 otic vesicle PATO:0000462 absent abnormal ZDB-GENE-011128-4 140423 182 jag1b ZFA:0000566 posterior crista BFO:0000050 part_of ZFA:0000051 otic vesicle PATO:0000638 apoptotic abnormal ZDB-GENE-011128-4 140423 182 jag1b ZFA:0000619 anterior crista BFO:0000050 part_of ZFA:0000051 otic vesicle PATO:0000462 absent abnormal ZDB-GENE-011128-4 140423 182 jag1b ZFA:0000217 inner ear PATO:0000574 decreased length abnormal ZDB-GENE-011128-4 140423 182 jag1b ZFA:0000220 lateral semicircular canal PATO:0000587 decreased size abnormal ZDB-GENE-011128-4 140423 182 jag1b ZFA:0000250 opercle PATO:0000406 curved abnormal ZDB-GENE-011128-4 140423 182 jag1b ZFA:0000250 opercle PATO:0000587 decreased size abnormal ZDB-GENE-011128-4 140423 182 jag1b ZFA:0000250 opercle PATO:0000599 decreased width abnormal ZDB-GENE-011128-4 140423 182 jag1b ZFA:0009366 hair cell BFO:0000050 part_of ZFA:0000566 posterior crista PATO:0000462 absent abnormal ZDB-GENE-011128-4 140423 182 jag1b ZFA:0009366 hair cell BFO:0000050 part_of ZFA:0000619 anterior crista PATO:0000462 absent abnormal ZDB-GENE-011128-4 140423 182 jag1b ZFA:0000672 hyomandibula PATO:0000051 morphology abnormal ZDB-GENE-011128-4 140423 182 jag1b ZFA:0000672 hyomandibula PATO:0000587 decreased size abnormal ZDB-GENE-011128-4 140423 182 jag1b ZFA:0001081 thyroid primordium PATO:0000646 malformed abnormal ZDB-GENE-011128-4 140423 182 jag1b ZFA:0001094 whole organism PATO:0001422 dead abnormal ZDB-GENE-011128-4 140423 182 jag1b ZFA:0001158 endocrine system PATO:0002001 has fewer parts of type abnormal ZFA:0001072 thyroid follicle ZDB-GENE-011128-4 140423 182 jag1b ZFA:0001205 Meckel's cartilage PATO:0000587 decreased size abnormal ZDB-GENE-011128-4 140423 182 jag1b ZFA:0001227 mandibular arch skeleton PATO:0000051 morphology abnormal ZDB-GENE-011128-4 140423 182 jag1b ZFA:0001399 palatoquadrate cartilage PATO:0000051 morphology abnormal ZDB-GENE-011128-4 140423 182 jag1b ZFA:0001399 palatoquadrate cartilage PATO:0000587 decreased size abnormal ZDB-GENE-011128-4 140423 182 jag1b ZFA:0001399 palatoquadrate cartilage PATO:0000646 malformed abnormal ZDB-GENE-011128-4 140423 182 jag1b ZFA:0001399 palatoquadrate cartilage PATO:0000936 truncated abnormal ZDB-GENE-011128-4 140423 182 jag1b ZFA:0001400 ceratohyal cartilage PATO:0000587 decreased size abnormal ZDB-GENE-011128-4 140423 182 jag1b ZFA:0001422 hyosymplectic cartilage PATO:0000646 malformed abnormal ZDB-GENE-011128-4 140423 182 jag1b ZFA:0001422 hyosymplectic cartilage PATO:0001617 deformed abnormal ZDB-GENE-011128-4 140423 182 jag1b ZFA:0001715 otic vesicle protrusion PATO:0000052 shape abnormal ZDB-GENE-011128-4 140423 182 jag1b ZFA:0001715 otic vesicle protrusion PATO:0000646 malformed abnormal ZDB-GENE-011128-4 140423 182 jag1b ZFA:0005386 foramen PATO:0000586 increased size abnormal ZDB-GENE-011128-4 140423 182 jag1b ZFA:0007054 pillar of the anterior semicircular canal PATO:0000591 increased thickness abnormal ZDB-GENE-011128-4 140423 182 jag1b ZFA:0007055 pillar of the lateral semicircular canal PATO:0000591 increased thickness abnormal ZDB-GENE-011128-7 140424 3000 gucy2f GO:0007601 visual perception PATO:0002302 decreased process quality abnormal ZDB-GENE-011128-7 140424 3000 gucy2f ZFA:0000152 retina PATO:0001780 dystrophic abnormal ZDB-GENE-011128-7 140424 3000 gucy2f ZFA:0001466 photoreceptor outer segment layer PATO:0002364 shortened abnormal ZDB-GENE-011128-7 140424 3000 gucy2f ZFA:0009262 retinal cone cell PATO:0001997 decreased amount abnormal ZDB-GENE-011128-9 140426 3000 gucy2d GO:0007601 visual perception PATO:0000001 quality abnormal ZDB-GENE-011128-9 140426 3000 gucy2d GO:0007632 visual behavior PATO:0000001 quality abnormal ZDB-GENE-011128-9 140426 3000 gucy2d GO:0007634 optokinetic behavior PATO:0000297 arrested abnormal ZDB-GENE-011128-9 140426 3000 gucy2d GO:0071632 optomotor response PATO:0000297 arrested abnormal ZDB-GENE-011207-1 140616 6663 sox10 GO:0002244 hematopoietic progenitor cell differentiation PATO:0002052 decreased occurrence abnormal ZDB-GENE-011207-1 140616 6663 sox10 GO:0008347 glial cell migration PATO:0001507 disrupted abnormal ZDB-GENE-011207-1 140616 6663 sox10 GO:0014037 Schwann cell differentiation PATO:0000297 arrested abnormal ZDB-GENE-011207-1 140616 6663 sox10 GO:0014044 Schwann cell development PATO:0000297 arrested abnormal ZDB-GENE-011207-1 140616 6663 sox10 GO:0014044 Schwann cell development PATO:0001507 disrupted abnormal ZDB-GENE-011207-1 140616 6663 sox10 GO:0032288 myelin assembly PATO:0001507 disrupted abnormal ZDB-GENE-011207-1 140616 6663 sox10 GO:0036484 trunk neural crest cell migration PATO:0000297 arrested abnormal ZDB-GENE-011207-1 140616 6663 sox10 GO:0042472 inner ear morphogenesis PATO:0002302 decreased process quality abnormal ZDB-GENE-011207-1 140616 6663 sox10 GO:0043473 pigmentation PATO:0001507 disrupted abnormal ZDB-GENE-011207-1 140616 6663 sox10 GO:0048589 developmental growth PATO:0000911 decreased rate abnormal ZDB-GENE-011207-1 140616 6663 sox10 GO:0048709 oligodendrocyte differentiation PATO:0000297 arrested abnormal ZDB-GENE-011207-1 140616 6663 sox10 GO:0048752 semicircular canal morphogenesis PATO:0001507 disrupted abnormal ZDB-GENE-011207-1 140616 6663 sox10 GO:0060879 semicircular canal fusion PATO:0000297 arrested abnormal ZDB-GENE-011207-1 140616 6663 sox10 GO:0097324 melanocyte migration PATO:0001507 disrupted abnormal ZDB-GENE-011207-1 140616 6663 sox10 GO:0120054 intestinal motility PATO:0001236 process quality abnormal ZDB-GENE-011207-1 140616 6663 sox10 ZFA:0000030 macula utricle PATO:0001241 physical object quality abnormal ZDB-GENE-011207-1 140616 6663 sox10 BSPO:0000071 anterior region BFO:0000050 part_of ZFA:0000051 otic vesicle PATO:0001241 physical object quality abnormal ZDB-GENE-011207-1 140616 6663 sox10 ZFA:0009034 epithelial cell BFO:0000050 part_of ZFA:0000051 otic vesicle PATO:0000638 apoptotic abnormal ZDB-GENE-011207-1 140616 6663 sox10 ZFA:0009366 hair cell BFO:0000050 part_of ZFA:0000051 otic vesicle PATO:0000470 increased amount abnormal ZDB-GENE-011207-1 140616 6663 sox10 ZFA:0000051 otic vesicle PATO:0000052 shape abnormal ZDB-GENE-011207-1 140616 6663 sox10 ZFA:0000051 otic vesicle PATO:0000587 decreased size abnormal ZDB-GENE-011207-1 140616 6663 sox10 ZFA:0000051 otic vesicle PATO:0001602 distended abnormal ZDB-GENE-011207-1 140616 6663 sox10 BSPO:0000063 dorsal side BFO:0000050 part_of ZFA:0000075 spinal cord PATO:0000638 apoptotic abnormal ZDB-GENE-011207-1 140616 6663 sox10 GO:0008283 cell population proliferation BFO:0000066 occurs_in ZFA:0000112 gut PATO:0002051 increased occurrence abnormal ZDB-GENE-011207-1 140616 6663 sox10 ZFA:0009327 neutrophil BFO:0000050 part_of ZFA:0000112 gut PATO:0000470 increased amount abnormal ZDB-GENE-011207-1 140616 6663 sox10 ZFA:0000166 lateral crista PATO:0001241 physical object quality abnormal ZDB-GENE-011207-1 140616 6663 sox10 ZFA:0000168 anterior macula PATO:0000642 fused with abnormal ZFA:0000558 posterior macula ZDB-GENE-011207-1 140616 6663 sox10 ZFA:0000168 anterior macula PATO:0000628 mislocalised abnormal ZDB-GENE-011207-1 140616 6663 sox10 GO:0030424 axon BFO:0000050 part_of ZFA:0000175 posterior lateral line nerve PATO:0001997 decreased amount abnormal ZDB-GENE-011207-1 140616 6663 sox10 GO:0034706 sodium channel complex BFO:0000050 part_of ZFA:0000175 posterior lateral line nerve PATO:0000616 asymmetrical abnormal ZDB-GENE-011207-1 140616 6663 sox10 GO:0034706 sodium channel complex BFO:0000050 part_of ZFA:0000175 posterior lateral line nerve PATO:0001154 elongated abnormal ZDB-GENE-011207-1 140616 6663 sox10 GO:0034706 sodium channel complex BFO:0000050 part_of ZFA:0000175 posterior lateral line nerve PATO:0001567 undistributed abnormal ZDB-GENE-011207-1 140616 6663 sox10 GO:0034706 sodium channel complex BFO:0000050 part_of ZFA:0000175 posterior lateral line nerve PATO:0001997 decreased amount abnormal ZDB-GENE-011207-1 140616 6663 sox10 GO:0043209 myelin sheath BFO:0000050 part_of ZFA:0000175 posterior lateral line nerve PATO:0000462 absent abnormal ZDB-GENE-011207-1 140616 6663 sox10 ZFA:0009135 myelinating Schwann cell BFO:0000050 part_of ZFA:0000175 posterior lateral line nerve PATO:0000462 absent abnormal ZDB-GENE-011207-1 140616 6663 sox10 ZFA:0000175 posterior lateral line nerve PATO:0000628 mislocalised abnormal ZDB-GENE-011207-1 140616 6663 sox10 ZFA:0000175 posterior lateral line nerve PATO:0001959 defasciculated abnormal ZDB-GENE-011207-1 140616 6663 sox10 ZFA:0000200 dorsal root ganglion PATO:0000462 absent abnormal ZDB-GENE-011207-1 140616 6663 sox10 ZFA:0000200 dorsal root ganglion PATO:0000470 increased amount abnormal ZDB-GENE-011207-1 140616 6663 sox10 ZFA:0000200 dorsal root ganglion PATO:0000628 mislocalised abnormal ZDB-GENE-011207-1 140616 6663 sox10 ZFA:0000200 dorsal root ganglion PATO:0001997 decreased amount abnormal ZDB-GENE-011207-1 140616 6663 sox10 ZFA:0000217 inner ear PATO:0000001 quality abnormal ZDB-GENE-011207-1 140616 6663 sox10 ZFA:0000217 inner ear PATO:0000587 decreased size abnormal ZDB-GENE-011207-1 140616 6663 sox10 ZFA:0000217 inner ear PATO:0000646 malformed abnormal ZDB-GENE-011207-1 140616 6663 sox10 ZFA:0000225 lateral crista primordium PATO:0001241 physical object quality abnormal ZDB-GENE-011207-1 140616 6663 sox10 ZFA:0000225 lateral crista primordium PATO:0001483 aplastic abnormal ZDB-GENE-011207-1 140616 6663 sox10 ZFA:0000243 neuromast PATO:0000001 quality abnormal ZDB-GENE-011207-1 140616 6663 sox10 ZFA:0000262 posterior semicircular canal PATO:0001483 aplastic abnormal ZDB-GENE-011207-1 140616 6663 sox10 ZFA:0000282 sensory system PATO:0000001 quality abnormal ZDB-GENE-011207-1 140616 6663 sox10 ZFA:0000314 anterior semicircular canal PATO:0001483 aplastic abnormal ZDB-GENE-011207-1 140616 6663 sox10 ZFA:0000368 integument PATO:0002000 lacks all parts of type abnormal ZFA:0009090 pigment cell ZDB-GENE-011207-1 140616 6663 sox10 ZFA:0009366 hair cell BFO:0000050 part_of ZFA:0000386 macula PATO:0000628 mislocalised abnormal ZDB-GENE-011207-1 140616 6663 sox10 ZFA:0000411 posterior crista primordium PATO:0001241 physical object quality abnormal ZDB-GENE-011207-1 140616 6663 sox10 ZFA:0000431 semicircular canal PATO:0000051 morphology abnormal ZDB-GENE-011207-1 140616 6663 sox10 ZFA:0000431 semicircular canal PATO:0000592 decreased thickness abnormal ZDB-GENE-011207-1 140616 6663 sox10 ZFA:0000431 semicircular canal PATO:0000646 malformed abnormal ZDB-GENE-011207-1 140616 6663 sox10 ZFA:0000431 semicircular canal PATO:0000937 disorganized abnormal ZDB-GENE-011207-1 140616 6663 sox10 ZFA:0000431 semicircular canal PATO:0001241 physical object quality abnormal ZDB-GENE-011207-1 140616 6663 sox10 ZFA:0009359 microvillous olfactory receptor neuron BFO:0000050 part_of ZFA:0000554 olfactory epithelium PATO:0000937 disorganized abnormal ZDB-GENE-011207-1 140616 6663 sox10 ZFA:0000554 olfactory epithelium PATO:0001999 lacks parts or has fewer parts of type abnormal ZFA:0009359 microvillous olfactory receptor neuron BFO:0000050 part_of ZFA:0000554 olfactory epithelium ZDB-GENE-011207-1 140616 6663 sox10 ZFA:0000558 posterior macula PATO:0000628 mislocalised abnormal ZDB-GENE-011207-1 140616 6663 sox10 ZFA:0000559 otolith organ PATO:0000587 decreased size abnormal ZDB-GENE-011207-1 140616 6663 sox10 ZFA:0009366 hair cell BFO:0000050 part_of ZFA:0000566 posterior crista PATO:0000470 increased amount abnormal ZDB-GENE-011207-1 140616 6663 sox10 ZFA:0000566 posterior crista PATO:0001241 physical object quality abnormal ZDB-GENE-011207-1 140616 6663 sox10 ZFA:0009248 neuron BFO:0000050 part_of ZFA:0000588 statoacoustic (VIII) ganglion PATO:0000638 apoptotic abnormal ZDB-GENE-011207-1 140616 6663 sox10 ZFA:0009366 hair cell BFO:0000050 part_of ZFA:0000619 anterior crista PATO:0000470 increased amount abnormal ZDB-GENE-011207-1 140616 6663 sox10 ZFA:0000619 anterior crista PATO:0001241 physical object quality abnormal ZDB-GENE-011207-1 140616 6663 sox10 ZFA:0000940 posterior lateral line neuromast PATO:0000001 quality abnormal ZDB-GENE-011207-1 140616 6663 sox10 ZFA:0009073 glial cell BFO:0000050 part_of ZFA:0000944 posterior lateral line PATO:0000462 absent abnormal ZDB-GENE-011207-1 140616 6663 sox10 CHEBI:89634 Melanin BFO:0000050 part_of ZFA:0001094 whole organism PATO:0001997 decreased amount abnormal ZDB-GENE-011207-1 140616 6663 sox10 ZFA:0001094 whole organism PATO:0002000 lacks all parts of type abnormal ZFA:0009091 melanocyte ZDB-GENE-011207-1 140616 6663 sox10 ZFA:0001094 whole organism PATO:0002000 lacks all parts of type abnormal ZFA:0009198 xanthophore ZDB-GENE-011207-1 140616 6663 sox10 ZFA:0001094 whole organism PATO:0002000 lacks all parts of type abnormal ZFA:0009199 iridophore ZDB-GENE-011207-1 140616 6663 sox10 ZFA:0001094 whole organism PATO:0002000 lacks all parts of type abnormal ZFA:0009249 melanoblast ZDB-GENE-011207-1 140616 6663 sox10 ZFA:0001094 whole organism PATO:0000169 viability abnormal ZDB-GENE-011207-1 140616 6663 sox10 ZFA:0001094 whole organism PATO:0000718 lethal (sensu genetics) abnormal ZDB-GENE-011207-1 140616 6663 sox10 ZFA:0001094 whole organism PATO:0002251 decreased pigmentation abnormal ZDB-GENE-011207-1 140616 6663 sox10 ZFA:0009090 pigment cell BFO:0000050 part_of ZFA:0001114 head PATO:0000462 absent abnormal ZDB-GENE-011207-1 140616 6663 sox10 ZFA:0009090 pigment cell BFO:0000050 part_of ZFA:0001115 trunk PATO:0000462 absent abnormal ZDB-GENE-011207-1 140616 6663 sox10 ZFA:0009249 melanoblast BFO:0000050 part_of ZFA:0001117 post-vent region PATO:0001997 decreased amount abnormal ZDB-GENE-011207-1 140616 6663 sox10 ZFA:0009073 glial cell BFO:0000050 part_of ZFA:0001155 enteric nervous system PATO:0001997 decreased amount abnormal ZDB-GENE-011207-1 140616 6663 sox10 ZFA:0009248 neuron BFO:0000050 part_of ZFA:0001155 enteric nervous system PATO:0000462 absent abnormal ZDB-GENE-011207-1 140616 6663 sox10 ZFA:0009248 neuron BFO:0000050 part_of ZFA:0001155 enteric nervous system PATO:0001997 decreased amount abnormal ZDB-GENE-011207-1 140616 6663 sox10 ZFA:0001273 ventral mandibular arch PATO:0000051 morphology abnormal ZDB-GENE-011207-1 140616 6663 sox10 ZFA:0001329 retinal inner plexiform layer PATO:0000051 morphology abnormal ZDB-GENE-011207-1 140616 6663 sox10 ZFA:0001329 retinal inner plexiform layer PATO:0001781 irregular thickness abnormal ZDB-GENE-011207-1 140616 6663 sox10 ZFA:0001334 presumptive enteric nervous system PATO:0001483 aplastic abnormal ZDB-GENE-011207-1 140616 6663 sox10 GO:0030432 peristalsis BFO:0000066 occurs_in ZFA:0001338 intestine PATO:0002051 increased occurrence abnormal ZDB-GENE-011207-1 140616 6663 sox10 ZFA:0001460 pharyngeal arch cartilage PATO:0000051 morphology abnormal ZDB-GENE-011207-1 140616 6663 sox10 ZFA:0001469 lateral line PATO:0000001 quality abnormal ZDB-GENE-011207-1 140616 6663 sox10 ZFA:0001516 ceratobranchial cartilage PATO:0000462 absent abnormal ZDB-GENE-011207-1 140616 6663 sox10 ZFA:0001617 otolith PATO:0000375 decreased distance abnormal ZFA:0001617 otolith ZDB-GENE-011207-1 140616 6663 sox10 ZFA:0001617 otolith PATO:0000001 quality abnormal ZDB-GENE-011207-1 140616 6663 sox10 ZFA:0001617 otolith PATO:0000587 decreased size abnormal ZDB-GENE-011207-1 140616 6663 sox10 ZFA:0001634 perichondrium PATO:0000937 disorganized abnormal ZDB-GENE-011207-1 140616 6663 sox10 ZFA:0005775 enteric neuron PATO:0000462 absent abnormal ZDB-GENE-011207-1 140616 6663 sox10 ZFA:0005850 nucleus of the caudal commissure PATO:0001997 decreased amount abnormal ZDB-GENE-011207-1 140616 6663 sox10 ZFA:0007067 vagal ganglion PATO:0000646 malformed abnormal ZDB-GENE-011207-1 140616 6663 sox10 ZFA:0009046 T cell PATO:0001997 decreased amount abnormal ZDB-GENE-011207-1 140616 6663 sox10 GO:0030424 axon BFO:0000050 part_of ZFA:0009052 motor neuron PATO:0000141 structure abnormal ZDB-GENE-011207-1 140616 6663 sox10 GO:0030424 axon BFO:0000050 part_of ZFA:0009052 motor neuron PATO:0001959 defasciculated abnormal ZDB-GENE-011207-1 140616 6663 sox10 GO:0030175 filopodium BFO:0000050 part_of ZFA:0009073 glial cell PATO:0000303 increased speed abnormal ZDB-GENE-011207-1 140616 6663 sox10 GO:0030175 filopodium BFO:0000050 part_of ZFA:0009073 glial cell PATO:0000573 increased length abnormal ZDB-GENE-011207-1 140616 6663 sox10 ZFA:0009073 glial cell PATO:0000628 mislocalised abnormal ZDB-GENE-011207-1 140616 6663 sox10 ZFA:0009090 pigment cell PATO:0000001 quality abnormal ZDB-GENE-011207-1 140616 6663 sox10 ZFA:0009090 pigment cell PATO:0000060 spatial pattern abnormal ZDB-GENE-011207-1 140616 6663 sox10 ZFA:0009090 pigment cell PATO:0000330 irregular spatial pattern abnormal ZDB-GENE-011207-1 140616 6663 sox10 ZFA:0009091 melanocyte PATO:0000001 quality abnormal ZDB-GENE-011207-1 140616 6663 sox10 ZFA:0009091 melanocyte PATO:0000462 absent abnormal ZDB-GENE-011207-1 140616 6663 sox10 ZFA:0009091 melanocyte PATO:0001997 decreased amount abnormal ZDB-GENE-011207-1 140616 6663 sox10 GO:0042552 myelination BFO:0000066 occurs_in ZFA:0009135 myelinating Schwann cell PATO:0001507 disrupted abnormal ZDB-GENE-011207-1 140616 6663 sox10 ZFA:0009135 myelinating Schwann cell PATO:0000051 morphology abnormal ZDB-GENE-011207-1 140616 6663 sox10 ZFA:0009135 myelinating Schwann cell PATO:0000462 absent abnormal ZDB-GENE-011207-1 140616 6663 sox10 ZFA:0009165 neural crest cell PATO:0000638 apoptotic abnormal ZDB-GENE-011207-1 140616 6663 sox10 ZFA:0009165 neural crest cell PATO:0001997 decreased amount abnormal ZDB-GENE-011207-1 140616 6663 sox10 ZFA:0009198 xanthophore PATO:0000001 quality abnormal ZDB-GENE-011207-1 140616 6663 sox10 ZFA:0009198 xanthophore PATO:0000051 morphology abnormal ZDB-GENE-011207-1 140616 6663 sox10 ZFA:0009198 xanthophore PATO:0001422 dead abnormal ZDB-GENE-011207-1 140616 6663 sox10 ZFA:0009199 iridophore PATO:0001997 decreased amount abnormal ZDB-GENE-011207-1 140616 6663 sox10 ZFA:0009249 melanoblast PATO:0000462 absent abnormal ZDB-GENE-011207-1 140616 6663 sox10 ZFA:0009249 melanoblast PATO:0001997 decreased amount abnormal ZDB-GENE-011207-1 140616 6663 sox10 GO:0044297 cell body BFO:0000050 part_of ZFA:0009280 Muller cell PATO:0000060 spatial pattern abnormal ZDB-GENE-011207-1 140616 6663 sox10 GO:0044297 cell body BFO:0000050 part_of ZFA:0009280 Muller cell PATO:0000140 position abnormal ZDB-GENE-011207-1 140616 6663 sox10 GO:0097386 glial cell projection BFO:0000050 part_of ZFA:0009280 Muller cell PATO:0001590 overlap with abnormal GO:0097386 glial cell projection BFO:0000050 part_of ZFA:0009280 Muller cell ZDB-GENE-011207-1 140616 6663 sox10 ZFA:0009280 Muller cell PATO:0001241 physical object quality abnormal ZDB-GENE-011207-1 140616 6663 sox10 ZFA:0009354 hematopoietic multipotent progenitor cell PATO:0001997 decreased amount abnormal ZDB-GENE-011210-1 140621 836 casp3a GO:0055113 epiboly involved in gastrulation with mouth forming second PATO:0000297 arrested abnormal ZDB-GENE-011210-1 140621 836 casp3a GO:0055113 epiboly involved in gastrulation with mouth forming second PATO:0001507 disrupted abnormal ZDB-GENE-011210-1 140621 836 casp3a ZFA:0001094 whole organism PATO:0000620 wholly dorsalized abnormal ZDB-GENE-011210-1 140621 836 casp3a GO:0004197 cysteine-type endopeptidase activity BFO:0000050 part_of ZFA:0009310 retinal ganglion cell PATO:0002052 decreased occurrence abnormal ZDB-GENE-011210-1 140621 836 casp3a GO:0016322 neuron remodeling BFO:0000066 occurs_in ZFA:0009310 retinal ganglion cell PATO:0002302 decreased process quality abnormal ZDB-GENE-011210-1 140621 836 casp3a GO:0030424 axon BFO:0000050 part_of ZFA:0009310 retinal ganglion cell PATO:0001241 physical object quality abnormal ZDB-GENE-011210-1 140621 836 casp3a GO:0044303 axon collateral BFO:0000050 part_of ZFA:0009310 retinal ganglion cell PATO:0001241 physical object quality abnormal ZDB-GENE-011210-1 140621 836 casp3a GO:0048669 collateral sprouting in absence of injury BFO:0000066 occurs_in ZFA:0009310 retinal ganglion cell PATO:0000057 occurrence abnormal ZDB-GENE-011210-2 140614 7494 xbp1 GO:0001889 liver development PATO:0001507 disrupted abnormal ZDB-GENE-011210-2 140614 7494 xbp1 GO:0035188 hatching PATO:0000297 arrested abnormal ZDB-GENE-011210-2 140614 7494 xbp1 GO:0048785 hatching gland development PATO:0000297 arrested abnormal ZDB-GENE-011210-2 140614 7494 xbp1 ZFA:0000123 liver PATO:0000587 decreased size abnormal ZDB-GENE-011210-2 140614 7494 xbp1 ZFA:0000329 chorion PATO:0000467 present abnormal ZDB-GENE-011210-2 140614 7494 xbp1 ZFA:0001249 exocrine pancreas PATO:0000587 decreased size abnormal ZDB-GENE-011210-2 140614 7494 xbp1 GO:0030141 secretory granule BFO:0000050 part_of ZFA:0009151 hatching gland cell PATO:0000587 decreased size abnormal ZDB-GENE-011210-2 140614 7494 xbp1 GO:0030141 secretory granule BFO:0000050 part_of ZFA:0009151 hatching gland cell PATO:0001997 decreased amount abnormal ZDB-GENE-011210-2 140614 7494 xbp1 ZFA:0009327 neutrophil PATO:0001997 decreased amount abnormal ZDB-GENE-011212-1 140615 9415 fads2 CHEBI:17351 linoleic acid BFO:0000050 part_of ZFA:0000123 liver PATO:0000470 increased amount abnormal ZDB-GENE-011212-1 140615 9415 fads2 CHEBI:26208 polyunsaturated fatty acid BFO:0000050 part_of ZFA:0000123 liver PATO:0000470 increased amount abnormal ZDB-GENE-011212-1 140615 9415 fads2 CHEBI:26607 saturated fatty acid BFO:0000050 part_of ZFA:0000123 liver PATO:0001997 decreased amount abnormal ZDB-GENE-011212-1 140615 9415 fads2 CHEBI:27432 alpha-linolenic acid BFO:0000050 part_of ZFA:0000123 liver PATO:0000470 increased amount abnormal ZDB-GENE-011212-1 140615 9415 fads2 CHEBI:28661 gamma-linolenic acid BFO:0000050 part_of ZFA:0000123 liver PATO:0001997 decreased amount abnormal ZDB-GENE-011212-1 140615 9415 fads2 CHEBI:32389 all-cis-octadeca-6,9,12,15-tetraenoic acid BFO:0000050 part_of ZFA:0000123 liver PATO:0001997 decreased amount abnormal ZDB-GENE-011212-1 140615 9415 fads2 CHEBI:36005 docosahexaenoic acid BFO:0000050 part_of ZFA:0000123 liver PATO:0001997 decreased amount abnormal ZDB-GENE-011212-1 140615 9415 fads2 CHEBI:61204 docosapentaenoic acid BFO:0000050 part_of ZFA:0000123 liver PATO:0000470 increased amount abnormal ZDB-GENE-011212-1 140615 9415 fads2 ZFA:0000303 female organism PATO:0001834 decreased fertility abnormal ZDB-GENE-011212-1 140615 9415 fads2 GO:0006636 unsaturated fatty acid biosynthetic process BFO:0000066 occurs_in ZFA:0001570 unfertilized egg PATO:0001507 disrupted abnormal ZDB-GENE-011212-3 140599 7431 vim GO:0031101 fin regeneration PATO:0001236 process quality abnormal ZDB-GENE-011212-3 140599 7431 vim GO:0031101 fin regeneration PATO:0002302 decreased process quality abnormal ZDB-GENE-011212-3 140599 7431 vim GO:0042060 wound healing PATO:0002302 decreased process quality abnormal ZDB-GENE-011212-3 140599 7431 vim ZFA:0001269 regenerating fin PATO:0002058 decreased area abnormal ZDB-GENE-011212-5 140620 5631 prps1a GO:0010842 retina layer formation PATO:0000297 arrested abnormal ZDB-GENE-011212-5 140620 5631 prps1a GO:0010842 retina layer formation PATO:0000502 delayed abnormal ZDB-GENE-011212-5 140620 5631 prps1a GO:0010842 retina layer formation PATO:0001236 process quality abnormal ZDB-GENE-011212-5 140620 5631 prps1a GO:0048798 swim bladder inflation PATO:0001236 process quality abnormal ZDB-GENE-011212-5 140620 5631 prps1a GO:0048884 neuromast development PATO:0001507 disrupted abnormal ZDB-GENE-011212-5 140620 5631 prps1a GO:0060041 retina development in camera-type eye PATO:0000502 delayed abnormal ZDB-GENE-011212-5 140620 5631 prps1a GO:0060041 retina development in camera-type eye PATO:0001236 process quality abnormal ZDB-GENE-011212-5 140620 5631 prps1a GO:0005884 actin filament BFO:0000050 part_of ZFA:0000107 eye PATO:0000937 disorganized abnormal ZDB-GENE-011212-5 140620 5631 prps1a ZFA:0000107 eye PATO:0000587 decreased size abnormal ZDB-GENE-011212-5 140620 5631 prps1a ZFA:0000144 retinal pigmented epithelium PATO:0000592 decreased thickness abnormal ZDB-GENE-011212-5 140620 5631 prps1a ZFA:0000098 proliferative region BFO:0000050 part_of ZFA:0000152 retina PATO:0000470 increased amount abnormal ZDB-GENE-011212-5 140620 5631 prps1a ZFA:0000098 proliferative region BFO:0000050 part_of ZFA:0000152 retina PATO:0000628 mislocalised abnormal ZDB-GENE-011212-5 140620 5631 prps1a ZFA:0009000 cell BFO:0000050 part_of ZFA:0000152 retina PATO:0001997 decreased amount abnormal ZDB-GENE-011212-5 140620 5631 prps1a ZFA:0000152 retina PATO:0000587 decreased size abnormal ZDB-GENE-011212-5 140620 5631 prps1a ZFA:0000940 posterior lateral line neuromast PATO:0002001 has fewer parts of type abnormal ZFA:0009367 neuromast hair cell ZDB-GENE-011212-5 140620 5631 prps1a ZFA:0001114 head PATO:0000587 decreased size abnormal ZDB-GENE-011212-5 140620 5631 prps1a ZFA:0009198 xanthophore PATO:0001997 decreased amount abnormal ZDB-GENE-011212-5 140620 5631 prps1a ZFA:0009199 iridophore PATO:0001997 decreased amount abnormal ZDB-GENE-011212-5 140620 5631 prps1a ZFA:0009367 neuromast hair cell PATO:0001997 decreased amount abnormal ZDB-GENE-011212-6 140618 7020 tfap2a GO:0002072 optic cup morphogenesis involved in camera-type eye development PATO:0001236 process quality abnormal ZDB-GENE-011212-6 140618 7020 tfap2a GO:0002244 hematopoietic progenitor cell differentiation PATO:0002052 decreased occurrence abnormal ZDB-GENE-011212-6 140618 7020 tfap2a GO:0007422 peripheral nervous system development PATO:0001507 disrupted abnormal ZDB-GENE-011212-6 140618 7020 tfap2a GO:0030318 melanocyte differentiation PATO:0001507 disrupted abnormal ZDB-GENE-011212-6 140618 7020 tfap2a GO:0036484 trunk neural crest cell migration PATO:0000297 arrested abnormal ZDB-GENE-011212-6 140618 7020 tfap2a GO:0043473 pigmentation PATO:0000502 delayed abnormal ZDB-GENE-011212-6 140618 7020 tfap2a GO:0043473 pigmentation PATO:0001507 disrupted abnormal ZDB-GENE-011212-6 140618 7020 tfap2a GO:0048483 autonomic nervous system development PATO:0001507 disrupted abnormal ZDB-GENE-011212-6 140618 7020 tfap2a GO:0048703 embryonic viscerocranium morphogenesis PATO:0002302 decreased process quality abnormal ZDB-GENE-011212-6 140618 7020 tfap2a GO:0061386 closure of optic fissure PATO:0002052 decreased occurrence abnormal ZDB-GENE-011212-6 140618 7020 tfap2a ZFA:0000008 brain PATO:0000001 quality abnormal ZDB-GENE-011212-6 140618 7020 tfap2a ZFA:0000029 hindbrain PATO:0000001 quality abnormal ZDB-GENE-011212-6 140618 7020 tfap2a GO:0007219 Notch signaling pathway BFO:0000066 occurs_in ZFA:0000051 otic vesicle PATO:0002304 increased process quality abnormal ZDB-GENE-011212-6 140618 7020 tfap2a GO:0008543 fibroblast growth factor receptor signaling pathway BFO:0000066 occurs_in ZFA:0000051 otic vesicle PATO:0002304 increased process quality abnormal ZDB-GENE-011212-6 140618 7020 tfap2a GO:0014018 neuroblast fate specification BFO:0000066 occurs_in ZFA:0000051 otic vesicle PATO:0002052 decreased occurrence abnormal ZDB-GENE-011212-6 140618 7020 tfap2a GO:0022008 neurogenesis BFO:0000066 occurs_in ZFA:0000051 otic vesicle PATO:0002052 decreased occurrence abnormal ZDB-GENE-011212-6 140618 7020 tfap2a ZFA:0000051 otic vesicle PATO:0002001 has fewer parts of type abnormal ZFA:0009168 neuroblast (sensu Vertebrata) BFO:0000050 part_of ZFA:0000051 otic vesicle ZDB-GENE-011212-6 140618 7020 tfap2a ZFA:0000095 pharyngeal arch 3-7 skeleton PATO:0002001 has fewer parts of type abnormal ZFA:0001516 ceratobranchial cartilage ZDB-GENE-011212-6 140618 7020 tfap2a ZFA:0000095 pharyngeal arch 3-7 skeleton PATO:0000001 quality abnormal ZDB-GENE-011212-6 140618 7020 tfap2a ZFA:0000095 pharyngeal arch 3-7 skeleton PATO:0000051 morphology abnormal ZDB-GENE-011212-6 140618 7020 tfap2a ZFA:0000095 pharyngeal arch 3-7 skeleton PATO:0000587 decreased size abnormal ZDB-GENE-011212-6 140618 7020 tfap2a ZFA:0000107 eye PATO:0000587 decreased size abnormal ZDB-GENE-011212-6 140618 7020 tfap2a ZFA:0000114 heart PATO:0001450 edematous abnormal ZDB-GENE-011212-6 140618 7020 tfap2a GO:0006915 apoptotic process BFO:0000066 occurs_in ZFA:0000135 notochord PATO:0002051 increased occurrence abnormal ZDB-GENE-011212-6 140618 7020 tfap2a ZFA:0009248 neuron BFO:0000050 part_of ZFA:0000142 peripheral nervous system PATO:0001566 distributed abnormal ZDB-GENE-011212-6 140618 7020 tfap2a ZFA:0000144 retinal pigmented epithelium PATO:0000628 mislocalised abnormal ZDB-GENE-011212-6 140618 7020 tfap2a ZFA:0000144 retinal pigmented epithelium PATO:0001598 protruding abnormal ZDB-GENE-011212-6 140618 7020 tfap2a ZFA:0009248 neuron BFO:0000050 part_of ZFA:0000200 dorsal root ganglion PATO:0001997 decreased amount abnormal ZDB-GENE-011212-6 140618 7020 tfap2a ZFA:0000354 gill PATO:0000587 decreased size abnormal ZDB-GENE-011212-6 140618 7020 tfap2a ZFA:0000396 nervous system PATO:0000001 quality abnormal ZDB-GENE-011212-6 140618 7020 tfap2a ZFA:0009061 adrenergic neuron BFO:0000050 part_of ZFA:0000539 locus coeruleus PATO:0000462 absent abnormal ZDB-GENE-011212-6 140618 7020 tfap2a ZFA:0009061 adrenergic neuron BFO:0000050 part_of ZFA:0000545 medulla oblongata PATO:0000462 absent abnormal ZDB-GENE-011212-6 140618 7020 tfap2a ZFA:0000547 mouth PATO:0000001 quality abnormal ZDB-GENE-011212-6 140618 7020 tfap2a GO:0030182 neuron differentiation BFO:0000066 occurs_in ZFA:0000588 statoacoustic (VIII) ganglion PATO:0000911 decreased rate abnormal ZDB-GENE-011212-6 140618 7020 tfap2a ZFA:0000588 statoacoustic (VIII) ganglion PATO:0002002 has extra parts of type abnormal ZFA:0009168 neuroblast (sensu Vertebrata) BFO:0000050 part_of ZFA:0000588 statoacoustic (VIII) ganglion ZDB-GENE-011212-6 140618 7020 tfap2a ZFA:0000588 statoacoustic (VIII) ganglion PATO:0002001 has fewer parts of type abnormal ZFA:0009248 neuron BFO:0000050 part_of ZFA:0000588 statoacoustic (VIII) ganglion ZDB-GENE-011212-6 140618 7020 tfap2a ZFA:0000621 quadrate PATO:0000574 decreased length abnormal ZDB-GENE-011212-6 140618 7020 tfap2a ZFA:0000621 quadrate PATO:0000587 decreased size abnormal ZDB-GENE-011212-6 140618 7020 tfap2a BSPO:0000084 ventral region BFO:0000050 part_of ZFA:0001058 caudal fin PATO:0002251 decreased pigmentation abnormal ZDB-GENE-011212-6 140618 7020 tfap2a ZFA:0009091 melanocyte BFO:0000050 part_of ZFA:0001058 caudal fin PATO:0001997 decreased amount abnormal ZDB-GENE-011212-6 140618 7020 tfap2a ZFA:0001094 whole organism PATO:0002000 lacks all parts of type abnormal ZFA:0009248 neuron BFO:0000050 part_of ZFA:0001576 sympathetic nervous system ZDB-GENE-011212-6 140618 7020 tfap2a ZFA:0001094 whole organism PATO:0000718 lethal (sensu genetics) abnormal ZDB-GENE-011212-6 140618 7020 tfap2a ZFA:0009091 melanocyte BFO:0000050 part_of ZFA:0001114 head PATO:0000328 low saturation abnormal ZDB-GENE-011212-6 140618 7020 tfap2a ZFA:0009091 melanocyte BFO:0000050 part_of ZFA:0001114 head PATO:0001997 decreased amount abnormal ZDB-GENE-011212-6 140618 7020 tfap2a ZFA:0009091 melanocyte BFO:0000050 part_of ZFA:0001115 trunk PATO:0000328 low saturation abnormal ZDB-GENE-011212-6 140618 7020 tfap2a ZFA:0009091 melanocyte BFO:0000050 part_of ZFA:0001115 trunk PATO:0001997 decreased amount abnormal ZDB-GENE-011212-6 140618 7020 tfap2a ZFA:0009248 neuron BFO:0000050 part_of ZFA:0001155 enteric nervous system PATO:0001997 decreased amount abnormal ZDB-GENE-011212-6 140618 7020 tfap2a BSPO:0000070 anatomical region BFO:0000050 part_of ZFA:0001202 optic cup PATO:0002001 has fewer parts of type abnormal ZFA:0009165 neural crest cell ZDB-GENE-011212-6 140618 7020 tfap2a ZFA:0001205 Meckel's cartilage PATO:0000642 fused with abnormal ZFA:0001205 Meckel's cartilage ZDB-GENE-011212-6 140618 7020 tfap2a ZFA:0001205 Meckel's cartilage PATO:0000574 decreased length abnormal ZDB-GENE-011212-6 140618 7020 tfap2a ZFA:0001205 Meckel's cartilage PATO:0000587 decreased size abnormal ZDB-GENE-011212-6 140618 7020 tfap2a ZFA:0001205 Meckel's cartilage PATO:0000646 malformed abnormal ZDB-GENE-011212-6 140618 7020 tfap2a ZFA:0001205 Meckel's cartilage PATO:0002143 sloped downward abnormal ZDB-GENE-011212-6 140618 7020 tfap2a ZFA:0001227 mandibular arch skeleton PATO:0000587 decreased size abnormal ZDB-GENE-011212-6 140618 7020 tfap2a ZFA:0001227 mandibular arch skeleton PATO:0000646 malformed abnormal ZDB-GENE-011212-6 140618 7020 tfap2a ZFA:0001227 mandibular arch skeleton PATO:0000937 disorganized abnormal ZDB-GENE-011212-6 140618 7020 tfap2a ZFA:0001227 mandibular arch skeleton PATO:0001598 protruding abnormal ZDB-GENE-011212-6 140618 7020 tfap2a ZFA:0001227 mandibular arch skeleton PATO:0001920 mislocalised ventrally abnormal ZDB-GENE-011212-6 140618 7020 tfap2a ZFA:0001228 pharyngeal arch 3 skeleton PATO:0000587 decreased size abnormal ZDB-GENE-011212-6 140618 7020 tfap2a ZFA:0001229 pharyngeal arch 7 skeleton PATO:0000587 decreased size abnormal ZDB-GENE-011212-6 140618 7020 tfap2a ZFA:0001230 pharyngeal arch 6 skeleton PATO:0000462 absent abnormal ZDB-GENE-011212-6 140618 7020 tfap2a ZFA:0001231 pharyngeal arch 4 skeleton PATO:0000462 absent abnormal ZDB-GENE-011212-6 140618 7020 tfap2a ZFA:0001232 pharyngeal arch 5 skeleton PATO:0000462 absent abnormal ZDB-GENE-011212-6 140618 7020 tfap2a ZFA:0001276 pharyngeal arch 2 skeleton PATO:0000051 morphology abnormal ZDB-GENE-011212-6 140618 7020 tfap2a ZFA:0001276 pharyngeal arch 2 skeleton PATO:0000587 decreased size abnormal ZDB-GENE-011212-6 140618 7020 tfap2a ZFA:0001284 optic fissure PATO:0000609 closure incomplete abnormal ZDB-GENE-011212-6 140618 7020 tfap2a ZFA:0001306 pharyngeal arch PATO:0000646 malformed abnormal ZDB-GENE-011212-6 140618 7020 tfap2a ZFA:0001399 palatoquadrate cartilage PATO:0000628 mislocalised abnormal ZDB-GENE-011212-6 140618 7020 tfap2a ZFA:0001399 palatoquadrate cartilage PATO:0000937 disorganized abnormal ZDB-GENE-011212-6 140618 7020 tfap2a ZFA:0001400 ceratohyal cartilage PATO:0000587 decreased size abnormal ZDB-GENE-011212-6 140618 7020 tfap2a ZFA:0001400 ceratohyal cartilage PATO:0000645 hypoplastic abnormal ZDB-GENE-011212-6 140618 7020 tfap2a ZFA:0001400 ceratohyal cartilage PATO:0002155 medially rotated abnormal ZDB-GENE-011212-6 140618 7020 tfap2a ZFA:0001405 ethmoid cartilage PATO:0001786 split abnormal ZDB-GENE-011212-6 140618 7020 tfap2a ZFA:0001422 hyosymplectic cartilage PATO:0000587 decreased size abnormal ZDB-GENE-011212-6 140618 7020 tfap2a ZFA:0001460 pharyngeal arch cartilage PATO:0000587 decreased size abnormal ZDB-GENE-011212-6 140618 7020 tfap2a ZFA:0001507 trabecula cranii PATO:0000574 decreased length abnormal ZDB-GENE-011212-6 140618 7020 tfap2a ZFA:0001507 trabecula cranii PATO:0000592 decreased thickness abnormal ZDB-GENE-011212-6 140618 7020 tfap2a ZFA:0001508 trabecula communis PATO:0000462 absent abnormal ZDB-GENE-011212-6 140618 7020 tfap2a ZFA:0001510 basihyal cartilage PATO:0000574 decreased length abnormal ZDB-GENE-011212-6 140618 7020 tfap2a ZFA:0001510 basihyal cartilage PATO:0000587 decreased size abnormal ZDB-GENE-011212-6 140618 7020 tfap2a ZFA:0001510 basihyal cartilage PATO:0001923 mislocalised laterally abnormal ZDB-GENE-011212-6 140618 7020 tfap2a ZFA:0001516 ceratobranchial cartilage PATO:0000587 decreased size abnormal ZDB-GENE-011212-6 140618 7020 tfap2a ZFA:0001516 ceratobranchial cartilage PATO:0001997 decreased amount abnormal ZDB-GENE-011212-6 140618 7020 tfap2a ZFA:0001580 neurocranium PATO:0000587 decreased size abnormal ZDB-GENE-011212-6 140618 7020 tfap2a ZFA:0001611 pharyngeal arch 2 PATO:0000937 disorganized abnormal ZDB-GENE-011212-6 140618 7020 tfap2a ZFA:0001613 pharyngeal arch 3-7 PATO:0000587 decreased size abnormal ZDB-GENE-011212-6 140618 7020 tfap2a GO:0035778 pronephric nephron tubule epithelial cell differentiation BFO:0000066 occurs_in ZFA:0001621 pronephric proximal straight tubule PATO:0000057 occurrence abnormal ZDB-GENE-011212-6 140618 7020 tfap2a GO:0005634 nucleus BFO:0000050 part_of ZFA:0001622 pronephric distal early tubule PATO:0000587 decreased size abnormal ZDB-GENE-011212-6 140618 7020 tfap2a GO:0035778 pronephric nephron tubule epithelial cell differentiation BFO:0000066 occurs_in ZFA:0001622 pronephric distal early tubule PATO:0000057 occurrence ameliorated ZDB-GENE-011212-6 140618 7020 tfap2a GO:0035778 pronephric nephron tubule epithelial cell differentiation BFO:0000066 occurs_in ZFA:0001622 pronephric distal early tubule PATO:0002052 decreased occurrence abnormal ZDB-GENE-011212-6 140618 7020 tfap2a GO:0072067 early distal convoluted tubule development BFO:0000066 occurs_in ZFA:0001622 pronephric distal early tubule PATO:0002052 decreased occurrence abnormal ZDB-GENE-011212-6 140618 7020 tfap2a ZFA:0009374 kidney epithelial cell BFO:0000050 part_of ZFA:0001622 pronephric distal early tubule PATO:0000587 decreased size abnormal ZDB-GENE-011212-6 140618 7020 tfap2a GO:0035778 pronephric nephron tubule epithelial cell differentiation BFO:0000066 occurs_in ZFA:0001624 pronephric distal late tubule PATO:0000057 occurrence abnormal ZDB-GENE-011212-6 140618 7020 tfap2a GO:0035778 pronephric nephron tubule epithelial cell differentiation BFO:0000066 occurs_in ZFA:0001624 pronephric distal late tubule PATO:0002052 decreased occurrence abnormal ZDB-GENE-011212-6 140618 7020 tfap2a ZFA:0005342 anterior catecholaminergic tract PATO:0000587 decreased size abnormal ZDB-GENE-011212-6 140618 7020 tfap2a ZFA:0009046 T cell PATO:0001997 decreased amount abnormal ZDB-GENE-011212-6 140618 7020 tfap2a ZFA:0009090 pigment cell PATO:0001997 decreased amount abnormal ZDB-GENE-011212-6 140618 7020 tfap2a ZFA:0009091 melanocyte PATO:0000330 irregular spatial pattern abnormal ZDB-GENE-011212-6 140618 7020 tfap2a ZFA:0009091 melanocyte PATO:0001997 decreased amount abnormal ZDB-GENE-011212-6 140618 7020 tfap2a ZFA:0009354 hematopoietic multipotent progenitor cell PATO:0001997 decreased amount abnormal ZDB-GENE-011213-1 140613 57801 her9 GO:0042672 retinal cone cell fate specification PATO:0001236 process quality abnormal ZDB-GENE-011213-1 140613 57801 her9 GO:0071632 optomotor response PATO:0002302 decreased process quality abnormal ZDB-GENE-011213-1 140613 57801 her9 GO:0120303 visually-mediated background adaptation PATO:0002302 decreased process quality abnormal ZDB-GENE-011213-1 140613 57801 her9 GO:1904888 cranial skeletal system development PATO:0001507 disrupted abnormal ZDB-GENE-011213-1 140613 57801 her9 ZFA:0009073 glial cell BFO:0000050 part_of ZFA:0000008 brain PATO:0001997 decreased amount abnormal ZDB-GENE-011213-1 140613 57801 her9 GO:0006915 apoptotic process BFO:0000066 occurs_in ZFA:0000024 retinal ganglion cell layer PATO:0002051 increased occurrence abnormal ZDB-GENE-011213-1 140613 57801 her9 ZFA:0000054 pericardium PATO:0001450 edematous abnormal ZDB-GENE-011213-1 140613 57801 her9 ZFA:0000076 swim bladder PATO:0001483 aplastic abnormal ZDB-GENE-011213-1 140613 57801 her9 ZFA:0000107 eye PATO:0000587 decreased size abnormal ZDB-GENE-011213-1 140613 57801 her9 GO:0006915 apoptotic process BFO:0000066 occurs_in ZFA:0000119 retinal inner nuclear layer PATO:0002051 increased occurrence abnormal ZDB-GENE-011213-1 140613 57801 her9 ZFA:0000123 liver PATO:0000586 increased size abnormal ZDB-GENE-011213-1 140613 57801 her9 ZFA:0001094 whole organism PATO:0000169 viability abnormal ZDB-GENE-011213-1 140613 57801 her9 ZFA:0001094 whole organism PATO:0000587 decreased size abnormal ZDB-GENE-011213-1 140613 57801 her9 ZFA:0001094 whole organism PATO:0001422 dead abnormal ZDB-GENE-011213-1 140613 57801 her9 ZFA:0001094 whole organism PATO:0001592 increased curvature abnormal ZDB-GENE-011213-1 140613 57801 her9 ZFA:0001094 whole organism PATO:0002251 decreased pigmentation abnormal ZDB-GENE-011213-1 140613 57801 her9 ZFA:0001127 visual system PATO:0001624 decreased functionality abnormal ZDB-GENE-011213-1 140613 57801 her9 ZFA:0009073 glial cell BFO:0000050 part_of ZFA:0001155 enteric nervous system PATO:0001997 decreased amount abnormal ZDB-GENE-011213-1 140613 57801 her9 GO:0006915 apoptotic process BFO:0000066 occurs_in ZFA:0001289 ciliary marginal zone PATO:0002051 increased occurrence abnormal ZDB-GENE-011213-1 140613 57801 her9 ZFA:0001289 ciliary marginal zone PATO:0000587 decreased size abnormal ZDB-GENE-011213-1 140613 57801 her9 GO:0006915 apoptotic process BFO:0000066 occurs_in ZFA:0001464 retinal outer nuclear layer PATO:0002051 increased occurrence abnormal ZDB-GENE-011213-1 140613 57801 her9 GO:0120199 cone photoreceptor outer segment BFO:0000050 part_of ZFA:0005945 long double cone cell PATO:0000051 morphology abnormal ZDB-GENE-011213-1 140613 57801 her9 GO:0120199 cone photoreceptor outer segment BFO:0000050 part_of ZFA:0005946 short double cone cell PATO:0000051 morphology abnormal ZDB-GENE-011213-1 140613 57801 her9 ZFA:0005948 short single cone cell PATO:0001997 decreased amount abnormal ZDB-GENE-011213-1 140613 57801 her9 GO:0120199 cone photoreceptor outer segment BFO:0000050 part_of ZFA:0009262 retinal cone cell PATO:0000574 decreased length abnormal ZDB-GENE-011213-1 140613 57801 her9 ZFA:0009262 retinal cone cell PATO:0001997 decreased amount abnormal ZDB-GENE-011213-1 140613 57801 her9 GO:0120200 rod photoreceptor outer segment BFO:0000050 part_of ZFA:0009275 retinal rod cell PATO:0000051 morphology abnormal ZDB-GENE-011213-1 140613 57801 her9 ZFA:0009275 retinal rod cell PATO:0001997 decreased amount abnormal ZDB-GENE-011213-1 140613 57801 her9 GO:0044297 cell body BFO:0000050 part_of ZFA:0009280 Muller cell PATO:0000140 position abnormal ZDB-GENE-011213-1 140613 57801 her9 GO:0097386 glial cell projection BFO:0000050 part_of ZFA:0009280 Muller cell PATO:0001997 decreased amount abnormal ZDB-GENE-011213-1 140613 57801 her9 ZFA:0009280 Muller cell PATO:0000937 disorganized abnormal ZDB-GENE-011213-1 140613 57801 her9 ZFA:0009280 Muller cell PATO:0001997 decreased amount abnormal ZDB-GENE-011213-1 140613 57801 her9 ZFA:0009310 retinal ganglion cell PATO:0001997 decreased amount abnormal ZDB-GENE-011220-2 140633 8864 per2 GO:0007626 locomotory behavior PATO:0001507 disrupted abnormal ZDB-GENE-011220-2 140633 8864 per2 GO:0007632 visual behavior PATO:0002052 decreased occurrence abnormal ZDB-GENE-011220-2 140633 8864 per2 GO:0007634 optokinetic behavior PATO:0002052 decreased occurrence abnormal ZDB-GENE-011220-2 140633 8864 per2 GO:0009416 response to light stimulus PATO:0001507 disrupted abnormal ZDB-GENE-011220-2 140633 8864 per2 GO:0032922 circadian regulation of gene expression PATO:0001507 disrupted abnormal ZDB-GENE-011220-2 140633 8864 per2 GO:0045475 locomotor rhythm PATO:0001236 process quality abnormal ZDB-GENE-011220-2 140633 8864 per2 GO:0071632 optomotor response PATO:0002052 decreased occurrence abnormal ZDB-GENE-011220-2 140633 8864 per2 GO:0098684 photoreceptor ribbon synapse BFO:0000050 part_of ZFA:0000107 eye PATO:0000051 morphology abnormal ZDB-GENE-011220-2 140633 8864 per2 ZFA:0001285 intersegmental vessel PATO:0000573 increased length abnormal ZDB-GENE-011221-1 140631 342977 nanos3 GO:0007281 germ cell development PATO:0001507 disrupted abnormal ZDB-GENE-011221-1 140631 342977 nanos3 GO:0008354 germ cell migration PATO:0001507 disrupted abnormal ZDB-GENE-011221-1 140631 342977 nanos3 GO:0036099 female germ-line stem cell population maintenance PATO:0001507 disrupted abnormal ZDB-GENE-011221-1 140631 342977 nanos3 ZFA:0001109 oocyte PATO:0000462 absent abnormal ZDB-GENE-011221-1 140631 342977 nanos3 ZFA:0009288 primordial germ cell PATO:0000628 mislocalised abnormal ZDB-GENE-011221-1 140631 342977 nanos3 ZFA:0009288 primordial germ cell PATO:0000638 apoptotic abnormal ZDB-GENE-011221-1 140631 342977 nanos3 ZFA:0009288 primordial germ cell PATO:0001997 decreased amount abnormal ZDB-GENE-020102-1 140747 7852 cxcr4a GO:0001570 vasculogenesis PATO:0001236 process quality abnormal ZDB-GENE-020102-1 140747 7852 cxcr4a GO:0001947 heart looping PATO:0001236 process quality abnormal ZDB-GENE-020102-1 140747 7852 cxcr4a GO:0001947 heart looping PATO:0002052 decreased occurrence abnormal ZDB-GENE-020102-1 140747 7852 cxcr4a GO:0002040 sprouting angiogenesis PATO:0001236 process quality abnormal ZDB-GENE-020102-1 140747 7852 cxcr4a GO:0002042 cell migration involved in sprouting angiogenesis PATO:0001507 disrupted abnormal ZDB-GENE-020102-1 140747 7852 cxcr4a GO:0003140 determination of left/right asymmetry in lateral mesoderm PATO:0001236 process quality abnormal ZDB-GENE-020102-1 140747 7852 cxcr4a GO:0003140 determination of left/right asymmetry in lateral mesoderm PATO:0002052 decreased occurrence abnormal ZDB-GENE-020102-1 140747 7852 cxcr4a GO:0007519 skeletal muscle tissue development PATO:0001507 disrupted abnormal ZDB-GENE-020102-1 140747 7852 cxcr4a GO:0008015 blood circulation PATO:0000297 arrested abnormal ZDB-GENE-020102-1 140747 7852 cxcr4a GO:0030239 myofibril assembly PATO:0001507 disrupted abnormal ZDB-GENE-020102-1 140747 7852 cxcr4a GO:0042074 cell migration involved in gastrulation PATO:0000502 delayed abnormal ZDB-GENE-020102-1 140747 7852 cxcr4a GO:0042074 cell migration involved in gastrulation PATO:0001236 process quality abnormal ZDB-GENE-020102-1 140747 7852 cxcr4a GO:0042074 cell migration involved in gastrulation PATO:0001507 disrupted abnormal ZDB-GENE-020102-1 140747 7852 cxcr4a GO:0043534 blood vessel endothelial cell migration PATO:0001236 process quality abnormal ZDB-GENE-020102-1 140747 7852 cxcr4a GO:0055001 muscle cell development PATO:0001507 disrupted abnormal ZDB-GENE-020102-1 140747 7852 cxcr4a GO:0060030 dorsal convergence PATO:0000502 delayed abnormal ZDB-GENE-020102-1 140747 7852 cxcr4a GO:0060030 dorsal convergence PATO:0001507 disrupted abnormal ZDB-GENE-020102-1 140747 7852 cxcr4a GO:0071910 determination of liver left/right asymmetry PATO:0001236 process quality abnormal ZDB-GENE-020102-1 140747 7852 cxcr4a GO:0071910 determination of liver left/right asymmetry PATO:0002052 decreased occurrence abnormal ZDB-GENE-020102-1 140747 7852 cxcr4a GO:0003351 epithelial cilium movement involved in extracellular fluid movement BFO:0000066 occurs_in ZFA:0000001 Kupffer's vesicle PATO:0001236 process quality abnormal ZDB-GENE-020102-1 140747 7852 cxcr4a GO:0005929 cilium BFO:0000050 part_of ZFA:0000001 Kupffer's vesicle PATO:0000574 decreased length abnormal ZDB-GENE-020102-1 140747 7852 cxcr4a GO:0005929 cilium BFO:0000050 part_of ZFA:0000001 Kupffer's vesicle PATO:0001997 decreased amount abnormal ZDB-GENE-020102-1 140747 7852 cxcr4a ZFA:0009000 cell BFO:0000050 part_of ZFA:0000001 Kupffer's vesicle PATO:0001997 decreased amount abnormal ZDB-GENE-020102-1 140747 7852 cxcr4a ZFA:0000001 Kupffer's vesicle PATO:0000462 absent abnormal ZDB-GENE-020102-1 140747 7852 cxcr4a ZFA:0000001 Kupffer's vesicle PATO:0000587 decreased size abnormal ZDB-GENE-020102-1 140747 7852 cxcr4a ZFA:0009181 vascular associated smooth muscle cell BFO:0000050 part_of ZFA:0000014 dorsal aorta PATO:0001997 decreased amount abnormal ZDB-GENE-020102-1 140747 7852 cxcr4a ZFA:0000014 dorsal aorta PATO:0000600 increased width abnormal ZDB-GENE-020102-1 140747 7852 cxcr4a GO:0042074 cell migration involved in gastrulation BFO:0000066 occurs_in ZFA:0000017 endoderm PATO:0001236 process quality abnormal ZDB-GENE-020102-1 140747 7852 cxcr4a ZFA:0000017 endoderm PATO:0001921 mislocalised anteriorly abnormal ZDB-GENE-020102-1 140747 7852 cxcr4a GO:0008283 cell population proliferation BFO:0000066 occurs_in ZFA:0000023 forerunner cell group PATO:0002052 decreased occurrence abnormal ZDB-GENE-020102-1 140747 7852 cxcr4a GO:0044843 cell cycle G1/S phase transition BFO:0000066 occurs_in ZFA:0000023 forerunner cell group PATO:0000297 arrested abnormal ZDB-GENE-020102-1 140747 7852 cxcr4a ZFA:0000112 gut PATO:0000051 morphology abnormal ZDB-GENE-020102-1 140747 7852 cxcr4a ZFA:0000112 gut PATO:0001784 bifurcated abnormal ZDB-GENE-020102-1 140747 7852 cxcr4a ZFA:0000123 liver PATO:0000587 decreased size abnormal ZDB-GENE-020102-1 140747 7852 cxcr4a ZFA:0000123 liver PATO:0001473 duplicated abnormal ZDB-GENE-020102-1 140747 7852 cxcr4a ZFA:0009102 pancreatic B cell BFO:0000050 part_of ZFA:0000140 pancreas PATO:0001630 dispersed abnormal ZDB-GENE-020102-1 140747 7852 cxcr4a ZFA:0000140 pancreas PATO:0000051 morphology abnormal ZDB-GENE-020102-1 140747 7852 cxcr4a ZFA:0000140 pancreas PATO:0000587 decreased size abnormal ZDB-GENE-020102-1 140747 7852 cxcr4a ZFA:0000140 pancreas PATO:0001473 duplicated abnormal ZDB-GENE-020102-1 140747 7852 cxcr4a ZFA:0000155 somite PATO:0000051 morphology abnormal ZDB-GENE-020102-1 140747 7852 cxcr4a ZFA:0000155 somite PATO:0001396 cellular quality abnormal ZDB-GENE-020102-1 140747 7852 cxcr4a ZFA:0005603 lymphangiogenic sprout BFO:0000050 part_of ZFA:0000173 bulbus arteriosus PATO:0001997 decreased amount abnormal ZDB-GENE-020102-1 140747 7852 cxcr4a ZFA:0005603 lymphangiogenic sprout BFO:0000050 part_of ZFA:0000173 bulbus arteriosus PATO:0005001 variability of count abnormal ZDB-GENE-020102-1 140747 7852 cxcr4a ZFA:0005604 angiogenic sprout BFO:0000050 part_of ZFA:0001052 primordial hindbrain channel PATO:0000628 mislocalised abnormal ZDB-GENE-020102-1 140747 7852 cxcr4a ZFA:0005604 angiogenic sprout BFO:0000050 part_of ZFA:0001052 primordial hindbrain channel PATO:0001997 decreased amount abnormal ZDB-GENE-020102-1 140747 7852 cxcr4a ZFA:0001054 lateral dorsal aorta PATO:0000051 morphology abnormal ZDB-GENE-020102-1 140747 7852 cxcr4a ZFA:0001054 lateral dorsal aorta PATO:0000646 malformed abnormal ZDB-GENE-020102-1 140747 7852 cxcr4a ZFA:0001054 lateral dorsal aorta PATO:0010001 disconnected abnormal ZDB-GENE-020102-1 140747 7852 cxcr4a ZFA:0001054 lateral dorsal aorta PATO:0040026 structurally discontinuous abnormal ZDB-GENE-020102-1 140747 7852 cxcr4a GO:0030175 filopodium BFO:0000050 part_of ZFA:0001194 cranial neural crest PATO:0000574 decreased length abnormal ZDB-GENE-020102-1 140747 7852 cxcr4a ZFA:0001260 endocrine pancreas PATO:0000628 mislocalised abnormal ZDB-GENE-020102-1 140747 7852 cxcr4a ZFA:0001260 endocrine pancreas PATO:0000646 malformed abnormal ZDB-GENE-020102-1 140747 7852 cxcr4a ZFA:0005604 angiogenic sprout BFO:0000050 part_of ZFA:0001285 intersegmental vessel PATO:0000628 mislocalised abnormal ZDB-GENE-020102-1 140747 7852 cxcr4a ZFA:0005604 angiogenic sprout BFO:0000050 part_of ZFA:0001285 intersegmental vessel PATO:0001997 decreased amount abnormal ZDB-GENE-020102-1 140747 7852 cxcr4a ZFA:0001338 intestine PATO:0001473 duplicated abnormal ZDB-GENE-020102-1 140747 7852 cxcr4a GO:0005813 centrosome BFO:0000050 part_of ZFA:0001462 somite border PATO:0000060 spatial pattern abnormal ZDB-GENE-020102-1 140747 7852 cxcr4a GO:0060231 mesenchymal to epithelial transition BFO:0000066 occurs_in ZFA:0001462 somite border PATO:0002052 decreased occurrence abnormal ZDB-GENE-020102-1 140747 7852 cxcr4a ZFA:0009034 epithelial cell BFO:0000050 part_of ZFA:0001462 somite border PATO:0000051 morphology abnormal ZDB-GENE-020102-1 140747 7852 cxcr4a ZFA:0001462 somite border PATO:0000051 morphology abnormal ZDB-GENE-020102-1 140747 7852 cxcr4a ZFA:0001462 somite border PATO:0000646 malformed abnormal ZDB-GENE-020102-1 140747 7852 cxcr4a ZFA:0005002 basilar artery PATO:0000462 absent abnormal ZDB-GENE-020102-1 140747 7852 cxcr4a ZFA:0005002 basilar artery PATO:0001896 unlumenized abnormal ZDB-GENE-020102-1 140747 7852 cxcr4a ZFA:0005002 basilar artery PATO:0002291 agenesis abnormal ZDB-GENE-020102-1 140747 7852 cxcr4a ZFA:0005020 central artery PATO:0001241 physical object quality abnormal ZDB-GENE-020102-1 140747 7852 cxcr4a GO:0001946 lymphangiogenesis BFO:0000066 occurs_in ZFA:0005110 thoracic duct PATO:0002302 decreased process quality abnormal ZDB-GENE-020102-1 140747 7852 cxcr4a ZFA:0005950 bulbus arteriosus lymph vessel PATO:0000060 spatial pattern abnormal ZDB-GENE-020102-1 140747 7852 cxcr4a ZFA:0005951 cardiac ventricle lymph vessel PATO:0000462 absent abnormal ZDB-GENE-020102-1 140747 7852 cxcr4a ZFA:0005951 cardiac ventricle lymph vessel PATO:0002291 agenesis abnormal ZDB-GENE-020102-1 140747 7852 cxcr4a ZFA:0009036 blood vessel endothelial cell PATO:0000628 mislocalised abnormal ZDB-GENE-020102-1 140747 7852 cxcr4a GO:0030175 filopodium BFO:0000050 part_of ZFA:0009139 endodermal cell PATO:0000133 orientation abnormal BSPO:0000016 dorsal-ventral axis BFO:0000050 part_of ZFA:0001094 whole organism ZDB-GENE-020102-1 140747 7852 cxcr4a GO:0030175 filopodium BFO:0000050 part_of ZFA:0009139 endodermal cell PATO:0001997 decreased amount abnormal ZDB-GENE-020102-1 140747 7852 cxcr4a ZFA:0009139 endodermal cell PATO:0002168 displaced to abnormal ZFA:0000038 margin ZDB-GENE-020102-1 140747 7852 cxcr4a ZFA:0009139 endodermal cell PATO:0000411 circular abnormal ZDB-GENE-020102-1 140747 7852 cxcr4a ZFA:0009139 endodermal cell PATO:0001921 mislocalised anteriorly abnormal ZDB-GENE-020102-1 140747 7852 cxcr4a ZFA:0009139 endodermal cell PATO:0002181 displaced abnormal ZDB-GENE-020104-1 792391 6928 hnf1ba GO:0001889 liver development PATO:0001507 disrupted abnormal ZDB-GENE-020104-1 792391 6928 hnf1ba GO:0003002 regionalization PATO:0001507 disrupted abnormal ZDB-GENE-020104-1 792391 6928 hnf1ba GO:0003161 cardiac conduction system development PATO:0001507 disrupted abnormal ZDB-GENE-020104-1 792391 6928 hnf1ba GO:0003323 type B pancreatic cell development PATO:0001507 disrupted abnormal ZDB-GENE-020104-1 792391 6928 hnf1ba GO:0007492 endoderm development PATO:0001507 disrupted abnormal ZDB-GENE-020104-1 792391 6928 hnf1ba GO:0021575 hindbrain morphogenesis PATO:0001507 disrupted abnormal ZDB-GENE-020104-1 792391 6928 hnf1ba GO:0030902 hindbrain development PATO:0001236 process quality abnormal ZDB-GENE-020104-1 792391 6928 hnf1ba GO:0030902 hindbrain development PATO:0001507 disrupted abnormal ZDB-GENE-020104-1 792391 6928 hnf1ba GO:0031016 pancreas development PATO:0001507 disrupted abnormal ZDB-GENE-020104-1 792391 6928 hnf1ba GO:0035148 tube formation PATO:0001507 disrupted abnormal ZDB-GENE-020104-1 792391 6928 hnf1ba GO:0039020 pronephric nephron tubule development PATO:0002302 decreased process quality abnormal ZDB-GENE-020104-1 792391 6928 hnf1ba GO:0048546 digestive tract morphogenesis PATO:0001507 disrupted abnormal ZDB-GENE-020104-1 792391 6928 hnf1ba GO:0055117 regulation of cardiac muscle contraction PATO:0001507 disrupted abnormal ZDB-GENE-020104-1 792391 6928 hnf1ba GO:0061008 hepaticobiliary system development PATO:0001507 disrupted abnormal ZDB-GENE-020104-1 792391 6928 hnf1ba ZFA:0000009 cardiac ventricle PATO:0001691 non-contractile abnormal ZDB-GENE-020104-1 792391 6928 hnf1ba ZFA:0000017 endoderm PATO:0000051 morphology abnormal ZDB-GENE-020104-1 792391 6928 hnf1ba ZFA:0000029 hindbrain PATO:0000051 morphology abnormal ZDB-GENE-020104-1 792391 6928 hnf1ba ZFA:0000029 hindbrain PATO:0000330 irregular spatial pattern abnormal ZDB-GENE-020104-1 792391 6928 hnf1ba ZFA:0000051 otic vesicle PATO:0000411 circular abnormal ZDB-GENE-020104-1 792391 6928 hnf1ba ZFA:0000051 otic vesicle PATO:0000587 decreased size abnormal ZDB-GENE-020104-1 792391 6928 hnf1ba ZFA:0000051 otic vesicle PATO:0000615 wholly anteriorized abnormal ZDB-GENE-020104-1 792391 6928 hnf1ba ZFA:0000054 pericardium PATO:0001450 edematous abnormal ZDB-GENE-020104-1 792391 6928 hnf1ba GO:0071679 commissural neuron axon guidance BFO:0000066 occurs_in ZFA:0000059 postoptic commissure PATO:0001507 disrupted abnormal ZDB-GENE-020104-1 792391 6928 hnf1ba ZFA:0000059 postoptic commissure PATO:0001959 defasciculated abnormal ZDB-GENE-020104-1 792391 6928 hnf1ba ZFA:0000069 rhombomere 6 PATO:0000051 morphology abnormal ZDB-GENE-020104-1 792391 6928 hnf1ba ZFA:0000069 rhombomere 6 PATO:0000462 absent abnormal ZDB-GENE-020104-1 792391 6928 hnf1ba ZFA:0000076 swim bladder PATO:0002291 agenesis abnormal ZDB-GENE-020104-1 792391 6928 hnf1ba ZFA:0000107 eye PATO:0000587 decreased size abnormal ZDB-GENE-020104-1 792391 6928 hnf1ba GO:0071679 commissural neuron axon guidance BFO:0000066 occurs_in ZFA:0000109 forebrain PATO:0001507 disrupted abnormal ZDB-GENE-020104-1 792391 6928 hnf1ba ZFA:0000112 gut PATO:0000051 morphology abnormal ZDB-GENE-020104-1 792391 6928 hnf1ba ZFA:0000112 gut PATO:0000645 hypoplastic abnormal ZDB-GENE-020104-1 792391 6928 hnf1ba ZFA:0000123 liver PATO:0000001 quality abnormal ZDB-GENE-020104-1 792391 6928 hnf1ba ZFA:0000123 liver PATO:0000587 decreased size abnormal ZDB-GENE-020104-1 792391 6928 hnf1ba ZFA:0000123 liver PATO:0000645 hypoplastic abnormal ZDB-GENE-020104-1 792391 6928 hnf1ba ZFA:0000123 liver PATO:0001483 aplastic abnormal ZDB-GENE-020104-1 792391 6928 hnf1ba ZFA:0000123 liver PATO:0002291 agenesis abnormal ZDB-GENE-020104-1 792391 6928 hnf1ba ZFA:0000140 pancreas PATO:0000587 decreased size abnormal ZDB-GENE-020104-1 792391 6928 hnf1ba ZFA:0000140 pancreas PATO:0000645 hypoplastic abnormal ZDB-GENE-020104-1 792391 6928 hnf1ba ZFA:0000140 pancreas PATO:0001483 aplastic abnormal ZDB-GENE-020104-1 792391 6928 hnf1ba ZFA:0000140 pancreas PATO:0001956 variability of size abnormal ZDB-GENE-020104-1 792391 6928 hnf1ba ZFA:0000140 pancreas PATO:0002291 agenesis abnormal ZDB-GENE-020104-1 792391 6928 hnf1ba BSPO:0000078 distal region BFO:0000050 part_of ZFA:0000151 pronephros PATO:0002303 decreased object quality abnormal ZDB-GENE-020104-1 792391 6928 hnf1ba ZFA:0000151 pronephros PATO:0000001 quality abnormal ZDB-GENE-020104-1 792391 6928 hnf1ba ZFA:0000151 pronephros PATO:0001673 cystic abnormal ZDB-GENE-020104-1 792391 6928 hnf1ba ZFA:0000217 inner ear PATO:0000001 quality abnormal ZDB-GENE-020104-1 792391 6928 hnf1ba ZFA:0000431 semicircular canal PATO:0000052 shape abnormal ZDB-GENE-020104-1 792391 6928 hnf1ba GO:0071679 commissural neuron axon guidance BFO:0000066 occurs_in ZFA:0000435 cranial nerve II PATO:0001507 disrupted abnormal ZDB-GENE-020104-1 792391 6928 hnf1ba ZFA:0000435 cranial nerve II PATO:0000587 decreased size abnormal ZDB-GENE-020104-1 792391 6928 hnf1ba ZFA:0000435 cranial nerve II PATO:0000592 decreased thickness abnormal ZDB-GENE-020104-1 792391 6928 hnf1ba ZFA:0000435 cranial nerve II PATO:0001959 defasciculated abnormal ZDB-GENE-020104-1 792391 6928 hnf1ba ZFA:0000529 kidney PATO:0001673 cystic abnormal ZDB-GENE-020104-1 792391 6928 hnf1ba ZFA:0000823 rhombomere 5 PATO:0000051 morphology abnormal ZDB-GENE-020104-1 792391 6928 hnf1ba ZFA:0000823 rhombomere 5 PATO:0000462 absent abnormal ZDB-GENE-020104-1 792391 6928 hnf1ba ZFA:0000823 rhombomere 5 PATO:0000587 decreased size abnormal ZDB-GENE-020104-1 792391 6928 hnf1ba ZFA:0000823 rhombomere 5 PATO:0001483 aplastic abnormal ZDB-GENE-020104-1 792391 6928 hnf1ba ZFA:0001032 rhombomere 4 PATO:0000586 increased size abnormal ZDB-GENE-020104-1 792391 6928 hnf1ba ZFA:0001076 intestinal bulb PATO:0000141 structure abnormal ZDB-GENE-020104-1 792391 6928 hnf1ba GO:0071679 commissural neuron axon guidance BFO:0000066 occurs_in ZFA:0001108 anterior commissure PATO:0001507 disrupted abnormal ZDB-GENE-020104-1 792391 6928 hnf1ba ZFA:0001108 anterior commissure PATO:0001959 defasciculated abnormal ZDB-GENE-020104-1 792391 6928 hnf1ba ZFA:0001114 head PATO:0000587 decreased size abnormal ZDB-GENE-020104-1 792391 6928 hnf1ba ZFA:0001260 endocrine pancreas PATO:0000001 quality abnormal ZDB-GENE-020104-1 792391 6928 hnf1ba ZFA:0001390 pancreatic bud PATO:0001483 aplastic abnormal ZDB-GENE-020104-1 792391 6928 hnf1ba ZFA:0001439 anatomical system PATO:0000001 quality abnormal ZDB-GENE-020104-1 792391 6928 hnf1ba ZFA:0001558 pronephric tubule PATO:0001241 physical object quality abnormal ZDB-GENE-020104-1 792391 6928 hnf1ba ZFA:0001617 otolith PATO:0000052 shape abnormal ZDB-GENE-020104-1 792391 6928 hnf1ba ZFA:0005070 atrioventricular node PATO:0000608 closed abnormal ZDB-GENE-020104-1 792391 6928 hnf1ba ZFA:0005070 atrioventricular node PATO:0001624 decreased functionality abnormal ZDB-GENE-020104-1 792391 6928 hnf1ba ZFA:0005169 intrahepatic bile duct PATO:0000574 decreased length abnormal ZDB-GENE-020104-1 792391 6928 hnf1ba ZFA:0005169 intrahepatic bile duct PATO:0000645 hypoplastic abnormal ZDB-GENE-020104-1 792391 6928 hnf1ba ZFA:0005169 intrahepatic bile duct PATO:0001571 dilated abnormal ZDB-GENE-020104-1 792391 6928 hnf1ba ZFA:0005755 islet PATO:0000937 disorganized abnormal ZDB-GENE-020104-1 792391 6928 hnf1ba ZFA:0009102 pancreatic B cell PATO:0000937 disorganized abnormal ZDB-GENE-020104-1 792391 6928 hnf1ba ZFA:0009102 pancreatic B cell PATO:0001997 decreased amount abnormal ZDB-GENE-020104-1 792391 6928 hnf1ba ZFA:0009102 pancreatic B cell PATO:0002058 decreased area abnormal ZDB-GENE-020104-1 792391 6928 hnf1ba ZFA:0009111 hepatocyte PATO:0002100 undifferentiated abnormal ZDB-GENE-020104-1 792391 6928 hnf1ba ZFA:0009366 hair cell PATO:0000628 mislocalised abnormal ZDB-GENE-020107-1 140818 5786 ptpra GO:0008015 blood circulation PATO:0001507 disrupted abnormal ZDB-GENE-020107-1 140818 5786 ptpra GO:0010842 retina layer formation PATO:0001507 disrupted abnormal ZDB-GENE-020107-1 140818 5786 ptpra GO:0042074 cell migration involved in gastrulation PATO:0000911 decreased rate abnormal ZDB-GENE-020107-1 140818 5786 ptpra GO:0060027 convergent extension involved in gastrulation PATO:0001507 disrupted abnormal ZDB-GENE-020107-1 140818 5786 ptpra GO:0060030 dorsal convergence PATO:0000911 decreased rate abnormal ZDB-GENE-020107-1 140818 5786 ptpra GO:0060031 mediolateral intercalation PATO:0001507 disrupted abnormal ZDB-GENE-020107-1 140818 5786 ptpra ZFA:0000046 retinal neural layer PATO:0000645 hypoplastic abnormal ZDB-GENE-020107-1 140818 5786 ptpra ZFA:0000054 pericardium PATO:0001450 edematous abnormal ZDB-GENE-020107-1 140818 5786 ptpra ZFA:0000084 yolk PATO:0001450 edematous abnormal ZDB-GENE-020107-1 140818 5786 ptpra ZFA:0000106 extension PATO:0000574 decreased length abnormal ZDB-GENE-020107-1 140818 5786 ptpra ZFA:0000107 eye PATO:0000587 decreased size abnormal ZDB-GENE-020107-1 140818 5786 ptpra ZFA:0009000 cell BFO:0000050 part_of ZFA:0000152 retina PATO:0001997 decreased amount abnormal ZDB-GENE-020107-1 140818 5786 ptpra ZFA:0000152 retina PATO:0000937 disorganized abnormal ZDB-GENE-020107-1 140818 5786 ptpra ZFA:0000435 cranial nerve II PATO:0001959 defasciculated abnormal ZDB-GENE-020107-1 140818 5786 ptpra ZFA:0001094 whole organism PATO:0000574 decreased length abnormal ZDB-GENE-020107-1 140818 5786 ptpra ZFA:0001094 whole organism PATO:0001422 dead abnormal ZDB-GENE-020107-2 140819 5792 ptprfa GO:0009646 response to absence of light PATO:0002304 increased process quality abnormal ZDB-GENE-020107-2 140819 5792 ptprfa GO:0036268 swimming PATO:0000380 increased frequency abnormal ZDB-GENE-020107-2 140819 5792 ptprfa GO:0036268 swimming PATO:0040033 decreased linear velocity abnormal ZDB-GENE-020107-2 140819 5792 ptprfa GO:0036268 swimming PATO:0055001 decreased spatial extent of a process abnormal ZDB-GENE-020107-2 140819 5792 ptprfa GO:0060134 prepulse inhibition PATO:0002017 increased magnitude abnormal ZDB-GENE-020107-2 140819 5792 ptprfa GO:0097374 sensory neuron axon guidance PATO:0001507 disrupted abnormal ZDB-GENE-020107-2 140819 5792 ptprfa GO:0030424 axon BFO:0000050 part_of ZFA:0009150 Rohon-Beard neuron PATO:0002396 mislocalized adaxially abnormal ZDB-GENE-020107-2 140819 5792 ptprfa GO:0030424 axon BFO:0000050 part_of ZFA:0009150 Rohon-Beard neuron PATO:0002438 subdermal abnormal ZDB-GENE-020108-2 798565 6261 ryr1a ZFA:0001086 muscle pioneer PATO:0001997 decreased amount abnormal ZDB-GENE-020108-2 798565 6261 ryr1a ZFA:0009116 slow muscle cell PATO:0001997 decreased amount abnormal ZDB-GENE-020108-2 798565 6261 ryr1a ZFA:0009117 fast muscle cell PATO:0001997 decreased amount abnormal ZDB-GENE-020111-2 140815 1050 cebpa GO:0001889 liver development PATO:0001236 process quality abnormal ZDB-GENE-020111-2 140815 1050 cebpa GO:0030851 granulocyte differentiation PATO:0001507 disrupted abnormal ZDB-GENE-020111-2 140815 1050 cebpa GO:0072332 intrinsic apoptotic signaling pathway by p53 class mediator PATO:0002051 increased occurrence abnormal ZDB-GENE-020111-2 140815 1050 cebpa ZFA:0009141 macrophage BFO:0000050 part_of ZFA:0000008 brain PATO:0000462 absent abnormal ZDB-GENE-020111-2 140815 1050 cebpa GO:0006915 apoptotic process BFO:0000066 occurs_in ZFA:0000123 liver PATO:0002304 increased process quality abnormal ZDB-GENE-020111-2 140815 1050 cebpa GO:0008283 cell population proliferation BFO:0000066 occurs_in ZFA:0000123 liver PATO:0002051 increased occurrence abnormal ZDB-GENE-020111-2 140815 1050 cebpa ZFA:0000123 liver PATO:0000587 decreased size abnormal ZDB-GENE-020111-2 140815 1050 cebpa ZFA:0009141 macrophage PATO:0000460 abnormal abnormal ZDB-GENE-020111-2 140815 1050 cebpa ZFA:0009141 macrophage PATO:0000462 absent abnormal ZDB-GENE-020111-2 140815 1050 cebpa ZFA:0009327 neutrophil PATO:0000462 absent abnormal ZDB-GENE-020111-2 140815 1050 cebpa GO:0000084 mitotic S phase BFO:0000066 occurs_in ZFA:0009356 myeloid lineage restricted progenitor cell PATO:0000297 arrested abnormal ZDB-GENE-020111-2 140815 1050 cebpa GO:0097529 myeloid leukocyte migration BFO:0000066 occurs_in ZFA:0009356 myeloid lineage restricted progenitor cell PATO:0002052 decreased occurrence abnormal ZDB-GENE-020111-2 140815 1050 cebpa ZFA:0009356 myeloid lineage restricted progenitor cell PATO:0002269 accumulation abnormal ZFA:0005029 rostral blood island ZDB-GENE-020111-2 140815 1050 cebpa ZFA:0009356 myeloid lineage restricted progenitor cell PATO:0001997 decreased amount abnormal ZDB-GENE-020114-1 142986 5747 ptk2ab GO:0002088 lens development in camera-type eye PATO:0001507 disrupted abnormal ZDB-GENE-020114-1 142986 5747 ptk2ab GO:0060026 convergent extension PATO:0010005 spatial distribution of a process abnormal ZDB-GENE-020114-1 142986 5747 ptk2ab GO:0070309 lens fiber cell morphogenesis PATO:0001507 disrupted abnormal ZDB-GENE-020114-1 142986 5747 ptk2ab GO:0090504 epiboly PATO:0000297 arrested abnormal ZDB-GENE-020114-1 142986 5747 ptk2ab GO:0090504 epiboly PATO:0000502 delayed abnormal ZDB-GENE-020114-1 142986 5747 ptk2ab GO:0090504 epiboly PATO:0001507 disrupted abnormal ZDB-GENE-020114-1 142986 5747 ptk2ab GO:0005634 nucleus BFO:0000050 part_of ZFA:0000035 lens PATO:0000470 increased amount abnormal ZDB-GENE-020114-1 142986 5747 ptk2ab ZFA:0009000 cell BFO:0000050 part_of ZFA:0000035 lens PATO:0001505 separated from abnormal ZFA:0001326 lens epithelium ZDB-GENE-020114-1 142986 5747 ptk2ab GO:0032432 actin filament bundle BFO:0000050 part_of ZFA:0000038 margin PATO:0001997 decreased amount abnormal ZDB-GENE-020114-1 142986 5747 ptk2ab GO:0016477 cell migration BFO:0000066 occurs_in ZFA:0000060 prechordal plate PATO:0001236 process quality abnormal ZDB-GENE-020114-1 142986 5747 ptk2ab GO:0016477 cell migration BFO:0000066 occurs_in ZFA:0000060 prechordal plate PATO:0001507 disrupted abnormal ZDB-GENE-020114-1 142986 5747 ptk2ab GO:0016477 cell migration BFO:0000066 occurs_in ZFA:0000060 prechordal plate PATO:0040033 decreased linear velocity abnormal ZDB-GENE-020114-1 142986 5747 ptk2ab ZFA:0000077 tail bud PATO:0000645 hypoplastic abnormal ZDB-GENE-020114-1 142986 5747 ptk2ab GO:0016477 cell migration BFO:0000066 occurs_in ZFA:0000086 EVL PATO:0000688 asynchronous abnormal ZDB-GENE-020114-1 142986 5747 ptk2ab GO:0005634 nucleus BFO:0000050 part_of ZFA:0000088 yolk syncytial layer PATO:0000060 spatial pattern abnormal ZDB-GENE-020114-1 142986 5747 ptk2ab GO:0016477 cell migration BFO:0000066 occurs_in ZFA:0000117 hypoblast PATO:0000911 decreased rate abnormal ZDB-GENE-020114-1 142986 5747 ptk2ab GO:0016477 cell migration BFO:0000066 occurs_in ZFA:0000117 hypoblast PATO:0001236 process quality abnormal ZDB-GENE-020114-1 142986 5747 ptk2ab GO:0016477 cell migration BFO:0000066 occurs_in ZFA:0000117 hypoblast PATO:0001507 disrupted abnormal ZDB-GENE-020114-1 142986 5747 ptk2ab GO:0016477 cell migration BFO:0000066 occurs_in ZFA:0000117 hypoblast PATO:0040033 decreased linear velocity abnormal ZDB-GENE-020114-1 142986 5747 ptk2ab ZFA:0000155 somite PATO:0000600 increased width abnormal ZDB-GENE-020114-1 142986 5747 ptk2ab ZFA:0000092 axis BFO:0000050 part_of ZFA:0001094 whole organism PATO:0000574 decreased length abnormal ZDB-GENE-020114-1 142986 5747 ptk2ab BSPO:0000006 anatomical margin BFO:0000050 part_of ZFA:0001176 blastoderm PATO:0000051 morphology abnormal ZDB-GENE-020114-1 142986 5747 ptk2ab BSPO:0000074 basal region BFO:0000050 part_of ZFA:0007125 midbrain hindbrain boundary constriction PATO:0000141 structure abnormal ZDB-GENE-020114-1 142986 5747 ptk2ab BSPO:0000074 basal region BFO:0000050 part_of ZFA:0007125 midbrain hindbrain boundary constriction PATO:0000600 increased width abnormal ZDB-GENE-020114-1 142986 5747 ptk2ab GO:0003382 epithelial cell morphogenesis BFO:0000066 occurs_in ZFA:0007125 midbrain hindbrain boundary constriction PATO:0001236 process quality abnormal ZDB-GENE-020114-1 142986 5747 ptk2ab GO:0021555 midbrain-hindbrain boundary morphogenesis BFO:0000066 occurs_in ZFA:0007125 midbrain hindbrain boundary constriction PATO:0001236 process quality abnormal ZDB-GENE-020117-1 142987 127343 dmbx1a GO:0010842 retina layer formation PATO:0001507 disrupted abnormal ZDB-GENE-020117-1 142987 127343 dmbx1a GO:0060041 retina development in camera-type eye PATO:0001507 disrupted abnormal ZDB-GENE-020117-1 142987 127343 dmbx1a GO:0070306 lens fiber cell differentiation PATO:0001507 disrupted abnormal ZDB-GENE-020117-1 142987 127343 dmbx1a ZFA:0000035 lens PATO:0000587 decreased size abnormal ZDB-GENE-020117-1 142987 127343 dmbx1a ZFA:0000152 retina PATO:0000592 decreased thickness abnormal ZDB-GENE-020117-1 142987 127343 dmbx1a ZFA:0000435 cranial nerve II PATO:0001959 defasciculated abnormal ZDB-GENE-020117-1 142987 127343 dmbx1a ZFA:0000445 optic tectum PATO:0000587 decreased size abnormal ZDB-GENE-020117-2 142985 2636 gbx1 GO:0007369 gastrulation PATO:0000502 delayed abnormal ZDB-GENE-020117-2 142985 2636 gbx1 GO:0021555 midbrain-hindbrain boundary morphogenesis PATO:0001507 disrupted abnormal ZDB-GENE-020117-2 142985 2636 gbx1 ZFA:0000008 brain PATO:0000051 morphology abnormal ZDB-GENE-020117-2 142985 2636 gbx1 BSPO:0000013 anterior-posterior axis BFO:0000050 part_of ZFA:0000029 hindbrain PATO:0000574 decreased length abnormal ZDB-GENE-020117-2 142985 2636 gbx1 BSPO:0000071 anterior region BFO:0000050 part_of ZFA:0000029 hindbrain PATO:0000587 decreased size abnormal ZDB-GENE-020117-2 142985 2636 gbx1 ZFA:0000075 spinal cord PATO:0000574 decreased length abnormal ZDB-GENE-020117-2 142985 2636 gbx1 ZFA:0000131 neural keel PATO:0000615 wholly anteriorized abnormal ZDB-GENE-020117-2 142985 2636 gbx1 ZFA:0000132 neural plate PATO:0000615 wholly anteriorized abnormal ZDB-GENE-020117-2 142985 2636 gbx1 ZFA:0001094 whole organism PATO:0000052 shape abnormal ZDB-GENE-020117-2 142985 2636 gbx1 ZFA:0001094 whole organism PATO:0000647 necrotic abnormal ZDB-GENE-020117-2 142985 2636 gbx1 ZFA:0007028 spinal cord neural keel PATO:0000574 decreased length abnormal ZDB-GENE-020117-2 142985 2636 gbx1 ZFA:0007044 midbrain hindbrain boundary neural plate PATO:0001922 mislocalised posteriorly abnormal ZDB-GENE-020117-2 142985 2636 gbx1 ZFA:0007045 midbrain hindbrain boundary neural keel PATO:0000051 morphology abnormal ZDB-GENE-020122-1 170446 4211 meis1b GO:0001525 angiogenesis PATO:0001507 disrupted abnormal ZDB-GENE-020122-1 170446 4211 meis1b GO:0001570 vasculogenesis PATO:0001507 disrupted abnormal ZDB-GENE-020122-1 170446 4211 meis1b GO:0001947 heart looping PATO:0001507 disrupted abnormal ZDB-GENE-020122-1 170446 4211 meis1b GO:0008015 blood circulation PATO:0001507 disrupted abnormal ZDB-GENE-020122-1 170446 4211 meis1b GO:0009880 embryonic pattern specification PATO:0001507 disrupted abnormal ZDB-GENE-020122-1 170446 4211 meis1b GO:0009953 dorsal/ventral pattern formation PATO:0001507 disrupted abnormal ZDB-GENE-020122-1 170446 4211 meis1b GO:0030097 hemopoiesis PATO:0002302 decreased process quality abnormal ZDB-GENE-020122-1 170446 4211 meis1b GO:0030218 erythrocyte differentiation PATO:0001507 disrupted abnormal ZDB-GENE-020122-1 170446 4211 meis1b GO:0035474 selective angioblast sprouting PATO:0001507 disrupted abnormal ZDB-GENE-020122-1 170446 4211 meis1b GO:0040036 regulation of fibroblast growth factor receptor signaling pathway PATO:0001507 disrupted abnormal ZDB-GENE-020122-1 170446 4211 meis1b GO:0048514 blood vessel morphogenesis PATO:0001507 disrupted abnormal ZDB-GENE-020122-1 170446 4211 meis1b GO:0048844 artery morphogenesis PATO:0001507 disrupted abnormal ZDB-GENE-020122-1 170446 4211 meis1b GO:0060047 heart contraction PATO:0000911 decreased rate abnormal ZDB-GENE-020122-1 170446 4211 meis1b GO:0060047 heart contraction PATO:0001507 disrupted abnormal ZDB-GENE-020122-1 170446 4211 meis1b GO:0060059 embryonic retina morphogenesis in camera-type eye PATO:0001507 disrupted abnormal ZDB-GENE-020122-1 170446 4211 meis1b GO:0072554 blood vessel lumenization PATO:0001507 disrupted abnormal ZDB-GENE-020122-1 170446 4211 meis1b ZFA:0000014 dorsal aorta PATO:0000642 fused with abnormal ZFA:0000477 posterior cardinal vein ZDB-GENE-020122-1 170446 4211 meis1b ZFA:0000014 dorsal aorta PATO:0000051 morphology abnormal ZDB-GENE-020122-1 170446 4211 meis1b ZFA:0000029 hindbrain PATO:0000051 morphology abnormal ZDB-GENE-020122-1 170446 4211 meis1b ZFA:0000054 pericardium PATO:0001450 edematous abnormal ZDB-GENE-020122-1 170446 4211 meis1b ZFA:0009141 macrophage BFO:0000050 part_of ZFA:0000094 blood island PATO:0001997 decreased amount abnormal ZDB-GENE-020122-1 170446 4211 meis1b ZFA:0009327 neutrophil BFO:0000050 part_of ZFA:0000094 blood island PATO:0001997 decreased amount abnormal ZDB-GENE-020122-1 170446 4211 meis1b ZFA:0000107 eye PATO:0000587 decreased size abnormal ZDB-GENE-020122-1 170446 4211 meis1b ZFA:0000114 heart PATO:0000625 inverted abnormal ZDB-GENE-020122-1 170446 4211 meis1b ZFA:0000152 retina PATO:0000051 morphology abnormal ZDB-GENE-020122-1 170446 4211 meis1b ZFA:0001681 grey matter BFO:0000050 part_of ZFA:0000445 optic tectum PATO:0001562 decreased mass abnormal ZDB-GENE-020122-1 170446 4211 meis1b ZFA:0000445 optic tectum PATO:0000587 decreased size abnormal ZDB-GENE-020122-1 170446 4211 meis1b ZFA:0001202 optic cup PATO:0000636 wholly ventralized abnormal ZDB-GENE-020122-1 170446 4211 meis1b ZFA:0001205 Meckel's cartilage PATO:0000642 fused with abnormal ZFA:0001399 palatoquadrate cartilage ZDB-GENE-020122-1 170446 4211 meis1b ZFA:0001205 Meckel's cartilage PATO:0000642 fused with abnormal ZFA:0001422 hyosymplectic cartilage ZDB-GENE-020122-1 170446 4211 meis1b ZFA:0001285 intersegmental vessel PATO:0000051 morphology abnormal ZDB-GENE-020122-1 170446 4211 meis1b ZFA:0001399 palatoquadrate cartilage PATO:0001599 rotated abnormal ZDB-GENE-020122-1 170446 4211 meis1b ZFA:0001399 palatoquadrate cartilage PATO:0002254 flattened abnormal ZDB-GENE-020122-1 170446 4211 meis1b ZFA:0001400 ceratohyal cartilage PATO:0000642 fused with abnormal ZFA:0001516 ceratobranchial cartilage ZDB-GENE-020122-1 170446 4211 meis1b ZFA:0001458 cranial cartilage PATO:0000051 morphology abnormal ZDB-GENE-020122-1 170446 4211 meis1b ZFA:0001458 cranial cartilage PATO:0000628 mislocalised abnormal ZDB-GENE-020122-1 170446 4211 meis1b ZFA:0001516 ceratobranchial cartilage PATO:0000642 fused with abnormal ZFA:0001516 ceratobranchial cartilage ZDB-GENE-020122-1 170446 4211 meis1b ZFA:0009044 blood cell PATO:0001997 decreased amount abnormal ZDB-GENE-020122-1 170446 4211 meis1b ZFA:0009256 nucleate erythrocyte PATO:0001997 decreased amount abnormal ZDB-GENE-020122-1 170446 4211 meis1b ZFA:0009323 thrombocyte PATO:0000462 absent abnormal ZDB-GENE-020122-2 170454 4212 meis2a ZFA:0001205 Meckel's cartilage PATO:0000642 fused with abnormal ZFA:0001399 palatoquadrate cartilage ZDB-GENE-020122-2 170454 4212 meis2a ZFA:0001458 cranial cartilage PATO:0000642 fused with abnormal ZFA:0001458 cranial cartilage ZDB-GENE-020122-2 170454 4212 meis2a ZFA:0001458 cranial cartilage PATO:0000628 mislocalised abnormal ZDB-GENE-020122-5 798151 5316 pknox1.1 GO:0008219 cell death PATO:0002051 increased occurrence abnormal ZDB-GENE-020122-5 798151 5316 pknox1.1 GO:0030902 hindbrain development PATO:0001507 disrupted abnormal ZDB-GENE-020122-5 798151 5316 pknox1.1 GO:0035284 brain segmentation PATO:0001507 disrupted abnormal ZDB-GENE-020122-5 798151 5316 pknox1.1 GO:0048798 swim bladder inflation PATO:0000297 arrested abnormal ZDB-GENE-020122-5 798151 5316 pknox1.1 ZFA:0000008 brain PATO:0000051 morphology abnormal ZDB-GENE-020122-5 798151 5316 pknox1.1 ZFA:0000008 brain PATO:0000638 apoptotic abnormal ZDB-GENE-020122-5 798151 5316 pknox1.1 ZFA:0000054 pericardium PATO:0001450 edematous abnormal ZDB-GENE-020122-5 798151 5316 pknox1.1 ZFA:0000076 swim bladder PATO:0001483 aplastic abnormal ZDB-GENE-020122-5 798151 5316 pknox1.1 ZFA:0000107 eye PATO:0000587 decreased size abnormal ZDB-GENE-020122-5 798151 5316 pknox1.1 ZFA:0000206 facial nerve motor nucleus PATO:0000628 mislocalised abnormal ZDB-GENE-020122-5 798151 5316 pknox1.1 ZFA:0009248 neuron BFO:0000050 part_of ZFA:0001064 rhombomere PATO:0002264 organization quality abnormal ZDB-GENE-020122-5 798151 5316 pknox1.1 ZFA:0001094 whole organism PATO:0002000 lacks all parts of type abnormal ZFA:0001227 mandibular arch skeleton ZDB-GENE-020122-5 798151 5316 pknox1.1 ZFA:0001094 whole organism PATO:0000169 viability abnormal ZDB-GENE-020122-5 798151 5316 pknox1.1 ZFA:0001114 head PATO:0000587 decreased size abnormal ZDB-GENE-020122-5 798151 5316 pknox1.1 ZFA:0001161 pectoral fin PATO:0001623 atrophied abnormal ZDB-GENE-020122-5 798151 5316 pknox1.1 ZFA:0001405 ethmoid cartilage PATO:0000587 decreased size abnormal ZDB-GENE-020122-5 798151 5316 pknox1.1 ZFA:0001405 ethmoid cartilage PATO:0001617 deformed abnormal ZDB-GENE-020122-5 798151 5316 pknox1.1 ZFA:0001507 trabecula cranii PATO:0000587 decreased size abnormal ZDB-GENE-020122-5 798151 5316 pknox1.1 ZFA:0001507 trabecula cranii PATO:0001617 deformed abnormal ZDB-GENE-020122-5 798151 5316 pknox1.1 ZFA:0009091 melanocyte PATO:0000060 spatial pattern abnormal ZDB-GENE-020122-5 798151 5316 pknox1.1 ZFA:0009191 CNS interneuron PATO:0001997 decreased amount abnormal ZDB-GENE-020123-1 170445 5316 pknox1.2 GO:0007492 endoderm development PATO:0001236 process quality abnormal ZDB-GENE-020123-1 170445 5316 pknox1.2 GO:0014033 neural crest cell differentiation PATO:0001236 process quality abnormal ZDB-GENE-020123-1 170445 5316 pknox1.2 GO:0048384 retinoic acid receptor signaling pathway PATO:0001236 process quality abnormal ZDB-GENE-020123-1 170445 5316 pknox1.2 GO:0048703 embryonic viscerocranium morphogenesis PATO:0001236 process quality abnormal ZDB-GENE-020123-1 170445 5316 pknox1.2 GO:0060037 pharyngeal system development PATO:0001236 process quality abnormal ZDB-GENE-020123-1 170445 5316 pknox1.2 ZFA:0000141 pectoral fin bud PATO:0001241 physical object quality abnormal ZDB-GENE-020123-1 170445 5316 pknox1.2 ZFA:0001131 pharyngeal pouch 3 PATO:0001483 aplastic abnormal ZDB-GENE-020123-1 170445 5316 pknox1.2 ZFA:0001132 pharyngeal pouch 6 PATO:0001483 aplastic abnormal ZDB-GENE-020123-1 170445 5316 pknox1.2 ZFA:0001133 pharyngeal pouch 5 PATO:0001483 aplastic abnormal ZDB-GENE-020123-1 170445 5316 pknox1.2 ZFA:0001134 pharyngeal pouch 4 PATO:0001483 aplastic abnormal ZDB-GENE-020123-1 170445 5316 pknox1.2 ZFA:0001205 Meckel's cartilage PATO:0000587 decreased size abnormal ZDB-GENE-020123-1 170445 5316 pknox1.2 ZFA:0001205 Meckel's cartilage PATO:0000646 malformed abnormal ZDB-GENE-020123-1 170445 5316 pknox1.2 ZFA:0001228 pharyngeal arch 3 skeleton PATO:0000587 decreased size abnormal ZDB-GENE-020123-1 170445 5316 pknox1.2 ZFA:0001229 pharyngeal arch 7 skeleton PATO:0001483 aplastic abnormal ZDB-GENE-020123-1 170445 5316 pknox1.2 ZFA:0001230 pharyngeal arch 6 skeleton PATO:0001483 aplastic abnormal ZDB-GENE-020123-1 170445 5316 pknox1.2 ZFA:0001231 pharyngeal arch 4 skeleton PATO:0001483 aplastic abnormal ZDB-GENE-020123-1 170445 5316 pknox1.2 ZFA:0001232 pharyngeal arch 5 skeleton PATO:0001483 aplastic abnormal ZDB-GENE-020123-1 170445 5316 pknox1.2 ZFA:0001400 ceratohyal cartilage PATO:0000587 decreased size abnormal ZDB-GENE-020123-1 170445 5316 pknox1.2 ZFA:0001400 ceratohyal cartilage PATO:0000646 malformed abnormal ZDB-GENE-020123-1 170445 5316 pknox1.2 ZFA:0001613 pharyngeal arch 3-7 PATO:0001241 physical object quality abnormal ZDB-GENE-020123-2 170457 9294 s1pr2 GO:0003007 heart morphogenesis PATO:0001236 process quality abnormal ZDB-GENE-020123-2 170457 9294 s1pr2 GO:0003007 heart morphogenesis PATO:0001507 disrupted abnormal ZDB-GENE-020123-2 170457 9294 s1pr2 GO:0003007 heart morphogenesis PATO:0002302 decreased process quality abnormal ZDB-GENE-020123-2 170457 9294 s1pr2 GO:0003143 embryonic heart tube morphogenesis PATO:0001507 disrupted abnormal ZDB-GENE-020123-2 170457 9294 s1pr2 GO:0003144 embryonic heart tube formation PATO:0002052 decreased occurrence abnormal ZDB-GENE-020123-2 170457 9294 s1pr2 GO:0003261 cardiac muscle progenitor cell migration to the midline involved in heart field formation PATO:0002052 decreased occurrence abnormal ZDB-GENE-020123-2 170457 9294 s1pr2 GO:0003315 heart rudiment formation PATO:0002302 decreased process quality abnormal ZDB-GENE-020123-2 170457 9294 s1pr2 GO:0003318 cell migration to the midline involved in heart development PATO:0002052 decreased occurrence abnormal ZDB-GENE-020123-2 170457 9294 s1pr2 GO:0003319 cardioblast migration to the midline involved in heart rudiment formation PATO:0001507 disrupted abnormal ZDB-GENE-020123-2 170457 9294 s1pr2 GO:0003319 cardioblast migration to the midline involved in heart rudiment formation PATO:0002302 decreased process quality abnormal ZDB-GENE-020123-2 170457 9294 s1pr2 GO:0008015 blood circulation PATO:0000297 arrested abnormal ZDB-GENE-020123-2 170457 9294 s1pr2 GO:0008015 blood circulation PATO:0001507 disrupted abnormal ZDB-GENE-020123-2 170457 9294 s1pr2 GO:0008078 mesodermal cell migration PATO:0000912 increased rate abnormal ZDB-GENE-020123-2 170457 9294 s1pr2 GO:0035676 anterior lateral line neuromast hair cell development PATO:0001507 disrupted abnormal ZDB-GENE-020123-2 170457 9294 s1pr2 GO:0035677 posterior lateral line neuromast hair cell development PATO:0001507 disrupted abnormal ZDB-GENE-020123-2 170457 9294 s1pr2 GO:0042074 cell migration involved in gastrulation PATO:0001507 disrupted abnormal ZDB-GENE-020123-2 170457 9294 s1pr2 GO:0060872 semicircular canal development PATO:0001507 disrupted abnormal ZDB-GENE-020123-2 170457 9294 s1pr2 GO:0060975 cardioblast migration to the midline involved in heart field formation PATO:0002052 decreased occurrence abnormal ZDB-GENE-020123-2 170457 9294 s1pr2 GO:0071600 otic vesicle morphogenesis PATO:0001507 disrupted abnormal ZDB-GENE-020123-2 170457 9294 s1pr2 BSPO:0000050 antero-medial region BFO:0000050 part_of ZFA:0000017 endoderm PATO:0002303 decreased object quality abnormal ZDB-GENE-020123-2 170457 9294 s1pr2 BSPO:0000071 anterior region BFO:0000050 part_of ZFA:0000017 endoderm PATO:0000600 increased width abnormal ZDB-GENE-020123-2 170457 9294 s1pr2 BSPO:0000071 anterior region BFO:0000050 part_of ZFA:0000017 endoderm PATO:0000638 apoptotic abnormal ZDB-GENE-020123-2 170457 9294 s1pr2 BSPO:0000071 anterior region BFO:0000050 part_of ZFA:0000017 endoderm PATO:0002112 perforate abnormal ZDB-GENE-020123-2 170457 9294 s1pr2 GO:0006915 apoptotic process BFO:0000066 occurs_in ZFA:0000017 endoderm PATO:0002051 increased occurrence abnormal ZDB-GENE-020123-2 170457 9294 s1pr2 GO:0060026 convergent extension BFO:0000066 occurs_in ZFA:0000017 endoderm PATO:0001236 process quality abnormal ZDB-GENE-020123-2 170457 9294 s1pr2 ZFA:0000054 pericardium PATO:0001450 edematous abnormal ZDB-GENE-020123-2 170457 9294 s1pr2 ZFA:0000054 pericardium PATO:0001851 swollen abnormal ZDB-GENE-020123-2 170457 9294 s1pr2 ZFA:0000060 prechordal plate PATO:0000407 flat abnormal ZDB-GENE-020123-2 170457 9294 s1pr2 ZFA:0000060 prechordal plate PATO:0000573 increased length abnormal ZDB-GENE-020123-2 170457 9294 s1pr2 ZFA:0000060 prechordal plate PATO:0000600 increased width abnormal ZDB-GENE-020123-2 170457 9294 s1pr2 ZFA:0000114 heart PATO:0000001 quality abnormal ZDB-GENE-020123-2 170457 9294 s1pr2 ZFA:0000114 heart PATO:0000052 shape abnormal ZDB-GENE-020123-2 170457 9294 s1pr2 ZFA:0000114 heart PATO:0000403 cleft abnormal ZDB-GENE-020123-2 170457 9294 s1pr2 ZFA:0000114 heart PATO:0000470 increased amount abnormal ZDB-GENE-020123-2 170457 9294 s1pr2 ZFA:0000114 heart PATO:0000646 malformed abnormal ZDB-GENE-020123-2 170457 9294 s1pr2 ZFA:0000114 heart PATO:0001450 edematous abnormal ZDB-GENE-020123-2 170457 9294 s1pr2 ZFA:0000114 heart PATO:0001473 duplicated abnormal ZDB-GENE-020123-2 170457 9294 s1pr2 ZFA:0000114 heart PATO:0001784 bifurcated abnormal ZDB-GENE-020123-2 170457 9294 s1pr2 ZFA:0000114 heart PATO:0002171 split bilaterally abnormal ZDB-GENE-020123-2 170457 9294 s1pr2 ZFA:0000115 heart rudiment PATO:0000646 malformed abnormal ZDB-GENE-020123-2 170457 9294 s1pr2 ZFA:0000115 heart rudiment PATO:0001784 bifurcated abnormal ZDB-GENE-020123-2 170457 9294 s1pr2 ZFA:0000115 heart rudiment PATO:0001786 split abnormal ZDB-GENE-020123-2 170457 9294 s1pr2 ZFA:0009138 mesodermal cell BFO:0000050 part_of ZFA:0000117 hypoblast PATO:0000060 spatial pattern abnormal ZDB-GENE-020123-2 170457 9294 s1pr2 ZFA:0000123 liver PATO:0000618 bilateral abnormal ZDB-GENE-020123-2 170457 9294 s1pr2 ZFA:0000131 neural keel PATO:0000573 increased length abnormal ZDB-GENE-020123-2 170457 9294 s1pr2 ZFA:0000360 heart tube PATO:0000470 increased amount abnormal ZDB-GENE-020123-2 170457 9294 s1pr2 ZFA:0000360 heart tube PATO:0001473 duplicated abnormal ZDB-GENE-020123-2 170457 9294 s1pr2 ZFA:0000360 heart tube PATO:0001784 bifurcated abnormal ZDB-GENE-020123-2 170457 9294 s1pr2 ZFA:0000360 heart tube PATO:0001923 mislocalised laterally abnormal ZDB-GENE-020123-2 170457 9294 s1pr2 ZFA:0000360 heart tube PATO:0002171 split bilaterally abnormal ZDB-GENE-020123-2 170457 9294 s1pr2 ZFA:0000428 saccule PATO:0000587 decreased size abnormal ZDB-GENE-020123-2 170457 9294 s1pr2 ZFA:0000431 semicircular canal PATO:0000051 morphology abnormal ZDB-GENE-020123-2 170457 9294 s1pr2 ZFA:0000431 semicircular canal PATO:0002080 broken into two pieces abnormal ZDB-GENE-020123-2 170457 9294 s1pr2 ZFA:0000700 utricle PATO:0000586 increased size abnormal ZDB-GENE-020123-2 170457 9294 s1pr2 ZFA:0000940 posterior lateral line neuromast PATO:0000587 decreased size abnormal ZDB-GENE-020123-2 170457 9294 s1pr2 ZFA:0000944 posterior lateral line PATO:0002001 has fewer parts of type abnormal ZFA:0000940 posterior lateral line neuromast ZDB-GENE-020123-2 170457 9294 s1pr2 ZFA:0000017 endoderm BFO:0000050 part_of ZFA:0001058 caudal fin PATO:0001928 blistered abnormal ZDB-GENE-020123-2 170457 9294 s1pr2 ZFA:0009183 epidermal cell BFO:0000050 part_of ZFA:0001058 caudal fin PATO:0001629 aggregated abnormal ZDB-GENE-020123-2 170457 9294 s1pr2 ZFA:0001058 caudal fin PATO:0001928 blistered abnormal ZDB-GENE-020123-2 170457 9294 s1pr2 ZFA:0001094 whole organism PATO:0000718 lethal (sensu genetics) abnormal ZDB-GENE-020123-2 170457 9294 s1pr2 ZFA:0001104 pharyngeal endoderm PATO:0000937 disorganized abnormal ZDB-GENE-020123-2 170457 9294 s1pr2 ZFA:0001104 pharyngeal endoderm PATO:0001922 mislocalised posteriorly abnormal ZDB-GENE-020123-2 170457 9294 s1pr2 ZFA:0001104 pharyngeal endoderm PATO:0001923 mislocalised laterally abnormal ZDB-GENE-020123-2 170457 9294 s1pr2 ZFA:0001486 epithelium BFO:0000050 part_of ZFA:0001117 post-vent region PATO:0001928 blistered abnormal ZDB-GENE-020123-2 170457 9294 s1pr2 ZFA:0001205 Meckel's cartilage PATO:0000645 hypoplastic abnormal ZDB-GENE-020123-2 170457 9294 s1pr2 ZFA:0001205 Meckel's cartilage PATO:0000646 malformed abnormal ZDB-GENE-020123-2 170457 9294 s1pr2 ZFA:0001205 Meckel's cartilage PATO:0000937 disorganized abnormal ZDB-GENE-020123-2 170457 9294 s1pr2 ZFA:0001205 Meckel's cartilage PATO:0001483 aplastic abnormal ZDB-GENE-020123-2 170457 9294 s1pr2 GO:0030282 bone mineralization BFO:0000066 occurs_in ZFA:0001216 splanchnocranium PATO:0001507 disrupted abnormal ZDB-GENE-020123-2 170457 9294 s1pr2 ZFA:0001227 mandibular arch skeleton PATO:0000052 shape abnormal ZDB-GENE-020123-2 170457 9294 s1pr2 ZFA:0001227 mandibular arch skeleton PATO:0000117 size abnormal ZDB-GENE-020123-2 170457 9294 s1pr2 ZFA:0001227 mandibular arch skeleton PATO:0000628 mislocalised abnormal ZDB-GENE-020123-2 170457 9294 s1pr2 ZFA:0001227 mandibular arch skeleton PATO:0000645 hypoplastic abnormal ZDB-GENE-020123-2 170457 9294 s1pr2 BSPO:0000013 anterior-posterior axis BFO:0000050 part_of ZFA:0001273 ventral mandibular arch PATO:0000574 decreased length abnormal ZDB-GENE-020123-2 170457 9294 s1pr2 ZFA:0001273 ventral mandibular arch PATO:0000051 morphology abnormal ZDB-GENE-020123-2 170457 9294 s1pr2 ZFA:0001320 endocardium PATO:0000651 unfused from abnormal ZFA:0001320 endocardium ZDB-GENE-020123-2 170457 9294 s1pr2 ZFA:0001320 endocardium PATO:0000628 mislocalised abnormal ZDB-GENE-020123-2 170457 9294 s1pr2 ZFA:0001321 neurocranial trabecula PATO:0000645 hypoplastic abnormal ZDB-GENE-020123-2 170457 9294 s1pr2 ZFA:0001379 pharyngeal ectoderm PATO:0000937 disorganized abnormal ZDB-GENE-020123-2 170457 9294 s1pr2 ZFA:0001379 pharyngeal ectoderm PATO:0002057 increased area abnormal ZDB-GENE-020123-2 170457 9294 s1pr2 ZFA:0001399 palatoquadrate cartilage PATO:0001483 aplastic abnormal ZDB-GENE-020123-2 170457 9294 s1pr2 ZFA:0001405 ethmoid cartilage PATO:0000645 hypoplastic abnormal ZDB-GENE-020123-2 170457 9294 s1pr2 ZFA:0001439 anatomical system PATO:0000001 quality abnormal ZDB-GENE-020123-2 170457 9294 s1pr2 ZFA:0009367 neuromast hair cell BFO:0000050 part_of ZFA:0001470 anterior lateral line PATO:0001997 decreased amount abnormal ZDB-GENE-020123-2 170457 9294 s1pr2 ZFA:0001612 pharyngeal arch 1 PATO:0000051 morphology abnormal ZDB-GENE-020123-2 170457 9294 s1pr2 ZFA:0001612 pharyngeal arch 1 PATO:0000574 decreased length abnormal ZDB-GENE-020123-2 170457 9294 s1pr2 ZFA:0001617 otolith PATO:0000586 increased size abnormal ZDB-GENE-020123-2 170457 9294 s1pr2 ZFA:0001617 otolith PATO:0000646 malformed abnormal ZDB-GENE-020123-2 170457 9294 s1pr2 ZFA:0005463 oral ectoderm PATO:0000645 hypoplastic abnormal ZDB-GENE-020123-2 170457 9294 s1pr2 ZFA:0005463 oral ectoderm PATO:0000937 disorganized abnormal ZDB-GENE-020123-2 170457 9294 s1pr2 ZFA:0005463 oral ectoderm PATO:0001921 mislocalised anteriorly abnormal ZDB-GENE-020123-2 170457 9294 s1pr2 ZFA:0005490 myocardial precursor PATO:0001923 mislocalised laterally abnormal ZDB-GENE-020123-2 170457 9294 s1pr2 ZFA:0005597 median fin PATO:0001928 blistered abnormal ZDB-GENE-020123-2 170457 9294 s1pr2 ZFA:0009183 epidermal cell PATO:0001629 aggregated abnormal ZDB-GENE-020123-2 170457 9294 s1pr2 ZFA:0009367 neuromast hair cell PATO:0000638 apoptotic abnormal ZDB-GENE-020125-1 798689 2890 gria1a GO:0001964 startle response PATO:0002017 increased magnitude abnormal ZDB-GENE-020125-1 798689 2890 gria1a GO:0009646 response to absence of light PATO:0002302 decreased process quality abnormal ZDB-GENE-020125-1 798689 2890 gria1a GO:0036268 swimming PATO:0000380 increased frequency abnormal ZDB-GENE-020125-1 798689 2890 gria1a GO:0036268 swimming PATO:0002051 increased occurrence abnormal ZDB-GENE-020125-1 798689 2890 gria1a GO:0036268 swimming PATO:0040033 decreased linear velocity abnormal ZDB-GENE-020125-1 798689 2890 gria1a GO:0036268 swimming PATO:0055001 decreased spatial extent of a process abnormal ZDB-GENE-020125-1 798689 2890 gria1a GO:0046959 habituation PATO:0000912 increased rate abnormal ZDB-GENE-020125-1 798689 2890 gria1a GO:0060134 prepulse inhibition PATO:0002017 increased magnitude abnormal ZDB-GENE-020125-2 403044 2890 gria1b GO:0001964 startle response PATO:0002017 increased magnitude abnormal ZDB-GENE-020125-2 403044 2890 gria1b GO:0009646 response to absence of light PATO:0002302 decreased process quality abnormal ZDB-GENE-020125-2 403044 2890 gria1b GO:0036268 swimming PATO:0000380 increased frequency abnormal ZDB-GENE-020125-2 403044 2890 gria1b GO:0036268 swimming PATO:0002051 increased occurrence abnormal ZDB-GENE-020125-2 403044 2890 gria1b GO:0036268 swimming PATO:0040033 decreased linear velocity abnormal ZDB-GENE-020125-2 403044 2890 gria1b GO:0036268 swimming PATO:0055001 decreased spatial extent of a process abnormal ZDB-GENE-020125-2 403044 2890 gria1b GO:0046959 habituation PATO:0000912 increased rate abnormal ZDB-GENE-020125-2 403044 2890 gria1b GO:0060134 prepulse inhibition PATO:0002017 increased magnitude abnormal ZDB-GENE-020125-3 170450 2891 gria2a GO:0001755 neural crest cell migration PATO:0001236 process quality abnormal ZDB-GENE-020125-3 170450 2891 gria2a GO:0006915 apoptotic process PATO:0002304 increased process quality abnormal ZDB-GENE-020125-3 170450 2891 gria2a GO:0006915 apoptotic process BFO:0000066 occurs_in ZFA:0000029 hindbrain PATO:0002304 increased process quality abnormal ZDB-GENE-020125-3 170450 2891 gria2a ZFA:0000075 spinal cord PATO:0002001 has fewer parts of type abnormal ZFA:0009052 motor neuron ZDB-GENE-020125-3 170450 2891 gria2a GO:0006915 apoptotic process BFO:0000066 occurs_in ZFA:0000107 eye PATO:0002304 increased process quality abnormal ZDB-GENE-020125-3 170450 2891 gria2a ZFA:0000110 fourth ventricle PATO:0000586 increased size abnormal ZDB-GENE-020125-3 170450 2891 gria2a GO:0006915 apoptotic process BFO:0000066 occurs_in ZFA:0000128 midbrain PATO:0002304 increased process quality abnormal ZDB-GENE-020125-3 170450 2891 gria2a ZFA:0000161 third ventricle PATO:0000586 increased size abnormal ZDB-GENE-020125-3 170450 2891 gria2a GO:0006915 apoptotic process BFO:0000066 occurs_in ZFA:0000671 horizontal myoseptum PATO:0002304 increased process quality abnormal ZDB-GENE-020125-3 170450 2891 gria2a ZFA:0000940 posterior lateral line neuromast PATO:0001997 decreased amount abnormal ZDB-GENE-020125-3 170450 2891 gria2a GO:0006915 apoptotic process BFO:0000066 occurs_in ZFA:0001114 head PATO:0002304 increased process quality abnormal ZDB-GENE-020125-3 170450 2891 gria2a ZFA:0001114 head PATO:0000587 decreased size abnormal ZDB-GENE-020125-3 170450 2891 gria2a GO:0006915 apoptotic process BFO:0000066 occurs_in ZFA:0001115 trunk PATO:0002304 increased process quality abnormal ZDB-GENE-020125-3 170450 2891 gria2a ZFA:0001306 pharyngeal arch PATO:0000462 absent abnormal ZDB-GENE-020125-3 170450 2891 gria2a ZFA:0001321 neurocranial trabecula PATO:0000587 decreased size abnormal ZDB-GENE-020125-3 170450 2891 gria2a ZFA:0001405 ethmoid cartilage PATO:0000462 absent abnormal ZDB-GENE-020125-3 170450 2891 gria2a ZFA:0001423 parachordal cartilage PATO:0000587 decreased size abnormal ZDB-GENE-020125-3 170450 2891 gria2a ZFA:0001458 cranial cartilage PATO:0000646 malformed abnormal ZDB-GENE-020125-3 170450 2891 gria2a ZFA:0001472 anterior lateral line neuromast PATO:0001997 decreased amount abnormal ZDB-GENE-020125-5 170452 2892 gria3a ZFA:0001094 whole organism PATO:0000051 morphology abnormal ZDB-GENE-020125-5 170452 2892 gria3a ZFA:0001094 whole organism PATO:0001422 dead abnormal ZDB-GENE-020125-7 407735 2893 gria4a BSPO:0000079 dorsal region BFO:0000050 part_of ZFA:0000075 spinal cord PATO:0002001 has fewer parts of type abnormal ZFA:0009169 glioblast (sensu Vertebrata) ZDB-GENE-020125-7 407735 2893 gria4a BSPO:0000079 dorsal region BFO:0000050 part_of ZFA:0000075 spinal cord PATO:0002002 has extra parts of type abnormal ZFA:0009169 glioblast (sensu Vertebrata) ZDB-GENE-020125-7 407735 2893 gria4a GO:0008347 glial cell migration BFO:0000066 occurs_in ZFA:0000075 spinal cord PATO:0002302 decreased process quality abnormal ZDB-GENE-020125-7 407735 2893 gria4a GO:0022010 central nervous system myelination BFO:0000066 occurs_in ZFA:0000075 spinal cord PATO:0002302 decreased process quality abnormal ZDB-GENE-020125-7 407735 2893 gria4a GO:1905232 cellular response to L-glutamate BFO:0000066 occurs_in ZFA:0009169 glioblast (sensu Vertebrata) PATO:0002302 decreased process quality abnormal ZDB-GENE-020129-1 170581 775 cacna1c GO:0001947 heart looping PATO:0001507 disrupted abnormal ZDB-GENE-020129-1 170581 775 cacna1c GO:0001964 startle response PATO:0002018 decreased magnitude abnormal ZDB-GENE-020129-1 170581 775 cacna1c GO:0008015 blood circulation PATO:0000297 arrested abnormal ZDB-GENE-020129-1 170581 775 cacna1c GO:0008283 cell population proliferation PATO:0002052 decreased occurrence abnormal ZDB-GENE-020129-1 170581 775 cacna1c GO:0009646 response to absence of light PATO:0002304 increased process quality abnormal ZDB-GENE-020129-1 170581 775 cacna1c GO:0036268 swimming PATO:0000381 decreased frequency abnormal ZDB-GENE-020129-1 170581 775 cacna1c GO:0036268 swimming PATO:0002052 decreased occurrence abnormal ZDB-GENE-020129-1 170581 775 cacna1c GO:0036268 swimming PATO:0040033 decreased linear velocity abnormal ZDB-GENE-020129-1 170581 775 cacna1c GO:0036268 swimming PATO:0055001 decreased spatial extent of a process abnormal ZDB-GENE-020129-1 170581 775 cacna1c GO:0046959 habituation PATO:0000911 decreased rate abnormal ZDB-GENE-020129-1 170581 775 cacna1c GO:0060047 heart contraction PATO:0000297 arrested abnormal ZDB-GENE-020129-1 170581 775 cacna1c GO:0060047 heart contraction PATO:0001236 process quality abnormal ZDB-GENE-020129-1 170581 775 cacna1c GO:0060047 heart contraction PATO:0001507 disrupted abnormal ZDB-GENE-020129-1 170581 775 cacna1c GO:0060047 heart contraction PATO:0001845 irregular rhythm abnormal ZDB-GENE-020129-1 170581 775 cacna1c GO:0060048 cardiac muscle contraction PATO:0001845 irregular rhythm abnormal ZDB-GENE-020129-1 170581 775 cacna1c GO:0060134 prepulse inhibition PATO:0002017 increased magnitude abnormal ZDB-GENE-020129-1 170581 775 cacna1c GO:0061337 cardiac conduction PATO:0000078 rhythm quality abnormal ZDB-GENE-020129-1 170581 775 cacna1c GO:0061371 determination of heart left/right asymmetry PATO:0001507 disrupted abnormal ZDB-GENE-020129-1 170581 775 cacna1c ZFA:0000008 brain PATO:0000587 decreased size abnormal ZDB-GENE-020129-1 170581 775 cacna1c ZFA:0000008 brain PATO:0001853 hydrocephalic abnormal ZDB-GENE-020129-1 170581 775 cacna1c ZFA:0009316 cardiac muscle cell BFO:0000050 part_of ZFA:0000009 cardiac ventricle PATO:0001691 non-contractile abnormal ZDB-GENE-020129-1 170581 775 cacna1c ZFA:0000009 cardiac ventricle PATO:0000051 morphology abnormal ZDB-GENE-020129-1 170581 775 cacna1c ZFA:0000009 cardiac ventricle PATO:0000587 decreased size abnormal ZDB-GENE-020129-1 170581 775 cacna1c ZFA:0000009 cardiac ventricle PATO:0001511 non-functional abnormal ZDB-GENE-020129-1 170581 775 cacna1c ZFA:0000054 pericardium PATO:0001450 edematous abnormal ZDB-GENE-020129-1 170581 775 cacna1c ZFA:0000084 yolk PATO:0001450 edematous abnormal ZDB-GENE-020129-1 170581 775 cacna1c ZFA:0000114 heart PATO:0000001 quality abnormal ZDB-GENE-020129-1 170581 775 cacna1c ZFA:0000114 heart PATO:0001579 contractility abnormal ZDB-GENE-020129-1 170581 775 cacna1c ZFA:0000114 heart PATO:0001581 decreased contractility abnormal ZDB-GENE-020129-1 170581 775 cacna1c ZFA:0000150 pronephric duct PATO:0001571 dilated abnormal ZDB-GENE-020129-1 170581 775 cacna1c ZFA:0000150 pronephric duct PATO:0001673 cystic abnormal ZDB-GENE-020129-1 170581 775 cacna1c CHEBI:17234 glucose BFO:0000050 part_of ZFA:0001094 whole organism PATO:0000470 increased amount abnormal ZDB-GENE-020129-1 170581 775 cacna1c ZFA:0009084 chondrocyte BFO:0000050 part_of ZFA:0001205 Meckel's cartilage PATO:0000587 decreased size abnormal ZDB-GENE-020129-1 170581 775 cacna1c ZFA:0001227 mandibular arch skeleton PATO:0000051 morphology abnormal ZDB-GENE-020129-1 170581 775 cacna1c ZFA:0001273 ventral mandibular arch PATO:0000587 decreased size abnormal ZDB-GENE-020129-1 170581 775 cacna1c ZFA:0001374 atrial myocardium PATO:0001579 contractility abnormal ZDB-GENE-020129-1 170581 775 cacna1c ZFA:0001439 anatomical system PATO:0000001 quality abnormal ZDB-GENE-020129-1 170581 775 cacna1c ZFA:0001557 pronephric glomerulus PATO:0000651 unfused from abnormal ZFA:0001557 pronephric glomerulus ZDB-GENE-020129-1 170581 775 cacna1c ZFA:0001673 pronephric podocyte PATO:0000651 unfused from abnormal ZFA:0001673 pronephric podocyte ZDB-GENE-020129-1 170581 775 cacna1c ZFA:0005061 ventricular myocardium PATO:0000592 decreased thickness abnormal ZDB-GENE-020129-1 170581 775 cacna1c ZFA:0005061 ventricular myocardium PATO:0001511 non-functional abnormal ZDB-GENE-020129-1 170581 775 cacna1c ZFA:0009316 cardiac muscle cell PATO:0000596 decreased volume abnormal ZDB-GENE-020213-2 170783 23609 mkrn2 ZFA:0001115 trunk PATO:0001469 curved ventral abnormal ZDB-GENE-020220-1 170846 351 appb GO:0001966 thigmotaxis PATO:0002052 decreased occurrence abnormal ZDB-GENE-020220-1 170846 351 appb GO:0002040 sprouting angiogenesis PATO:0002302 decreased process quality abnormal ZDB-GENE-020220-1 170846 351 appb GO:0007409 axonogenesis PATO:0001507 disrupted abnormal ZDB-GENE-020220-1 170846 351 appb GO:0007416 synapse assembly PATO:0001507 disrupted abnormal ZDB-GENE-020220-1 170846 351 appb GO:0007417 central nervous system development PATO:0001507 disrupted abnormal ZDB-GENE-020220-1 170846 351 appb GO:0008219 cell death PATO:0002051 increased occurrence abnormal ZDB-GENE-020220-1 170846 351 appb GO:0008345 larval locomotory behavior PATO:0000912 increased rate abnormal ZDB-GENE-020220-1 170846 351 appb GO:0021658 rhombomere 3 morphogenesis PATO:0001236 process quality abnormal ZDB-GENE-020220-1 170846 351 appb GO:0021661 rhombomere 4 morphogenesis PATO:0001236 process quality abnormal ZDB-GENE-020220-1 170846 351 appb GO:0030901 midbrain development PATO:0001507 disrupted abnormal ZDB-GENE-020220-1 170846 351 appb GO:0031175 neuron projection development PATO:0001507 disrupted abnormal ZDB-GENE-020220-1 170846 351 appb GO:0060027 convergent extension involved in gastrulation PATO:0001507 disrupted abnormal ZDB-GENE-020220-1 170846 351 appb ZFA:0000012 central nervous system PATO:0000051 morphology abnormal ZDB-GENE-020220-1 170846 351 appb GO:0007219 Notch signaling pathway BFO:0000066 occurs_in ZFA:0000029 hindbrain PATO:0002051 increased occurrence abnormal ZDB-GENE-020220-1 170846 351 appb GO:0021534 cell proliferation in hindbrain BFO:0000066 occurs_in ZFA:0000029 hindbrain PATO:0002052 decreased occurrence abnormal ZDB-GENE-020220-1 170846 351 appb GO:0030182 neuron differentiation BFO:0000066 occurs_in ZFA:0000029 hindbrain PATO:0002052 decreased occurrence abnormal ZDB-GENE-020220-1 170846 351 appb ZFA:0000029 hindbrain PATO:0001999 lacks parts or has fewer parts of type abnormal ZFA:0009149 Mauthner neuron ZDB-GENE-020220-1 170846 351 appb ZFA:0000084 yolk PATO:0000587 decreased size abnormal ZDB-GENE-020220-1 170846 351 appb GO:0042995 cell projection BFO:0000050 part_of ZFA:0000093 blastomere PATO:0000141 structure abnormal ZDB-GENE-020220-1 170846 351 appb ZFA:0000099 brain vasculature PATO:0002001 has fewer parts of type abnormal ZFA:0005020 central artery ZDB-GENE-020220-1 170846 351 appb ZFA:0009000 cell BFO:0000050 part_of ZFA:0000135 notochord PATO:0000411 circular abnormal ZDB-GENE-020220-1 170846 351 appb ZFA:0000135 notochord PATO:0000967 undulate abnormal ZDB-GENE-020220-1 170846 351 appb ZFA:0000155 somite PATO:0000599 decreased width abnormal ZDB-GENE-020220-1 170846 351 appb ZFA:0000155 somite PATO:0000600 increased width abnormal ZDB-GENE-020220-1 170846 351 appb ZFA:0000155 somite PATO:0001617 deformed abnormal ZDB-GENE-020220-1 170846 351 appb GO:0030424 axon BFO:0000050 part_of ZFA:0000206 facial nerve motor nucleus PATO:0000574 decreased length abnormal ZDB-GENE-020220-1 170846 351 appb ZFA:0000737 cranium PATO:0001450 edematous abnormal ZDB-GENE-020220-1 170846 351 appb ZFA:0000948 rhombomere 3 PATO:0000574 decreased length abnormal ZDB-GENE-020220-1 170846 351 appb ZFA:0001032 rhombomere 4 PATO:0000574 decreased length abnormal ZDB-GENE-020220-1 170846 351 appb ZFA:0001056 myotome PATO:0000600 increased width abnormal ZDB-GENE-020220-1 170846 351 appb ZFA:0001058 caudal fin PATO:0000405 curled abnormal ZDB-GENE-020220-1 170846 351 appb BSPO:0000013 anterior-posterior axis BFO:0000050 part_of ZFA:0001094 whole organism PATO:0000574 decreased length abnormal ZDB-GENE-020220-1 170846 351 appb GO:0007155 cell adhesion BFO:0000066 occurs_in ZFA:0001094 whole organism PATO:0002302 decreased process quality abnormal ZDB-GENE-020220-1 170846 351 appb GO:0090504 epiboly BFO:0000066 occurs_in ZFA:0001094 whole organism PATO:0000502 delayed abnormal ZDB-GENE-020220-1 170846 351 appb ZFA:0001094 whole organism PATO:0000574 decreased length abnormal ZDB-GENE-020220-1 170846 351 appb ZFA:0001094 whole organism PATO:0000587 decreased size abnormal ZDB-GENE-020220-1 170846 351 appb ZFA:0001115 trunk PATO:0001617 deformed abnormal ZDB-GENE-020220-1 170846 351 appb ZFA:0001117 post-vent region PATO:0000406 curved abnormal ZDB-GENE-020220-1 170846 351 appb ZFA:0001117 post-vent region PATO:0000574 decreased length abnormal ZDB-GENE-020220-1 170846 351 appb GO:0005911 cell-cell junction BFO:0000050 part_of ZFA:0001185 periderm PATO:0000470 increased amount abnormal ZDB-GENE-020220-1 170846 351 appb ZFA:0009000 cell BFO:0000050 part_of ZFA:0001185 periderm PATO:0000052 shape abnormal ZDB-GENE-020220-1 170846 351 appb ZFA:0009000 cell BFO:0000050 part_of ZFA:0001185 periderm PATO:0002057 increased area abnormal ZDB-GENE-020220-1 170846 351 appb GO:0030424 axon BFO:0000050 part_of ZFA:0001365 trigeminal motor nucleus PATO:0000574 decreased length abnormal ZDB-GENE-020220-1 170846 351 appb GO:0005856 cytoskeleton BFO:0000050 part_of ZFA:0009052 motor neuron PATO:0000937 disorganized abnormal ZDB-GENE-020220-1 170846 351 appb GO:0030424 axon BFO:0000050 part_of ZFA:0009052 motor neuron PATO:0002286 decreased branchiness abnormal ZDB-GENE-020220-1 170846 351 appb GO:0005874 microtubule BFO:0000050 part_of ZFA:0009149 Mauthner neuron PATO:0001997 decreased amount abnormal ZDB-GENE-020220-1 170846 351 appb GO:0015630 microtubule cytoskeleton BFO:0000050 part_of ZFA:0009149 Mauthner neuron PATO:0001790 decreased mass density abnormal ZDB-GENE-020220-1 170846 351 appb GO:0030424 axon BFO:0000050 part_of ZFA:0009243 CaP motoneuron PATO:0000574 decreased length abnormal ZDB-GENE-020220-1 170846 351 appb GO:0030424 axon BFO:0000050 part_of ZFA:0009243 CaP motoneuron PATO:0002285 increased branchiness abnormal ZDB-GENE-020220-1 170846 351 appb GO:0048675 axon extension BFO:0000066 occurs_in ZFA:0009243 CaP motoneuron PATO:0002302 decreased process quality abnormal ZDB-GENE-020220-1 170846 351 appb GO:0030424 axon BFO:0000050 part_of ZFA:0009244 primary motor neuron PATO:0002285 increased branchiness abnormal ZDB-GENE-020220-1 170846 351 appb GO:0048675 axon extension BFO:0000066 occurs_in ZFA:0009247 secondary motor neuron PATO:0002302 decreased process quality abnormal ZDB-GENE-020228-1 799873 83985 spns1 GO:0090398 cellular senescence PATO:0002017 increased magnitude abnormal ZDB-GENE-020228-1 799873 83985 spns1 GO:0090398 cellular senescence PATO:0002304 increased process quality abnormal ZDB-GENE-020228-1 799873 83985 spns1 GO:0097352 autophagosome maturation PATO:0001236 process quality abnormal ZDB-GENE-020228-1 799873 83985 spns1 ZFA:0000084 yolk PATO:0000647 necrotic abnormal ZDB-GENE-020228-1 799873 83985 spns1 ZFA:0000084 yolk PATO:0000963 opaque abnormal ZDB-GENE-020228-1 799873 83985 spns1 ZFA:0000084 yolk PATO:0001251 dark grey abnormal ZDB-GENE-020228-1 799873 83985 spns1 ZFA:0000106 extension PATO:0000462 absent abnormal ZDB-GENE-020228-1 799873 83985 spns1 ZFA:0000106 extension PATO:0000592 decreased thickness abnormal ZDB-GENE-020228-1 799873 83985 spns1 ZFA:0000123 liver PATO:0000025 composition abnormal ZDB-GENE-020228-1 799873 83985 spns1 GO:0005927 muscle tendon junction BFO:0000050 part_of ZFA:0001056 myotome PATO:0000937 disorganized abnormal ZDB-GENE-020228-1 799873 83985 spns1 GO:0042383 sarcolemma BFO:0000050 part_of ZFA:0001056 myotome PATO:0000982 permeable abnormal ZDB-GENE-020228-1 799873 83985 spns1 ZFA:0009115 skeletal muscle cell BFO:0000050 part_of ZFA:0001056 myotome PATO:0001453 detached from abnormal GO:0005927 muscle tendon junction BFO:0000050 part_of ZFA:0000610 vertical myoseptum ZDB-GENE-020228-1 799873 83985 spns1 ZFA:0009115 skeletal muscle cell BFO:0000050 part_of ZFA:0001056 myotome PATO:0000639 degenerate abnormal ZDB-GENE-020228-1 799873 83985 spns1 ZFA:0009115 skeletal muscle cell BFO:0000050 part_of ZFA:0001056 myotome PATO:0000937 disorganized abnormal ZDB-GENE-020228-1 799873 83985 spns1 ZFA:0009116 slow muscle cell BFO:0000050 part_of ZFA:0001056 myotome PATO:0000639 degenerate abnormal ZDB-GENE-020228-1 799873 83985 spns1 ZFA:0009117 fast muscle cell BFO:0000050 part_of ZFA:0001056 myotome PATO:0000639 degenerate abnormal ZDB-GENE-020228-1 799873 83985 spns1 ZFA:0001094 whole organism PATO:0000001 quality abnormal ZDB-GENE-020228-1 799873 83985 spns1 ZFA:0001094 whole organism PATO:0000169 viability abnormal ZDB-GENE-020228-1 799873 83985 spns1 ZFA:0001094 whole organism PATO:0000647 necrotic abnormal ZDB-GENE-020228-1 799873 83985 spns1 ZFA:0001094 whole organism PATO:0000718 lethal (sensu genetics) abnormal ZDB-GENE-020228-1 799873 83985 spns1 ZFA:0001094 whole organism PATO:0001450 edematous abnormal ZDB-GENE-020228-1 799873 83985 spns1 ZFA:0001094 whole organism PATO:0001604 decreased life span abnormal ZDB-GENE-020228-1 799873 83985 spns1 GO:0035751 regulation of lysosomal lumen pH BFO:0000066 occurs_in ZFA:0001115 trunk PATO:0002302 decreased process quality abnormal ZDB-GENE-020228-1 799873 83985 spns1 ZFA:0001115 trunk PATO:0000592 decreased thickness abnormal ZDB-GENE-020228-1 799873 83985 spns1 GO:0035751 regulation of lysosomal lumen pH BFO:0000066 occurs_in ZFA:0001117 post-vent region PATO:0002302 decreased process quality abnormal ZDB-GENE-020228-1 799873 83985 spns1 ZFA:0005145 muscle PATO:0000025 composition abnormal ZDB-GENE-020228-1 799873 83985 spns1 GO:0005764 lysosome BFO:0000050 part_of ZFA:0009000 cell PATO:0000470 increased amount abnormal ZDB-GENE-020228-1 799873 83985 spns1 GO:0005776 autophagosome BFO:0000050 part_of ZFA:0009000 cell PATO:0002269 accumulation abnormal GO:0048471 perinuclear region of cytoplasm BFO:0000050 part_of ZFA:0009000 cell ZDB-GENE-020228-1 799873 83985 spns1 GO:0005776 autophagosome BFO:0000050 part_of ZFA:0009000 cell PATO:0000470 increased amount abnormal ZDB-GENE-020228-1 799873 83985 spns1 GO:0044754 autolysosome BFO:0000050 part_of ZFA:0009000 cell PATO:0002269 accumulation abnormal GO:0048471 perinuclear region of cytoplasm BFO:0000050 part_of ZFA:0009000 cell ZDB-GENE-020228-1 799873 83985 spns1 GO:0044754 autolysosome BFO:0000050 part_of ZFA:0009000 cell PATO:0000470 increased amount abnormal ZDB-GENE-020228-1 799873 83985 spns1 GO:0090559 regulation of membrane permeability BFO:0000066 occurs_in ZFA:0009115 skeletal muscle cell PATO:0002302 decreased process quality abnormal ZDB-GENE-020318-2 171478 2170 fabp3 GO:0001654 eye development PATO:0001507 disrupted abnormal ZDB-GENE-020318-2 171478 2170 fabp3 GO:0001947 heart looping PATO:0001507 disrupted abnormal ZDB-GENE-020318-2 171478 2170 fabp3 GO:0003230 cardiac atrium development PATO:0001507 disrupted abnormal ZDB-GENE-020318-2 171478 2170 fabp3 GO:0006754 ATP biosynthetic process PATO:0002302 decreased process quality abnormal ZDB-GENE-020318-2 171478 2170 fabp3 GO:0006915 apoptotic process PATO:0002304 increased process quality abnormal ZDB-GENE-020318-2 171478 2170 fabp3 GO:0007507 heart development PATO:0001236 process quality abnormal ZDB-GENE-020318-2 171478 2170 fabp3 GO:0009790 embryo development PATO:0000502 delayed abnormal ZDB-GENE-020318-2 171478 2170 fabp3 GO:0060047 heart contraction PATO:0000911 decreased rate abnormal ZDB-GENE-020318-2 171478 2170 fabp3 ZFA:0000009 cardiac ventricle PATO:0000140 position abnormal ZDB-GENE-020318-2 171478 2170 fabp3 ZFA:0000009 cardiac ventricle PATO:0000592 decreased thickness abnormal ZDB-GENE-020318-2 171478 2170 fabp3 GO:0000262 mitochondrial chromosome BFO:0000050 part_of ZFA:0000037 anatomical structure PATO:0001997 decreased amount abnormal ZDB-GENE-020318-2 171478 2170 fabp3 ZFA:0000054 pericardium PATO:0001450 edematous abnormal ZDB-GENE-020318-2 171478 2170 fabp3 ZFA:0000114 heart PATO:0000051 morphology abnormal ZDB-GENE-020318-2 171478 2170 fabp3 ZFA:0000155 somite PATO:0000051 morphology abnormal ZDB-GENE-020318-2 171478 2170 fabp3 ZFA:0000173 bulbus arteriosus PATO:0000051 morphology abnormal ZDB-GENE-020318-2 171478 2170 fabp3 ZFA:0000471 atrium PATO:0000140 position abnormal ZDB-GENE-020318-2 171478 2170 fabp3 ZFA:0000471 atrium PATO:0000592 decreased thickness abnormal ZDB-GENE-020318-2 171478 2170 fabp3 ZFA:0001114 head PATO:0000587 decreased size abnormal ZDB-GENE-020318-2 171478 2170 fabp3 ZFA:0001114 head PATO:0000646 malformed abnormal ZDB-GENE-020320-5 171474 54756 il17rd GO:0048920 posterior lateral line neuromast primordium migration PATO:0000297 arrested abnormal ZDB-GENE-020320-5 171474 54756 il17rd ZFA:0005227 protoneuromast BFO:0000050 part_of ZFA:0001157 posterior lateral line primordium PATO:0000051 morphology abnormal ZDB-GENE-020402-1 192124 8001 glra3 GO:0001966 thigmotaxis PATO:0001236 process quality abnormal ZDB-GENE-020402-1 192124 8001 glra3 GO:0007638 mechanosensory behavior PATO:0001236 process quality abnormal ZDB-GENE-020416-5 192294 6911 tbx6 GO:0001756 somitogenesis PATO:0001236 process quality abnormal ZDB-GENE-020416-5 192294 6911 tbx6 GO:0001756 somitogenesis PATO:0001507 disrupted abnormal ZDB-GENE-020416-5 192294 6911 tbx6 GO:0001966 thigmotaxis PATO:0002302 decreased process quality abnormal ZDB-GENE-020416-5 192294 6911 tbx6 GO:0016203 muscle attachment PATO:0001236 process quality abnormal ZDB-GENE-020416-5 192294 6911 tbx6 GO:0021952 central nervous system projection neuron axonogenesis PATO:0001507 disrupted abnormal ZDB-GENE-020416-5 192294 6911 tbx6 GO:0048514 blood vessel morphogenesis PATO:0001507 disrupted abnormal ZDB-GENE-020416-5 192294 6911 tbx6 GO:0061053 somite development PATO:0002052 decreased occurrence abnormal ZDB-GENE-020416-5 192294 6911 tbx6 GO:0061055 myotome development PATO:0001236 process quality abnormal ZDB-GENE-020416-5 192294 6911 tbx6 GO:0061056 sclerotome development PATO:0001507 disrupted abnormal ZDB-GENE-020416-5 192294 6911 tbx6 ZFA:0000007 blood PATO:0001997 decreased amount abnormal ZDB-GENE-020416-5 192294 6911 tbx6 ZFA:0000126 centrum PATO:0000122 length abnormal ZDB-GENE-020416-5 192294 6911 tbx6 GO:0035282 segmentation BFO:0000066 occurs_in ZFA:0000155 somite PATO:0001507 disrupted abnormal ZDB-GENE-020416-5 192294 6911 tbx6 ZFA:0000003 adaxial cell BFO:0000050 part_of ZFA:0000155 somite PATO:0001997 decreased amount abnormal ZDB-GENE-020416-5 192294 6911 tbx6 ZFA:0000155 somite PATO:0000642 fused with abnormal ZFA:0000155 somite ZDB-GENE-020416-5 192294 6911 tbx6 ZFA:0000155 somite PATO:0001999 lacks parts or has fewer parts of type abnormal ZFA:0009117 fast muscle cell ZDB-GENE-020416-5 192294 6911 tbx6 ZFA:0000155 somite PATO:0000001 quality abnormal ZDB-GENE-020416-5 192294 6911 tbx6 ZFA:0000155 somite PATO:0000051 morphology abnormal ZDB-GENE-020416-5 192294 6911 tbx6 ZFA:0000155 somite PATO:0000052 shape abnormal ZDB-GENE-020416-5 192294 6911 tbx6 ZFA:0000155 somite PATO:0000937 disorganized abnormal ZDB-GENE-020416-5 192294 6911 tbx6 ZFA:0000155 somite PATO:0001617 deformed abnormal ZDB-GENE-020416-5 192294 6911 tbx6 ZFA:0000155 somite PATO:0001879 U-shaped abnormal ZDB-GENE-020416-5 192294 6911 tbx6 ZFA:0000155 somite PATO:0005020 irregularly shaped abnormal ZDB-GENE-020416-5 192294 6911 tbx6 ZFA:0000277 scale BFO:0000050 part_of ZFA:0000368 integument PATO:0000330 irregular spatial pattern abnormal ZDB-GENE-020416-5 192294 6911 tbx6 ZFA:0000473 trunk musculature PATO:0000051 morphology abnormal ZDB-GENE-020416-5 192294 6911 tbx6 ZFA:0000473 trunk musculature PATO:0000596 decreased volume abnormal ZDB-GENE-020416-5 192294 6911 tbx6 ZFA:0000473 trunk musculature PATO:0040025 lesioned abnormal ZDB-GENE-020416-5 192294 6911 tbx6 ZFA:0000519 hemal arch PATO:0000642 fused with abnormal ZFA:0000519 hemal arch ZDB-GENE-020416-5 192294 6911 tbx6 ZFA:0000519 hemal arch PATO:0000330 irregular spatial pattern abnormal ZDB-GENE-020416-5 192294 6911 tbx6 ZFA:0000519 hemal arch PATO:0000646 malformed abnormal ZDB-GENE-020416-5 192294 6911 tbx6 ZFA:0000671 horizontal myoseptum PATO:0000462 absent abnormal ZDB-GENE-020416-5 192294 6911 tbx6 BSPO:0000088 compartment boundary BFO:0000050 part_of ZFA:0001056 myotome PATO:0000937 disorganized abnormal ZDB-GENE-020416-5 192294 6911 tbx6 BSPO:0000088 compartment boundary BFO:0000050 part_of ZFA:0001056 myotome PATO:0001332 amorphous abnormal ZDB-GENE-020416-5 192294 6911 tbx6 GO:0035282 segmentation BFO:0000066 occurs_in ZFA:0001056 myotome PATO:0002302 decreased process quality abnormal ZDB-GENE-020416-5 192294 6911 tbx6 ZFA:0001056 myotome PATO:0000052 shape abnormal ZDB-GENE-020416-5 192294 6911 tbx6 ZFA:0001056 myotome PATO:0000587 decreased size abnormal ZDB-GENE-020416-5 192294 6911 tbx6 ZFA:0001066 neural arch PATO:0000642 fused with abnormal ZFA:0001066 neural arch ZDB-GENE-020416-5 192294 6911 tbx6 ZFA:0001066 neural arch PATO:0000330 irregular spatial pattern abnormal ZDB-GENE-020416-5 192294 6911 tbx6 ZFA:0001066 neural arch PATO:0000646 malformed abnormal ZDB-GENE-020416-5 192294 6911 tbx6 ZFA:0001080 sclerotome PATO:0000060 spatial pattern abnormal ZDB-GENE-020416-5 192294 6911 tbx6 ZFA:0001094 whole organism PATO:0000574 decreased length abnormal ZDB-GENE-020416-5 192294 6911 tbx6 BSPO:0000075 central region BFO:0000050 part_of ZFA:0001115 trunk PATO:0002001 has fewer parts of type abnormal ZFA:0001513 dermomyotome ZDB-GENE-020416-5 192294 6911 tbx6 BSPO:0000075 central region BFO:0000050 part_of ZFA:0001115 trunk PATO:0000141 structure abnormal ZDB-GENE-020416-5 192294 6911 tbx6 ZFA:0001117 post-vent region PATO:0000001 quality abnormal ZDB-GENE-020416-5 192294 6911 tbx6 ZFA:0001117 post-vent region PATO:0000052 shape abnormal ZDB-GENE-020416-5 192294 6911 tbx6 ZFA:0001117 post-vent region PATO:0000574 decreased length abnormal ZDB-GENE-020416-5 192294 6911 tbx6 GO:0048705 skeletal system morphogenesis BFO:0000066 occurs_in ZFA:0001189 vertebra PATO:0002302 decreased process quality abnormal ZDB-GENE-020416-5 192294 6911 tbx6 ZFA:0001189 vertebra PATO:0000642 fused with abnormal ZFA:0001189 vertebra ZDB-GENE-020416-5 192294 6911 tbx6 ZFA:0001189 vertebra PATO:0000141 structure abnormal ZDB-GENE-020416-5 192294 6911 tbx6 ZFA:0001285 intersegmental vessel PATO:0000646 malformed abnormal ZDB-GENE-020416-5 192294 6911 tbx6 ZFA:0001462 somite border PATO:0000051 morphology abnormal ZDB-GENE-020416-5 192294 6911 tbx6 ZFA:0001462 somite border PATO:0000060 spatial pattern abnormal ZDB-GENE-020416-5 192294 6911 tbx6 ZFA:0001462 somite border PATO:0000141 structure abnormal ZDB-GENE-020416-5 192294 6911 tbx6 ZFA:0001462 somite border PATO:0000330 irregular spatial pattern abnormal ZDB-GENE-020416-5 192294 6911 tbx6 ZFA:0001462 somite border PATO:0000462 absent abnormal ZDB-GENE-020416-5 192294 6911 tbx6 ZFA:0001462 somite border PATO:0000464 inconspicuous abnormal ZDB-GENE-020416-5 192294 6911 tbx6 ZFA:0001462 somite border PATO:0000937 disorganized abnormal ZDB-GENE-020416-5 192294 6911 tbx6 ZFA:0001462 somite border PATO:0001483 aplastic abnormal ZDB-GENE-020416-5 192294 6911 tbx6 ZFA:0001559 vertebral column PATO:0001592 increased curvature abnormal ZDB-GENE-020416-5 192294 6911 tbx6 GO:0030424 axon BFO:0000050 part_of ZFA:0005179 MiP motor neuron PATO:0000330 irregular spatial pattern abnormal ZDB-GENE-020416-5 192294 6911 tbx6 GO:0030424 axon BFO:0000050 part_of ZFA:0005179 MiP motor neuron PATO:0000574 decreased length abnormal ZDB-GENE-020416-5 192294 6911 tbx6 ZFA:0005277 skeletal muscle PATO:0002014 structure, cavities abnormal ZDB-GENE-020416-5 192294 6911 tbx6 ZFA:0009115 skeletal muscle cell PATO:0000052 shape abnormal ZDB-GENE-020416-5 192294 6911 tbx6 ZFA:0009115 skeletal muscle cell PATO:0000122 length abnormal ZDB-GENE-020416-5 192294 6911 tbx6 ZFA:0009115 skeletal muscle cell PATO:0000937 disorganized abnormal ZDB-GENE-020416-5 192294 6911 tbx6 ZFA:0009115 skeletal muscle cell PATO:0001997 decreased amount abnormal ZDB-GENE-020416-5 192294 6911 tbx6 ZFA:0009116 slow muscle cell PATO:0000642 fused with abnormal ZFA:0009116 slow muscle cell ZDB-GENE-020416-5 192294 6911 tbx6 ZFA:0009116 slow muscle cell PATO:0000591 increased thickness abnormal ZDB-GENE-020416-5 192294 6911 tbx6 ZFA:0009116 slow muscle cell PATO:0000628 mislocalised abnormal ZDB-GENE-020416-5 192294 6911 tbx6 ZFA:0009116 slow muscle cell PATO:0000937 disorganized abnormal ZDB-GENE-020416-5 192294 6911 tbx6 ZFA:0009116 slow muscle cell PATO:0001997 decreased amount abnormal ZDB-GENE-020416-5 192294 6911 tbx6 ZFA:0009117 fast muscle cell PATO:0000051 morphology abnormal ZDB-GENE-020416-5 192294 6911 tbx6 ZFA:0009117 fast muscle cell PATO:0000937 disorganized abnormal ZDB-GENE-020416-5 192294 6911 tbx6 ZFA:0009117 fast muscle cell PATO:0001997 decreased amount abnormal ZDB-GENE-020416-5 192294 6911 tbx6 GO:0030424 axon BFO:0000050 part_of ZFA:0009243 CaP motoneuron PATO:0000330 irregular spatial pattern abnormal ZDB-GENE-020416-5 192294 6911 tbx6 GO:0030424 axon BFO:0000050 part_of ZFA:0009243 CaP motoneuron PATO:0000470 increased amount abnormal ZDB-GENE-020416-5 192294 6911 tbx6 GO:0030424 axon BFO:0000050 part_of ZFA:0009243 CaP motoneuron PATO:0000574 decreased length abnormal ZDB-GENE-020418-1 192295 890 ccna2 ZFA:0000008 brain PATO:0000587 decreased size abnormal ZDB-GENE-020418-1 192295 890 ccna2 ZFA:0000012 central nervous system PATO:0000647 necrotic abnormal ZDB-GENE-020418-1 192295 890 ccna2 ZFA:0000054 pericardium PATO:0001450 edematous abnormal ZDB-GENE-020418-1 192295 890 ccna2 ZFA:0000107 eye PATO:0000587 decreased size abnormal ZDB-GENE-020418-1 192295 890 ccna2 ZFA:0000112 gut PATO:0000001 quality abnormal ZDB-GENE-020418-1 192295 890 ccna2 ZFA:0000112 gut PATO:0000645 hypoplastic abnormal ZDB-GENE-020418-1 192295 890 ccna2 ZFA:0000123 liver PATO:0000001 quality abnormal ZDB-GENE-020418-1 192295 890 ccna2 ZFA:0000123 liver PATO:0000587 decreased size abnormal ZDB-GENE-020418-1 192295 890 ccna2 ZFA:0000123 liver PATO:0000645 hypoplastic abnormal ZDB-GENE-020418-1 192295 890 ccna2 GO:0000084 mitotic S phase BFO:0000066 occurs_in ZFA:0000152 retina PATO:0002052 decreased occurrence abnormal ZDB-GENE-020418-1 192295 890 ccna2 GO:0035861 site of double-strand break BFO:0000050 part_of ZFA:0000152 retina PATO:0000470 increased amount abnormal ZDB-GENE-020418-1 192295 890 ccna2 ZFA:0000152 retina PATO:0000001 quality abnormal ZDB-GENE-020418-1 192295 890 ccna2 ZFA:0000396 nervous system PATO:0000001 quality abnormal ZDB-GENE-020418-1 192295 890 ccna2 ZFA:0001114 head PATO:0000599 decreased width abnormal ZDB-GENE-020418-1 192295 890 ccna2 ZFA:0001114 head PATO:0002258 pointed abnormal ZDB-GENE-020418-1 192295 890 ccna2 ZFA:0001227 mandibular arch skeleton PATO:0000587 decreased size abnormal ZDB-GENE-020418-2 192298 29927 sec61a1a GO:0021986 habenula development PATO:0001507 disrupted abnormal ZDB-GENE-020418-2 192298 29927 sec61a1a GO:0022008 neurogenesis PATO:0002051 increased occurrence abnormal ZDB-GENE-020418-2 192298 29927 sec61a1a GO:0048884 neuromast development PATO:0001507 disrupted abnormal ZDB-GENE-020418-2 192298 29927 sec61a1a GO:0050975 sensory perception of touch PATO:0001507 disrupted abnormal ZDB-GENE-020418-2 192298 29927 sec61a1a GO:0051301 cell division PATO:0002051 increased occurrence abnormal ZDB-GENE-020418-2 192298 29927 sec61a1a GO:0060384 innervation PATO:0001507 disrupted abnormal ZDB-GENE-020418-2 192298 29927 sec61a1a ZFA:0000054 pericardium PATO:0001450 edematous abnormal ZDB-GENE-020418-2 192298 29927 sec61a1a ZFA:0000095 pharyngeal arch 3-7 skeleton PATO:0000001 quality abnormal ZDB-GENE-020418-2 192298 29927 sec61a1a ZFA:0000100 cerebellum PATO:0002002 has extra parts of type abnormal ZFA:0009248 neuron ZDB-GENE-020418-2 192298 29927 sec61a1a ZFA:0000107 eye PATO:0000587 decreased size abnormal ZDB-GENE-020418-2 192298 29927 sec61a1a ZFA:0000112 gut PATO:0000001 quality abnormal ZDB-GENE-020418-2 192298 29927 sec61a1a ZFA:0000112 gut PATO:0000645 hypoplastic abnormal ZDB-GENE-020418-2 192298 29927 sec61a1a ZFA:0000114 heart PATO:0000001 quality abnormal ZDB-GENE-020418-2 192298 29927 sec61a1a ZFA:0000123 liver PATO:0000001 quality abnormal ZDB-GENE-020418-2 192298 29927 sec61a1a ZFA:0000123 liver PATO:0000645 hypoplastic abnormal ZDB-GENE-020418-2 192298 29927 sec61a1a ZFA:0001486 epithelium BFO:0000050 part_of ZFA:0000161 third ventricle PATO:0000051 morphology abnormal ZDB-GENE-020418-2 192298 29927 sec61a1a ZFA:0009038 columnar/cuboidal epithelial cell BFO:0000050 part_of ZFA:0000161 third ventricle PATO:0001531 cellular adhesivity abnormal ZFA:0009038 columnar/cuboidal epithelial cell BFO:0000050 part_of ZFA:0000161 third ventricle ZDB-GENE-020418-2 192298 29927 sec61a1a ZFA:0009038 columnar/cuboidal epithelial cell BFO:0000050 part_of ZFA:0000161 third ventricle PATO:0000411 circular abnormal ZDB-GENE-020418-2 192298 29927 sec61a1a BSPO:0000007 right side BFO:0000050 part_of ZFA:0000197 dorsal habenular nucleus PATO:0002002 has extra parts of type abnormal ZFA:0009248 neuron ZDB-GENE-020418-2 192298 29927 sec61a1a BSPO:0000082 lateral region BFO:0000050 part_of ZFA:0000197 dorsal habenular nucleus PATO:0002002 has extra parts of type abnormal ZFA:0009248 neuron ZDB-GENE-020418-2 192298 29927 sec61a1a BSPO:0000083 medial region BFO:0000050 part_of ZFA:0000197 dorsal habenular nucleus PATO:0002001 has fewer parts of type abnormal ZFA:0009248 neuron ZDB-GENE-020418-2 192298 29927 sec61a1a ZFA:0009248 neuron BFO:0000050 part_of ZFA:0000197 dorsal habenular nucleus PATO:0000060 spatial pattern abnormal ZDB-GENE-020418-2 192298 29927 sec61a1a ZFA:0000197 dorsal habenular nucleus PATO:0000051 morphology abnormal ZDB-GENE-020418-2 192298 29927 sec61a1a BSPO:0000000 left side BFO:0000050 part_of ZFA:0000213 habenula PATO:0002002 has extra parts of type abnormal ZFA:0009248 neuron ZDB-GENE-020418-2 192298 29927 sec61a1a BSPO:0000007 right side BFO:0000050 part_of ZFA:0000213 habenula PATO:0002002 has extra parts of type abnormal ZFA:0009248 neuron ZDB-GENE-020418-2 192298 29927 sec61a1a ZFA:0000282 sensory system PATO:0000001 quality abnormal ZDB-GENE-020418-2 192298 29927 sec61a1a ZFA:0000672 hyomandibula PATO:0000587 decreased size abnormal ZDB-GENE-020418-2 192298 29927 sec61a1a ZFA:0000940 posterior lateral line neuromast PATO:0002001 has fewer parts of type abnormal ZFA:0009367 neuromast hair cell ZDB-GENE-020418-2 192298 29927 sec61a1a BSPO:0000013 anterior-posterior axis BFO:0000050 part_of ZFA:0001094 whole organism PATO:0000574 decreased length abnormal ZDB-GENE-020418-2 192298 29927 sec61a1a BSPO:0000013 anterior-posterior axis BFO:0000050 part_of ZFA:0001094 whole organism PATO:0001468 curved dorsal abnormal ZDB-GENE-020418-2 192298 29927 sec61a1a ZFA:0001094 whole organism PATO:0000617 bent abnormal ZDB-GENE-020418-2 192298 29927 sec61a1a ZFA:0001114 head PATO:0000587 decreased size abnormal ZDB-GENE-020418-2 192298 29927 sec61a1a ZFA:0001114 head PATO:0000596 decreased volume abnormal ZDB-GENE-020418-2 192298 29927 sec61a1a ZFA:0001115 trunk PATO:0001468 curved dorsal abnormal ZDB-GENE-020418-2 192298 29927 sec61a1a ZFA:0001117 post-vent region PATO:0001468 curved dorsal abnormal ZDB-GENE-020418-2 192298 29927 sec61a1a GO:0031012 extracellular matrix BFO:0000050 part_of ZFA:0001227 mandibular arch skeleton PATO:0001609 sparse abnormal ZDB-GENE-020418-2 192298 29927 sec61a1a ZFA:0009084 chondrocyte BFO:0000050 part_of ZFA:0001227 mandibular arch skeleton PATO:0001396 cellular quality abnormal ZDB-GENE-020418-2 192298 29927 sec61a1a ZFA:0001227 mandibular arch skeleton PATO:0000587 decreased size abnormal ZDB-GENE-020418-2 192298 29927 sec61a1a ZFA:0001501 cartilage element PATO:0000051 morphology abnormal ZDB-GENE-020418-2 192298 29927 sec61a1a ZFA:0001611 pharyngeal arch 2 PATO:0000587 decreased size abnormal ZDB-GENE-020418-2 192298 29927 sec61a1a ZFA:0001612 pharyngeal arch 1 PATO:0000587 decreased size abnormal ZDB-GENE-020418-2 192298 29927 sec61a1a ZFA:0001617 otolith PATO:0000001 quality abnormal ZDB-GENE-020418-2 192298 29927 sec61a1a ZFA:0001617 otolith PATO:0000587 decreased size abnormal ZDB-GENE-020418-2 192298 29927 sec61a1a GO:0005911 cell-cell junction BFO:0000050 part_of ZFA:0009038 columnar/cuboidal epithelial cell PATO:0001997 decreased amount abnormal ZDB-GENE-020418-2 192298 29927 sec61a1a GO:0005783 endoplasmic reticulum BFO:0000050 part_of ZFA:0009084 chondrocyte PATO:0000596 decreased volume abnormal ZDB-GENE-020418-2 192298 29927 sec61a1a GO:0031941 filamentous actin BFO:0000050 part_of ZFA:0009306 neuroepithelial cell PATO:0001997 decreased amount abnormal ZDB-GENE-020419-1 192328 7307 u2af1 ZFA:0000008 brain PATO:0000001 quality abnormal ZDB-GENE-020419-1 192328 7307 u2af1 ZFA:0000012 central nervous system PATO:0000647 necrotic abnormal ZDB-GENE-020419-1 192328 7307 u2af1 ZFA:0000029 hindbrain PATO:0000001 quality abnormal ZDB-GENE-020419-1 192328 7307 u2af1 ZFA:0000042 midbrain hindbrain boundary PATO:0001485 condensed abnormal ZDB-GENE-020419-1 192328 7307 u2af1 ZFA:0000084 yolk PATO:0000411 circular abnormal ZDB-GENE-020419-1 192328 7307 u2af1 ZFA:0000106 extension PATO:0000592 decreased thickness abnormal ZDB-GENE-020419-1 192328 7307 u2af1 ZFA:0000107 eye PATO:0000587 decreased size abnormal ZDB-GENE-020419-1 192328 7307 u2af1 ZFA:0000110 fourth ventricle PATO:0001602 distended abnormal ZDB-GENE-020419-1 192328 7307 u2af1 ZFA:0000396 nervous system PATO:0000001 quality abnormal ZDB-GENE-020419-1 192328 7307 u2af1 ZFA:0000737 cranium PATO:0000645 hypoplastic abnormal ZDB-GENE-020419-1 192328 7307 u2af1 ZFA:0000737 cranium PATO:0000646 malformed abnormal ZDB-GENE-020419-1 192328 7307 u2af1 ZFA:0001094 whole organism PATO:0000169 viability abnormal ZDB-GENE-020419-1 192328 7307 u2af1 ZFA:0001114 head PATO:0000587 decreased size abnormal ZDB-GENE-020419-1 192328 7307 u2af1 ZFA:0001115 trunk PATO:0000592 decreased thickness abnormal ZDB-GENE-020419-11 192335 529 atp6v1e1b GO:0009605 response to external stimulus PATO:0000001 quality abnormal ZDB-GENE-020419-11 192335 529 atp6v1e1b GO:0043473 pigmentation PATO:0001507 disrupted abnormal ZDB-GENE-020419-11 192335 529 atp6v1e1b GO:0048570 notochord morphogenesis PATO:0002302 decreased process quality abnormal ZDB-GENE-020419-11 192335 529 atp6v1e1b GO:0050881 musculoskeletal movement PATO:0000001 quality abnormal ZDB-GENE-020419-11 192335 529 atp6v1e1b GO:0050975 sensory perception of touch PATO:0001507 disrupted abnormal ZDB-GENE-020419-11 192335 529 atp6v1e1b GO:0060036 notochord cell vacuolation PATO:0002302 decreased process quality abnormal ZDB-GENE-020419-11 192335 529 atp6v1e1b GO:0060042 retina morphogenesis in camera-type eye PATO:0001236 process quality abnormal ZDB-GENE-020419-11 192335 529 atp6v1e1b ZFA:0000095 pharyngeal arch 3-7 skeleton PATO:0000001 quality abnormal ZDB-GENE-020419-11 192335 529 atp6v1e1b ZFA:0000107 eye PATO:0000587 decreased size abnormal ZDB-GENE-020419-11 192335 529 atp6v1e1b ZFA:0000112 gut PATO:0000645 hypoplastic abnormal ZDB-GENE-020419-11 192335 529 atp6v1e1b GO:0005773 vacuole BFO:0000050 part_of ZFA:0000135 notochord PATO:0001444 broken abnormal ZDB-GENE-020419-11 192335 529 atp6v1e1b ZFA:0000144 retinal pigmented epithelium PATO:0000001 quality abnormal ZDB-GENE-020419-11 192335 529 atp6v1e1b ZFA:0000144 retinal pigmented epithelium PATO:0001241 physical object quality abnormal ZDB-GENE-020419-11 192335 529 atp6v1e1b ZFA:0000144 retinal pigmented epithelium PATO:0001354 translucent abnormal ZDB-GENE-020419-11 192335 529 atp6v1e1b ZFA:0000217 inner ear PATO:0000587 decreased size abnormal ZDB-GENE-020419-11 192335 529 atp6v1e1b ZFA:0000282 sensory system PATO:0000001 quality abnormal ZDB-GENE-020419-11 192335 529 atp6v1e1b ZFA:0001069 ventral fin fold PATO:0000587 decreased size abnormal ZDB-GENE-020419-11 192335 529 atp6v1e1b ZFA:0001094 whole organism PATO:0001422 dead abnormal ZDB-GENE-020419-11 192335 529 atp6v1e1b ZFA:0001114 head PATO:0000587 decreased size abnormal ZDB-GENE-020419-11 192335 529 atp6v1e1b ZFA:0001114 head PATO:0002251 decreased pigmentation abnormal ZDB-GENE-020419-11 192335 529 atp6v1e1b ZFA:0001115 trunk PATO:0000592 decreased thickness abnormal ZDB-GENE-020419-11 192335 529 atp6v1e1b ZFA:0001115 trunk PATO:0002251 decreased pigmentation abnormal ZDB-GENE-020419-11 192335 529 atp6v1e1b ZFA:0001117 post-vent region PATO:0002251 decreased pigmentation abnormal ZDB-GENE-020419-11 192335 529 atp6v1e1b ZFA:0001227 mandibular arch skeleton PATO:0000052 shape abnormal ZDB-GENE-020419-11 192335 529 atp6v1e1b ZFA:0001613 pharyngeal arch 3-7 PATO:0000052 shape abnormal ZDB-GENE-020419-11 192335 529 atp6v1e1b ZFA:0001617 otolith PATO:0000001 quality abnormal ZDB-GENE-020419-11 192335 529 atp6v1e1b ZFA:0001617 otolith PATO:0000587 decreased size abnormal ZDB-GENE-020419-11 192335 529 atp6v1e1b ZFA:0009091 melanocyte BFO:0000050 part_of ZFA:0005220 larval melanophore stripe PATO:0001354 translucent abnormal ZDB-GENE-020419-11 192335 529 atp6v1e1b ZFA:0009090 pigment cell PATO:0000001 quality abnormal ZDB-GENE-020419-11 192335 529 atp6v1e1b ZFA:0009090 pigment cell PATO:0001608 patchy abnormal ZDB-GENE-020419-11 192335 529 atp6v1e1b ZFA:0009091 melanocyte PATO:0000586 increased size abnormal ZDB-GENE-020419-11 192335 529 atp6v1e1b ZFA:0009091 melanocyte PATO:0000639 degenerate abnormal ZDB-GENE-020419-11 192335 529 atp6v1e1b ZFA:0009091 melanocyte PATO:0000646 malformed abnormal ZDB-GENE-020419-11 192335 529 atp6v1e1b ZFA:0009091 melanocyte PATO:0001354 translucent abnormal ZDB-GENE-020419-11 192335 529 atp6v1e1b ZFA:0009091 melanocyte PATO:0002251 decreased pigmentation abnormal ZDB-GENE-020419-11 192335 529 atp6v1e1b GO:0001750 photoreceptor outer segment BFO:0000050 part_of ZFA:0009154 eye photoreceptor cell PATO:0000587 decreased size abnormal ZDB-GENE-020419-12 192297 6193 rps5 ZFA:0000008 brain PATO:0000647 necrotic abnormal ZDB-GENE-020419-12 192297 6193 rps5 ZFA:0000012 central nervous system PATO:0000647 necrotic abnormal ZDB-GENE-020419-12 192297 6193 rps5 ZFA:0000084 yolk PATO:0000411 circular abnormal ZDB-GENE-020419-12 192297 6193 rps5 ZFA:0000084 yolk PATO:0001511 non-functional abnormal ZDB-GENE-020419-12 192297 6193 rps5 ZFA:0000106 extension PATO:0000592 decreased thickness abnormal ZDB-GENE-020419-12 192297 6193 rps5 ZFA:0000107 eye PATO:0000587 decreased size abnormal ZDB-GENE-020419-12 192297 6193 rps5 ZFA:0000110 fourth ventricle PATO:0001602 distended abnormal ZDB-GENE-020419-12 192297 6193 rps5 ZFA:0000112 gut PATO:0000645 hypoplastic abnormal ZDB-GENE-020419-12 192297 6193 rps5 ZFA:0000123 liver PATO:0000645 hypoplastic abnormal ZDB-GENE-020419-12 192297 6193 rps5 GO:0005694 chromosome BFO:0000050 part_of ZFA:0000142 peripheral nervous system PATO:0000070 amount abnormal ZDB-GENE-020419-12 192297 6193 rps5 ZFA:0001114 head PATO:0000587 decreased size abnormal ZDB-GENE-020419-12 192297 6193 rps5 ZFA:0001115 trunk PATO:0000592 decreased thickness abnormal ZDB-GENE-020419-13 192311 51593 srrt ZFA:0000008 brain PATO:0000647 necrotic abnormal ZDB-GENE-020419-13 192311 51593 srrt ZFA:0000012 central nervous system PATO:0000647 necrotic abnormal ZDB-GENE-020419-13 192311 51593 srrt ZFA:0000054 pericardium PATO:0001450 edematous abnormal ZDB-GENE-020419-13 192311 51593 srrt ZFA:0000107 eye PATO:0000587 decreased size abnormal ZDB-GENE-020419-13 192311 51593 srrt ZFA:0000114 heart PATO:0000001 quality abnormal ZDB-GENE-020419-13 192311 51593 srrt ZFA:0001094 whole organism PATO:0001468 curved dorsal abnormal ZDB-GENE-020419-13 192311 51593 srrt ZFA:0001114 head PATO:0000587 decreased size abnormal ZDB-GENE-020419-13 192311 51593 srrt ZFA:0001115 trunk PATO:0000647 necrotic abnormal ZDB-GENE-020419-13 192311 51593 srrt ZFA:0001227 mandibular arch skeleton PATO:0000591 increased thickness abnormal ZDB-GENE-020419-14 192331 6632 snrpd1 GO:0090398 cellular senescence PATO:0002017 increased magnitude abnormal ZDB-GENE-020419-14 192331 6632 snrpd1 ZFA:0000012 central nervous system PATO:0000647 necrotic abnormal ZDB-GENE-020419-14 192331 6632 snrpd1 ZFA:0000084 yolk PATO:0000411 circular abnormal ZDB-GENE-020419-14 192331 6632 snrpd1 ZFA:0000106 extension PATO:0000592 decreased thickness abnormal ZDB-GENE-020419-14 192331 6632 snrpd1 ZFA:0000110 fourth ventricle PATO:0001602 distended abnormal ZDB-GENE-020419-14 192331 6632 snrpd1 ZFA:0000114 heart PATO:0000647 necrotic abnormal ZDB-GENE-020419-14 192331 6632 snrpd1 ZFA:0000396 nervous system PATO:0000001 quality abnormal ZDB-GENE-020419-14 192331 6632 snrpd1 ZFA:0001094 whole organism PATO:0000169 viability abnormal ZDB-GENE-020419-14 192331 6632 snrpd1 ZFA:0001115 trunk PATO:0000647 necrotic abnormal ZDB-GENE-020419-15 192329 5514 ppp1r10 ZFA:0000008 brain PATO:0000647 necrotic abnormal ZDB-GENE-020419-15 192329 5514 ppp1r10 ZFA:0000107 eye PATO:0000587 decreased size abnormal ZDB-GENE-020419-16 192320 5427 pole2 ZFA:0000008 brain PATO:0000647 necrotic abnormal ZDB-GENE-020419-16 192320 5427 pole2 ZFA:0000012 central nervous system PATO:0000647 necrotic abnormal ZDB-GENE-020419-16 192320 5427 pole2 ZFA:0000084 yolk PATO:0000411 circular abnormal ZDB-GENE-020419-16 192320 5427 pole2 ZFA:0000106 extension PATO:0000592 decreased thickness abnormal ZDB-GENE-020419-16 192320 5427 pole2 ZFA:0000107 eye PATO:0000587 decreased size abnormal ZDB-GENE-020419-16 192320 5427 pole2 ZFA:0000110 fourth ventricle PATO:0001602 distended abnormal ZDB-GENE-020419-16 192320 5427 pole2 ZFA:0001094 whole organism PATO:0000169 viability abnormal ZDB-GENE-020419-16 192320 5427 pole2 ZFA:0001114 head PATO:0000587 decreased size abnormal ZDB-GENE-020419-16 192320 5427 pole2 ZFA:0001115 trunk PATO:0000647 necrotic abnormal ZDB-GENE-020419-17 798429 100287932 timm23a ZFA:0000054 pericardium PATO:0001450 edematous abnormal ZDB-GENE-020419-17 798429 100287932 timm23a ZFA:0000084 yolk PATO:0000411 circular abnormal ZDB-GENE-020419-17 798429 100287932 timm23a ZFA:0000084 yolk PATO:0000950 grey abnormal ZDB-GENE-020419-17 798429 100287932 timm23a ZFA:0000107 eye PATO:0000587 decreased size abnormal ZDB-GENE-020419-17 798429 100287932 timm23a ZFA:0000112 gut PATO:0000645 hypoplastic abnormal ZDB-GENE-020419-17 798429 100287932 timm23a ZFA:0000123 liver PATO:0000645 hypoplastic abnormal ZDB-GENE-020419-17 798429 100287932 timm23a ZFA:0001114 head PATO:0000587 decreased size abnormal ZDB-GENE-020419-18 100002261 6879 taf7 ZFA:0000107 eye PATO:0000587 decreased size abnormal ZDB-GENE-020419-18 100002261 6879 taf7 ZFA:0000112 gut PATO:0000645 hypoplastic abnormal ZDB-GENE-020419-18 100002261 6879 taf7 ZFA:0000123 liver PATO:0000645 hypoplastic abnormal ZDB-GENE-020419-18 100002261 6879 taf7 ZFA:0000282 sensory system PATO:0000001 quality abnormal ZDB-GENE-020419-18 100002261 6879 taf7 ZFA:0001114 head PATO:0000587 decreased size abnormal ZDB-GENE-020419-19 192307 1452 csnk1a1 GO:0060047 heart contraction PATO:0000911 decreased rate abnormal ZDB-GENE-020419-19 192307 1452 csnk1a1 ZFA:0000009 cardiac ventricle PATO:0001571 dilated abnormal ZDB-GENE-020419-19 192307 1452 csnk1a1 ZFA:0009075 astrocyte BFO:0000050 part_of ZFA:0000059 postoptic commissure PATO:0000628 mislocalised abnormal ZDB-GENE-020419-19 192307 1452 csnk1a1 ZFA:0000059 postoptic commissure PATO:0000051 morphology abnormal ZDB-GENE-020419-19 192307 1452 csnk1a1 ZFA:0000095 pharyngeal arch 3-7 skeleton PATO:0000001 quality abnormal ZDB-GENE-020419-19 192307 1452 csnk1a1 GO:0071679 commissural neuron axon guidance BFO:0000066 occurs_in ZFA:0000109 forebrain PATO:0001507 disrupted abnormal ZDB-GENE-020419-19 192307 1452 csnk1a1 ZFA:0009075 astrocyte BFO:0000050 part_of ZFA:0000109 forebrain PATO:0000051 morphology abnormal ZDB-GENE-020419-19 192307 1452 csnk1a1 ZFA:0000292 surface structure PATO:0000001 quality abnormal ZDB-GENE-020419-19 192307 1452 csnk1a1 ZFA:0000435 cranial nerve II PATO:0001959 defasciculated abnormal ZDB-GENE-020419-19 192307 1452 csnk1a1 ZFA:0000471 atrium PATO:0001571 dilated abnormal ZDB-GENE-020419-19 192307 1452 csnk1a1 ZFA:0009075 astrocyte BFO:0000050 part_of ZFA:0001108 anterior commissure PATO:0000628 mislocalised abnormal ZDB-GENE-020419-19 192307 1452 csnk1a1 ZFA:0001108 anterior commissure PATO:0000051 morphology abnormal ZDB-GENE-020419-19 192307 1452 csnk1a1 ZFA:0001114 head PATO:0000587 decreased size abnormal ZDB-GENE-020419-19 192307 1452 csnk1a1 ZFA:0001161 pectoral fin PATO:0000001 quality abnormal ZDB-GENE-020419-19 192307 1452 csnk1a1 ZFA:0001161 pectoral fin PATO:0000052 shape abnormal ZDB-GENE-020419-19 192307 1452 csnk1a1 ZFA:0001161 pectoral fin PATO:0001643 stubby abnormal ZDB-GENE-020419-19 192307 1452 csnk1a1 ZFA:0001205 Meckel's cartilage PATO:0000574 decreased length abnormal ZDB-GENE-020419-19 192307 1452 csnk1a1 ZFA:0001227 mandibular arch skeleton PATO:0000052 shape abnormal ZDB-GENE-020419-19 192307 1452 csnk1a1 ZFA:0001227 mandibular arch skeleton PATO:0000587 decreased size abnormal ZDB-GENE-020419-19 192307 1452 csnk1a1 ZFA:0001400 ceratohyal cartilage PATO:0000051 morphology abnormal ZDB-GENE-020419-19 192307 1452 csnk1a1 ZFA:0001501 cartilage element PATO:0000574 decreased length abnormal ZDB-GENE-020419-19 192307 1452 csnk1a1 ZFA:0001501 cartilage element PATO:0000700 rough abnormal ZDB-GENE-020419-19 192307 1452 csnk1a1 ZFA:0001501 cartilage element PATO:0001810 wrinkled abnormal ZDB-GENE-020419-2 192299 11224 rpl35 GO:0009790 embryo development PATO:0000502 delayed abnormal ZDB-GENE-020419-2 192299 11224 rpl35 ZFA:0000006 ball PATO:0000586 increased size abnormal ZDB-GENE-020419-2 192299 11224 rpl35 ZFA:0000006 ball PATO:0000963 opaque abnormal ZDB-GENE-020419-2 192299 11224 rpl35 ZFA:0000008 brain PATO:0000001 quality abnormal ZDB-GENE-020419-2 192299 11224 rpl35 ZFA:0000008 brain PATO:0001483 aplastic abnormal ZDB-GENE-020419-2 192299 11224 rpl35 ZFA:0000012 central nervous system PATO:0000647 necrotic abnormal ZDB-GENE-020419-2 192299 11224 rpl35 ZFA:0000029 hindbrain PATO:0000001 quality abnormal ZDB-GENE-020419-2 192299 11224 rpl35 ZFA:0000029 hindbrain PATO:0000967 undulate abnormal ZDB-GENE-020419-2 192299 11224 rpl35 ZFA:0000042 midbrain hindbrain boundary PATO:0000592 decreased thickness abnormal ZDB-GENE-020419-2 192299 11224 rpl35 ZFA:0000084 yolk PATO:0000411 circular abnormal ZDB-GENE-020419-2 192299 11224 rpl35 ZFA:0000106 extension PATO:0000574 decreased length abnormal ZDB-GENE-020419-2 192299 11224 rpl35 ZFA:0000106 extension PATO:0000592 decreased thickness abnormal ZDB-GENE-020419-2 192299 11224 rpl35 ZFA:0000107 eye PATO:0000587 decreased size abnormal ZDB-GENE-020419-2 192299 11224 rpl35 ZFA:0000108 fin PATO:0001483 aplastic abnormal ZDB-GENE-020419-2 192299 11224 rpl35 ZFA:0000109 forebrain PATO:0001598 protruding abnormal ZDB-GENE-020419-2 192299 11224 rpl35 ZFA:0000110 fourth ventricle PATO:0000586 increased size abnormal ZDB-GENE-020419-2 192299 11224 rpl35 ZFA:0000110 fourth ventricle PATO:0001602 distended abnormal ZDB-GENE-020419-2 192299 11224 rpl35 ZFA:0000138 otic placode PATO:0000587 decreased size abnormal ZDB-GENE-020419-2 192299 11224 rpl35 ZFA:0000138 otic placode PATO:0001483 aplastic abnormal ZDB-GENE-020419-2 192299 11224 rpl35 GO:0005694 chromosome BFO:0000050 part_of ZFA:0000142 peripheral nervous system PATO:0000070 amount abnormal ZDB-GENE-020419-2 192299 11224 rpl35 ZFA:0007009 nerve BFO:0000050 part_of ZFA:0000142 peripheral nervous system PATO:0002011 neoplastic abnormal ZDB-GENE-020419-2 192299 11224 rpl35 ZFA:0000152 retina PATO:0000587 decreased size abnormal ZDB-GENE-020419-2 192299 11224 rpl35 ZFA:0000396 nervous system PATO:0000001 quality abnormal ZDB-GENE-020419-2 192299 11224 rpl35 ZFA:0000445 optic tectum PATO:0000586 increased size abnormal ZDB-GENE-020419-2 192299 11224 rpl35 ZFA:0000445 optic tectum PATO:0000963 opaque abnormal ZDB-GENE-020419-2 192299 11224 rpl35 ZFA:0000559 otolith organ PATO:0001617 deformed abnormal ZDB-GENE-020419-2 192299 11224 rpl35 MPATH:218 neoplasm BFO:0000050 part_of ZFA:0001094 whole organism PATO:0000470 increased amount abnormal ZDB-GENE-020419-2 192299 11224 rpl35 MPATH:370 primitive neurectodermal tumor BFO:0000050 part_of ZFA:0001094 whole organism PATO:0000470 increased amount abnormal ZDB-GENE-020419-2 192299 11224 rpl35 MPATH:437 neurofibrosarcoma BFO:0000050 part_of ZFA:0001094 whole organism PATO:0000470 increased amount abnormal ZDB-GENE-020419-2 192299 11224 rpl35 ZFA:0001094 whole organism PATO:0000169 viability abnormal ZDB-GENE-020419-2 192299 11224 rpl35 ZFA:0001094 whole organism PATO:0000574 decreased length abnormal ZDB-GENE-020419-2 192299 11224 rpl35 ZFA:0001094 whole organism PATO:0000587 decreased size abnormal ZDB-GENE-020419-2 192299 11224 rpl35 ZFA:0001114 head PATO:0000587 decreased size abnormal ZDB-GENE-020419-2 192299 11224 rpl35 ZFA:0001115 trunk PATO:0000592 decreased thickness abnormal ZDB-GENE-020419-2 192299 11224 rpl35 ZFA:0001117 post-vent region PATO:0000617 bent abnormal ZDB-GENE-020419-2 192299 11224 rpl35 ZFA:0001117 post-vent region PATO:0001617 deformed abnormal ZDB-GENE-020419-2 192299 11224 rpl35 ZFA:0009256 nucleate erythrocyte PATO:0001997 decreased amount abnormal ZDB-GENE-020419-20 192300 6222 rps18 ZFA:0000008 brain PATO:0000001 quality abnormal ZDB-GENE-020419-20 192300 6222 rps18 ZFA:0000029 hindbrain PATO:0000001 quality abnormal ZDB-GENE-020419-20 192300 6222 rps18 ZFA:0000054 pericardium PATO:0001450 edematous abnormal ZDB-GENE-020419-20 192300 6222 rps18 ZFA:0000084 yolk PATO:0000411 circular abnormal ZDB-GENE-020419-20 192300 6222 rps18 ZFA:0000106 extension PATO:0000592 decreased thickness abnormal ZDB-GENE-020419-20 192300 6222 rps18 ZFA:0000107 eye PATO:0000587 decreased size abnormal ZDB-GENE-020419-20 192300 6222 rps18 ZFA:0000110 fourth ventricle PATO:0001602 distended abnormal ZDB-GENE-020419-20 192300 6222 rps18 ZFA:0000112 gut PATO:0000645 hypoplastic abnormal ZDB-GENE-020419-20 192300 6222 rps18 ZFA:0000123 liver PATO:0000645 hypoplastic abnormal ZDB-GENE-020419-20 192300 6222 rps18 GO:0005694 chromosome BFO:0000050 part_of ZFA:0000142 peripheral nervous system PATO:0000070 amount abnormal ZDB-GENE-020419-20 192300 6222 rps18 ZFA:0007009 nerve BFO:0000050 part_of ZFA:0000142 peripheral nervous system PATO:0002011 neoplastic abnormal ZDB-GENE-020419-20 192300 6222 rps18 ZFA:0000396 nervous system PATO:0000001 quality abnormal ZDB-GENE-020419-20 192300 6222 rps18 ZFA:0001114 head PATO:0000587 decreased size abnormal ZDB-GENE-020419-21 192332 10051 smc4 ZFA:0000008 brain PATO:0000647 necrotic abnormal ZDB-GENE-020419-21 192332 10051 smc4 ZFA:0000012 central nervous system PATO:0000647 necrotic abnormal ZDB-GENE-020419-21 192332 10051 smc4 ZFA:0000054 pericardium PATO:0001450 edematous abnormal ZDB-GENE-020419-21 192332 10051 smc4 ZFA:0000107 eye PATO:0000587 decreased size abnormal ZDB-GENE-020419-21 192332 10051 smc4 ZFA:0000112 gut PATO:0000645 hypoplastic abnormal ZDB-GENE-020419-21 192332 10051 smc4 ZFA:0000114 heart PATO:0000001 quality abnormal ZDB-GENE-020419-21 192332 10051 smc4 ZFA:0000123 liver PATO:0000645 hypoplastic abnormal ZDB-GENE-020419-21 192332 10051 smc4 ZFA:0001114 head PATO:0000587 decreased size abnormal ZDB-GENE-020419-22 192318 10262 sf3b4 ZFA:0000008 brain PATO:0000647 necrotic abnormal ZDB-GENE-020419-22 192318 10262 sf3b4 ZFA:0000012 central nervous system PATO:0000647 necrotic abnormal ZDB-GENE-020419-22 192318 10262 sf3b4 ZFA:0000084 yolk PATO:0000411 circular abnormal ZDB-GENE-020419-22 192318 10262 sf3b4 ZFA:0000107 eye PATO:0000587 decreased size abnormal ZDB-GENE-020419-22 192318 10262 sf3b4 ZFA:0000112 gut PATO:0000645 hypoplastic abnormal ZDB-GENE-020419-22 192318 10262 sf3b4 ZFA:0000123 liver PATO:0000645 hypoplastic abnormal ZDB-GENE-020419-22 192318 10262 sf3b4 ZFA:0001094 whole organism PATO:0000169 viability abnormal ZDB-GENE-020419-22 192318 10262 sf3b4 ZFA:0001114 head PATO:0000587 decreased size abnormal ZDB-GENE-020419-22 192318 10262 sf3b4 ZFA:0001115 trunk PATO:0000574 decreased length abnormal ZDB-GENE-020419-22 192318 10262 sf3b4 ZFA:0001115 trunk PATO:0000647 necrotic abnormal ZDB-GENE-020419-23 192336 527 atp6v0ca GO:0030318 melanocyte differentiation PATO:0001507 disrupted abnormal ZDB-GENE-020419-23 192336 527 atp6v0ca GO:0043473 pigmentation PATO:0001507 disrupted abnormal ZDB-GENE-020419-23 192336 527 atp6v0ca GO:0043473 pigmentation PATO:0002052 decreased occurrence abnormal ZDB-GENE-020419-23 192336 527 atp6v0ca GO:0048069 eye pigmentation PATO:0001507 disrupted abnormal ZDB-GENE-020419-23 192336 527 atp6v0ca GO:0048570 notochord morphogenesis PATO:0002302 decreased process quality abnormal ZDB-GENE-020419-23 192336 527 atp6v0ca GO:0060036 notochord cell vacuolation PATO:0002302 decreased process quality abnormal ZDB-GENE-020419-23 192336 527 atp6v0ca GO:0060042 retina morphogenesis in camera-type eye PATO:0001236 process quality abnormal ZDB-GENE-020419-23 192336 527 atp6v0ca GO:0060059 embryonic retina morphogenesis in camera-type eye PATO:0001507 disrupted abnormal ZDB-GENE-020419-23 192336 527 atp6v0ca GO:0090398 cellular senescence PATO:0002017 increased magnitude abnormal ZDB-GENE-020419-23 192336 527 atp6v0ca ZFA:0000008 brain PATO:0000647 necrotic abnormal ZDB-GENE-020419-23 192336 527 atp6v0ca ZFA:0000012 central nervous system PATO:0000647 necrotic abnormal ZDB-GENE-020419-23 192336 527 atp6v0ca ZFA:0000107 eye PATO:0000014 color abnormal ZDB-GENE-020419-23 192336 527 atp6v0ca ZFA:0000107 eye PATO:0000587 decreased size abnormal ZDB-GENE-020419-23 192336 527 atp6v0ca ZFA:0000108 fin PATO:0000646 malformed abnormal ZDB-GENE-020419-23 192336 527 atp6v0ca ZFA:0000112 gut PATO:0000587 decreased size abnormal ZDB-GENE-020419-23 192336 527 atp6v0ca ZFA:0000112 gut PATO:0000645 hypoplastic abnormal ZDB-GENE-020419-23 192336 527 atp6v0ca ZFA:0000123 liver PATO:0000587 decreased size abnormal ZDB-GENE-020419-23 192336 527 atp6v0ca ZFA:0000123 liver PATO:0000645 hypoplastic abnormal ZDB-GENE-020419-23 192336 527 atp6v0ca GO:0005773 vacuole BFO:0000050 part_of ZFA:0000135 notochord PATO:0001444 broken abnormal ZDB-GENE-020419-23 192336 527 atp6v0ca ZFA:0000144 retinal pigmented epithelium PATO:0000001 quality abnormal ZDB-GENE-020419-23 192336 527 atp6v0ca ZFA:0000144 retinal pigmented epithelium PATO:0000051 morphology abnormal ZDB-GENE-020419-23 192336 527 atp6v0ca ZFA:0000144 retinal pigmented epithelium PATO:0000646 malformed abnormal ZDB-GENE-020419-23 192336 527 atp6v0ca ZFA:0000144 retinal pigmented epithelium PATO:0001241 physical object quality abnormal ZDB-GENE-020419-23 192336 527 atp6v0ca ZFA:0000144 retinal pigmented epithelium PATO:0001354 translucent abnormal ZDB-GENE-020419-23 192336 527 atp6v0ca ZFA:0000292 surface structure PATO:0000001 quality abnormal ZDB-GENE-020419-23 192336 527 atp6v0ca ZFA:0000396 nervous system PATO:0000001 quality abnormal ZDB-GENE-020419-23 192336 527 atp6v0ca ZFA:0001094 whole organism PATO:0000169 viability abnormal ZDB-GENE-020419-23 192336 527 atp6v0ca ZFA:0001094 whole organism PATO:0000328 low saturation abnormal ZDB-GENE-020419-23 192336 527 atp6v0ca ZFA:0001094 whole organism PATO:0000617 bent abnormal ZDB-GENE-020419-23 192336 527 atp6v0ca ZFA:0001094 whole organism PATO:0000718 lethal (sensu genetics) abnormal ZDB-GENE-020419-23 192336 527 atp6v0ca ZFA:0001094 whole organism PATO:0002249 unpigmented abnormal ZDB-GENE-020419-23 192336 527 atp6v0ca ZFA:0001094 whole organism PATO:0002251 decreased pigmentation abnormal ZDB-GENE-020419-23 192336 527 atp6v0ca ZFA:0001114 head PATO:0000587 decreased size abnormal ZDB-GENE-020419-23 192336 527 atp6v0ca ZFA:0001114 head PATO:0002251 decreased pigmentation abnormal ZDB-GENE-020419-23 192336 527 atp6v0ca ZFA:0001161 pectoral fin PATO:0000001 quality abnormal ZDB-GENE-020419-23 192336 527 atp6v0ca ZFA:0001161 pectoral fin PATO:0001799 ruffled abnormal ZDB-GENE-020419-23 192336 527 atp6v0ca ZFA:0009091 melanocyte BFO:0000050 part_of ZFA:0005220 larval melanophore stripe PATO:0001354 translucent abnormal ZDB-GENE-020419-23 192336 527 atp6v0ca GO:0005764 lysosome BFO:0000050 part_of ZFA:0009000 cell PATO:0001997 decreased amount abnormal ZDB-GENE-020419-23 192336 527 atp6v0ca GO:0005776 autophagosome BFO:0000050 part_of ZFA:0009000 cell PATO:0000470 increased amount abnormal ZDB-GENE-020419-23 192336 527 atp6v0ca ZFA:0009090 pigment cell PATO:0000001 quality abnormal ZDB-GENE-020419-23 192336 527 atp6v0ca ZFA:0009091 melanocyte PATO:0000001 quality abnormal ZDB-GENE-020419-23 192336 527 atp6v0ca ZFA:0009091 melanocyte PATO:0000462 absent abnormal ZDB-GENE-020419-23 192336 527 atp6v0ca ZFA:0009091 melanocyte PATO:0000586 increased size abnormal ZDB-GENE-020419-23 192336 527 atp6v0ca ZFA:0009091 melanocyte PATO:0000646 malformed abnormal ZDB-GENE-020419-23 192336 527 atp6v0ca ZFA:0009091 melanocyte PATO:0001354 translucent abnormal ZDB-GENE-020419-23 192336 527 atp6v0ca ZFA:0009091 melanocyte PATO:0001512 punctate abnormal ZDB-GENE-020419-23 192336 527 atp6v0ca ZFA:0009091 melanocyte PATO:0001997 decreased amount abnormal ZDB-GENE-020419-23 192336 527 atp6v0ca GO:0001750 photoreceptor outer segment BFO:0000050 part_of ZFA:0009154 eye photoreceptor cell PATO:0000587 decreased size abnormal ZDB-GENE-020419-24 192338 4171 mcm2 GO:0031514 motile cilium BFO:0000050 part_of ZFA:0000001 Kupffer's vesicle PATO:0000574 decreased length abnormal ZDB-GENE-020419-24 192338 4171 mcm2 GO:0044458 motile cilium assembly BFO:0000066 occurs_in ZFA:0000001 Kupffer's vesicle PATO:0002302 decreased process quality abnormal ZDB-GENE-020419-24 192338 4171 mcm2 ZFA:0000008 brain PATO:0000647 necrotic abnormal ZDB-GENE-020419-24 192338 4171 mcm2 ZFA:0000012 central nervous system PATO:0000647 necrotic abnormal ZDB-GENE-020419-24 192338 4171 mcm2 ZFA:0000107 eye PATO:0000587 decreased size abnormal ZDB-GENE-020419-24 192338 4171 mcm2 ZFA:0000112 gut PATO:0000645 hypoplastic abnormal ZDB-GENE-020419-24 192338 4171 mcm2 GO:0001947 heart looping BFO:0000066 occurs_in ZFA:0000114 heart PATO:0002052 decreased occurrence abnormal ZDB-GENE-020419-24 192338 4171 mcm2 ZFA:0000114 heart PATO:0001450 edematous abnormal ZDB-GENE-020419-24 192338 4171 mcm2 GO:0003140 determination of left/right asymmetry in lateral mesoderm BFO:0000066 occurs_in ZFA:0000121 lateral plate mesoderm PATO:0002052 decreased occurrence abnormal ZDB-GENE-020419-24 192338 4171 mcm2 ZFA:0000123 liver PATO:0000645 hypoplastic abnormal ZDB-GENE-020419-24 192338 4171 mcm2 GO:0031514 motile cilium BFO:0000050 part_of ZFA:0000150 pronephric duct PATO:0000574 decreased length abnormal ZDB-GENE-020419-24 192338 4171 mcm2 GO:0031514 motile cilium BFO:0000050 part_of ZFA:0000150 pronephric duct PATO:0000937 disorganized abnormal ZDB-GENE-020419-24 192338 4171 mcm2 ZFA:0000150 pronephric duct PATO:0001714 increased diameter abnormal ZDB-GENE-020419-24 192338 4171 mcm2 ZFA:0000152 retina PATO:0000001 quality abnormal ZDB-GENE-020419-24 192338 4171 mcm2 GO:0008283 cell population proliferation BFO:0000066 occurs_in ZFA:0001078 thymus PATO:0002052 decreased occurrence abnormal ZDB-GENE-020419-24 192338 4171 mcm2 ZFA:0009034 epithelial cell BFO:0000050 part_of ZFA:0001078 thymus PATO:0001997 decreased amount abnormal ZDB-GENE-020419-24 192338 4171 mcm2 ZFA:0001078 thymus PATO:0000587 decreased size abnormal ZDB-GENE-020419-24 192338 4171 mcm2 GO:0007224 smoothened signaling pathway BFO:0000066 occurs_in ZFA:0001094 whole organism PATO:0002052 decreased occurrence abnormal ZDB-GENE-020419-24 192338 4171 mcm2 ZFA:0001114 head PATO:0000587 decreased size abnormal ZDB-GENE-020419-24 192338 4171 mcm2 ZFA:0001115 trunk PATO:0000967 undulate abnormal ZDB-GENE-020419-24 192338 4171 mcm2 GO:0035469 determination of pancreatic left/right asymmetry BFO:0000066 occurs_in ZFA:0001260 endocrine pancreas PATO:0002052 decreased occurrence abnormal ZDB-GENE-020419-24 192338 4171 mcm2 ZFA:0001260 endocrine pancreas PATO:0000628 mislocalised abnormal ZDB-GENE-020419-24 192338 4171 mcm2 ZFA:0001613 pharyngeal arch 3-7 PATO:0001483 aplastic abnormal ZDB-GENE-020419-25 192301 6152 rpl24 ZFA:0000006 ball PATO:0000586 increased size abnormal ZDB-GENE-020419-25 192301 6152 rpl24 ZFA:0000079 telencephalon PATO:0001617 deformed abnormal ZDB-GENE-020419-25 192301 6152 rpl24 ZFA:0000084 yolk PATO:0001511 non-functional abnormal ZDB-GENE-020419-25 192301 6152 rpl24 ZFA:0000106 extension PATO:0000574 decreased length abnormal ZDB-GENE-020419-25 192301 6152 rpl24 ZFA:0000106 extension PATO:0000592 decreased thickness abnormal ZDB-GENE-020419-25 192301 6152 rpl24 ZFA:0000106 extension PATO:0001617 deformed abnormal ZDB-GENE-020419-25 192301 6152 rpl24 ZFA:0000107 eye PATO:0000587 decreased size abnormal ZDB-GENE-020419-25 192301 6152 rpl24 ZFA:0000110 fourth ventricle PATO:0000963 opaque abnormal ZDB-GENE-020419-25 192301 6152 rpl24 ZFA:0000112 gut PATO:0000645 hypoplastic abnormal ZDB-GENE-020419-25 192301 6152 rpl24 ZFA:0000123 liver PATO:0000645 hypoplastic abnormal ZDB-GENE-020419-25 192301 6152 rpl24 ZFA:0000138 otic placode PATO:0000052 shape abnormal ZDB-GENE-020419-25 192301 6152 rpl24 ZFA:0000138 otic placode PATO:0000587 decreased size abnormal ZDB-GENE-020419-25 192301 6152 rpl24 ZFA:0000445 optic tectum PATO:0000586 increased size abnormal ZDB-GENE-020419-25 192301 6152 rpl24 ZFA:0001114 head PATO:0000587 decreased size abnormal ZDB-GENE-020419-25 192301 6152 rpl24 ZFA:0001117 post-vent region PATO:0000617 bent abnormal ZDB-GENE-020419-26 192330 6631 snrpc GO:0000380 alternative mRNA splicing, via spliceosome PATO:0001236 process quality abnormal ZDB-GENE-020419-26 192330 6631 snrpc GO:0000381 regulation of alternative mRNA splicing, via spliceosome PATO:0001507 disrupted abnormal ZDB-GENE-020419-26 192330 6631 snrpc ZFA:0000008 brain PATO:0000647 necrotic abnormal ZDB-GENE-020419-26 192330 6631 snrpc ZFA:0000012 central nervous system PATO:0000647 necrotic abnormal ZDB-GENE-020419-26 192330 6631 snrpc ZFA:0000054 pericardium PATO:0001450 edematous abnormal ZDB-GENE-020419-26 192330 6631 snrpc ZFA:0000107 eye PATO:0000587 decreased size abnormal ZDB-GENE-020419-26 192330 6631 snrpc ZFA:0000107 eye PATO:0000647 necrotic abnormal ZDB-GENE-020419-26 192330 6631 snrpc ZFA:0000112 gut PATO:0000645 hypoplastic abnormal ZDB-GENE-020419-26 192330 6631 snrpc ZFA:0000123 liver PATO:0000645 hypoplastic abnormal ZDB-GENE-020419-26 192330 6631 snrpc ZFA:0001094 whole organism PATO:0001468 curved dorsal abnormal ZDB-GENE-020419-26 192330 6631 snrpc ZFA:0001094 whole organism PATO:0001911 circling abnormal ZDB-GENE-020419-26 192330 6631 snrpc ZFA:0001094 whole organism PATO:0002251 decreased pigmentation abnormal ZDB-GENE-020419-26 192330 6631 snrpc ZFA:0001114 head PATO:0000587 decreased size abnormal ZDB-GENE-020419-26 192330 6631 snrpc ZFA:0001114 head PATO:0000647 necrotic abnormal ZDB-GENE-020419-26 192330 6631 snrpc ZFA:0001115 trunk PATO:0000592 decreased thickness abnormal ZDB-GENE-020419-26 192330 6631 snrpc ZFA:0001115 trunk PATO:0000617 bent abnormal ZDB-GENE-020419-26 192330 6631 snrpc ZFA:0001115 trunk PATO:0000647 necrotic abnormal ZDB-GENE-020419-26 192330 6631 snrpc ZFA:0001115 trunk PATO:0001468 curved dorsal abnormal ZDB-GENE-020419-27 192333 4176 mcm7 GO:0048884 neuromast development PATO:0001507 disrupted abnormal ZDB-GENE-020419-27 192333 4176 mcm7 GO:0031514 motile cilium BFO:0000050 part_of ZFA:0000001 Kupffer's vesicle PATO:0000574 decreased length abnormal ZDB-GENE-020419-27 192333 4176 mcm7 ZFA:0000008 brain PATO:0000647 necrotic abnormal ZDB-GENE-020419-27 192333 4176 mcm7 ZFA:0000012 central nervous system PATO:0000647 necrotic abnormal ZDB-GENE-020419-27 192333 4176 mcm7 ZFA:0000054 pericardium PATO:0001450 edematous abnormal ZDB-GENE-020419-27 192333 4176 mcm7 ZFA:0000107 eye PATO:0000587 decreased size abnormal ZDB-GENE-020419-27 192333 4176 mcm7 ZFA:0000107 eye PATO:0000647 necrotic abnormal ZDB-GENE-020419-27 192333 4176 mcm7 ZFA:0000112 gut PATO:0000001 quality abnormal ZDB-GENE-020419-27 192333 4176 mcm7 ZFA:0000112 gut PATO:0000645 hypoplastic abnormal ZDB-GENE-020419-27 192333 4176 mcm7 ZFA:0000114 heart PATO:0001450 edematous abnormal ZDB-GENE-020419-27 192333 4176 mcm7 GO:0003140 determination of left/right asymmetry in lateral mesoderm BFO:0000066 occurs_in ZFA:0000121 lateral plate mesoderm PATO:0002052 decreased occurrence abnormal ZDB-GENE-020419-27 192333 4176 mcm7 ZFA:0000123 liver PATO:0000001 quality abnormal ZDB-GENE-020419-27 192333 4176 mcm7 ZFA:0000123 liver PATO:0000645 hypoplastic abnormal ZDB-GENE-020419-27 192333 4176 mcm7 ZFA:0000396 nervous system PATO:0000001 quality abnormal ZDB-GENE-020419-27 192333 4176 mcm7 ZFA:0000940 posterior lateral line neuromast PATO:0002001 has fewer parts of type abnormal ZFA:0009367 neuromast hair cell ZDB-GENE-020419-27 192333 4176 mcm7 ZFA:0001094 whole organism PATO:0000052 shape abnormal ZDB-GENE-020419-27 192333 4176 mcm7 ZFA:0001094 whole organism PATO:0000617 bent abnormal ZDB-GENE-020419-27 192333 4176 mcm7 ZFA:0001114 head PATO:0000587 decreased size abnormal ZDB-GENE-020419-27 192333 4176 mcm7 ZFA:0001114 head PATO:0000647 necrotic abnormal ZDB-GENE-020419-27 192333 4176 mcm7 ZFA:0001114 head PATO:0001450 edematous abnormal ZDB-GENE-020419-27 192333 4176 mcm7 ZFA:0001115 trunk PATO:0000592 decreased thickness abnormal ZDB-GENE-020419-27 192333 4176 mcm7 ZFA:0001115 trunk PATO:0000617 bent abnormal ZDB-GENE-020419-27 192333 4176 mcm7 ZFA:0001115 trunk PATO:0000647 necrotic abnormal ZDB-GENE-020419-27 192333 4176 mcm7 ZFA:0001115 trunk PATO:0001468 curved dorsal abnormal ZDB-GENE-020419-27 192333 4176 mcm7 ZFA:0001439 anatomical system PATO:0000001 quality abnormal ZDB-GENE-020419-28 192305 159 adssl GO:0051320 S phase PATO:0000498 increased duration abnormal ZDB-GENE-020419-28 192305 159 adssl ZFA:0000008 brain PATO:0000647 necrotic abnormal ZDB-GENE-020419-28 192305 159 adssl ZFA:0000012 central nervous system PATO:0000647 necrotic abnormal ZDB-GENE-020419-28 192305 159 adssl ZFA:0000054 pericardium PATO:0001450 edematous abnormal ZDB-GENE-020419-28 192305 159 adssl ZFA:0000107 eye PATO:0000587 decreased size abnormal ZDB-GENE-020419-28 192305 159 adssl ZFA:0000112 gut PATO:0000645 hypoplastic abnormal ZDB-GENE-020419-28 192305 159 adssl ZFA:0000123 liver PATO:0000645 hypoplastic abnormal ZDB-GENE-020419-28 192305 159 adssl ZFA:0001114 head PATO:0000587 decreased size abnormal ZDB-GENE-020419-28 192305 159 adssl ZFA:0001115 trunk PATO:0000647 necrotic abnormal ZDB-GENE-020419-29 192340 950 scarb2a ZFA:0000008 brain PATO:0000001 quality abnormal ZDB-GENE-020419-29 192340 950 scarb2a ZFA:0000029 hindbrain PATO:0000001 quality abnormal ZDB-GENE-020419-29 192340 950 scarb2a ZFA:0000029 hindbrain PATO:0000330 irregular spatial pattern abnormal ZDB-GENE-020419-29 192340 950 scarb2a ZFA:0000029 hindbrain PATO:0001925 surface feature shape abnormal ZDB-GENE-020419-29 192340 950 scarb2a ZFA:0000112 gut PATO:0000001 quality abnormal ZDB-GENE-020419-29 192340 950 scarb2a ZFA:0000112 gut PATO:0000645 hypoplastic abnormal ZDB-GENE-020419-29 192340 950 scarb2a ZFA:0000123 liver PATO:0000001 quality abnormal ZDB-GENE-020419-29 192340 950 scarb2a ZFA:0000123 liver PATO:0000645 hypoplastic abnormal ZDB-GENE-020419-29 192340 950 scarb2a GO:0005604 basement membrane BFO:0000050 part_of ZFA:0000135 notochord PATO:0000591 increased thickness abnormal ZDB-GENE-020419-29 192340 950 scarb2a GO:0005604 basement membrane BFO:0000050 part_of ZFA:0000135 notochord PATO:0000646 malformed abnormal ZDB-GENE-020419-29 192340 950 scarb2a GO:0005604 basement membrane BFO:0000050 part_of ZFA:0000135 notochord PATO:0000941 vacuolated abnormal ZDB-GENE-020419-29 192340 950 scarb2a GO:0005773 vacuole BFO:0000050 part_of ZFA:0000135 notochord PATO:0000140 position abnormal ZDB-GENE-020419-29 192340 950 scarb2a GO:0005773 vacuole BFO:0000050 part_of ZFA:0000135 notochord PATO:0000587 decreased size abnormal ZDB-GENE-020419-29 192340 950 scarb2a GO:0005773 vacuole BFO:0000050 part_of ZFA:0000135 notochord PATO:0000646 malformed abnormal ZDB-GENE-020419-29 192340 950 scarb2a ZFA:0000135 notochord PATO:0000001 quality abnormal ZDB-GENE-020419-29 192340 950 scarb2a ZFA:0000135 notochord PATO:0000051 morphology abnormal ZDB-GENE-020419-29 192340 950 scarb2a ZFA:0001094 whole organism PATO:0000617 bent abnormal ZDB-GENE-020419-29 192340 950 scarb2a ZFA:0001114 head PATO:0000052 shape abnormal ZDB-GENE-020419-29 192340 950 scarb2a ZFA:0001114 head PATO:0000587 decreased size abnormal ZDB-GENE-020419-29 192340 950 scarb2a ZFA:0001114 head PATO:0001872 cuboid abnormal ZDB-GENE-020419-29 192340 950 scarb2a ZFA:0001115 trunk PATO:0000406 curved abnormal ZDB-GENE-020419-29 192340 950 scarb2a ZFA:0001115 trunk PATO:0001468 curved dorsal abnormal ZDB-GENE-020419-29 192340 950 scarb2a ZFA:0001115 trunk PATO:0002251 decreased pigmentation abnormal ZDB-GENE-020419-29 192340 950 scarb2a ZFA:0001117 post-vent region PATO:0002251 decreased pigmentation abnormal ZDB-GENE-020419-29 192340 950 scarb2a ZFA:0009090 pigment cell PATO:0000001 quality abnormal ZDB-GENE-020419-29 192340 950 scarb2a ZFA:0009091 melanocyte PATO:0000001 quality abnormal ZDB-GENE-020419-3 192334 26229 b3gat3 GO:0001503 ossification PATO:0000502 delayed abnormal ZDB-GENE-020419-3 192334 26229 b3gat3 GO:0015012 heparan sulfate proteoglycan biosynthetic process PATO:0002052 decreased occurrence abnormal ZDB-GENE-020419-3 192334 26229 b3gat3 GO:0030203 glycosaminoglycan metabolic process PATO:0001507 disrupted abnormal ZDB-GENE-020419-3 192334 26229 b3gat3 GO:0030206 chondroitin sulfate biosynthetic process PATO:0001236 process quality abnormal ZDB-GENE-020419-3 192334 26229 b3gat3 GO:0050650 chondroitin sulfate proteoglycan biosynthetic process PATO:0002052 decreased occurrence abnormal ZDB-GENE-020419-3 192334 26229 b3gat3 GO:0051923 sulfation PATO:0002052 decreased occurrence abnormal ZDB-GENE-020419-3 192334 26229 b3gat3 GO:0060350 endochondral bone morphogenesis PATO:0000502 delayed abnormal ZDB-GENE-020419-3 192334 26229 b3gat3 ZFA:0000095 pharyngeal arch 3-7 skeleton PATO:0000001 quality abnormal ZDB-GENE-020419-3 192334 26229 b3gat3 ZFA:0000184 cleithrum PATO:0000587 decreased size abnormal ZDB-GENE-020419-3 192334 26229 b3gat3 ZFA:0000184 cleithrum PATO:0000646 malformed abnormal ZDB-GENE-020419-3 192334 26229 b3gat3 ZFA:0000250 opercle PATO:0000587 decreased size abnormal ZDB-GENE-020419-3 192334 26229 b3gat3 ZFA:0000250 opercle PATO:0000646 malformed abnormal ZDB-GENE-020419-3 192334 26229 b3gat3 BSPO:0000013 anterior-posterior axis BFO:0000050 part_of ZFA:0001094 whole organism PATO:0000969 dwarf-like abnormal ZDB-GENE-020419-3 192334 26229 b3gat3 ZFA:0001114 head PATO:0000587 decreased size abnormal ZDB-GENE-020419-3 192334 26229 b3gat3 ZFA:0001114 head PATO:0001872 cuboid abnormal ZDB-GENE-020419-3 192334 26229 b3gat3 ZFA:0009084 chondrocyte BFO:0000050 part_of ZFA:0001205 Meckel's cartilage PATO:0000937 disorganized abnormal ZDB-GENE-020419-3 192334 26229 b3gat3 ZFA:0001205 Meckel's cartilage PATO:0000141 structure abnormal ZDB-GENE-020419-3 192334 26229 b3gat3 ZFA:0001227 mandibular arch skeleton PATO:0000051 morphology abnormal ZDB-GENE-020419-3 192334 26229 b3gat3 ZFA:0001227 mandibular arch skeleton PATO:0000052 shape abnormal ZDB-GENE-020419-3 192334 26229 b3gat3 ZFA:0001227 mandibular arch skeleton PATO:0000574 decreased length abnormal ZDB-GENE-020419-3 192334 26229 b3gat3 ZFA:0001227 mandibular arch skeleton PATO:0001485 condensed abnormal ZDB-GENE-020419-3 192334 26229 b3gat3 ZFA:0009084 chondrocyte BFO:0000050 part_of ZFA:0001400 ceratohyal cartilage PATO:0000937 disorganized abnormal ZDB-GENE-020419-3 192334 26229 b3gat3 ZFA:0001400 ceratohyal cartilage PATO:0000141 structure abnormal ZDB-GENE-020419-3 192334 26229 b3gat3 GO:0005581 collagen trimer BFO:0000050 part_of ZFA:0001458 cranial cartilage PATO:0000051 morphology abnormal ZDB-GENE-020419-3 192334 26229 b3gat3 GO:0005584 collagen type I trimer BFO:0000050 part_of ZFA:0001458 cranial cartilage PATO:0001997 decreased amount abnormal ZDB-GENE-020419-3 192334 26229 b3gat3 GO:0005585 collagen type II trimer BFO:0000050 part_of ZFA:0001458 cranial cartilage PATO:0001997 decreased amount abnormal ZDB-GENE-020419-3 192334 26229 b3gat3 GO:0005589 collagen type VI trimer BFO:0000050 part_of ZFA:0001458 cranial cartilage PATO:0000462 absent abnormal ZDB-GENE-020419-3 192334 26229 b3gat3 GO:0031012 extracellular matrix BFO:0000050 part_of ZFA:0001458 cranial cartilage PATO:0000025 composition abnormal ZDB-GENE-020419-3 192334 26229 b3gat3 ZFA:0001458 cranial cartilage PATO:0000051 morphology abnormal ZDB-GENE-020419-3 192334 26229 b3gat3 ZFA:0001458 cranial cartilage PATO:0001617 deformed abnormal ZDB-GENE-020419-3 192334 26229 b3gat3 ZFA:0009084 chondrocyte BFO:0000050 part_of ZFA:0001460 pharyngeal arch cartilage PATO:0000411 circular abnormal ZDB-GENE-020419-3 192334 26229 b3gat3 ZFA:0009084 chondrocyte BFO:0000050 part_of ZFA:0001460 pharyngeal arch cartilage PATO:0000937 disorganized abnormal ZDB-GENE-020419-3 192334 26229 b3gat3 ZFA:0001460 pharyngeal arch cartilage PATO:0000574 decreased length abnormal ZDB-GENE-020419-3 192334 26229 b3gat3 ZFA:0001460 pharyngeal arch cartilage PATO:0000591 increased thickness abnormal ZDB-GENE-020419-3 192334 26229 b3gat3 ZFA:0001460 pharyngeal arch cartilage PATO:0000614 oriented abnormal ZDB-GENE-020419-3 192334 26229 b3gat3 ZFA:0001613 pharyngeal arch 3-7 PATO:0000052 shape abnormal ZDB-GENE-020419-30 192339 11269 ddx19b ZFA:0000008 brain PATO:0000647 necrotic abnormal ZDB-GENE-020419-30 192339 11269 ddx19b ZFA:0000012 central nervous system PATO:0000647 necrotic abnormal ZDB-GENE-020419-30 192339 11269 ddx19b ZFA:0000107 eye PATO:0000587 decreased size abnormal ZDB-GENE-020419-30 192339 11269 ddx19b ZFA:0000396 nervous system PATO:0000001 quality abnormal ZDB-GENE-020419-30 192339 11269 ddx19b ZFA:0001094 whole organism PATO:0000169 viability abnormal ZDB-GENE-020419-30 192339 11269 ddx19b ZFA:0001094 whole organism PATO:0000406 curved abnormal ZDB-GENE-020419-30 192339 11269 ddx19b ZFA:0001094 whole organism PATO:0000647 necrotic abnormal ZDB-GENE-020419-30 192339 55308 ddx19b ZFA:0000008 brain PATO:0000647 necrotic abnormal ZDB-GENE-020419-30 192339 55308 ddx19b ZFA:0000012 central nervous system PATO:0000647 necrotic abnormal ZDB-GENE-020419-30 192339 55308 ddx19b ZFA:0000107 eye PATO:0000587 decreased size abnormal ZDB-GENE-020419-30 192339 55308 ddx19b ZFA:0000396 nervous system PATO:0000001 quality abnormal ZDB-GENE-020419-30 192339 55308 ddx19b ZFA:0001094 whole organism PATO:0000169 viability abnormal ZDB-GENE-020419-30 192339 55308 ddx19b ZFA:0001094 whole organism PATO:0000406 curved abnormal ZDB-GENE-020419-30 192339 55308 ddx19b ZFA:0001094 whole organism PATO:0000647 necrotic abnormal ZDB-GENE-020419-31 192325 22916 ncbp2 ZFA:0000008 brain PATO:0000647 necrotic abnormal ZDB-GENE-020419-31 192325 22916 ncbp2 ZFA:0000012 central nervous system PATO:0000647 necrotic abnormal ZDB-GENE-020419-31 192325 22916 ncbp2 ZFA:0000054 pericardium PATO:0001450 edematous abnormal ZDB-GENE-020419-31 192325 22916 ncbp2 ZFA:0000107 eye PATO:0000587 decreased size abnormal ZDB-GENE-020419-31 192325 22916 ncbp2 ZFA:0000107 eye PATO:0000647 necrotic abnormal ZDB-GENE-020419-31 192325 22916 ncbp2 ZFA:0000112 gut PATO:0000645 hypoplastic abnormal ZDB-GENE-020419-31 192325 22916 ncbp2 ZFA:0000114 heart PATO:0000001 quality abnormal ZDB-GENE-020419-31 192325 22916 ncbp2 ZFA:0000123 liver PATO:0000645 hypoplastic abnormal ZDB-GENE-020419-31 192325 22916 ncbp2 ZFA:0001114 head PATO:0000587 decreased size abnormal ZDB-GENE-020419-31 192325 22916 ncbp2 ZFA:0001114 head PATO:0000647 necrotic abnormal ZDB-GENE-020419-32 192302 3065 hdac1 GO:0001764 neuron migration PATO:0001507 disrupted abnormal ZDB-GENE-020419-32 192302 3065 hdac1 GO:0001889 liver development PATO:0001749 paedomorphic growth abnormal ZDB-GENE-020419-32 192302 3065 hdac1 GO:0001947 heart looping PATO:0001507 disrupted abnormal ZDB-GENE-020419-32 192302 3065 hdac1 GO:0003139 secondary heart field specification PATO:0002052 decreased occurrence abnormal ZDB-GENE-020419-32 192302 3065 hdac1 GO:0008015 blood circulation PATO:0001507 disrupted abnormal ZDB-GENE-020419-32 192302 3065 hdac1 GO:0009790 embryo development PATO:0000502 delayed abnormal ZDB-GENE-020419-32 192302 3065 hdac1 GO:0010842 retina layer formation PATO:0001507 disrupted abnormal ZDB-GENE-020419-32 192302 3065 hdac1 GO:0021654 rhombomere boundary formation PATO:0001507 disrupted abnormal ZDB-GENE-020419-32 192302 3065 hdac1 GO:0030318 melanocyte differentiation PATO:0000502 delayed abnormal ZDB-GENE-020419-32 192302 3065 hdac1 GO:0030902 hindbrain development PATO:0001507 disrupted abnormal ZDB-GENE-020419-32 192302 3065 hdac1 GO:0031017 exocrine pancreas development PATO:0001236 process quality abnormal ZDB-GENE-020419-32 192302 3065 hdac1 GO:0031017 exocrine pancreas development PATO:0001749 paedomorphic growth abnormal ZDB-GENE-020419-32 192302 3065 hdac1 GO:0035188 hatching PATO:0000502 delayed abnormal ZDB-GENE-020419-32 192302 3065 hdac1 GO:0043473 pigmentation PATO:0001507 disrupted abnormal ZDB-GENE-020419-32 192302 3065 hdac1 GO:0048884 neuromast development PATO:0001507 disrupted abnormal ZDB-GENE-020419-32 192302 3065 hdac1 GO:0051726 regulation of cell cycle PATO:0001507 disrupted abnormal ZDB-GENE-020419-32 192302 3065 hdac1 GO:0060042 retina morphogenesis in camera-type eye PATO:0001507 disrupted abnormal ZDB-GENE-020419-32 192302 3065 hdac1 GO:0060047 heart contraction PATO:0000911 decreased rate abnormal ZDB-GENE-020419-32 192302 3065 hdac1 GO:0060218 hematopoietic stem cell differentiation PATO:0001507 disrupted abnormal ZDB-GENE-020419-32 192302 3065 hdac1 GO:0097324 melanocyte migration PATO:0001507 disrupted abnormal ZDB-GENE-020419-32 192302 3065 hdac1 ZFA:0000007 blood PATO:0002269 accumulation abnormal ZFA:0005249 vasculature ZDB-GENE-020419-32 192302 3065 hdac1 ZFA:0000008 brain PATO:0000051 morphology abnormal ZDB-GENE-020419-32 192302 3065 hdac1 ZFA:0000008 brain PATO:0000141 structure abnormal ZDB-GENE-020419-32 192302 3065 hdac1 ZFA:0000008 brain PATO:0000587 decreased size abnormal ZDB-GENE-020419-32 192302 3065 hdac1 ZFA:0009316 cardiac muscle cell BFO:0000050 part_of ZFA:0000009 cardiac ventricle PATO:0001997 decreased amount abnormal ZDB-GENE-020419-32 192302 3065 hdac1 ZFA:0000009 cardiac ventricle PATO:0000587 decreased size abnormal ZDB-GENE-020419-32 192302 3065 hdac1 ZFA:0000029 hindbrain PATO:0000001 quality abnormal ZDB-GENE-020419-32 192302 3065 hdac1 ZFA:0000035 lens PATO:0000001 quality abnormal ZDB-GENE-020419-32 192302 3065 hdac1 ZFA:0000046 retinal neural layer PATO:0000937 disorganized abnormal ZDB-GENE-020419-32 192302 3065 hdac1 ZFA:0000051 otic vesicle PATO:0000587 decreased size abnormal ZDB-GENE-020419-32 192302 3065 hdac1 ZFA:0000054 pericardium PATO:0001450 edematous abnormal ZDB-GENE-020419-32 192302 3065 hdac1 ZFA:0000076 swim bladder PATO:0001483 aplastic abnormal ZDB-GENE-020419-32 192302 3065 hdac1 ZFA:0001463 melanophore stripe BFO:0000050 part_of ZFA:0000084 yolk PATO:0000462 absent abnormal ZDB-GENE-020419-32 192302 3065 hdac1 ZFA:0000084 yolk PATO:0000052 shape abnormal ZDB-GENE-020419-32 192302 3065 hdac1 ZFA:0000084 yolk PATO:0000950 grey abnormal ZDB-GENE-020419-32 192302 3065 hdac1 ZFA:0000084 yolk PATO:0001851 swollen abnormal ZDB-GENE-020419-32 192302 3065 hdac1 ZFA:0000095 pharyngeal arch 3-7 skeleton PATO:0000001 quality abnormal ZDB-GENE-020419-32 192302 3065 hdac1 ZFA:0000106 extension PATO:0000587 decreased size abnormal ZDB-GENE-020419-32 192302 3065 hdac1 ZFA:0000107 eye PATO:0000374 increased distance abnormal ZFA:0000051 otic vesicle ZDB-GENE-020419-32 192302 3065 hdac1 ZFA:0000107 eye PATO:0000375 decreased distance abnormal ZFA:0000107 eye ZDB-GENE-020419-32 192302 3065 hdac1 ZFA:0000107 eye PATO:0000001 quality abnormal ZDB-GENE-020419-32 192302 3065 hdac1 ZFA:0000107 eye PATO:0000587 decreased size abnormal ZDB-GENE-020419-32 192302 3065 hdac1 ZFA:0009000 cell BFO:0000050 part_of ZFA:0000112 gut PATO:0000470 increased amount abnormal ZDB-GENE-020419-32 192302 3065 hdac1 ZFA:0000112 gut PATO:0000600 increased width abnormal ZDB-GENE-020419-32 192302 3065 hdac1 GO:0008015 blood circulation BFO:0000066 occurs_in ZFA:0000114 heart PATO:0002302 decreased process quality abnormal ZDB-GENE-020419-32 192302 3065 hdac1 ZFA:0000114 heart PATO:0000001 quality abnormal ZDB-GENE-020419-32 192302 3065 hdac1 ZFA:0000114 heart PATO:0000587 decreased size abnormal ZDB-GENE-020419-32 192302 3065 hdac1 ZFA:0000114 heart PATO:0001199 linear abnormal ZDB-GENE-020419-32 192302 3065 hdac1 ZFA:0000114 heart PATO:0001450 edematous abnormal ZDB-GENE-020419-32 192302 3065 hdac1 ZFA:0000114 heart PATO:0001624 decreased functionality abnormal ZDB-GENE-020419-32 192302 3065 hdac1 ZFA:0000123 liver PATO:0000051 morphology abnormal ZDB-GENE-020419-32 192302 3065 hdac1 ZFA:0000123 liver PATO:0000587 decreased size abnormal ZDB-GENE-020419-32 192302 3065 hdac1 BSPO:0000071 anterior region BFO:0000050 part_of ZFA:0000135 notochord PATO:0000600 increased width abnormal ZDB-GENE-020419-32 192302 3065 hdac1 ZFA:0000135 notochord PATO:0000001 quality abnormal ZDB-GENE-020419-32 192302 3065 hdac1 ZFA:0000135 notochord PATO:0000574 decreased length abnormal ZDB-GENE-020419-32 192302 3065 hdac1 ZFA:0000135 notochord PATO:0000600 increased width abnormal ZDB-GENE-020419-32 192302 3065 hdac1 ZFA:0000140 pancreas PATO:0000051 morphology abnormal ZDB-GENE-020419-32 192302 3065 hdac1 ZFA:0000140 pancreas PATO:0000587 decreased size abnormal ZDB-GENE-020419-32 192302 3065 hdac1 ZFA:0000144 retinal pigmented epithelium PATO:0001444 broken abnormal ZDB-GENE-020419-32 192302 3065 hdac1 ZFA:0000144 retinal pigmented epithelium PATO:0001608 patchy abnormal ZDB-GENE-020419-32 192302 3065 hdac1 ZFA:0000144 retinal pigmented epithelium PATO:0002251 decreased pigmentation abnormal ZDB-GENE-020419-32 192302 3065 hdac1 GO:0008283 cell population proliferation BFO:0000066 occurs_in ZFA:0000152 retina PATO:0002051 increased occurrence abnormal ZDB-GENE-020419-32 192302 3065 hdac1 GO:0072332 intrinsic apoptotic signaling pathway by p53 class mediator BFO:0000066 occurs_in ZFA:0000152 retina PATO:0002051 increased occurrence abnormal ZDB-GENE-020419-32 192302 3065 hdac1 ZFA:0009000 cell BFO:0000050 part_of ZFA:0000152 retina PATO:0000638 apoptotic abnormal ZDB-GENE-020419-32 192302 3065 hdac1 ZFA:0000152 retina PATO:0000141 structure abnormal ZDB-GENE-020419-32 192302 3065 hdac1 ZFA:0000152 retina PATO:0000937 disorganized abnormal ZDB-GENE-020419-32 192302 3065 hdac1 ZFA:0000152 retina PATO:0002112 perforate abnormal ZDB-GENE-020419-32 192302 3065 hdac1 ZFA:0000155 somite PATO:0001879 U-shaped abnormal ZDB-GENE-020419-32 192302 3065 hdac1 ZFA:0000155 somite PATO:0001997 decreased amount abnormal ZDB-GENE-020419-32 192302 3065 hdac1 ZFA:0005274 smooth muscle BFO:0000050 part_of ZFA:0000173 bulbus arteriosus PATO:0000462 absent abnormal ZDB-GENE-020419-32 192302 3065 hdac1 ZFA:0009316 cardiac muscle cell BFO:0000050 part_of ZFA:0000173 bulbus arteriosus PATO:0001997 decreased amount abnormal ZDB-GENE-020419-32 192302 3065 hdac1 ZFA:0000200 dorsal root ganglion PATO:0000628 mislocalised abnormal ZDB-GENE-020419-32 192302 3065 hdac1 ZFA:0000206 facial nerve motor nucleus PATO:0000051 morphology abnormal ZDB-GENE-020419-32 192302 3065 hdac1 ZFA:0000257 pectoral fin cartilage PATO:0000462 absent abnormal ZDB-GENE-020419-32 192302 3065 hdac1 ZFA:0000396 nervous system PATO:0000001 quality abnormal ZDB-GENE-020419-32 192302 3065 hdac1 ZFA:0000445 optic tectum PATO:0000587 decreased size abnormal ZDB-GENE-020419-32 192302 3065 hdac1 ZFA:0000471 atrium PATO:0000586 increased size abnormal ZDB-GENE-020419-32 192302 3065 hdac1 ZFA:0000471 atrium PATO:0000587 decreased size abnormal ZDB-GENE-020419-32 192302 3065 hdac1 ZFA:0000471 atrium PATO:0002210 bulbous abnormal ZDB-GENE-020419-32 192302 3065 hdac1 ZFA:0009248 neuron BFO:0000050 part_of ZFA:0000588 statoacoustic (VIII) ganglion PATO:0001997 decreased amount abnormal ZDB-GENE-020419-32 192302 3065 hdac1 ZFA:0000940 posterior lateral line neuromast PATO:0002001 has fewer parts of type abnormal ZFA:0009367 neuromast hair cell ZDB-GENE-020419-32 192302 3065 hdac1 ZFA:0001058 caudal fin PATO:0001999 lacks parts or has fewer parts of type abnormal ZFA:0000200 dorsal root ganglion ZDB-GENE-020419-32 192302 3065 hdac1 ZFA:0001058 caudal fin PATO:0001469 curved ventral abnormal ZDB-GENE-020419-32 192302 3065 hdac1 ZFA:0009023 common lymphoid progenitor BFO:0000050 part_of ZFA:0001077 thymus primordium PATO:0000462 absent abnormal ZDB-GENE-020419-32 192302 3065 hdac1 ZFA:0001094 whole organism PATO:0000406 curved abnormal ZDB-GENE-020419-32 192302 3065 hdac1 ZFA:0001094 whole organism PATO:0000574 decreased length abnormal ZDB-GENE-020419-32 192302 3065 hdac1 ZFA:0001094 whole organism PATO:0000587 decreased size abnormal ZDB-GENE-020419-32 192302 3065 hdac1 ZFA:0001094 whole organism PATO:0001469 curved ventral abnormal ZDB-GENE-020419-32 192302 3065 hdac1 ZFA:0001094 whole organism PATO:0001604 decreased life span abnormal ZDB-GENE-020419-32 192302 3065 hdac1 ZFA:0001094 whole organism PATO:0002251 decreased pigmentation abnormal ZDB-GENE-020419-32 192302 3065 hdac1 GO:0008015 blood circulation BFO:0000066 occurs_in ZFA:0001114 head PATO:0000297 arrested abnormal ZDB-GENE-020419-32 192302 3065 hdac1 ZFA:0001114 head PATO:0000587 decreased size abnormal ZDB-GENE-020419-32 192302 3065 hdac1 ZFA:0001115 trunk PATO:0000406 curved abnormal ZDB-GENE-020419-32 192302 3065 hdac1 ZFA:0001115 trunk PATO:0000574 decreased length abnormal ZDB-GENE-020419-32 192302 3065 hdac1 ZFA:0001115 trunk PATO:0000639 degenerate abnormal ZDB-GENE-020419-32 192302 3065 hdac1 ZFA:0001115 trunk PATO:0001469 curved ventral abnormal ZDB-GENE-020419-32 192302 3065 hdac1 GO:0008015 blood circulation BFO:0000066 occurs_in ZFA:0001117 post-vent region PATO:0000297 arrested abnormal ZDB-GENE-020419-32 192302 3065 hdac1 ZFA:0009165 neural crest cell BFO:0000050 part_of ZFA:0001117 post-vent region PATO:0000467 present abnormal ZDB-GENE-020419-32 192302 3065 hdac1 ZFA:0001117 post-vent region PATO:0000406 curved abnormal ZDB-GENE-020419-32 192302 3065 hdac1 ZFA:0001117 post-vent region PATO:0000647 necrotic abnormal ZDB-GENE-020419-32 192302 3065 hdac1 ZFA:0001161 pectoral fin PATO:0000001 quality abnormal ZDB-GENE-020419-32 192302 3065 hdac1 ZFA:0001161 pectoral fin PATO:0000587 decreased size abnormal ZDB-GENE-020419-32 192302 3065 hdac1 ZFA:0001161 pectoral fin PATO:0000645 hypoplastic abnormal ZDB-GENE-020419-32 192302 3065 hdac1 ZFA:0001161 pectoral fin PATO:0001483 aplastic abnormal ZDB-GENE-020419-32 192302 3065 hdac1 ZFA:0001205 Meckel's cartilage PATO:0000462 absent abnormal ZDB-GENE-020419-32 192302 3065 hdac1 ZFA:0001227 mandibular arch skeleton PATO:0000587 decreased size abnormal ZDB-GENE-020419-32 192302 3065 hdac1 ZFA:0001227 mandibular arch skeleton PATO:0001483 aplastic abnormal ZDB-GENE-020419-32 192302 3065 hdac1 GO:0008283 cell population proliferation BFO:0000066 occurs_in ZFA:0001249 exocrine pancreas PATO:0002052 decreased occurrence abnormal ZDB-GENE-020419-32 192302 3065 hdac1 GO:0040007 growth BFO:0000066 occurs_in ZFA:0001249 exocrine pancreas PATO:0002052 decreased occurrence abnormal ZDB-GENE-020419-32 192302 3065 hdac1 ZFA:0009045 epithelial cell of pancreas BFO:0000050 part_of ZFA:0001249 exocrine pancreas PATO:0001997 decreased amount abnormal ZDB-GENE-020419-32 192302 3065 hdac1 ZFA:0001249 exocrine pancreas PATO:0000051 morphology abnormal ZDB-GENE-020419-32 192302 3065 hdac1 ZFA:0001249 exocrine pancreas PATO:0001483 aplastic abnormal ZDB-GENE-020419-32 192302 3065 hdac1 ZFA:0001259 forebrain ventricle PATO:0000051 morphology abnormal ZDB-GENE-020419-32 192302 3065 hdac1 ZFA:0001259 forebrain ventricle PATO:0000586 increased size abnormal ZDB-GENE-020419-32 192302 3065 hdac1 ZFA:0001284 optic fissure PATO:0000609 closure incomplete abnormal ZDB-GENE-020419-32 192302 3065 hdac1 ZFA:0001284 optic fissure PATO:0000610 open abnormal ZDB-GENE-020419-32 192302 3065 hdac1 GO:0008283 cell population proliferation BFO:0000066 occurs_in ZFA:0001289 ciliary marginal zone PATO:0002051 increased occurrence abnormal ZDB-GENE-020419-32 192302 3065 hdac1 ZFA:0001399 palatoquadrate cartilage PATO:0000462 absent abnormal ZDB-GENE-020419-32 192302 3065 hdac1 ZFA:0001400 ceratohyal cartilage PATO:0000462 absent abnormal ZDB-GENE-020419-32 192302 3065 hdac1 ZFA:0001422 hyosymplectic cartilage PATO:0000462 absent abnormal ZDB-GENE-020419-32 192302 3065 hdac1 ZFA:0001458 cranial cartilage PATO:0001483 aplastic abnormal ZDB-GENE-020419-32 192302 3065 hdac1 ZFA:0009091 melanocyte BFO:0000050 part_of ZFA:0001463 melanophore stripe PATO:0001997 decreased amount abnormal ZDB-GENE-020419-32 192302 3065 hdac1 ZFA:0001463 melanophore stripe PATO:0001997 decreased amount abnormal ZDB-GENE-020419-32 192302 3065 hdac1 ZFA:0001501 cartilage element PATO:0000051 morphology abnormal ZDB-GENE-020419-32 192302 3065 hdac1 ZFA:0001516 ceratobranchial cartilage PATO:0000462 absent abnormal ZDB-GENE-020419-32 192302 3065 hdac1 ZFA:0001611 pharyngeal arch 2 PATO:0000646 malformed abnormal ZDB-GENE-020419-32 192302 3065 hdac1 ZFA:0009084 chondrocyte BFO:0000050 part_of ZFA:0001612 pharyngeal arch 1 PATO:0000052 shape abnormal ZDB-GENE-020419-32 192302 3065 hdac1 ZFA:0001612 pharyngeal arch 1 PATO:0002001 has fewer parts of type abnormal ZFA:0009084 chondrocyte ZDB-GENE-020419-32 192302 3065 hdac1 ZFA:0001612 pharyngeal arch 1 PATO:0000646 malformed abnormal ZDB-GENE-020419-32 192302 3065 hdac1 GO:0008219 cell death BFO:0000066 occurs_in ZFA:0001613 pharyngeal arch 3-7 PATO:0002304 increased process quality abnormal ZDB-GENE-020419-32 192302 3065 hdac1 ZFA:0001613 pharyngeal arch 3-7 PATO:0000462 absent abnormal ZDB-GENE-020419-32 192302 3065 hdac1 ZFA:0001617 otolith PATO:0000375 decreased distance abnormal ZFA:0001617 otolith ZDB-GENE-020419-32 192302 3065 hdac1 ZFA:0001617 otolith PATO:0000001 quality abnormal ZDB-GENE-020419-32 192302 3065 hdac1 ZFA:0001617 otolith PATO:0000587 decreased size abnormal ZDB-GENE-020419-32 192302 3065 hdac1 GO:0060038 cardiac muscle cell proliferation BFO:0000066 occurs_in ZFA:0001712 presumptive bulbus arteriosus PATO:0002052 decreased occurrence abnormal ZDB-GENE-020419-32 192302 3065 hdac1 ZFA:0009014 hematopoietic stem cell BFO:0000050 part_of ZFA:0005028 ventral wall of dorsal aorta PATO:0000462 absent abnormal ZDB-GENE-020419-32 192302 3065 hdac1 ZFA:0005274 smooth muscle PATO:0000462 absent abnormal ZDB-GENE-020419-32 192302 3065 hdac1 ZFA:0005496 snout PATO:0000411 circular abnormal ZDB-GENE-020419-32 192302 3065 hdac1 ZFA:0005496 snout PATO:0002364 shortened abnormal ZDB-GENE-020419-32 192302 3065 hdac1 ZFA:0005741 pancreatic acinar gland PATO:0000462 absent abnormal ZDB-GENE-020419-32 192302 3065 hdac1 ZFA:0009052 motor neuron PATO:0000628 mislocalised abnormal ZDB-GENE-020419-32 192302 3065 hdac1 ZFA:0009067 CNS neuron (sensu Vertebrata) PATO:0001997 decreased amount abnormal ZDB-GENE-020419-32 192302 3065 hdac1 ZFA:0009090 pigment cell PATO:0000001 quality abnormal ZDB-GENE-020419-32 192302 3065 hdac1 ZFA:0009090 pigment cell PATO:0000330 irregular spatial pattern abnormal ZDB-GENE-020419-32 192302 3065 hdac1 ZFA:0009091 melanocyte PATO:0000140 position abnormal ZDB-GENE-020419-32 192302 3065 hdac1 ZFA:0009091 melanocyte PATO:0000628 mislocalised abnormal ZDB-GENE-020419-32 192302 3065 hdac1 ZFA:0009091 melanocyte PATO:0001488 cellular motility abnormal ZDB-GENE-020419-32 192302 3065 hdac1 ZFA:0009091 melanocyte PATO:0001997 decreased amount abnormal ZDB-GENE-020419-32 192302 3065 hdac1 ZFA:0009096 endocrine cell PATO:0000628 mislocalised abnormal ZDB-GENE-020419-32 192302 3065 hdac1 ZFA:0009139 endodermal cell PATO:0001997 decreased amount abnormal ZDB-GENE-020419-33 100005887 57617 vps18 GO:0043473 pigmentation PATO:0001507 disrupted abnormal ZDB-GENE-020419-33 100005887 57617 vps18 GO:0048570 notochord morphogenesis PATO:0002302 decreased process quality abnormal ZDB-GENE-020419-33 100005887 57617 vps18 GO:0060036 notochord cell vacuolation PATO:0002302 decreased process quality abnormal ZDB-GENE-020419-33 100005887 57617 vps18 ZFA:0000112 gut PATO:0000645 hypoplastic abnormal ZDB-GENE-020419-33 100005887 57617 vps18 ZFA:0000123 liver PATO:0000001 quality abnormal ZDB-GENE-020419-33 100005887 57617 vps18 ZFA:0000123 liver PATO:0000586 increased size abnormal ZDB-GENE-020419-33 100005887 57617 vps18 GO:0005773 vacuole BFO:0000050 part_of ZFA:0000135 notochord PATO:0000937 disorganized abnormal ZDB-GENE-020419-33 100005887 57617 vps18 GO:0005773 vacuole BFO:0000050 part_of ZFA:0000135 notochord PATO:0001444 broken abnormal ZDB-GENE-020419-33 100005887 57617 vps18 GO:0048770 pigment granule BFO:0000050 part_of ZFA:0000152 retina PATO:0001609 sparse abnormal ZDB-GENE-020419-33 100005887 57617 vps18 GO:0048770 pigment granule BFO:0000050 part_of ZFA:0000368 integument PATO:0001609 sparse abnormal ZDB-GENE-020419-33 100005887 57617 vps18 ZFA:0001094 whole organism PATO:0002249 unpigmented abnormal ZDB-GENE-020419-33 100005887 57617 vps18 ZFA:0001115 trunk PATO:0002001 has fewer parts of type abnormal ZFA:0009091 melanocyte ZDB-GENE-020419-33 100005887 57617 vps18 ZFA:0001115 trunk PATO:0002001 has fewer parts of type abnormal ZFA:0009199 iridophore ZDB-GENE-020419-33 100005887 57617 vps18 ZFA:0001115 trunk PATO:0002251 decreased pigmentation abnormal ZDB-GENE-020419-33 100005887 57617 vps18 GO:0005902 microvillus BFO:0000050 part_of ZFA:0005163 bile canaliculus PATO:0000574 decreased length abnormal ZDB-GENE-020419-33 100005887 57617 vps18 GO:0005902 microvillus BFO:0000050 part_of ZFA:0005163 bile canaliculus PATO:0001609 sparse abnormal ZDB-GENE-020419-33 100005887 57617 vps18 ZFA:0005163 bile canaliculus PATO:0000648 obstructed abnormal ZDB-GENE-020419-33 100005887 57617 vps18 ZFA:0005163 bile canaliculus PATO:0001602 distended abnormal ZDB-GENE-020419-33 100005887 57617 vps18 ZFA:0009090 pigment cell PATO:0000001 quality abnormal ZDB-GENE-020419-33 100005887 57617 vps18 ZFA:0009091 melanocyte PATO:0000001 quality abnormal ZDB-GENE-020419-33 100005887 57617 vps18 ZFA:0009091 melanocyte PATO:0001997 decreased amount abnormal ZDB-GENE-020419-33 100005887 57617 vps18 GO:0005764 lysosome BFO:0000050 part_of ZFA:0009111 hepatocyte PATO:0001997 decreased amount abnormal ZDB-GENE-020419-33 100005887 57617 vps18 GO:0005773 vacuole BFO:0000050 part_of ZFA:0009111 hepatocyte PATO:0000470 increased amount abnormal ZDB-GENE-020419-33 100005887 57617 vps18 ZFA:0009111 hepatocyte PATO:0000374 increased distance abnormal ZFA:0009111 hepatocyte ZDB-GENE-020419-33 100005887 57617 vps18 ZFA:0009111 hepatocyte PATO:0000586 increased size abnormal ZDB-GENE-020419-33 100005887 57617 vps18 ZFA:0009199 iridophore PATO:0000001 quality abnormal ZDB-GENE-020419-33 100005887 57617 vps18 ZFA:0009199 iridophore PATO:0001997 decreased amount abnormal ZDB-GENE-020419-34 192314 51514 dtl GO:0090398 cellular senescence PATO:0002017 increased magnitude abnormal ZDB-GENE-020419-34 192314 51514 dtl ZFA:0000008 brain PATO:0000647 necrotic abnormal ZDB-GENE-020419-34 192314 51514 dtl ZFA:0000012 central nervous system PATO:0000647 necrotic abnormal ZDB-GENE-020419-34 192314 51514 dtl GO:0000922 spindle pole BFO:0000050 part_of ZFA:0000098 proliferative region PATO:0000470 increased amount abnormal ZDB-GENE-020419-34 192314 51514 dtl ZFA:0000106 extension PATO:0000592 decreased thickness abnormal ZDB-GENE-020419-34 192314 51514 dtl ZFA:0001094 whole organism PATO:0000169 viability abnormal ZDB-GENE-020419-34 192314 51514 dtl ZFA:0001094 whole organism PATO:0000617 bent abnormal ZDB-GENE-020419-34 192314 51514 dtl ZFA:0001094 whole organism PATO:0000647 necrotic abnormal ZDB-GENE-020419-34 192314 51514 dtl ZFA:0001094 whole organism PATO:0000718 lethal (sensu genetics) abnormal ZDB-GENE-020419-34 192314 51514 dtl ZFA:0001094 whole organism PATO:0001468 curved dorsal abnormal ZDB-GENE-020419-34 192314 51514 dtl ZFA:0001114 head PATO:0000407 flat abnormal ZDB-GENE-020419-35 192312 84549 mak16 ZFA:0000012 central nervous system PATO:0000647 necrotic abnormal ZDB-GENE-020419-35 192312 84549 mak16 GO:0030424 axon BFO:0000050 part_of ZFA:0000029 hindbrain PATO:0000628 mislocalised abnormal ZDB-GENE-020419-35 192312 84549 mak16 ZFA:0009147 glial cell (sensu Vertebrata) BFO:0000050 part_of ZFA:0000029 hindbrain PATO:0000628 mislocalised abnormal ZDB-GENE-020419-35 192312 84549 mak16 ZFA:0000054 pericardium PATO:0001450 edematous abnormal ZDB-GENE-020419-35 192312 84549 mak16 GO:0071679 commissural neuron axon guidance BFO:0000066 occurs_in ZFA:0000059 postoptic commissure PATO:0001507 disrupted abnormal ZDB-GENE-020419-35 192312 84549 mak16 ZFA:0009075 astrocyte BFO:0000050 part_of ZFA:0000059 postoptic commissure PATO:0000628 mislocalised abnormal ZDB-GENE-020419-35 192312 84549 mak16 ZFA:0000059 postoptic commissure PATO:0000051 morphology abnormal ZDB-GENE-020419-35 192312 84549 mak16 ZFA:0000059 postoptic commissure PATO:0001959 defasciculated abnormal ZDB-GENE-020419-35 192312 84549 mak16 ZFA:0000075 spinal cord PATO:0002000 lacks all parts of type abnormal ZFA:0009292 radial glial cell BFO:0000050 part_of ZFA:0001083 ventricular zone ZDB-GENE-020419-35 192312 84549 mak16 ZFA:0000084 yolk PATO:0000001 quality abnormal ZDB-GENE-020419-35 192312 84549 mak16 ZFA:0000084 yolk PATO:0000411 circular abnormal ZDB-GENE-020419-35 192312 84549 mak16 ZFA:0000084 yolk PATO:0000950 grey abnormal ZDB-GENE-020419-35 192312 84549 mak16 ZFA:0000106 extension PATO:0000592 decreased thickness abnormal ZDB-GENE-020419-35 192312 84549 mak16 ZFA:0000106 extension PATO:0001483 aplastic abnormal ZDB-GENE-020419-35 192312 84549 mak16 ZFA:0000107 eye PATO:0000587 decreased size abnormal ZDB-GENE-020419-35 192312 84549 mak16 GO:0071679 commissural neuron axon guidance BFO:0000066 occurs_in ZFA:0000109 forebrain PATO:0001507 disrupted abnormal ZDB-GENE-020419-35 192312 84549 mak16 ZFA:0000112 gut PATO:0000645 hypoplastic abnormal ZDB-GENE-020419-35 192312 84549 mak16 ZFA:0000123 liver PATO:0000645 hypoplastic abnormal ZDB-GENE-020419-35 192312 84549 mak16 ZFA:0000396 nervous system PATO:0000001 quality abnormal ZDB-GENE-020419-35 192312 84549 mak16 ZFA:0000435 cranial nerve II PATO:0000462 absent abnormal ZDB-GENE-020419-35 192312 84549 mak16 ZFA:0000435 cranial nerve II PATO:0000587 decreased size abnormal ZDB-GENE-020419-35 192312 84549 mak16 ZFA:0000435 cranial nerve II PATO:0001959 defasciculated abnormal ZDB-GENE-020419-35 192312 84549 mak16 ZFA:0001094 whole organism PATO:0001469 curved ventral abnormal ZDB-GENE-020419-35 192312 84549 mak16 GO:0071679 commissural neuron axon guidance BFO:0000066 occurs_in ZFA:0001108 anterior commissure PATO:0001507 disrupted abnormal ZDB-GENE-020419-35 192312 84549 mak16 ZFA:0009075 astrocyte BFO:0000050 part_of ZFA:0001108 anterior commissure PATO:0000628 mislocalised abnormal ZDB-GENE-020419-35 192312 84549 mak16 ZFA:0001108 anterior commissure PATO:0000051 morphology abnormal ZDB-GENE-020419-35 192312 84549 mak16 ZFA:0001108 anterior commissure PATO:0001959 defasciculated abnormal ZDB-GENE-020419-35 192312 84549 mak16 ZFA:0001114 head PATO:0000587 decreased size abnormal ZDB-GENE-020419-35 192312 84549 mak16 ZFA:0007009 nerve BFO:0000050 part_of ZFA:0001115 trunk PATO:0000936 truncated abnormal ZDB-GENE-020419-35 192312 84549 mak16 ZFA:0001115 trunk PATO:0002001 has fewer parts of type abnormal ZFA:0009147 glial cell (sensu Vertebrata) BFO:0000050 part_of ZFA:0007009 nerve ZDB-GENE-020419-35 192312 84549 mak16 ZFA:0001115 trunk PATO:0002001 has fewer parts of type abnormal GO:0030424 axon BFO:0000050 part_of ZFA:0009052 motor neuron ZDB-GENE-020419-35 192312 84549 mak16 ZFA:0001115 trunk PATO:0000592 decreased thickness abnormal ZDB-GENE-020419-35 192312 84549 mak16 GO:0042995 cell projection BFO:0000050 part_of ZFA:0009292 radial glial cell PATO:0000937 disorganized abnormal ZDB-GENE-020419-36 192313 86 actl6a ZFA:0000008 brain PATO:0000647 necrotic abnormal ZDB-GENE-020419-36 192313 86 actl6a ZFA:0000012 central nervous system PATO:0000647 necrotic abnormal ZDB-GENE-020419-36 192313 86 actl6a ZFA:0000054 pericardium PATO:0001450 edematous abnormal ZDB-GENE-020419-36 192313 86 actl6a ZFA:0000084 yolk PATO:0001450 edematous abnormal ZDB-GENE-020419-36 192313 86 actl6a ZFA:0000107 eye PATO:0000587 decreased size abnormal ZDB-GENE-020419-36 192313 86 actl6a ZFA:0000112 gut PATO:0000645 hypoplastic abnormal ZDB-GENE-020419-36 192313 86 actl6a ZFA:0000114 heart PATO:0000001 quality abnormal ZDB-GENE-020419-36 192313 86 actl6a ZFA:0000123 liver PATO:0000645 hypoplastic abnormal ZDB-GENE-020419-36 192313 86 actl6a ZFA:0001094 whole organism PATO:0000647 necrotic abnormal ZDB-GENE-020419-36 192313 86 actl6a ZFA:0001114 head PATO:0000587 decreased size abnormal ZDB-GENE-020419-36 192313 86 actl6a ZFA:0001114 head PATO:0001450 edematous abnormal ZDB-GENE-020419-37 192315 80146 uxs1 GO:0001503 ossification PATO:0000502 delayed abnormal ZDB-GENE-020419-37 192315 80146 uxs1 GO:0003428 chondrocyte intercalation involved in growth plate cartilage morphogenesis PATO:0001507 disrupted abnormal ZDB-GENE-020419-37 192315 80146 uxs1 GO:0015012 heparan sulfate proteoglycan biosynthetic process PATO:0002052 decreased occurrence abnormal ZDB-GENE-020419-37 192315 80146 uxs1 GO:0030203 glycosaminoglycan metabolic process PATO:0001507 disrupted abnormal ZDB-GENE-020419-37 192315 80146 uxs1 GO:0030206 chondroitin sulfate biosynthetic process PATO:0001236 process quality abnormal ZDB-GENE-020419-37 192315 80146 uxs1 GO:0034330 cell junction organization PATO:0001507 disrupted abnormal ZDB-GENE-020419-37 192315 80146 uxs1 GO:0050650 chondroitin sulfate proteoglycan biosynthetic process PATO:0002052 decreased occurrence abnormal ZDB-GENE-020419-37 192315 80146 uxs1 GO:0051923 sulfation PATO:0002052 decreased occurrence abnormal ZDB-GENE-020419-37 192315 80146 uxs1 GO:0060350 endochondral bone morphogenesis PATO:0000502 delayed abnormal ZDB-GENE-020419-37 192315 80146 uxs1 ZFA:0000095 pharyngeal arch 3-7 skeleton PATO:0000001 quality abnormal ZDB-GENE-020419-37 192315 80146 uxs1 ZFA:0000250 opercle PATO:0000587 decreased size abnormal ZDB-GENE-020419-37 192315 80146 uxs1 ZFA:0000292 surface structure PATO:0000001 quality abnormal ZDB-GENE-020419-37 192315 80146 uxs1 ZFA:0000561 parasphenoid PATO:0000587 decreased size abnormal ZDB-GENE-020419-37 192315 80146 uxs1 ZFA:0000578 ceratohyal bone PATO:0000462 absent abnormal ZDB-GENE-020419-37 192315 80146 uxs1 ZFA:0000672 hyomandibula PATO:0000462 absent abnormal ZDB-GENE-020419-37 192315 80146 uxs1 BSPO:0000013 anterior-posterior axis BFO:0000050 part_of ZFA:0001094 whole organism PATO:0000969 dwarf-like abnormal ZDB-GENE-020419-37 192315 80146 uxs1 ZFA:0001094 whole organism PATO:0000574 decreased length abnormal ZDB-GENE-020419-37 192315 80146 uxs1 ZFA:0001114 head PATO:0000411 circular abnormal ZDB-GENE-020419-37 192315 80146 uxs1 ZFA:0001114 head PATO:0000587 decreased size abnormal ZDB-GENE-020419-37 192315 80146 uxs1 ZFA:0001161 pectoral fin PATO:0000587 decreased size abnormal ZDB-GENE-020419-37 192315 80146 uxs1 BSPO:0000055 anterior side BFO:0000050 part_of ZFA:0001205 Meckel's cartilage PATO:0000375 decreased distance abnormal BSPO:0000056 posterior side BFO:0000050 part_of ZFA:0001400 ceratohyal cartilage ZDB-GENE-020419-37 192315 80146 uxs1 ZFA:0001205 Meckel's cartilage PATO:0000574 decreased length abnormal ZDB-GENE-020419-37 192315 80146 uxs1 ZFA:0001205 Meckel's cartilage PATO:0001483 aplastic abnormal ZDB-GENE-020419-37 192315 80146 uxs1 ZFA:0001227 mandibular arch skeleton PATO:0001485 condensed abnormal ZDB-GENE-020419-37 192315 80146 uxs1 ZFA:0001239 ceratobranchial 5 bone PATO:0000587 decreased size abnormal ZDB-GENE-020419-37 192315 80146 uxs1 ZFA:0001273 ventral mandibular arch PATO:0000587 decreased size abnormal ZDB-GENE-020419-37 192315 80146 uxs1 ZFA:0001399 palatoquadrate cartilage PATO:0001483 aplastic abnormal ZDB-GENE-020419-37 192315 80146 uxs1 ZFA:0001400 ceratohyal cartilage PATO:0000574 decreased length abnormal ZDB-GENE-020419-37 192315 80146 uxs1 ZFA:0001400 ceratohyal cartilage PATO:0001483 aplastic abnormal ZDB-GENE-020419-37 192315 80146 uxs1 CHEBI:53231 poly(ethylene imine) BFO:0000050 part_of ZFA:0001458 cranial cartilage PATO:0000060 spatial pattern abnormal ZDB-GENE-020419-37 192315 80146 uxs1 GO:0005581 collagen trimer BFO:0000050 part_of ZFA:0001458 cranial cartilage PATO:0000051 morphology abnormal ZDB-GENE-020419-37 192315 80146 uxs1 GO:0005583 fibrillar collagen trimer BFO:0000050 part_of ZFA:0001458 cranial cartilage PATO:0000462 absent abnormal ZDB-GENE-020419-37 192315 80146 uxs1 GO:0005584 collagen type I trimer BFO:0000050 part_of ZFA:0001458 cranial cartilage PATO:0001997 decreased amount abnormal ZDB-GENE-020419-37 192315 80146 uxs1 GO:0005585 collagen type II trimer BFO:0000050 part_of ZFA:0001458 cranial cartilage PATO:0000462 absent abnormal ZDB-GENE-020419-37 192315 80146 uxs1 GO:0005589 collagen type VI trimer BFO:0000050 part_of ZFA:0001458 cranial cartilage PATO:0000462 absent abnormal ZDB-GENE-020419-37 192315 80146 uxs1 GO:0031012 extracellular matrix BFO:0000050 part_of ZFA:0001458 cranial cartilage PATO:0000025 composition abnormal ZDB-GENE-020419-37 192315 80146 uxs1 GO:0031012 extracellular matrix BFO:0000050 part_of ZFA:0001458 cranial cartilage PATO:0000587 decreased size abnormal ZDB-GENE-020419-37 192315 80146 uxs1 ZFA:0001458 cranial cartilage PATO:0000051 morphology abnormal ZDB-GENE-020419-37 192315 80146 uxs1 ZFA:0001458 cranial cartilage PATO:0001617 deformed abnormal ZDB-GENE-020419-37 192315 80146 uxs1 ZFA:0009084 chondrocyte BFO:0000050 part_of ZFA:0001460 pharyngeal arch cartilage PATO:0000411 circular abnormal ZDB-GENE-020419-37 192315 80146 uxs1 ZFA:0009084 chondrocyte BFO:0000050 part_of ZFA:0001460 pharyngeal arch cartilage PATO:0000619 crowded abnormal ZDB-GENE-020419-37 192315 80146 uxs1 ZFA:0009084 chondrocyte BFO:0000050 part_of ZFA:0001460 pharyngeal arch cartilage PATO:0000937 disorganized abnormal ZDB-GENE-020419-37 192315 80146 uxs1 ZFA:0001460 pharyngeal arch cartilage PATO:0000574 decreased length abnormal ZDB-GENE-020419-37 192315 80146 uxs1 ZFA:0001460 pharyngeal arch cartilage PATO:0000591 increased thickness abnormal ZDB-GENE-020419-37 192315 80146 uxs1 ZFA:0001460 pharyngeal arch cartilage PATO:0000614 oriented abnormal ZDB-GENE-020419-37 192315 80146 uxs1 ZFA:0001460 pharyngeal arch cartilage PATO:0001483 aplastic abnormal ZDB-GENE-020419-37 192315 80146 uxs1 ZFA:0001461 chondrocranium cartilage PATO:0001483 aplastic abnormal ZDB-GENE-020419-37 192315 80146 uxs1 ZFA:0001501 cartilage element PATO:0000051 morphology abnormal ZDB-GENE-020419-37 192315 80146 uxs1 ZFA:0001516 ceratobranchial cartilage PATO:0001483 aplastic abnormal ZDB-GENE-020419-37 192315 80146 uxs1 ZFA:0001630 perichondral bone PATO:0001483 aplastic abnormal ZDB-GENE-020419-37 192315 80146 uxs1 ZFA:0001634 perichondrium PATO:0001483 aplastic abnormal ZDB-GENE-020419-37 192315 80146 uxs1 GO:0005583 fibrillar collagen trimer BFO:0000050 part_of ZFA:0009084 chondrocyte PATO:0001997 decreased amount abnormal ZDB-GENE-020419-37 192315 80146 uxs1 GO:0005886 plasma membrane BFO:0000050 part_of ZFA:0009084 chondrocyte PATO:0000701 smooth abnormal ZDB-GENE-020419-37 192315 80146 uxs1 GO:0031012 extracellular matrix BFO:0000050 part_of ZFA:0009084 chondrocyte PATO:0001485 condensed abnormal ZDB-GENE-020419-37 192315 80146 uxs1 GO:0031012 extracellular matrix BFO:0000050 part_of ZFA:0009084 chondrocyte PATO:0002058 decreased area abnormal ZDB-GENE-020419-37 192315 80146 uxs1 GO:0031253 cell projection membrane BFO:0000050 part_of ZFA:0009084 chondrocyte PATO:0000462 absent abnormal ZDB-GENE-020419-37 192315 80146 uxs1 ZFA:0009084 chondrocyte PATO:0000642 fused with abnormal ZFA:0009084 chondrocyte ZDB-GENE-020419-37 192315 80146 uxs1 ZFA:0009084 chondrocyte PATO:0001667 attached to abnormal ZFA:0009084 chondrocyte ZDB-GENE-020419-37 192315 80146 uxs1 ZFA:0009084 chondrocyte PATO:0000051 morphology abnormal ZDB-GENE-020419-39 192317 6491 stil GO:0000087 mitotic M phase PATO:0001333 temporally extended abnormal ZDB-GENE-020419-39 192317 6491 stil GO:0007051 spindle organization PATO:0001507 disrupted abnormal ZDB-GENE-020419-39 192317 6491 stil GO:0007079 mitotic chromosome movement towards spindle pole PATO:0001507 disrupted abnormal ZDB-GENE-020419-39 192317 6491 stil GO:0007080 mitotic metaphase chromosome alignment PATO:0001507 disrupted abnormal ZDB-GENE-020419-39 192317 6491 stil GO:0007601 visual perception PATO:0001236 process quality abnormal ZDB-GENE-020419-39 192317 6491 stil GO:0007632 visual behavior PATO:0001236 process quality abnormal ZDB-GENE-020419-39 192317 6491 stil GO:0051225 spindle assembly PATO:0001507 disrupted abnormal ZDB-GENE-020419-39 192317 6491 stil GO:0008219 cell death BFO:0000066 occurs_in ZFA:0000008 brain PATO:0002051 increased occurrence abnormal ZDB-GENE-020419-39 192317 6491 stil ZFA:0000008 brain PATO:0000587 decreased size abnormal ZDB-GENE-020419-39 192317 6491 stil ZFA:0000008 brain PATO:0000647 necrotic abnormal ZDB-GENE-020419-39 192317 6491 stil ZFA:0000008 brain PATO:0002037 degeneration abnormal ZDB-GENE-020419-39 192317 6491 stil ZFA:0000012 central nervous system PATO:0000647 necrotic abnormal ZDB-GENE-020419-39 192317 6491 stil ZFA:0000035 lens PATO:0001646 protruding out of abnormal ZFA:0000107 eye ZDB-GENE-020419-39 192317 6491 stil ZFA:0000046 retinal neural layer PATO:0000937 disorganized abnormal ZDB-GENE-020419-39 192317 6491 stil ZFA:0000054 pericardium PATO:0001450 edematous abnormal ZDB-GENE-020419-39 192317 6491 stil GO:0000278 mitotic cell cycle BFO:0000066 occurs_in ZFA:0000075 spinal cord PATO:0002051 increased occurrence abnormal ZDB-GENE-020419-39 192317 6491 stil GO:0008219 cell death BFO:0000066 occurs_in ZFA:0000107 eye PATO:0002051 increased occurrence abnormal ZDB-GENE-020419-39 192317 6491 stil ZFA:0000107 eye PATO:0000587 decreased size abnormal ZDB-GENE-020419-39 192317 6491 stil ZFA:0000107 eye PATO:0002037 degeneration abnormal ZDB-GENE-020419-39 192317 6491 stil ZFA:0000112 gut PATO:0000645 hypoplastic abnormal ZDB-GENE-020419-39 192317 6491 stil ZFA:0000114 heart PATO:0000001 quality abnormal ZDB-GENE-020419-39 192317 6491 stil ZFA:0000114 heart PATO:0001450 edematous abnormal ZDB-GENE-020419-39 192317 6491 stil ZFA:0009000 cell BFO:0000050 part_of ZFA:0000119 retinal inner nuclear layer PATO:0001851 swollen abnormal ZDB-GENE-020419-39 192317 6491 stil ZFA:0000119 retinal inner nuclear layer PATO:0002078 hollow abnormal ZDB-GENE-020419-39 192317 6491 stil ZFA:0000123 liver PATO:0000645 hypoplastic abnormal ZDB-GENE-020419-39 192317 6491 stil GO:0000087 mitotic M phase BFO:0000066 occurs_in ZFA:0000152 retina PATO:0000498 increased duration abnormal ZDB-GENE-020419-39 192317 6491 stil GO:0000236 mitotic prometaphase BFO:0000066 occurs_in ZFA:0000152 retina PATO:0000297 arrested abnormal ZDB-GENE-020419-39 192317 6491 stil GO:0000236 mitotic prometaphase BFO:0000066 occurs_in ZFA:0000152 retina PATO:0000498 increased duration abnormal ZDB-GENE-020419-39 192317 6491 stil GO:0000278 mitotic cell cycle BFO:0000066 occurs_in ZFA:0000152 retina PATO:0000297 arrested abnormal ZDB-GENE-020419-39 192317 6491 stil GO:0000278 mitotic cell cycle BFO:0000066 occurs_in ZFA:0000152 retina PATO:0000498 increased duration abnormal ZDB-GENE-020419-39 192317 6491 stil GO:0000278 mitotic cell cycle BFO:0000066 occurs_in ZFA:0000152 retina PATO:0002051 increased occurrence abnormal ZDB-GENE-020419-39 192317 6491 stil GO:0000279 M phase BFO:0000066 occurs_in ZFA:0000152 retina PATO:0000498 increased duration abnormal ZDB-GENE-020419-39 192317 6491 stil GO:0006915 apoptotic process BFO:0000066 occurs_in ZFA:0000152 retina PATO:0002051 increased occurrence abnormal ZDB-GENE-020419-39 192317 6491 stil GO:0051301 cell division BFO:0000066 occurs_in ZFA:0000152 retina PATO:0000498 increased duration abnormal ZDB-GENE-020419-39 192317 6491 stil ZFA:0000152 retina PATO:0002001 has fewer parts of type abnormal ZFA:0009000 cell BFO:0000050 part_of ZFA:0000152 retina ZDB-GENE-020419-39 192317 6491 stil ZFA:0000152 retina PATO:0001999 lacks parts or has fewer parts of type abnormal GO:0005813 centrosome BFO:0000050 part_of ZFA:0009000 cell ZDB-GENE-020419-39 192317 6491 stil ZFA:0000152 retina PATO:0000587 decreased size abnormal ZDB-GENE-020419-39 192317 6491 stil ZFA:0000152 retina PATO:0000937 disorganized abnormal ZDB-GENE-020419-39 192317 6491 stil ZFA:0000396 nervous system PATO:0000001 quality abnormal ZDB-GENE-020419-39 192317 6491 stil ZFA:0001058 caudal fin PATO:0000406 curved abnormal ZDB-GENE-020419-39 192317 6491 stil ZFA:0001094 whole organism PATO:0000587 decreased size abnormal ZDB-GENE-020419-39 192317 6491 stil ZFA:0001094 whole organism PATO:0000617 bent abnormal ZDB-GENE-020419-39 192317 6491 stil ZFA:0001094 whole organism PATO:0000718 lethal (sensu genetics) abnormal ZDB-GENE-020419-39 192317 6491 stil ZFA:0001094 whole organism PATO:0001422 dead abnormal ZDB-GENE-020419-39 192317 6491 stil ZFA:0001094 whole organism PATO:0001468 curved dorsal abnormal ZDB-GENE-020419-39 192317 6491 stil ZFA:0009248 neuron BFO:0000050 part_of ZFA:0001114 head PATO:0000638 apoptotic abnormal ZDB-GENE-020419-39 192317 6491 stil ZFA:0001114 head PATO:0000587 decreased size abnormal ZDB-GENE-020419-39 192317 6491 stil ZFA:0001115 trunk PATO:0001468 curved dorsal abnormal ZDB-GENE-020419-39 192317 6491 stil ZFA:0001115 trunk PATO:0001469 curved ventral abnormal ZDB-GENE-020419-39 192317 6491 stil ZFA:0001115 trunk PATO:0001878 sigmoid abnormal ZDB-GENE-020419-39 192317 6491 stil ZFA:0001117 post-vent region PATO:0000406 curved abnormal ZDB-GENE-020419-39 192317 6491 stil GO:0043005 neuron projection BFO:0000050 part_of ZFA:0001356 terminal nerve PATO:0000937 disorganized abnormal ZDB-GENE-020419-39 192317 6491 stil GO:0043005 neuron projection BFO:0000050 part_of ZFA:0001356 terminal nerve PATO:0002286 decreased branchiness abnormal ZDB-GENE-020419-39 192317 6491 stil ZFA:0007009 nerve PATO:0002037 degeneration abnormal ZDB-GENE-020419-39 192317 6491 stil GO:0000930 gamma-tubulin complex BFO:0000050 part_of ZFA:0009000 cell PATO:0000628 mislocalised abnormal ZDB-GENE-020419-39 192317 6491 stil GO:0005819 spindle BFO:0000050 part_of ZFA:0009000 cell PATO:0000937 disorganized abnormal ZDB-GENE-020419-39 192317 6491 stil GO:0031616 spindle pole centrosome BFO:0000050 part_of ZFA:0009000 cell PATO:0000462 absent abnormal ZDB-GENE-020419-4 192323 4172 mcm3 GO:0048798 swim bladder inflation PATO:0001507 disrupted abnormal ZDB-GENE-020419-4 192323 4172 mcm3 ZFA:0000107 eye PATO:0000587 decreased size abnormal ZDB-GENE-020419-4 192323 4172 mcm3 ZFA:0000112 gut PATO:0000645 hypoplastic abnormal ZDB-GENE-020419-4 192323 4172 mcm3 ZFA:0000123 liver PATO:0000645 hypoplastic abnormal ZDB-GENE-020419-4 192323 4172 mcm3 ZFA:0000152 retina PATO:0000001 quality abnormal ZDB-GENE-020419-4 192323 4172 mcm3 ZFA:0000282 sensory system PATO:0000001 quality abnormal ZDB-GENE-020419-4 192323 4172 mcm3 ZFA:0000445 optic tectum PATO:0000647 necrotic abnormal ZDB-GENE-020419-4 192323 4172 mcm3 ZFA:0001114 head PATO:0000587 decreased size abnormal ZDB-GENE-020419-40 791894 9212 aurkb GO:0000910 cytokinesis PATO:0001507 disrupted abnormal ZDB-GENE-020419-40 791894 9212 aurkb GO:0007059 chromosome segregation PATO:0001507 disrupted abnormal ZDB-GENE-020419-40 791894 9212 aurkb ZFA:0000008 brain PATO:0000647 necrotic abnormal ZDB-GENE-020419-40 791894 9212 aurkb ZFA:0000012 central nervous system PATO:0000647 necrotic abnormal ZDB-GENE-020419-40 791894 9212 aurkb ZFA:0000076 swim bladder PATO:0001478 collapsed abnormal ZDB-GENE-020419-40 791894 9212 aurkb GO:0060293 germ plasm BFO:0000050 part_of ZFA:0000093 blastomere PATO:0000628 mislocalised abnormal ZDB-GENE-020419-40 791894 9212 aurkb ZFA:0000396 nervous system PATO:0000001 quality abnormal ZDB-GENE-020419-40 791894 9212 aurkb ZFA:0000547 mouth PATO:0001598 protruding abnormal ZDB-GENE-020419-40 791894 9212 aurkb ZFA:0001094 whole organism PATO:0000169 viability abnormal ZDB-GENE-020419-40 791894 9212 aurkb ZFA:0001094 whole organism PATO:0000647 necrotic abnormal ZDB-GENE-020419-40 791894 9212 aurkb ZFA:0001114 head PATO:0000407 flat abnormal ZDB-GENE-020419-40 791894 9212 aurkb GO:0032154 cleavage furrow BFO:0000050 part_of ZFA:0001176 blastoderm PATO:0000462 absent abnormal ZDB-GENE-020419-40 791894 9212 aurkb GO:0032154 cleavage furrow BFO:0000050 part_of ZFA:0001176 blastoderm PATO:0000574 decreased length abnormal ZDB-GENE-020419-40 791894 9212 aurkb GO:0032154 cleavage furrow BFO:0000050 part_of ZFA:0001176 blastoderm PATO:0000646 malformed abnormal ZDB-GENE-020419-40 791894 9212 aurkb ZFA:0001176 blastoderm PATO:0000051 morphology abnormal ZDB-GENE-020419-40 791894 9212 aurkb GO:0005634 nucleus BFO:0000050 part_of ZFA:0009000 cell PATO:0001485 condensed abnormal ZDB-GENE-020419-40 791894 9212 aurkb GO:0030496 midbody BFO:0000050 part_of ZFA:0009000 cell PATO:0001790 decreased mass density abnormal ZDB-GENE-020419-5 192327 7203 cct3 ZFA:0000008 brain PATO:0000051 morphology abnormal ZDB-GENE-020419-5 192327 7203 cct3 ZFA:0000012 central nervous system PATO:0000647 necrotic abnormal ZDB-GENE-020419-5 192327 7203 cct3 ZFA:0000084 yolk PATO:0000001 quality abnormal ZDB-GENE-020419-5 192327 7203 cct3 ZFA:0000084 yolk PATO:0000411 circular abnormal ZDB-GENE-020419-5 192327 7203 cct3 ZFA:0000084 yolk PATO:0000950 grey abnormal ZDB-GENE-020419-5 192327 7203 cct3 ZFA:0000106 extension PATO:0000592 decreased thickness abnormal ZDB-GENE-020419-5 192327 7203 cct3 ZFA:0000106 extension PATO:0001483 aplastic abnormal ZDB-GENE-020419-5 192327 7203 cct3 ZFA:0000107 eye PATO:0000001 quality abnormal ZDB-GENE-020419-5 192327 7203 cct3 ZFA:0000107 eye PATO:0000587 decreased size abnormal ZDB-GENE-020419-5 192327 7203 cct3 ZFA:0000112 gut PATO:0000645 hypoplastic abnormal ZDB-GENE-020419-5 192327 7203 cct3 ZFA:0000114 heart PATO:0001450 edematous abnormal ZDB-GENE-020419-5 192327 7203 cct3 ZFA:0000123 liver PATO:0000645 hypoplastic abnormal ZDB-GENE-020419-5 192327 7203 cct3 GO:0006915 apoptotic process BFO:0000066 occurs_in ZFA:0000152 retina PATO:0002051 increased occurrence abnormal ZDB-GENE-020419-5 192327 7203 cct3 ZFA:0000152 retina PATO:0000639 degenerate abnormal ZDB-GENE-020419-5 192327 7203 cct3 ZFA:0000282 sensory system PATO:0000001 quality abnormal ZDB-GENE-020419-5 192327 7203 cct3 ZFA:0000396 nervous system PATO:0000001 quality abnormal ZDB-GENE-020419-5 192327 7203 cct3 GO:0031175 neuron projection development BFO:0000066 occurs_in ZFA:0000445 optic tectum PATO:0002052 decreased occurrence abnormal ZDB-GENE-020419-5 192327 7203 cct3 ZFA:0000445 optic tectum PATO:0002001 has fewer parts of type abnormal GO:0043005 neuron projection BFO:0000050 part_of ZFA:0000445 optic tectum ZDB-GENE-020419-5 192327 7203 cct3 ZFA:0009115 skeletal muscle cell BFO:0000050 part_of ZFA:0001056 myotome PATO:0002001 has fewer parts of type abnormal GO:0098723 skeletal muscle myofibril BFO:0000050 part_of ZFA:0009115 skeletal muscle cell ZDB-GENE-020419-5 192327 7203 cct3 ZFA:0001114 head PATO:0000587 decreased size abnormal ZDB-GENE-020419-5 192327 7203 cct3 GO:0014866 skeletal myofibril assembly BFO:0000066 occurs_in ZFA:0005277 skeletal muscle PATO:0002052 decreased occurrence abnormal ZDB-GENE-020419-5 192327 7203 cct3 GO:0030018 Z disc BFO:0000050 part_of ZFA:0009115 skeletal muscle cell PATO:0000646 malformed abnormal ZDB-GENE-020419-5 192327 7203 cct3 GO:0045214 sarcomere organization BFO:0000066 occurs_in ZFA:0009115 skeletal muscle cell PATO:0002302 decreased process quality abnormal ZDB-GENE-020419-5 192327 7203 cct3 GO:0098723 skeletal muscle myofibril BFO:0000050 part_of ZFA:0009115 skeletal muscle cell PATO:0001997 decreased amount abnormal ZDB-GENE-020419-6 192326 10576 cct2 GO:0032402 melanosome transport PATO:0001507 disrupted abnormal ZDB-GENE-020419-6 192326 10576 cct2 ZFA:0000001 Kupffer's vesicle PATO:0000587 decreased size abnormal ZDB-GENE-020419-6 192326 10576 cct2 ZFA:0000006 ball PATO:0000586 increased size abnormal ZDB-GENE-020419-6 192326 10576 cct2 ZFA:0000008 brain PATO:0000051 morphology abnormal ZDB-GENE-020419-6 192326 10576 cct2 ZFA:0000054 pericardium PATO:0001450 edematous abnormal ZDB-GENE-020419-6 192326 10576 cct2 GO:0035265 organ growth BFO:0000066 occurs_in ZFA:0000107 eye PATO:0001433 growth quality of occurrent abnormal ZDB-GENE-020419-6 192326 10576 cct2 ZFA:0000107 eye PATO:0000411 circular abnormal ZDB-GENE-020419-6 192326 10576 cct2 ZFA:0000107 eye PATO:0000587 decreased size abnormal ZDB-GENE-020419-6 192326 10576 cct2 ZFA:0000112 gut PATO:0000645 hypoplastic abnormal ZDB-GENE-020419-6 192326 10576 cct2 ZFA:0000114 heart PATO:0000001 quality abnormal ZDB-GENE-020419-6 192326 10576 cct2 ZFA:0000114 heart PATO:0001450 edematous abnormal ZDB-GENE-020419-6 192326 10576 cct2 ZFA:0000123 liver PATO:0000645 hypoplastic abnormal ZDB-GENE-020419-6 192326 10576 cct2 GO:0006915 apoptotic process BFO:0000066 occurs_in ZFA:0000152 retina PATO:0002051 increased occurrence abnormal ZDB-GENE-020419-6 192326 10576 cct2 ZFA:0009115 skeletal muscle cell BFO:0000050 part_of ZFA:0001056 myotome PATO:0002001 has fewer parts of type abnormal GO:0098723 skeletal muscle myofibril BFO:0000050 part_of ZFA:0009115 skeletal muscle cell ZDB-GENE-020419-6 192326 10576 cct2 ZFA:0001094 whole organism PATO:0000617 bent abnormal ZDB-GENE-020419-6 192326 10576 cct2 ZFA:0001114 head PATO:0000587 decreased size abnormal ZDB-GENE-020419-6 192326 10576 cct2 ZFA:0001114 head PATO:0000647 necrotic abnormal ZDB-GENE-020419-6 192326 10576 cct2 ZFA:0001115 trunk PATO:0000647 necrotic abnormal ZDB-GENE-020419-6 192326 10576 cct2 GO:0008283 cell population proliferation BFO:0000066 occurs_in ZFA:0001289 ciliary marginal zone PATO:0002052 decreased occurrence abnormal ZDB-GENE-020419-6 192326 10576 cct2 GO:0008283 cell population proliferation BFO:0000066 occurs_in ZFA:0001326 lens epithelium PATO:0002052 decreased occurrence abnormal ZDB-GENE-020419-6 192326 10576 cct2 GO:0014866 skeletal myofibril assembly BFO:0000066 occurs_in ZFA:0005277 skeletal muscle PATO:0002052 decreased occurrence abnormal ZDB-GENE-020419-6 192326 10576 cct2 GO:0098723 skeletal muscle myofibril BFO:0000050 part_of ZFA:0009115 skeletal muscle cell PATO:0001997 decreased amount abnormal ZDB-GENE-020419-7 192324 10574 cct7 ZFA:0000054 pericardium PATO:0001450 edematous abnormal ZDB-GENE-020419-7 192324 10574 cct7 ZFA:0000107 eye PATO:0000587 decreased size abnormal ZDB-GENE-020419-7 192324 10574 cct7 ZFA:0000112 gut PATO:0000645 hypoplastic abnormal ZDB-GENE-020419-7 192324 10574 cct7 ZFA:0000114 heart PATO:0000001 quality abnormal ZDB-GENE-020419-7 192324 10574 cct7 ZFA:0000123 liver PATO:0000645 hypoplastic abnormal ZDB-GENE-020419-7 192324 10574 cct7 ZFA:0001114 head PATO:0000587 decreased size abnormal ZDB-GENE-020419-9 192321 292 slc25a5 ZFA:0000107 eye PATO:0000587 decreased size abnormal ZDB-GENE-020419-9 192321 292 slc25a5 ZFA:0000112 gut PATO:0000001 quality abnormal ZDB-GENE-020419-9 192321 292 slc25a5 ZFA:0000112 gut PATO:0000645 hypoplastic abnormal ZDB-GENE-020419-9 192321 292 slc25a5 ZFA:0000123 liver PATO:0000001 quality abnormal ZDB-GENE-020419-9 192321 292 slc25a5 ZFA:0000123 liver PATO:0000645 hypoplastic abnormal ZDB-GENE-020419-9 192321 292 slc25a5 ZFA:0001114 head PATO:0000587 decreased size abnormal ZDB-GENE-020423-1 195819 6173 rpl36a GO:0009790 embryo development PATO:0001236 process quality abnormal ZDB-GENE-020423-1 195819 6173 rpl36a ZFA:0000006 ball PATO:0000586 increased size abnormal ZDB-GENE-020423-1 195819 6173 rpl36a ZFA:0000008 brain PATO:0000647 necrotic abnormal ZDB-GENE-020423-1 195819 6173 rpl36a ZFA:0000012 central nervous system PATO:0000647 necrotic abnormal ZDB-GENE-020423-1 195819 6173 rpl36a ZFA:0000029 hindbrain PATO:0000963 opaque abnormal ZDB-GENE-020423-1 195819 6173 rpl36a ZFA:0000035 lens PATO:0000586 increased size abnormal ZDB-GENE-020423-1 195819 6173 rpl36a ZFA:0000042 midbrain hindbrain boundary PATO:0001485 condensed abnormal ZDB-GENE-020423-1 195819 6173 rpl36a ZFA:0000084 yolk PATO:0000411 circular abnormal ZDB-GENE-020423-1 195819 6173 rpl36a GO:0060417 yolk BFO:0000050 part_of ZFA:0000106 extension PATO:0000462 absent abnormal ZDB-GENE-020423-1 195819 6173 rpl36a ZFA:0000106 extension PATO:0000592 decreased thickness abnormal ZDB-GENE-020423-1 195819 6173 rpl36a ZFA:0000106 extension PATO:0001617 deformed abnormal ZDB-GENE-020423-1 195819 6173 rpl36a ZFA:0000107 eye PATO:0000587 decreased size abnormal ZDB-GENE-020423-1 195819 6173 rpl36a ZFA:0000108 fin PATO:0001617 deformed abnormal ZDB-GENE-020423-1 195819 6173 rpl36a ZFA:0000110 fourth ventricle PATO:0000963 opaque abnormal ZDB-GENE-020423-1 195819 6173 rpl36a ZFA:0000110 fourth ventricle PATO:0001602 distended abnormal ZDB-GENE-020423-1 195819 6173 rpl36a ZFA:0000138 otic placode PATO:0000587 decreased size abnormal ZDB-GENE-020423-1 195819 6173 rpl36a GO:0005694 chromosome BFO:0000050 part_of ZFA:0000142 peripheral nervous system PATO:0000070 amount abnormal ZDB-GENE-020423-1 195819 6173 rpl36a ZFA:0007009 nerve BFO:0000050 part_of ZFA:0000142 peripheral nervous system PATO:0002011 neoplastic abnormal ZDB-GENE-020423-1 195819 6173 rpl36a ZFA:0000445 optic tectum PATO:0000586 increased size abnormal ZDB-GENE-020423-1 195819 6173 rpl36a ZFA:0001094 whole organism PATO:0000169 viability abnormal ZDB-GENE-020423-1 195819 6173 rpl36a ZFA:0001094 whole organism PATO:0000587 decreased size abnormal ZDB-GENE-020423-1 195819 6173 rpl36a ZFA:0001114 head PATO:0000587 decreased size abnormal ZDB-GENE-020423-1 195819 6173 rpl36a ZFA:0001115 trunk PATO:0000592 decreased thickness abnormal ZDB-GENE-020423-1 195819 6173 rpl36a ZFA:0001261 ventricular system PATO:0000586 increased size abnormal ZDB-GENE-020423-1 195819 6173 rpl36a ZFA:0009256 nucleate erythrocyte PATO:0001997 decreased amount abnormal ZDB-GENE-020423-2 195824 537 atp6ap1b GO:0001947 heart looping PATO:0001236 process quality abnormal ZDB-GENE-020423-2 195824 537 atp6ap1b GO:0001947 heart looping PATO:0002052 decreased occurrence abnormal ZDB-GENE-020423-2 195824 537 atp6ap1b GO:0003140 determination of left/right asymmetry in lateral mesoderm PATO:0002052 decreased occurrence abnormal ZDB-GENE-020423-2 195824 537 atp6ap1b GO:0003406 retinal pigment epithelium development PATO:0001236 process quality abnormal ZDB-GENE-020423-2 195824 537 atp6ap1b GO:0008057 eye pigment granule organization PATO:0001236 process quality abnormal ZDB-GENE-020423-2 195824 537 atp6ap1b GO:0008283 cell population proliferation PATO:0001236 process quality abnormal ZDB-GENE-020423-2 195824 537 atp6ap1b GO:0032438 melanosome organization PATO:0001236 process quality abnormal ZDB-GENE-020423-2 195824 537 atp6ap1b GO:0035622 intrahepatic bile duct development PATO:0001507 disrupted abnormal ZDB-GENE-020423-2 195824 537 atp6ap1b GO:0045176 apical protein localization PATO:0001507 disrupted abnormal ZDB-GENE-020423-2 195824 537 atp6ap1b GO:0046666 retinal cell programmed cell death PATO:0000912 increased rate abnormal ZDB-GENE-020423-2 195824 537 atp6ap1b GO:0048066 developmental pigmentation PATO:0001236 process quality abnormal ZDB-GENE-020423-2 195824 537 atp6ap1b GO:0048069 eye pigmentation PATO:0001236 process quality abnormal ZDB-GENE-020423-2 195824 537 atp6ap1b GO:0048797 swim bladder formation PATO:0001236 process quality abnormal ZDB-GENE-020423-2 195824 537 atp6ap1b GO:0051402 neuron apoptotic process PATO:0000912 increased rate abnormal ZDB-GENE-020423-2 195824 537 atp6ap1b GO:0060042 retina morphogenesis in camera-type eye PATO:0001236 process quality abnormal ZDB-GENE-020423-2 195824 537 atp6ap1b GO:0005929 cilium BFO:0000050 part_of ZFA:0000001 Kupffer's vesicle PATO:0000574 decreased length abnormal ZDB-GENE-020423-2 195824 537 atp6ap1b GO:0005929 cilium BFO:0000050 part_of ZFA:0000001 Kupffer's vesicle PATO:0001997 decreased amount abnormal ZDB-GENE-020423-2 195824 537 atp6ap1b ZFA:0009000 cell BFO:0000050 part_of ZFA:0000001 Kupffer's vesicle PATO:0001997 decreased amount abnormal ZDB-GENE-020423-2 195824 537 atp6ap1b ZFA:0000001 Kupffer's vesicle PATO:0000587 decreased size abnormal ZDB-GENE-020423-2 195824 537 atp6ap1b GO:0005737 cytoplasm BFO:0000050 part_of ZFA:0000023 forerunner cell group PATO:0001843 decreased acidity abnormal ZDB-GENE-020423-2 195824 537 atp6ap1b GO:0008283 cell population proliferation BFO:0000066 occurs_in ZFA:0000023 forerunner cell group PATO:0002052 decreased occurrence abnormal ZDB-GENE-020423-2 195824 537 atp6ap1b ZFA:0009000 cell BFO:0000050 part_of ZFA:0000023 forerunner cell group PATO:0001997 decreased amount abnormal ZDB-GENE-020423-2 195824 537 atp6ap1b ZFA:0000107 eye PATO:0000587 decreased size abnormal ZDB-GENE-020423-2 195824 537 atp6ap1b ZFA:0000112 gut PATO:0000001 quality abnormal ZDB-GENE-020423-2 195824 537 atp6ap1b ZFA:0000112 gut PATO:0000645 hypoplastic abnormal ZDB-GENE-020423-2 195824 537 atp6ap1b ZFA:0000123 liver PATO:0000001 quality abnormal ZDB-GENE-020423-2 195824 537 atp6ap1b ZFA:0000123 liver PATO:0000645 hypoplastic abnormal ZDB-GENE-020423-2 195824 537 atp6ap1b GO:0042470 melanosome BFO:0000050 part_of ZFA:0000144 retinal pigmented epithelium PATO:0000587 decreased size abnormal ZDB-GENE-020423-2 195824 537 atp6ap1b GO:0042470 melanosome BFO:0000050 part_of ZFA:0000144 retinal pigmented epithelium PATO:0000646 malformed abnormal ZDB-GENE-020423-2 195824 537 atp6ap1b GO:0042470 melanosome BFO:0000050 part_of ZFA:0000144 retinal pigmented epithelium PATO:0001444 broken abnormal ZDB-GENE-020423-2 195824 537 atp6ap1b ZFA:0000144 retinal pigmented epithelium PATO:0000001 quality abnormal ZDB-GENE-020423-2 195824 537 atp6ap1b ZFA:0000144 retinal pigmented epithelium PATO:0000591 increased thickness abnormal ZDB-GENE-020423-2 195824 537 atp6ap1b ZFA:0000144 retinal pigmented epithelium PATO:0000646 malformed abnormal ZDB-GENE-020423-2 195824 537 atp6ap1b ZFA:0000144 retinal pigmented epithelium PATO:0000941 vacuolated abnormal ZDB-GENE-020423-2 195824 537 atp6ap1b ZFA:0000144 retinal pigmented epithelium PATO:0001241 physical object quality abnormal ZDB-GENE-020423-2 195824 537 atp6ap1b ZFA:0000144 retinal pigmented epithelium PATO:0001354 translucent abnormal ZDB-GENE-020423-2 195824 537 atp6ap1b ZFA:0000144 retinal pigmented epithelium PATO:0002274 mottled abnormal ZDB-GENE-020423-2 195824 537 atp6ap1b ZFA:0000152 retina PATO:0000646 malformed abnormal ZDB-GENE-020423-2 195824 537 atp6ap1b GO:0060091 kinocilium BFO:0000050 part_of ZFA:0000243 neuromast PATO:0000574 decreased length abnormal ZDB-GENE-020423-2 195824 537 atp6ap1b ZFA:0000243 neuromast PATO:0000587 decreased size abnormal ZDB-GENE-020423-2 195824 537 atp6ap1b ZFA:0001094 whole organism PATO:0000169 viability abnormal ZDB-GENE-020423-2 195824 537 atp6ap1b ZFA:0001094 whole organism PATO:0002251 decreased pigmentation abnormal ZDB-GENE-020423-2 195824 537 atp6ap1b ZFA:0001114 head PATO:0000587 decreased size abnormal ZDB-GENE-020423-2 195824 537 atp6ap1b ZFA:0001114 head PATO:0002251 decreased pigmentation abnormal ZDB-GENE-020423-2 195824 537 atp6ap1b ZFA:0001464 retinal outer nuclear layer PATO:0000937 disorganized abnormal ZDB-GENE-020423-2 195824 537 atp6ap1b ZFA:0005169 intrahepatic bile duct PATO:0001602 distended abnormal ZDB-GENE-020423-2 195824 537 atp6ap1b ZFA:0005169 intrahepatic bile duct PATO:0001997 decreased amount abnormal ZDB-GENE-020423-2 195824 537 atp6ap1b ZFA:0009091 melanocyte BFO:0000050 part_of ZFA:0005220 larval melanophore stripe PATO:0001354 translucent abnormal ZDB-GENE-020423-2 195824 537 atp6ap1b ZFA:0009000 cell BFO:0000050 part_of ZFA:0009032 ciliated cell PATO:0001997 decreased amount abnormal ZDB-GENE-020423-2 195824 537 atp6ap1b ZFA:0009090 pigment cell PATO:0000001 quality abnormal ZDB-GENE-020423-2 195824 537 atp6ap1b ZFA:0009091 melanocyte PATO:0000586 increased size abnormal ZDB-GENE-020423-2 195824 537 atp6ap1b ZFA:0009091 melanocyte PATO:0000639 degenerate abnormal ZDB-GENE-020423-2 195824 537 atp6ap1b ZFA:0009091 melanocyte PATO:0000646 malformed abnormal ZDB-GENE-020423-2 195824 537 atp6ap1b ZFA:0009091 melanocyte PATO:0001354 translucent abnormal ZDB-GENE-020423-2 195824 537 atp6ap1b ZFA:0009091 melanocyte PATO:0002247 degree of pigmentation abnormal ZDB-GENE-020423-2 195824 537 atp6ap1b ZFA:0009091 melanocyte PATO:0002251 decreased pigmentation abnormal ZDB-GENE-020423-2 195824 537 atp6ap1b GO:0001750 photoreceptor outer segment BFO:0000050 part_of ZFA:0009154 eye photoreceptor cell PATO:0000646 malformed abnormal ZDB-GENE-020423-2 195824 537 atp6ap1b GO:0001750 photoreceptor outer segment BFO:0000050 part_of ZFA:0009154 eye photoreceptor cell PATO:0001154 elongated abnormal ZDB-GENE-020423-2 195824 537 atp6ap1b ZFA:0009154 eye photoreceptor cell PATO:0000646 malformed abnormal ZDB-GENE-020423-2 195824 537 atp6ap1b GO:0021772 olfactory bulb development BFO:0000066 occurs_in ZFA:0009358 ciliated olfactory receptor neuron PATO:0002052 decreased occurrence abnormal ZDB-GENE-020423-3 195822 1937 eef1g GO:0048797 swim bladder formation PATO:0000502 delayed abnormal ZDB-GENE-020423-3 195822 1937 eef1g GO:0048798 swim bladder inflation PATO:0000297 arrested abnormal ZDB-GENE-020423-3 195822 1937 eef1g ZFA:0000076 swim bladder PATO:0000001 quality abnormal ZDB-GENE-020423-3 195822 1937 eef1g ZFA:0001094 whole organism PATO:0000169 viability abnormal ZDB-GENE-020423-3 195822 1937 eef1g ZFA:0001094 whole organism PATO:0000583 decreased weight abnormal ZDB-GENE-020423-3 195822 1937 eef1g ZFA:0001094 whole organism PATO:0000587 decreased size abnormal ZDB-GENE-020423-4 195823 4666 naca GO:0006936 muscle contraction PATO:0002052 decreased occurrence abnormal ZDB-GENE-020423-4 195823 4666 naca GO:0006955 immune response PATO:0000001 quality abnormal ZDB-GENE-020423-4 195823 4666 naca GO:0008015 blood circulation PATO:0000911 decreased rate abnormal ZDB-GENE-020423-4 195823 4666 naca GO:0008015 blood circulation PATO:0001507 disrupted abnormal ZDB-GENE-020423-4 195823 4666 naca GO:0008015 blood circulation PATO:0002302 decreased process quality abnormal ZDB-GENE-020423-4 195823 4666 naca GO:0030098 lymphocyte differentiation PATO:0002302 decreased process quality abnormal ZDB-GENE-020423-4 195823 4666 naca GO:0030218 erythrocyte differentiation PATO:0002302 decreased process quality abnormal ZDB-GENE-020423-4 195823 4666 naca GO:0030851 granulocyte differentiation PATO:0002302 decreased process quality abnormal ZDB-GENE-020423-4 195823 4666 naca GO:0040011 locomotion PATO:0002052 decreased occurrence abnormal ZDB-GENE-020423-4 195823 4666 naca GO:0048797 swim bladder formation PATO:0000297 arrested abnormal ZDB-GENE-020423-4 195823 4666 naca GO:0060216 definitive hemopoiesis PATO:0001507 disrupted abnormal ZDB-GENE-020423-4 195823 4666 naca GO:0071688 striated muscle myosin thick filament assembly PATO:0001507 disrupted abnormal ZDB-GENE-020423-4 195823 4666 naca GO:0071689 muscle thin filament assembly PATO:0001507 disrupted abnormal ZDB-GENE-020423-4 195823 4666 naca ZFA:0000008 brain PATO:0000647 necrotic abnormal ZDB-GENE-020423-4 195823 4666 naca ZFA:0000054 pericardium PATO:0001450 edematous abnormal ZDB-GENE-020423-4 195823 4666 naca ZFA:0000084 yolk PATO:0000411 circular abnormal ZDB-GENE-020423-4 195823 4666 naca ZFA:0000084 yolk PATO:0000950 grey abnormal ZDB-GENE-020423-4 195823 4666 naca ZFA:0000084 yolk PATO:0001851 swollen abnormal ZDB-GENE-020423-4 195823 4666 naca ZFA:0009199 iridophore BFO:0000050 part_of ZFA:0000107 eye PATO:0000937 disorganized abnormal ZDB-GENE-020423-4 195823 4666 naca ZFA:0000114 heart PATO:0000001 quality abnormal ZDB-GENE-020423-4 195823 4666 naca ZFA:0000114 heart PATO:0001450 edematous abnormal ZDB-GENE-020423-4 195823 4666 naca ZFA:0001078 thymus PATO:0002000 lacks all parts of type abnormal ZFA:0009355 lymphoid progenitor cell ZDB-GENE-020423-4 195823 4666 naca ZFA:0001094 whole organism PATO:0000169 viability abnormal ZDB-GENE-020423-4 195823 4666 naca ZFA:0001094 whole organism PATO:0000763 paralysed abnormal ZDB-GENE-020423-4 195823 4666 naca ZFA:0001094 whole organism PATO:0001422 dead abnormal ZDB-GENE-020423-4 195823 4666 naca ZFA:0001094 whole organism PATO:0001604 decreased life span abnormal ZDB-GENE-020423-4 195823 4666 naca ZFA:0001114 head PATO:0000587 decreased size abnormal ZDB-GENE-020423-4 195823 4666 naca ZFA:0001114 head PATO:0000647 necrotic abnormal ZDB-GENE-020423-4 195823 4666 naca ZFA:0001115 trunk PATO:0000617 bent abnormal ZDB-GENE-020423-4 195823 4666 naca ZFA:0001115 trunk PATO:0000647 necrotic abnormal ZDB-GENE-020423-4 195823 4666 naca ZFA:0001115 trunk PATO:0001469 curved ventral abnormal ZDB-GENE-020423-4 195823 4666 naca ZFA:0001227 mandibular arch skeleton PATO:0001483 aplastic abnormal ZDB-GENE-020423-4 195823 4666 naca ZFA:0001273 ventral mandibular arch PATO:0001501 immature abnormal ZDB-GENE-020423-4 195823 4666 naca ZFA:0009226 stromal cell BFO:0000050 part_of ZFA:0001286 caudal vein plexus PATO:0000638 apoptotic abnormal ZDB-GENE-020423-4 195823 4666 naca ZFA:0001286 caudal vein plexus PATO:0002001 has fewer parts of type abnormal ZFA:0009014 hematopoietic stem cell ZDB-GENE-020423-4 195823 4666 naca ZFA:0001286 caudal vein plexus PATO:0000592 decreased thickness abnormal ZDB-GENE-020423-4 195823 4666 naca GO:0008219 cell death BFO:0000066 occurs_in ZFA:0005023 hematopoietic system PATO:0002051 increased occurrence abnormal ZDB-GENE-020423-4 195823 4666 naca ZFA:0009014 hematopoietic stem cell PATO:0000462 absent abnormal ZDB-GENE-020423-4 195823 4666 naca ZFA:0009014 hematopoietic stem cell PATO:0001997 decreased amount abnormal ZDB-GENE-020423-4 195823 4666 naca ZFA:0009048 granulocyte PATO:0000462 absent abnormal ZDB-GENE-020423-4 195823 4666 naca GO:0030016 myofibril BFO:0000050 part_of ZFA:0009116 slow muscle cell PATO:0000937 disorganized abnormal ZDB-GENE-020423-4 195823 4666 naca GO:0030016 myofibril BFO:0000050 part_of ZFA:0009117 fast muscle cell PATO:0000937 disorganized abnormal ZDB-GENE-020423-4 195823 4666 naca GO:0030017 sarcomere BFO:0000050 part_of ZFA:0009117 fast muscle cell PATO:0001997 decreased amount abnormal ZDB-GENE-020423-4 195823 4666 naca ZFA:0009327 neutrophil PATO:0000628 mislocalised abnormal ZDB-GENE-020423-4 195823 4666 naca ZFA:0009327 neutrophil PATO:0001997 decreased amount abnormal ZDB-GENE-020423-5 195820 2492 fshr GO:0001541 ovarian follicle development PATO:0000297 arrested abnormal ZDB-GENE-020423-5 195820 2492 fshr GO:0007283 spermatogenesis PATO:0000502 delayed abnormal ZDB-GENE-020423-5 195820 2492 fshr GO:0007530 sex determination PATO:0001236 process quality abnormal ZDB-GENE-020423-5 195820 2492 fshr ZFA:0000242 male organism PATO:0000470 increased amount abnormal ZDB-GENE-020423-5 195820 2492 fshr ZFA:0000303 female organism PATO:0000892 female sterile abnormal ZDB-GENE-020423-5 195820 2492 fshr ZFA:0000303 female organism PATO:0000956 sterile abnormal ZDB-GENE-020423-5 195820 2492 fshr ZFA:0000303 female organism PATO:0001997 decreased amount abnormal ZDB-GENE-020423-5 195820 2492 fshr ZFA:0000403 ovary PATO:0000587 decreased size abnormal ZDB-GENE-020423-5 195820 2492 fshr GO:0040007 growth BFO:0000066 occurs_in ZFA:0000598 testis PATO:0002302 decreased process quality abnormal ZDB-GENE-020423-5 195820 2492 fshr ZFA:0000598 testis PATO:0001501 immature abnormal ZDB-GENE-020423-5 195820 2492 fshr ZFA:0001094 whole organism PATO:0000047 biological sex abnormal ZDB-GENE-020423-5 195820 2492 fshr ZFA:0001263 ovarian follicle stage I PATO:0000587 decreased size abnormal ZDB-GENE-020423-5 195820 2492 fshr ZFA:0001263 ovarian follicle stage I PATO:0001501 immature abnormal ZDB-GENE-020423-5 195820 2492 fshr ZFA:0001264 ovarian follicle stage IV PATO:0000462 absent abnormal ZDB-GENE-020423-5 195820 2492 fshr ZFA:0001265 ovarian follicle stage II PATO:0000462 absent abnormal ZDB-GENE-020423-5 195820 2492 fshr ZFA:0001266 ovarian follicle stage III PATO:0000462 absent abnormal ZDB-GENE-020423-5 195820 2492 fshr ZFA:0009016 germ line cell PATO:0000587 decreased size abnormal ZDB-GENE-020423-5 195820 2492 fshr ZFA:0009016 germ line cell PATO:0001997 decreased amount abnormal ZDB-GENE-020424-3 195815 4000 lmna GO:0000084 mitotic S phase PATO:0001309 duration abnormal ZDB-GENE-020424-3 195815 4000 lmna GO:0000087 mitotic M phase PATO:0001309 duration abnormal ZDB-GENE-020424-3 195815 4000 lmna GO:0002027 regulation of heart rate PATO:0001507 disrupted abnormal ZDB-GENE-020424-3 195815 4000 lmna GO:0008015 blood circulation PATO:0001507 disrupted abnormal ZDB-GENE-020424-3 195815 4000 lmna GO:0036269 swimming behavior PATO:0001236 process quality abnormal ZDB-GENE-020424-3 195815 4000 lmna GO:0045444 fat cell differentiation PATO:0002052 decreased occurrence abnormal ZDB-GENE-020424-3 195815 4000 lmna GO:0060047 heart contraction PATO:0000911 decreased rate abnormal ZDB-GENE-020424-3 195815 4000 lmna GO:0090398 cellular senescence PATO:0002051 increased occurrence abnormal ZDB-GENE-020424-3 195815 4000 lmna ZFA:0000008 brain PATO:0000638 apoptotic abnormal ZDB-GENE-020424-3 195815 4000 lmna GO:0061337 cardiac conduction BFO:0000066 occurs_in ZFA:0000009 cardiac ventricle PATO:0002302 decreased process quality abnormal ZDB-GENE-020424-3 195815 4000 lmna ZFA:0000009 cardiac ventricle PATO:0001624 decreased functionality abnormal ZDB-GENE-020424-3 195815 4000 lmna ZFA:0000054 pericardium PATO:0001450 edematous abnormal ZDB-GENE-020424-3 195815 4000 lmna ZFA:0000114 heart PATO:0001581 decreased contractility abnormal ZDB-GENE-020424-3 195815 4000 lmna ZFA:0000114 heart PATO:0001624 decreased functionality abnormal ZDB-GENE-020424-3 195815 4000 lmna ZFA:0000154 sinus venosus PATO:0002270 increased accumulation abnormal ZFA:0000007 blood ZDB-GENE-020424-3 195815 4000 lmna ZFA:0009116 slow muscle cell BFO:0000050 part_of ZFA:0000155 somite PATO:0001167 damaged abnormal ZDB-GENE-020424-3 195815 4000 lmna ZFA:0000368 integument PATO:0000700 rough abnormal ZDB-GENE-020424-3 195815 4000 lmna ZFA:0009116 slow muscle cell BFO:0000050 part_of ZFA:0001056 myotome PATO:0000967 undulate abnormal ZDB-GENE-020424-3 195815 4000 lmna ZFA:0009116 slow muscle cell BFO:0000050 part_of ZFA:0001056 myotome PATO:0001997 decreased amount abnormal ZDB-GENE-020424-3 195815 4000 lmna ZFA:0001115 trunk PATO:0000638 apoptotic abnormal ZDB-GENE-020424-3 195815 4000 lmna ZFA:0001205 Meckel's cartilage PATO:0001652 alignment abnormal ZFA:0001399 palatoquadrate cartilage ZDB-GENE-020424-3 195815 4000 lmna GO:0061337 cardiac conduction BFO:0000066 occurs_in ZFA:0001315 atrioventricular canal PATO:0002302 decreased process quality abnormal ZDB-GENE-020424-3 195815 4000 lmna ZFA:0001400 ceratohyal cartilage PATO:0001922 mislocalised posteriorly abnormal ZDB-GENE-020424-3 195815 4000 lmna ZFA:0001460 pharyngeal arch cartilage PATO:0001241 physical object quality abnormal ZDB-GENE-020424-3 195815 4000 lmna ZFA:0009082 fat cell PATO:0001997 decreased amount abnormal ZDB-GENE-020424-3 195815 4000 lmna GO:0005634 nucleus BFO:0000050 part_of ZFA:0009316 cardiac muscle cell PATO:0000051 morphology abnormal ZDB-GENE-020426-1 195818 3832 kif11 ZFA:0000008 brain PATO:0000647 necrotic abnormal ZDB-GENE-020426-1 195818 3832 kif11 ZFA:0000012 central nervous system PATO:0000647 necrotic abnormal ZDB-GENE-020426-1 195818 3832 kif11 ZFA:0000054 pericardium PATO:0001450 edematous abnormal ZDB-GENE-020426-1 195818 3832 kif11 ZFA:0000075 spinal cord PATO:0002002 has extra parts of type abnormal ZFA:0009292 radial glial cell BFO:0000050 part_of ZFA:0001083 ventricular zone ZDB-GENE-020426-1 195818 3832 kif11 ZFA:0000092 axis PATO:0001592 increased curvature abnormal ZDB-GENE-020426-1 195818 3832 kif11 ZFA:0000107 eye PATO:0000587 decreased size abnormal ZDB-GENE-020426-1 195818 3832 kif11 GO:0071679 commissural neuron axon guidance BFO:0000066 occurs_in ZFA:0000109 forebrain PATO:0001507 disrupted abnormal ZDB-GENE-020426-1 195818 3832 kif11 ZFA:0000112 gut PATO:0000645 hypoplastic abnormal ZDB-GENE-020426-1 195818 3832 kif11 ZFA:0000217 inner ear PATO:0000001 quality abnormal ZDB-GENE-020426-1 195818 3832 kif11 ZFA:0000435 cranial nerve II PATO:0000462 absent abnormal ZDB-GENE-020426-1 195818 3832 kif11 ZFA:0000435 cranial nerve II PATO:0000587 decreased size abnormal ZDB-GENE-020426-1 195818 3832 kif11 ZFA:0000435 cranial nerve II PATO:0001959 defasciculated abnormal ZDB-GENE-020426-1 195818 3832 kif11 ZFA:0009147 glial cell (sensu Vertebrata) BFO:0000050 part_of ZFA:0000890 floor plate spinal cord region PATO:0000586 increased size abnormal ZDB-GENE-020426-1 195818 3832 kif11 ZFA:0001094 whole organism PATO:0000406 curved abnormal ZDB-GENE-020426-1 195818 3832 kif11 ZFA:0001094 whole organism PATO:0000617 bent abnormal ZDB-GENE-020426-1 195818 3832 kif11 ZFA:0001094 whole organism PATO:0001468 curved dorsal abnormal ZDB-GENE-020426-1 195818 3832 kif11 ZFA:0001114 head PATO:0000587 decreased size abnormal ZDB-GENE-020426-1 195818 3832 kif11 ZFA:0001115 trunk PATO:0001878 sigmoid abnormal ZDB-GENE-020426-1 195818 3832 kif11 GO:0006915 apoptotic process BFO:0000066 occurs_in ZFA:0001135 neural tube PATO:0002304 increased process quality abnormal ZDB-GENE-020426-1 195818 3832 kif11 ZFA:0001135 neural tube PATO:0002002 has extra parts of type abnormal ZFA:0009292 radial glial cell ZDB-GENE-020426-1 195818 3832 kif11 ZFA:0001259 forebrain ventricle PATO:0002002 has extra parts of type abnormal ZFA:0009075 astrocyte ZDB-GENE-020426-1 195818 3832 kif11 ZFA:0001285 intersegmental vessel PATO:0002364 shortened abnormal ZDB-GENE-020426-1 195818 3832 kif11 ZFA:0005025 dorsal longitudinal anastomotic vessel PATO:0000051 morphology abnormal ZDB-GENE-020426-1 195818 3832 kif11 ZFA:0005025 dorsal longitudinal anastomotic vessel PATO:0000462 absent abnormal ZDB-GENE-020426-1 195818 3832 kif11 ZFA:0005176 CoSA PATO:0001997 decreased amount abnormal ZDB-GENE-020426-1 195818 3832 kif11 GO:0007411 axon guidance BFO:0000066 occurs_in ZFA:0005177 VeLD PATO:0001236 process quality abnormal ZDB-GENE-020426-1 195818 3832 kif11 GO:0007411 axon guidance BFO:0000066 occurs_in ZFA:0005240 Kolmer-Agduhr neuron PATO:0001236 process quality abnormal ZDB-GENE-020426-1 195818 3832 kif11 ZFA:0005249 vasculature PATO:0002009 branchiness abnormal ZDB-GENE-020426-1 195818 3832 kif11 ZFA:0009052 motor neuron PATO:0001997 decreased amount abnormal ZDB-GENE-020426-1 195818 3832 kif11 ZFA:0009292 radial glial cell PATO:0002001 has fewer parts of type abnormal GO:0005818 aster BFO:0000050 part_of ZFA:0009292 radial glial cell ZDB-GENE-020430-3 245698 2319 flot2a GO:0055113 epiboly involved in gastrulation with mouth forming second PATO:0000297 arrested abnormal ZDB-GENE-020430-3 245698 2319 flot2a GO:0055113 epiboly involved in gastrulation with mouth forming second PATO:0000502 delayed abnormal ZDB-GENE-020430-3 245698 2319 flot2a ZFA:0000093 blastomere PATO:0002264 organization quality abnormal ZDB-GENE-020430-3 245698 2319 flot2a GO:0042074 cell migration involved in gastrulation BFO:0000066 occurs_in ZFA:0000711 DEL PATO:0000502 delayed abnormal ZDB-GENE-020430-3 245698 2319 flot2a GO:0042074 cell migration involved in gastrulation BFO:0000066 occurs_in ZFA:0000711 DEL PATO:0001236 process quality abnormal ZDB-GENE-020430-3 245698 2319 flot2a ZFA:0001058 caudal fin PATO:0000051 morphology abnormal ZDB-GENE-020430-3 245698 2319 flot2a BSPO:0000013 anterior-posterior axis BFO:0000050 part_of ZFA:0001094 whole organism PATO:0000574 decreased length abnormal ZDB-GENE-020503-1 245701 3480 igf1ra GO:0001654 eye development PATO:0001507 disrupted abnormal ZDB-GENE-020503-1 245701 3480 igf1ra GO:0003007 heart morphogenesis PATO:0000502 delayed abnormal ZDB-GENE-020503-1 245701 3480 igf1ra GO:0006936 muscle contraction PATO:0002052 decreased occurrence abnormal ZDB-GENE-020503-1 245701 3480 igf1ra GO:0009790 embryo development PATO:0000502 delayed abnormal ZDB-GENE-020503-1 245701 3480 igf1ra GO:0043583 ear development PATO:0001507 disrupted abnormal ZDB-GENE-020503-1 245701 3480 igf1ra GO:0060047 heart contraction PATO:0000911 decreased rate abnormal ZDB-GENE-020503-1 245701 3480 igf1ra ZFA:0000009 cardiac ventricle PATO:0000141 structure abnormal ZDB-GENE-020503-1 245701 3480 igf1ra ZFA:0000009 cardiac ventricle PATO:0000645 hypoplastic abnormal ZDB-GENE-020503-1 245701 3480 igf1ra ZFA:0000114 heart PATO:0000587 decreased size abnormal ZDB-GENE-020503-1 245701 3480 igf1ra ZFA:0000155 somite PATO:0001997 decreased amount abnormal ZDB-GENE-020503-1 245701 3480 igf1ra ZFA:0009366 hair cell BFO:0000050 part_of ZFA:0000217 inner ear PATO:0000462 absent abnormal ZDB-GENE-020503-1 245701 3480 igf1ra ZFA:0000225 lateral crista primordium PATO:0001483 aplastic abnormal ZDB-GENE-020503-1 245701 3480 igf1ra ZFA:0000411 posterior crista primordium PATO:0001483 aplastic abnormal ZDB-GENE-020503-1 245701 3480 igf1ra ZFA:0000468 anterior crista primordium PATO:0001483 aplastic abnormal ZDB-GENE-020503-1 245701 3480 igf1ra ZFA:0001094 whole organism PATO:0000574 decreased length abnormal ZDB-GENE-020503-1 245701 3480 igf1ra ZFA:0001094 whole organism PATO:0000587 decreased size abnormal ZDB-GENE-020503-1 245701 3480 igf1ra ZFA:0001094 whole organism PATO:0001422 dead abnormal ZDB-GENE-020503-1 245701 3480 igf1ra ZFA:0009116 slow muscle cell PATO:0001997 decreased amount abnormal ZDB-GENE-020503-1 245701 3480 igf1ra ZFA:0009117 fast muscle cell PATO:0001997 decreased amount abnormal ZDB-GENE-020503-1 245701 3480 igf1ra GO:0030424 axon BFO:0000050 part_of ZFA:0009243 CaP motoneuron PATO:0001624 decreased functionality abnormal ZDB-GENE-020503-1 245701 3480 igf1ra ZFA:0009310 retinal ganglion cell PATO:0000462 absent abnormal ZDB-GENE-020503-2 245702 3480 igf1rb GO:0001654 eye development PATO:0001507 disrupted abnormal ZDB-GENE-020503-2 245702 3480 igf1rb GO:0003007 heart morphogenesis PATO:0000502 delayed abnormal ZDB-GENE-020503-2 245702 3480 igf1rb GO:0006936 muscle contraction PATO:0000297 arrested abnormal ZDB-GENE-020503-2 245702 3480 igf1rb GO:0008354 germ cell migration PATO:0001507 disrupted abnormal ZDB-GENE-020503-2 245702 3480 igf1rb GO:0009790 embryo development PATO:0000502 delayed abnormal ZDB-GENE-020503-2 245702 3480 igf1rb GO:0043583 ear development PATO:0001507 disrupted abnormal ZDB-GENE-020503-2 245702 3480 igf1rb GO:0060047 heart contraction PATO:0000911 decreased rate abnormal ZDB-GENE-020503-2 245702 3480 igf1rb ZFA:0000009 cardiac ventricle PATO:0000141 structure abnormal ZDB-GENE-020503-2 245702 3480 igf1rb ZFA:0000009 cardiac ventricle PATO:0000645 hypoplastic abnormal ZDB-GENE-020503-2 245702 3480 igf1rb ZFA:0000114 heart PATO:0000587 decreased size abnormal ZDB-GENE-020503-2 245702 3480 igf1rb ZFA:0000155 somite PATO:0001997 decreased amount abnormal ZDB-GENE-020503-2 245702 3480 igf1rb ZFA:0009366 hair cell BFO:0000050 part_of ZFA:0000217 inner ear PATO:0000462 absent abnormal ZDB-GENE-020503-2 245702 3480 igf1rb ZFA:0000225 lateral crista primordium PATO:0001483 aplastic abnormal ZDB-GENE-020503-2 245702 3480 igf1rb ZFA:0000411 posterior crista primordium PATO:0001483 aplastic abnormal ZDB-GENE-020503-2 245702 3480 igf1rb ZFA:0000468 anterior crista primordium PATO:0001483 aplastic abnormal ZDB-GENE-020503-2 245702 3480 igf1rb ZFA:0001094 whole organism PATO:0000574 decreased length abnormal ZDB-GENE-020503-2 245702 3480 igf1rb ZFA:0001094 whole organism PATO:0000587 decreased size abnormal ZDB-GENE-020503-2 245702 3480 igf1rb ZFA:0001094 whole organism PATO:0001422 dead abnormal ZDB-GENE-020503-2 245702 3480 igf1rb ZFA:0009116 slow muscle cell PATO:0001997 decreased amount abnormal ZDB-GENE-020503-2 245702 3480 igf1rb ZFA:0009117 fast muscle cell PATO:0001997 decreased amount abnormal ZDB-GENE-020503-2 245702 3480 igf1rb GO:0030424 axon BFO:0000050 part_of ZFA:0009243 CaP motoneuron PATO:0001624 decreased functionality abnormal ZDB-GENE-020503-2 245702 3480 igf1rb ZFA:0009288 primordial germ cell PATO:0000629 misrouted abnormal ZDB-GENE-020503-2 245702 3480 igf1rb ZFA:0009288 primordial germ cell PATO:0001997 decreased amount abnormal ZDB-GENE-020503-2 245702 3480 igf1rb ZFA:0009310 retinal ganglion cell PATO:0000462 absent abnormal ZDB-GENE-020503-3 245699 3643 insra GO:0004346 glucose-6-phosphatase activity PATO:0002051 increased occurrence abnormal ZDB-GENE-020503-3 245699 3643 insra GO:0004611 phosphoenolpyruvate carboxykinase activity PATO:0002051 increased occurrence abnormal ZDB-GENE-020503-3 245699 3643 insra GO:0007631 feeding behavior PATO:0000912 increased rate abnormal ZDB-GENE-020503-3 245699 3643 insra GO:0040007 growth PATO:0001507 disrupted abnormal ZDB-GENE-020503-3 245699 3643 insra CHEBI:17234 glucose BFO:0000050 part_of ZFA:0000007 blood PATO:0000470 increased amount abnormal ZDB-GENE-020503-3 245699 3643 insra ZFA:0000042 midbrain hindbrain boundary PATO:0001617 deformed abnormal ZDB-GENE-020503-3 245699 3643 insra ZFA:0000107 eye PATO:0000587 decreased size abnormal ZDB-GENE-020503-3 245699 3643 insra ZFA:0000277 scale BFO:0000050 part_of ZFA:0000108 fin PATO:0000587 decreased size abnormal ZDB-GENE-020503-3 245699 3643 insra ZFA:0000109 forebrain PATO:0000587 decreased size abnormal ZDB-GENE-020503-3 245699 3643 insra CHEBI:17855 triglyceride BFO:0000050 part_of ZFA:0000123 liver PATO:0001997 decreased amount abnormal ZDB-GENE-020503-3 245699 3643 insra CHEBI:18059 lipid BFO:0000050 part_of ZFA:0000123 liver PATO:0001997 decreased amount abnormal ZDB-GENE-020503-3 245699 3643 insra GO:0004346 glucose-6-phosphatase activity BFO:0000050 part_of ZFA:0000123 liver PATO:0002051 increased occurrence abnormal ZDB-GENE-020503-3 245699 3643 insra GO:0004346 glucose-6-phosphatase activity BFO:0000050 part_of ZFA:0000123 liver PATO:0002052 decreased occurrence abnormal ZDB-GENE-020503-3 245699 3643 insra GO:0004611 phosphoenolpyruvate carboxykinase activity BFO:0000050 part_of ZFA:0000123 liver PATO:0002051 increased occurrence abnormal ZDB-GENE-020503-3 245699 3643 insra GO:0004743 pyruvate kinase activity BFO:0000050 part_of ZFA:0000123 liver PATO:0002051 increased occurrence abnormal ZDB-GENE-020503-3 245699 3643 insra GO:0004743 pyruvate kinase activity BFO:0000050 part_of ZFA:0000123 liver PATO:0002052 decreased occurrence abnormal ZDB-GENE-020503-3 245699 3643 insra ZFA:0000128 midbrain PATO:0000587 decreased size abnormal ZDB-GENE-020503-3 245699 3643 insra GO:0040007 growth BFO:0000066 occurs_in ZFA:0000277 scale PATO:0001507 disrupted abnormal ZDB-GENE-020503-3 245699 3643 insra CHEBI:17234 glucose BFO:0000050 part_of ZFA:0001094 whole organism PATO:0000470 increased amount abnormal ZDB-GENE-020503-3 245699 3643 insra CHEBI:17234 glucose BFO:0000050 part_of ZFA:0001094 whole organism PATO:0001997 decreased amount abnormal ZDB-GENE-020503-3 245699 3643 insra ZFA:0001094 whole organism PATO:0000573 increased length abnormal ZDB-GENE-020503-3 245699 3643 insra ZFA:0001094 whole organism PATO:0000582 increased weight abnormal ZDB-GENE-020503-3 245699 3643 insra ZFA:0001117 post-vent region PATO:0000406 curved abnormal ZDB-GENE-020503-3 245699 3643 insra GO:0004743 pyruvate kinase activity BFO:0000050 part_of ZFA:0005145 muscle PATO:0002052 decreased occurrence abnormal ZDB-GENE-020503-3 245699 3643 insra CHEBI:145810 insulin BFO:0000050 part_of ZFA:0005654 blood plasma PATO:0000470 increased amount abnormal ZDB-GENE-020503-3 245699 3643 insra CHEBI:16113 cholesterol BFO:0000050 part_of ZFA:0005654 blood plasma PATO:0001997 decreased amount abnormal ZDB-GENE-020503-3 245699 3643 insra CHEBI:16247 phospholipid BFO:0000050 part_of ZFA:0005654 blood plasma PATO:0001997 decreased amount abnormal ZDB-GENE-020503-3 245699 3643 insra CHEBI:17855 triglyceride BFO:0000050 part_of ZFA:0005654 blood plasma PATO:0001997 decreased amount abnormal ZDB-GENE-020503-3 245699 3643 insra CHEBI:35366 fatty acid BFO:0000050 part_of ZFA:0005654 blood plasma PATO:0001997 decreased amount abnormal ZDB-GENE-020503-4 245700 3643 insrb GO:0007631 feeding behavior PATO:0000912 increased rate abnormal ZDB-GENE-020503-4 245700 3643 insrb GO:0008610 lipid biosynthetic process PATO:0002051 increased occurrence abnormal ZDB-GENE-020503-4 245700 3643 insrb CHEBI:17234 glucose BFO:0000050 part_of ZFA:0000007 blood PATO:0000470 increased amount abnormal ZDB-GENE-020503-4 245700 3643 insrb ZFA:0000054 pericardium PATO:0001450 edematous abnormal ZDB-GENE-020503-4 245700 3643 insrb ZFA:0000107 eye PATO:0000587 decreased size abnormal ZDB-GENE-020503-4 245700 3643 insrb ZFA:0000109 forebrain PATO:0000587 decreased size abnormal ZDB-GENE-020503-4 245700 3643 insrb CHEBI:17855 triglyceride BFO:0000050 part_of ZFA:0000123 liver PATO:0000470 increased amount abnormal ZDB-GENE-020503-4 245700 3643 insrb CHEBI:18059 lipid BFO:0000050 part_of ZFA:0000123 liver PATO:0000470 increased amount abnormal ZDB-GENE-020503-4 245700 3643 insrb GO:0004346 glucose-6-phosphatase activity BFO:0000050 part_of ZFA:0000123 liver PATO:0002052 decreased occurrence abnormal ZDB-GENE-020503-4 245700 3643 insrb GO:0004611 phosphoenolpyruvate carboxykinase activity BFO:0000050 part_of ZFA:0000123 liver PATO:0002051 increased occurrence abnormal ZDB-GENE-020503-4 245700 3643 insrb GO:0004611 phosphoenolpyruvate carboxykinase activity BFO:0000050 part_of ZFA:0000123 liver PATO:0002052 decreased occurrence abnormal ZDB-GENE-020503-4 245700 3643 insrb GO:0004743 pyruvate kinase activity BFO:0000050 part_of ZFA:0000123 liver PATO:0002052 decreased occurrence abnormal ZDB-GENE-020503-4 245700 3643 insrb ZFA:0000128 midbrain PATO:0000587 decreased size abnormal ZDB-GENE-020503-4 245700 3643 insrb CHEBI:17234 glucose BFO:0000050 part_of ZFA:0001094 whole organism PATO:0000470 increased amount abnormal ZDB-GENE-020503-4 245700 3643 insrb CHEBI:17234 glucose BFO:0000050 part_of ZFA:0001094 whole organism PATO:0001997 decreased amount abnormal ZDB-GENE-020503-4 245700 3643 insrb ZFA:0001094 whole organism PATO:0000582 increased weight abnormal ZDB-GENE-020503-4 245700 3643 insrb ZFA:0001227 mandibular arch skeleton PATO:0000646 malformed abnormal ZDB-GENE-020503-4 245700 3643 insrb GO:0004743 pyruvate kinase activity BFO:0000050 part_of ZFA:0005145 muscle PATO:0002052 decreased occurrence abnormal ZDB-GENE-020503-4 245700 3643 insrb CHEBI:145810 insulin BFO:0000050 part_of ZFA:0005654 blood plasma PATO:0000470 increased amount abnormal ZDB-GENE-020503-4 245700 3643 insrb CHEBI:16113 cholesterol BFO:0000050 part_of ZFA:0005654 blood plasma PATO:0000470 increased amount abnormal ZDB-GENE-020503-4 245700 3643 insrb CHEBI:16247 phospholipid BFO:0000050 part_of ZFA:0005654 blood plasma PATO:0000470 increased amount abnormal ZDB-GENE-020503-4 245700 3643 insrb CHEBI:17855 triglyceride BFO:0000050 part_of ZFA:0005654 blood plasma PATO:0000470 increased amount abnormal ZDB-GENE-020503-4 245700 3643 insrb CHEBI:35366 fatty acid BFO:0000050 part_of ZFA:0005654 blood plasma PATO:0000470 increased amount abnormal ZDB-GENE-020503-4 245700 3643 insrb ZFA:0005759 visceral fat PATO:0000470 increased amount abnormal ZDB-GENE-020507-2 245946 27130 invs GO:0001889 liver development PATO:0001507 disrupted abnormal ZDB-GENE-020507-2 245946 27130 invs GO:0001947 heart looping PATO:0001236 process quality abnormal ZDB-GENE-020507-2 245946 27130 invs GO:0007368 determination of left/right symmetry PATO:0001507 disrupted abnormal ZDB-GENE-020507-2 245946 27130 invs GO:0035469 determination of pancreatic left/right asymmetry PATO:0001507 disrupted abnormal ZDB-GENE-020507-2 245946 27130 invs GO:0036372 opsin transport PATO:0001507 disrupted abnormal ZDB-GENE-020507-2 245946 27130 invs GO:0060972 left/right pattern formation PATO:0001507 disrupted abnormal ZDB-GENE-020507-2 245946 27130 invs ZFA:0000123 liver PATO:0000628 mislocalised abnormal ZDB-GENE-020507-2 245946 27130 invs ZFA:0000140 pancreas PATO:0000628 mislocalised abnormal ZDB-GENE-020507-2 245946 27130 invs ZFA:0000151 pronephros PATO:0001673 cystic abnormal ZDB-GENE-020507-2 245946 27130 invs ZFA:0000330 cloacal chamber PATO:0001617 deformed abnormal ZDB-GENE-020507-2 245946 27130 invs ZFA:0000529 kidney PATO:0001450 edematous abnormal ZDB-GENE-020507-2 245946 27130 invs ZFA:0001094 whole organism PATO:0001469 curved ventral abnormal ZDB-GENE-020507-2 245946 27130 invs ZFA:0001115 trunk PATO:0001469 curved ventral abnormal ZDB-GENE-020507-2 245946 27130 invs ZFA:0001117 post-vent region PATO:0000406 curved abnormal ZDB-GENE-020507-2 245946 27130 invs ZFA:0001117 post-vent region PATO:0001469 curved ventral abnormal ZDB-GENE-020507-2 245946 27130 invs ZFA:0001558 pronephric tubule BFO:0000050 part_of ZFA:0001557 pronephric glomerulus PATO:0001714 increased diameter abnormal ZDB-GENE-020507-2 245946 27130 invs ZFA:0001620 pronephric proximal convoluted tubule PATO:0001714 increased diameter abnormal ZDB-GENE-020507-3 245949 57216 vangl2 GO:0000132 establishment of mitotic spindle orientation PATO:0001507 disrupted abnormal ZDB-GENE-020507-3 245949 57216 vangl2 GO:0000902 cell morphogenesis PATO:0001507 disrupted abnormal ZDB-GENE-020507-3 245949 57216 vangl2 GO:0001702 gastrulation with mouth forming second PATO:0000001 quality abnormal ZDB-GENE-020507-3 245949 57216 vangl2 GO:0001756 somitogenesis PATO:0001507 disrupted abnormal ZDB-GENE-020507-3 245949 57216 vangl2 GO:0001764 neuron migration PATO:0001507 disrupted abnormal ZDB-GENE-020507-3 245949 57216 vangl2 GO:0001841 neural tube formation PATO:0001507 disrupted abnormal ZDB-GENE-020507-3 245949 57216 vangl2 GO:0001947 heart looping PATO:0001236 process quality abnormal ZDB-GENE-020507-3 245949 57216 vangl2 GO:0001947 heart looping PATO:0001507 disrupted abnormal ZDB-GENE-020507-3 245949 57216 vangl2 GO:0003140 determination of left/right asymmetry in lateral mesoderm PATO:0000057 occurrence abnormal ZDB-GENE-020507-3 245949 57216 vangl2 GO:0003140 determination of left/right asymmetry in lateral mesoderm PATO:0002052 decreased occurrence abnormal ZDB-GENE-020507-3 245949 57216 vangl2 GO:0003341 cilium movement PATO:0000381 decreased frequency abnormal ZDB-GENE-020507-3 245949 57216 vangl2 GO:0007015 actin filament organization PATO:0001507 disrupted abnormal ZDB-GENE-020507-3 245949 57216 vangl2 GO:0014812 muscle cell migration PATO:0001507 disrupted abnormal ZDB-GENE-020507-3 245949 57216 vangl2 GO:0021505 neural fold folding PATO:0000502 delayed abnormal ZDB-GENE-020507-3 245949 57216 vangl2 GO:0021561 facial nerve development PATO:0001507 disrupted abnormal ZDB-GENE-020507-3 245949 57216 vangl2 GO:0022007 convergent extension involved in neural plate elongation PATO:0001236 process quality abnormal ZDB-GENE-020507-3 245949 57216 vangl2 GO:0030010 establishment of cell polarity PATO:0001507 disrupted abnormal ZDB-GENE-020507-3 245949 57216 vangl2 GO:0035622 intrahepatic bile duct development PATO:0001507 disrupted abnormal ZDB-GENE-020507-3 245949 57216 vangl2 GO:0048840 otolith development PATO:0001507 disrupted abnormal ZDB-GENE-020507-3 245949 57216 vangl2 GO:0055002 striated muscle cell development PATO:0001507 disrupted abnormal ZDB-GENE-020507-3 245949 57216 vangl2 GO:0060026 convergent extension PATO:0001236 process quality abnormal ZDB-GENE-020507-3 245949 57216 vangl2 GO:0060026 convergent extension PATO:0001507 disrupted abnormal ZDB-GENE-020507-3 245949 57216 vangl2 GO:0060027 convergent extension involved in gastrulation PATO:0001236 process quality abnormal ZDB-GENE-020507-3 245949 57216 vangl2 GO:0060027 convergent extension involved in gastrulation PATO:0001507 disrupted abnormal ZDB-GENE-020507-3 245949 57216 vangl2 GO:0060028 convergent extension involved in axis elongation PATO:0001507 disrupted abnormal ZDB-GENE-020507-3 245949 57216 vangl2 GO:0060030 dorsal convergence PATO:0000502 delayed abnormal ZDB-GENE-020507-3 245949 57216 vangl2 GO:0060271 cilium assembly PATO:0001507 disrupted abnormal ZDB-GENE-020507-3 245949 57216 vangl2 GO:0060971 embryonic heart tube left/right pattern formation PATO:0002302 decreased process quality abnormal ZDB-GENE-020507-3 245949 57216 vangl2 GO:0060972 left/right pattern formation PATO:0001507 disrupted abnormal ZDB-GENE-020507-3 245949 57216 vangl2 GO:0061371 determination of heart left/right asymmetry PATO:0000057 occurrence abnormal ZDB-GENE-020507-3 245949 57216 vangl2 GO:0061371 determination of heart left/right asymmetry PATO:0002052 decreased occurrence abnormal ZDB-GENE-020507-3 245949 57216 vangl2 GO:0070121 Kupffer's vesicle development PATO:0001507 disrupted abnormal ZDB-GENE-020507-3 245949 57216 vangl2 GO:0071679 commissural neuron axon guidance PATO:0001236 process quality abnormal ZDB-GENE-020507-3 245949 57216 vangl2 GO:0071907 determination of digestive tract left/right asymmetry PATO:0000057 occurrence abnormal ZDB-GENE-020507-3 245949 57216 vangl2 GO:0071907 determination of digestive tract left/right asymmetry PATO:0002052 decreased occurrence abnormal ZDB-GENE-020507-3 245949 57216 vangl2 GO:0005634 nucleus BFO:0000050 part_of ZFA:0000001 Kupffer's vesicle PATO:0000374 increased distance abnormal GO:0016324 apical plasma membrane BFO:0000050 part_of ZFA:0000001 Kupffer's vesicle ZDB-GENE-020507-3 245949 57216 vangl2 GO:0005929 cilium BFO:0000050 part_of ZFA:0000001 Kupffer's vesicle PATO:0002490 anterior orientation abnormal ZDB-GENE-020507-3 245949 57216 vangl2 GO:0031514 motile cilium BFO:0000050 part_of ZFA:0000001 Kupffer's vesicle PATO:0000574 decreased length abnormal ZDB-GENE-020507-3 245949 57216 vangl2 GO:0031514 motile cilium BFO:0000050 part_of ZFA:0000001 Kupffer's vesicle PATO:0001906 movement quality abnormal ZDB-GENE-020507-3 245949 57216 vangl2 GO:0031514 motile cilium BFO:0000050 part_of ZFA:0000001 Kupffer's vesicle PATO:0001997 decreased amount abnormal ZDB-GENE-020507-3 245949 57216 vangl2 GO:0036064 ciliary basal body BFO:0000050 part_of ZFA:0000001 Kupffer's vesicle PATO:0001453 detached from abnormal GO:0016324 apical plasma membrane BFO:0000050 part_of ZFA:0000001 Kupffer's vesicle ZDB-GENE-020507-3 245949 57216 vangl2 GO:0036064 ciliary basal body BFO:0000050 part_of ZFA:0000001 Kupffer's vesicle PATO:0001921 mislocalised anteriorly abnormal ZDB-GENE-020507-3 245949 57216 vangl2 GO:0060287 epithelial cilium movement involved in determination of left/right asymmetry BFO:0000066 occurs_in ZFA:0000001 Kupffer's vesicle PATO:0001236 process quality abnormal ZDB-GENE-020507-3 245949 57216 vangl2 ZFA:0009032 ciliated cell BFO:0000050 part_of ZFA:0000001 Kupffer's vesicle PATO:0002448 oriented towards abnormal BSPO:0000071 anterior region BFO:0000050 part_of ZFA:0000001 Kupffer's vesicle ZDB-GENE-020507-3 245949 57216 vangl2 ZFA:0000001 Kupffer's vesicle PATO:0000586 increased size abnormal ZDB-GENE-020507-3 245949 57216 vangl2 ZFA:0000001 Kupffer's vesicle PATO:0001624 decreased functionality abnormal ZDB-GENE-020507-3 245949 57216 vangl2 ZFA:0000001 Kupffer's vesicle PATO:0001838 decreased fluid flow abnormal ZDB-GENE-020507-3 245949 57216 vangl2 ZFA:0000003 adaxial cell PATO:0000052 shape abnormal ZDB-GENE-020507-3 245949 57216 vangl2 BSPO:0000084 ventral region BFO:0000050 part_of ZFA:0000008 brain PATO:0001485 condensed abnormal ZDB-GENE-020507-3 245949 57216 vangl2 ZFA:0000008 brain PATO:0001853 hydrocephalic abnormal ZDB-GENE-020507-3 245949 57216 vangl2 GO:0042641 actomyosin BFO:0000050 part_of ZFA:0000009 cardiac ventricle PATO:0000060 spatial pattern abnormal ZDB-GENE-020507-3 245949 57216 vangl2 GO:0042641 actomyosin BFO:0000050 part_of ZFA:0000009 cardiac ventricle PATO:0002186 polarity abnormal ZDB-GENE-020507-3 245949 57216 vangl2 BSPO:0000084 ventral region BFO:0000050 part_of ZFA:0000012 central nervous system PATO:0000587 decreased size abnormal ZDB-GENE-020507-3 245949 57216 vangl2 ZFA:0000012 central nervous system PATO:0000639 degenerate abnormal ZDB-GENE-020507-3 245949 57216 vangl2 ZFA:0009000 cell BFO:0000050 part_of ZFA:0000016 ectoderm PATO:0000133 orientation abnormal ZFA:0000016 ectoderm ZDB-GENE-020507-3 245949 57216 vangl2 ZFA:0009000 cell BFO:0000050 part_of ZFA:0000016 ectoderm PATO:0000052 shape abnormal ZDB-GENE-020507-3 245949 57216 vangl2 GO:0001736 establishment of planar polarity BFO:0000066 occurs_in ZFA:0000022 floor plate PATO:0001236 process quality abnormal ZDB-GENE-020507-3 245949 57216 vangl2 GO:0007163 establishment or maintenance of cell polarity BFO:0000066 occurs_in ZFA:0000022 floor plate PATO:0002052 decreased occurrence abnormal ZDB-GENE-020507-3 245949 57216 vangl2 GO:0031514 motile cilium BFO:0000050 part_of ZFA:0000022 floor plate PATO:0000613 disoriented abnormal ZDB-GENE-020507-3 245949 57216 vangl2 GO:0036064 ciliary basal body BFO:0000050 part_of ZFA:0000022 floor plate PATO:0001769 positional polarity abnormal ZDB-GENE-020507-3 245949 57216 vangl2 ZFA:0009032 ciliated cell BFO:0000050 part_of ZFA:0000022 floor plate PATO:0000470 increased amount abnormal ZDB-GENE-020507-3 245949 57216 vangl2 ZFA:0000022 floor plate PATO:0000001 quality abnormal ZDB-GENE-020507-3 245949 57216 vangl2 ZFA:0000022 floor plate PATO:0000600 increased width abnormal ZDB-GENE-020507-3 245949 57216 vangl2 ZFA:0000022 floor plate PATO:0001602 distended abnormal ZDB-GENE-020507-3 245949 57216 vangl2 GO:0097475 motor neuron migration BFO:0000066 occurs_in ZFA:0000029 hindbrain PATO:0001236 process quality abnormal ZDB-GENE-020507-3 245949 57216 vangl2 ZFA:0009033 ependymal cell BFO:0000050 part_of ZFA:0000029 hindbrain PATO:0001999 lacks parts or has fewer parts of type abnormal GO:0031514 motile cilium BFO:0000050 part_of ZFA:0009033 ependymal cell ZDB-GENE-020507-3 245949 57216 vangl2 ZFA:0000054 pericardium PATO:0001450 edematous abnormal ZDB-GENE-020507-3 245949 57216 vangl2 ZFA:0000069 rhombomere 6 PATO:0002000 lacks all parts of type abnormal ZFA:0005731 branchiomotor neuron ZDB-GENE-020507-3 245949 57216 vangl2 ZFA:0000075 spinal cord PATO:0001473 duplicated abnormal ZDB-GENE-020507-3 245949 57216 vangl2 ZFA:0000091 axial chorda mesoderm PATO:0000574 decreased length abnormal ZDB-GENE-020507-3 245949 57216 vangl2 ZFA:0000091 axial chorda mesoderm PATO:0000600 increased width abnormal ZDB-GENE-020507-3 245949 57216 vangl2 ZFA:0000092 axis PATO:0000574 decreased length abnormal ZDB-GENE-020507-3 245949 57216 vangl2 ZFA:0000106 extension PATO:0000574 decreased length abnormal ZDB-GENE-020507-3 245949 57216 vangl2 ZFA:0000106 extension PATO:0000600 increased width abnormal ZDB-GENE-020507-3 245949 57216 vangl2 ZFA:0000107 eye PATO:0000375 decreased distance abnormal ZFA:0000107 eye ZDB-GENE-020507-3 245949 57216 vangl2 ZFA:0000107 eye PATO:0000642 fused with abnormal ZFA:0000107 eye ZDB-GENE-020507-3 245949 57216 vangl2 ZFA:0000107 eye PATO:0002259 adjacent to abnormal ZFA:0000107 eye ZDB-GENE-020507-3 245949 57216 vangl2 ZFA:0000107 eye PATO:0000599 decreased width abnormal ZDB-GENE-020507-3 245949 57216 vangl2 ZFA:0000110 fourth ventricle PATO:0001473 duplicated abnormal ZDB-GENE-020507-3 245949 57216 vangl2 GO:0042641 actomyosin BFO:0000050 part_of ZFA:0000114 heart PATO:0000060 spatial pattern abnormal ZDB-GENE-020507-3 245949 57216 vangl2 ZFA:0000131 neural keel PATO:0000591 increased thickness abnormal ZDB-GENE-020507-3 245949 57216 vangl2 ZFA:0000131 neural keel PATO:0000600 increased width abnormal ZDB-GENE-020507-3 245949 57216 vangl2 ZFA:0000132 neural plate PATO:0000600 increased width abnormal ZDB-GENE-020507-3 245949 57216 vangl2 ZFA:0000133 neural rod PATO:0000051 morphology abnormal ZDB-GENE-020507-3 245949 57216 vangl2 ZFA:0000133 neural rod PATO:0000591 increased thickness abnormal ZDB-GENE-020507-3 245949 57216 vangl2 ZFA:0000133 neural rod PATO:0000600 increased width abnormal ZDB-GENE-020507-3 245949 57216 vangl2 CARO:0000010 anatomical boundary BFO:0000050 part_of ZFA:0000135 notochord PATO:0002180 straight abnormal ZDB-GENE-020507-3 245949 57216 vangl2 ZFA:0009000 cell BFO:0000050 part_of ZFA:0000135 notochord PATO:0000133 orientation abnormal ZFA:0000135 notochord ZDB-GENE-020507-3 245949 57216 vangl2 ZFA:0009000 cell BFO:0000050 part_of ZFA:0000135 notochord PATO:0000052 shape abnormal ZDB-GENE-020507-3 245949 57216 vangl2 ZFA:0000135 notochord PATO:0000001 quality abnormal ZDB-GENE-020507-3 245949 57216 vangl2 ZFA:0000135 notochord PATO:0000574 decreased length abnormal ZDB-GENE-020507-3 245949 57216 vangl2 ZFA:0000135 notochord PATO:0000600 increased width abnormal ZDB-GENE-020507-3 245949 57216 vangl2 ZFA:0000135 notochord PATO:0000967 undulate abnormal ZDB-GENE-020507-3 245949 57216 vangl2 GO:0005929 cilium BFO:0000050 part_of ZFA:0000150 pronephric duct PATO:0000937 disorganized abnormal ZDB-GENE-020507-3 245949 57216 vangl2 GO:0005929 cilium BFO:0000050 part_of ZFA:0000150 pronephric duct PATO:0001624 decreased functionality abnormal ZDB-GENE-020507-3 245949 57216 vangl2 ZFA:0005242 multi-ciliated epithelial cell BFO:0000050 part_of ZFA:0000150 pronephric duct PATO:0000937 disorganized abnormal ZDB-GENE-020507-3 245949 57216 vangl2 ZFA:0009032 ciliated cell BFO:0000050 part_of ZFA:0000150 pronephric duct PATO:0002448 oriented towards abnormal BSPO:0000071 anterior region BFO:0000050 part_of ZFA:0000150 pronephric duct ZDB-GENE-020507-3 245949 57216 vangl2 ZFA:0009032 ciliated cell BFO:0000050 part_of ZFA:0000151 pronephros PATO:0001997 decreased amount abnormal ZDB-GENE-020507-3 245949 57216 vangl2 ZFA:0000151 pronephros PATO:0001673 cystic abnormal ZDB-GENE-020507-3 245949 57216 vangl2 GO:0031941 filamentous actin BFO:0000050 part_of ZFA:0000155 somite PATO:0000937 disorganized abnormal ZDB-GENE-020507-3 245949 57216 vangl2 ZFA:0000155 somite PATO:0000642 fused with abnormal ZFA:0000155 somite ZDB-GENE-020507-3 245949 57216 vangl2 ZFA:0000155 somite PATO:0000051 morphology abnormal ZDB-GENE-020507-3 245949 57216 vangl2 ZFA:0000155 somite PATO:0000117 size abnormal ZDB-GENE-020507-3 245949 57216 vangl2 ZFA:0000155 somite PATO:0000407 flat abnormal ZDB-GENE-020507-3 245949 57216 vangl2 ZFA:0000155 somite PATO:0000574 decreased length abnormal ZDB-GENE-020507-3 245949 57216 vangl2 ZFA:0000155 somite PATO:0000600 increased width abnormal ZDB-GENE-020507-3 245949 57216 vangl2 ZFA:0000155 somite PATO:0001485 condensed abnormal ZDB-GENE-020507-3 245949 57216 vangl2 ZFA:0009052 motor neuron BFO:0000050 part_of ZFA:0000206 facial nerve motor nucleus PATO:0000628 mislocalised abnormal ZDB-GENE-020507-3 245949 57216 vangl2 ZFA:0000206 facial nerve motor nucleus PATO:0000628 mislocalised abnormal ZDB-GENE-020507-3 245949 57216 vangl2 ZFA:0000208 gall bladder PATO:0001792 left side of abnormal ZFA:0001094 whole organism ZDB-GENE-020507-3 245949 57216 vangl2 ZFA:0000208 gall bladder PATO:0001923 mislocalised laterally abnormal ZDB-GENE-020507-3 245949 57216 vangl2 ZFA:0000217 inner ear PATO:0002083 altered number of abnormal ZFA:0001617 otolith ZDB-GENE-020507-3 245949 57216 vangl2 ZFA:0000255 paraxial mesoderm PATO:0000574 decreased length abnormal ZDB-GENE-020507-3 245949 57216 vangl2 ZFA:0000255 paraxial mesoderm PATO:0000600 increased width abnormal ZDB-GENE-020507-3 245949 57216 vangl2 ZFA:0009032 ciliated cell BFO:0000050 part_of ZFA:0000330 cloacal chamber PATO:0001997 decreased amount abnormal ZDB-GENE-020507-3 245949 57216 vangl2 ZFA:0000330 cloacal chamber PATO:0000646 malformed abnormal ZDB-GENE-020507-3 245949 57216 vangl2 ZFA:0001501 cartilage element BFO:0000050 part_of ZFA:0000737 cranium PATO:0002364 shortened abnormal ZDB-GENE-020507-3 245949 57216 vangl2 ZFA:0000823 rhombomere 5 PATO:0002000 lacks all parts of type abnormal ZFA:0005731 branchiomotor neuron ZDB-GENE-020507-3 245949 57216 vangl2 GO:0032421 stereocilium bundle BFO:0000050 part_of ZFA:0000940 posterior lateral line neuromast PATO:0000133 orientation abnormal ZFA:0000940 posterior lateral line neuromast ZDB-GENE-020507-3 245949 57216 vangl2 ZFA:0000949 rhombomere 7 PATO:0002000 lacks all parts of type abnormal ZFA:0005731 branchiomotor neuron ZDB-GENE-020507-3 245949 57216 vangl2 ZFA:0005731 branchiomotor neuron BFO:0000050 part_of ZFA:0001032 rhombomere 4 PATO:0000628 mislocalised abnormal ZDB-GENE-020507-3 245949 57216 vangl2 ZFA:0005731 branchiomotor neuron BFO:0000050 part_of ZFA:0001032 rhombomere 4 PATO:0001921 mislocalised anteriorly abnormal ZDB-GENE-020507-3 245949 57216 vangl2 ZFA:0001056 myotome PATO:0000574 decreased length abnormal ZDB-GENE-020507-3 245949 57216 vangl2 ZFA:0001064 rhombomere PATO:0001485 condensed abnormal ZDB-GENE-020507-3 245949 57216 vangl2 ZFA:0001070 presumptive pronephric mesoderm PATO:0001923 mislocalised laterally abnormal ZDB-GENE-020507-3 245949 57216 vangl2 BSPO:0000013 anterior-posterior axis BFO:0000050 part_of ZFA:0001094 whole organism PATO:0000574 decreased length abnormal ZDB-GENE-020507-3 245949 57216 vangl2 BSPO:0000013 anterior-posterior axis BFO:0000050 part_of ZFA:0001094 whole organism PATO:0001592 increased curvature abnormal ZDB-GENE-020507-3 245949 57216 vangl2 BSPO:0000013 anterior-posterior axis BFO:0000050 part_of ZFA:0001094 whole organism PATO:0002364 shortened abnormal ZDB-GENE-020507-3 245949 57216 vangl2 BSPO:0001001 medial-lateral axis BFO:0000050 part_of ZFA:0001094 whole organism PATO:0000573 increased length abnormal ZDB-GENE-020507-3 245949 57216 vangl2 ZFA:0001094 whole organism PATO:0000051 morphology abnormal ZDB-GENE-020507-3 245949 57216 vangl2 ZFA:0001094 whole organism PATO:0000052 shape abnormal ZDB-GENE-020507-3 245949 57216 vangl2 ZFA:0001094 whole organism PATO:0000169 viability abnormal ZDB-GENE-020507-3 245949 57216 vangl2 ZFA:0001094 whole organism PATO:0000406 curved abnormal ZDB-GENE-020507-3 245949 57216 vangl2 ZFA:0001094 whole organism PATO:0000574 decreased length abnormal ZDB-GENE-020507-3 245949 57216 vangl2 ZFA:0001094 whole organism PATO:0000617 bent abnormal ZDB-GENE-020507-3 245949 57216 vangl2 ZFA:0001094 whole organism PATO:0000718 lethal (sensu genetics) abnormal ZDB-GENE-020507-3 245949 57216 vangl2 ZFA:0001094 whole organism PATO:0001592 increased curvature abnormal ZDB-GENE-020507-3 245949 57216 vangl2 ZFA:0001114 head PATO:0001853 hydrocephalic abnormal ZDB-GENE-020507-3 245949 57216 vangl2 ZFA:0001115 trunk PATO:0000406 curved abnormal ZDB-GENE-020507-3 245949 57216 vangl2 ZFA:0001115 trunk PATO:0000574 decreased length abnormal ZDB-GENE-020507-3 245949 57216 vangl2 ZFA:0001115 trunk PATO:0001592 increased curvature abnormal ZDB-GENE-020507-3 245949 57216 vangl2 ZFA:0000135 notochord BFO:0000050 part_of ZFA:0001117 post-vent region PATO:0001910 folded abnormal ZDB-GENE-020507-3 245949 57216 vangl2 ZFA:0001117 post-vent region PATO:0000001 quality abnormal ZDB-GENE-020507-3 245949 57216 vangl2 ZFA:0001117 post-vent region PATO:0000051 morphology abnormal ZDB-GENE-020507-3 245949 57216 vangl2 ZFA:0001117 post-vent region PATO:0000574 decreased length abnormal ZDB-GENE-020507-3 245949 57216 vangl2 ZFA:0001117 post-vent region PATO:0000936 truncated abnormal ZDB-GENE-020507-3 245949 57216 vangl2 ZFA:0001117 post-vent region PATO:0001468 curved dorsal abnormal ZDB-GENE-020507-3 245949 57216 vangl2 ZFA:0001117 post-vent region PATO:0001469 curved ventral abnormal ZDB-GENE-020507-3 245949 57216 vangl2 ZFA:0001135 neural tube PATO:0000001 quality abnormal ZDB-GENE-020507-3 245949 57216 vangl2 ZFA:0001135 neural tube PATO:0000591 increased thickness abnormal ZDB-GENE-020507-3 245949 57216 vangl2 ZFA:0001135 neural tube PATO:0000600 increased width abnormal ZDB-GENE-020507-3 245949 57216 vangl2 ZFA:0001205 Meckel's cartilage PATO:0001617 deformed abnormal ZDB-GENE-020507-3 245949 57216 vangl2 GO:0042641 actomyosin BFO:0000050 part_of ZFA:0001319 myocardium PATO:0001671 increased distribution abnormal ZDB-GENE-020507-3 245949 57216 vangl2 ZFA:0001400 ceratohyal cartilage PATO:0001617 deformed abnormal ZDB-GENE-020507-3 245949 57216 vangl2 ZFA:0001460 pharyngeal arch cartilage PATO:0001617 deformed abnormal ZDB-GENE-020507-3 245949 57216 vangl2 ZFA:0001557 pronephric glomerulus PATO:0000651 unfused from abnormal ZFA:0001557 pronephric glomerulus ZDB-GENE-020507-3 245949 57216 vangl2 ZFA:0001559 vertebral column PATO:0001592 increased curvature abnormal ZDB-GENE-020507-3 245949 57216 vangl2 ZFA:0001559 vertebral column PATO:0001787 rotational curvature abnormal ZDB-GENE-020507-3 245949 57216 vangl2 ZFA:0001617 otolith PATO:0000070 amount abnormal ZDB-GENE-020507-3 245949 57216 vangl2 GO:0030424 axon BFO:0000050 part_of ZFA:0005175 CoPA PATO:0000629 misrouted abnormal ZDB-GENE-020507-3 245949 57216 vangl2 GO:0030424 axon BFO:0000050 part_of ZFA:0005175 CoPA PATO:0001922 mislocalised posteriorly abnormal ZDB-GENE-020507-3 245949 57216 vangl2 GO:0033564 anterior/posterior axon guidance BFO:0000066 occurs_in ZFA:0005175 CoPA PATO:0002302 decreased process quality abnormal ZDB-GENE-020507-3 245949 57216 vangl2 GO:0097380 dorsal spinal cord interneuron anterior axon guidance BFO:0000066 occurs_in ZFA:0005175 CoPA PATO:0002302 decreased process quality abnormal ZDB-GENE-020507-3 245949 57216 vangl2 GO:0001764 neuron migration BFO:0000066 occurs_in ZFA:0005731 branchiomotor neuron PATO:0002052 decreased occurrence abnormal ZDB-GENE-020507-3 245949 57216 vangl2 GO:0042995 cell projection BFO:0000050 part_of ZFA:0005731 branchiomotor neuron PATO:0002497 lateral orientation abnormal ZDB-GENE-020507-3 245949 57216 vangl2 ZFA:0005906 Reissner's fiber PATO:0000646 malformed abnormal ZDB-GENE-020507-3 245949 57216 vangl2 GO:0030010 establishment of cell polarity BFO:0000066 occurs_in ZFA:0005919 dorsal-ventral polarized posterior lateral line neuromast PATO:0001507 disrupted abnormal ZDB-GENE-020507-3 245949 57216 vangl2 ZFA:0009367 neuromast hair cell BFO:0000050 part_of ZFA:0005919 dorsal-ventral polarized posterior lateral line neuromast PATO:0000613 disoriented abnormal ZDB-GENE-020507-3 245949 57216 vangl2 ZFA:0009367 neuromast hair cell BFO:0000050 part_of ZFA:0005919 dorsal-ventral polarized posterior lateral line neuromast PATO:0001951 whorled abnormal ZDB-GENE-020507-3 245949 57216 vangl2 ZFA:0005919 dorsal-ventral polarized posterior lateral line neuromast PATO:0001769 positional polarity abnormal ZDB-GENE-020507-3 245949 57216 vangl2 GO:0030010 establishment of cell polarity BFO:0000066 occurs_in ZFA:0005920 anterior-posterior polarized posterior lateral line neuromast PATO:0001507 disrupted abnormal ZDB-GENE-020507-3 245949 57216 vangl2 ZFA:0009367 neuromast hair cell BFO:0000050 part_of ZFA:0005920 anterior-posterior polarized posterior lateral line neuromast PATO:0000613 disoriented abnormal ZDB-GENE-020507-3 245949 57216 vangl2 ZFA:0009367 neuromast hair cell BFO:0000050 part_of ZFA:0005920 anterior-posterior polarized posterior lateral line neuromast PATO:0001951 whorled abnormal ZDB-GENE-020507-3 245949 57216 vangl2 ZFA:0005920 anterior-posterior polarized posterior lateral line neuromast PATO:0000614 oriented abnormal ZDB-GENE-020507-3 245949 57216 vangl2 ZFA:0005920 anterior-posterior polarized posterior lateral line neuromast PATO:0001769 positional polarity abnormal ZDB-GENE-020507-3 245949 57216 vangl2 ZFA:0007085 migratory neural crest PATO:0001891 ovate abnormal ZDB-GENE-020507-3 245949 57216 vangl2 GO:0031012 extracellular matrix BFO:0000050 part_of ZFA:0009000 cell PATO:0000587 decreased size abnormal ZDB-GENE-020507-3 245949 57216 vangl2 GO:0031012 extracellular matrix BFO:0000050 part_of ZFA:0009000 cell PATO:0002264 organization quality abnormal ZDB-GENE-020507-3 245949 57216 vangl2 GO:0072686 mitotic spindle BFO:0000050 part_of ZFA:0009032 ciliated cell PATO:0002327 increased angle to abnormal BSPO:0000014 apical-basal axis relative to substrate BFO:0000050 part_of ZFA:0000151 pronephros ZDB-GENE-020507-3 245949 57216 vangl2 ZFA:0009116 slow muscle cell PATO:0000574 decreased length abnormal ZDB-GENE-020507-3 245949 57216 vangl2 ZFA:0009116 slow muscle cell PATO:0000937 disorganized abnormal ZDB-GENE-020507-3 245949 57216 vangl2 ZFA:0009306 neuroepithelial cell PATO:0000628 mislocalised abnormal ZDB-GENE-020507-3 245949 57216 vangl2 BSPO:0000074 basal region BFO:0000050 part_of ZFA:0009316 cardiac muscle cell PATO:0001617 deformed abnormal ZDB-GENE-020507-3 245949 57216 vangl2 GO:0048561 establishment of animal organ orientation BFO:0000066 occurs_in ZFA:0009316 cardiac muscle cell PATO:0001236 process quality abnormal ZDB-GENE-020507-3 245949 57216 vangl2 ZFA:0009316 cardiac muscle cell PATO:0000133 orientation abnormal ZFA:0000360 heart tube ZDB-GENE-020507-3 245949 57216 vangl2 ZFA:0009316 cardiac muscle cell PATO:0000051 morphology abnormal ZDB-GENE-020507-3 245949 57216 vangl2 ZFA:0009316 cardiac muscle cell PATO:0000701 smooth abnormal ZDB-GENE-020508-1 100000769 1409 cryaa GO:0002088 lens development in camera-type eye PATO:0001236 process quality abnormal ZDB-GENE-020508-1 100000769 1409 cryaa ZFA:0000035 lens PATO:0000051 morphology abnormal ZDB-GENE-020508-1 100000769 1409 cryaa ZFA:0000035 lens PATO:0000141 structure abnormal ZDB-GENE-020508-1 100000769 1409 cryaa ZFA:0000035 lens BFO:0000050 part_of ZFA:0000107 eye PATO:0000587 decreased size abnormal ZDB-GENE-020508-1 100000769 1409 cryaa ZFA:0000035 lens BFO:0000050 part_of ZFA:0000107 eye PATO:0000963 opaque abnormal ZDB-GENE-020509-1 171094 284086 nek8 GO:0001947 heart looping PATO:0000462 absent abnormal ZDB-GENE-020509-1 171094 284086 nek8 GO:0001947 heart looping PATO:0001507 disrupted abnormal ZDB-GENE-020509-1 171094 284086 nek8 ZFA:0000114 heart PATO:0000140 position abnormal ZDB-GENE-020509-1 171094 284086 nek8 ZFA:0000114 heart PATO:0002268 centered abnormal ZDB-GENE-020509-1 171094 284086 nek8 ZFA:0009000 cell BFO:0000050 part_of ZFA:0000150 pronephric duct PATO:0001453 detached from abnormal ZFA:0005313 pronephric glomerular basement membrane BFO:0000050 part_of ZFA:0000151 pronephros ZDB-GENE-020509-1 171094 284086 nek8 ZFA:0000151 pronephros PATO:0001673 cystic abnormal ZDB-GENE-020509-1 171094 284086 nek8 BSPO:0000013 anterior-posterior axis BFO:0000050 part_of ZFA:0001094 whole organism PATO:0001469 curved ventral abnormal ZDB-GENE-020509-1 171094 284086 nek8 ZFA:0001115 trunk PATO:0001469 curved ventral abnormal ZDB-GENE-020509-1 171094 284086 nek8 ZFA:0001117 post-vent region PATO:0000406 curved abnormal ZDB-GENE-020509-1 171094 284086 nek8 ZFA:0001558 pronephric tubule BFO:0000050 part_of ZFA:0001557 pronephric glomerulus PATO:0001714 increased diameter abnormal ZDB-GENE-020509-1 171094 284086 nek8 ZFA:0001557 pronephric glomerulus PATO:0001673 cystic abnormal ZDB-GENE-020509-1 171094 284086 nek8 ZFA:0001620 pronephric proximal convoluted tubule PATO:0001714 increased diameter abnormal ZDB-GENE-020509-2 245948 2637 gbx2 GO:0006915 apoptotic process PATO:0002051 increased occurrence abnormal ZDB-GENE-020509-2 245948 2637 gbx2 GO:0021534 cell proliferation in hindbrain PATO:0002052 decreased occurrence abnormal ZDB-GENE-020509-2 245948 2637 gbx2 GO:0021846 cell proliferation in forebrain PATO:0002052 decreased occurrence abnormal ZDB-GENE-020509-2 245948 2637 gbx2 GO:0030902 hindbrain development PATO:0001507 disrupted abnormal ZDB-GENE-020509-2 245948 2637 gbx2 BSPO:0000071 anterior region BFO:0000050 part_of ZFA:0000029 hindbrain PATO:0000936 truncated abnormal ZDB-GENE-020509-2 245948 2637 gbx2 GO:0043025 neuronal cell body BFO:0000050 part_of ZFA:0000697 cranial nerve V PATO:0000140 position abnormal ZDB-GENE-020509-2 245948 2637 gbx2 ZFA:0009052 motor neuron BFO:0000050 part_of ZFA:0000697 cranial nerve V PATO:0000937 disorganized abnormal ZDB-GENE-020509-2 245948 2637 gbx2 ZFA:0000822 rhombomere 2 PATO:0000638 apoptotic abnormal ZDB-GENE-020509-2 245948 2637 gbx2 ZFA:0000823 rhombomere 5 PATO:0000638 apoptotic abnormal ZDB-GENE-020509-2 245948 2637 gbx2 ZFA:0000948 rhombomere 3 PATO:0000599 decreased width abnormal ZDB-GENE-020509-2 245948 2637 gbx2 ZFA:0000948 rhombomere 3 PATO:0000638 apoptotic abnormal ZDB-GENE-020509-2 245948 2637 gbx2 ZFA:0001032 rhombomere 4 PATO:0000638 apoptotic abnormal ZDB-GENE-020509-2 245948 2637 gbx2 ZFA:0001094 whole organism PATO:0002001 has fewer parts of type abnormal ZFA:0009199 iridophore ZDB-GENE-020513-1 246090 114757 cygb1 GO:0008015 blood circulation PATO:0001507 disrupted abnormal ZDB-GENE-020513-1 246090 114757 cygb1 GO:0035188 hatching PATO:0001507 disrupted abnormal ZDB-GENE-020513-1 246090 114757 cygb1 GO:0048798 swim bladder inflation PATO:0001507 disrupted abnormal ZDB-GENE-020513-1 246090 114757 cygb1 GO:0008219 cell death BFO:0000066 occurs_in ZFA:0000029 hindbrain PATO:0002304 increased process quality abnormal ZDB-GENE-020513-1 246090 114757 cygb1 ZFA:0000029 hindbrain PATO:0002254 flattened abnormal ZDB-GENE-020513-1 246090 114757 cygb1 ZFA:0000054 pericardium PATO:0001450 edematous abnormal ZDB-GENE-020513-1 246090 114757 cygb1 GO:0006915 apoptotic process BFO:0000066 occurs_in ZFA:0000075 spinal cord PATO:0002304 increased process quality abnormal ZDB-GENE-020513-1 246090 114757 cygb1 GO:0008219 cell death BFO:0000066 occurs_in ZFA:0000075 spinal cord PATO:0002304 increased process quality abnormal ZDB-GENE-020513-1 246090 114757 cygb1 GO:0008219 cell death BFO:0000066 occurs_in ZFA:0000079 telencephalon PATO:0002304 increased process quality abnormal ZDB-GENE-020513-1 246090 114757 cygb1 ZFA:0000092 axis PATO:0000617 bent abnormal ZDB-GENE-020513-1 246090 114757 cygb1 GO:0006915 apoptotic process BFO:0000066 occurs_in ZFA:0000107 eye PATO:0002304 increased process quality abnormal ZDB-GENE-020513-1 246090 114757 cygb1 GO:0008219 cell death BFO:0000066 occurs_in ZFA:0000107 eye PATO:0002304 increased process quality abnormal ZDB-GENE-020513-1 246090 114757 cygb1 ZFA:0000107 eye PATO:0000587 decreased size abnormal ZDB-GENE-020513-1 246090 114757 cygb1 GO:0006915 apoptotic process BFO:0000066 occurs_in ZFA:0000128 midbrain PATO:0002304 increased process quality abnormal ZDB-GENE-020513-1 246090 114757 cygb1 GO:0008219 cell death BFO:0000066 occurs_in ZFA:0000128 midbrain PATO:0002304 increased process quality abnormal ZDB-GENE-020513-1 246090 114757 cygb1 ZFA:0000128 midbrain PATO:0002254 flattened abnormal ZDB-GENE-020513-1 246090 114757 cygb1 GO:0008283 cell population proliferation BFO:0000066 occurs_in ZFA:0001094 whole organism PATO:0002304 increased process quality abnormal ZDB-GENE-020513-1 246090 114757 cygb1 ZFA:0001094 whole organism PATO:0001422 dead abnormal ZDB-GENE-020513-1 246090 114757 cygb1 ZFA:0001094 whole organism PATO:0002283 decreased mobility abnormal ZDB-GENE-020513-1 246090 114757 cygb1 ZFA:0001114 head PATO:0002254 flattened abnormal ZDB-GENE-020513-1 246090 114757 cygb1 ZFA:0001205 Meckel's cartilage PATO:0000587 decreased size abnormal ZDB-GENE-020513-1 246090 114757 cygb1 ZFA:0001272 palatoquadrate arch PATO:0000640 dysplastic abnormal ZDB-GENE-020513-1 246090 114757 cygb1 ZFA:0001273 ventral mandibular arch PATO:0000640 dysplastic abnormal ZDB-GENE-020513-1 246090 114757 cygb1 ZFA:0001399 palatoquadrate cartilage PATO:0002327 increased angle to abnormal ZFA:0001399 palatoquadrate cartilage ZDB-GENE-020513-1 246090 114757 cygb1 ZFA:0001507 trabecula cranii PATO:0000587 decreased size abnormal ZDB-GENE-020513-1 246090 114757 cygb1 ZFA:0001516 ceratobranchial cartilage PATO:0000587 decreased size abnormal ZDB-GENE-020515-1 246093 3399 id3 ZFA:0000008 brain PATO:0000051 morphology abnormal ZDB-GENE-020515-1 246093 3399 id3 ZFA:0000042 midbrain hindbrain boundary PATO:0000646 malformed abnormal ZDB-GENE-020515-1 246093 3399 id3 ZFA:0000054 pericardium PATO:0001450 edematous abnormal ZDB-GENE-020515-1 246093 3399 id3 ZFA:0000110 fourth ventricle PATO:0000586 increased size abnormal ZDB-GENE-020515-1 246093 3399 id3 ZFA:0000445 optic tectum PATO:0000587 decreased size abnormal ZDB-GENE-020515-1 246093 3399 id3 ZFA:0000633 caudal tuberculum PATO:0002001 has fewer parts of type abnormal ZFA:0009301 dopaminergic neuron ZDB-GENE-020515-1 246093 3399 id3 ZFA:0001114 head PATO:0000587 decreased size abnormal ZDB-GENE-020515-1 246093 3399 id3 ZFA:0001115 trunk PATO:0000587 decreased size abnormal ZDB-GENE-020516-1 246091 4081 mab21l1 GO:0048593 camera-type eye morphogenesis PATO:0002302 decreased process quality abnormal ZDB-GENE-020516-1 246091 4081 mab21l1 GO:0061303 cornea development in camera-type eye PATO:0002302 decreased process quality abnormal ZDB-GENE-020516-1 246091 4081 mab21l1 ZFA:0000035 lens PATO:0000639 degenerate abnormal ZDB-GENE-020516-1 246091 4081 mab21l1 ZFA:0000035 lens PATO:0000646 malformed abnormal ZDB-GENE-020516-1 246091 4081 mab21l1 ZFA:0000107 eye PATO:0000587 decreased size abnormal ZDB-GENE-020516-1 246091 4081 mab21l1 GO:0006915 apoptotic process BFO:0000066 occurs_in ZFA:0000640 cornea PATO:0002051 increased occurrence abnormal ZDB-GENE-020516-1 246091 4081 mab21l1 ZFA:0000640 cornea PATO:0000592 decreased thickness abnormal ZDB-GENE-020516-1 246091 4081 mab21l1 ZFA:0000640 cornea PATO:0000963 opaque abnormal ZDB-GENE-020516-1 246091 4081 mab21l1 ZFA:0001283 pupil PATO:0000587 decreased size abnormal ZDB-GENE-020516-1 246091 4081 mab21l1 ZFA:0001283 pupil PATO:0000646 malformed abnormal ZDB-GENE-020516-1 246091 4081 mab21l1 ZFA:0001326 lens epithelium PATO:0000646 malformed abnormal ZDB-GENE-020516-1 246091 4081 mab21l1 ZFA:0001676 annular ligament PATO:0000587 decreased size abnormal ZDB-GENE-020516-1 246091 4081 mab21l1 ZFA:0001683 corneal epithelium PATO:0000592 decreased thickness abnormal ZDB-GENE-020516-1 246091 4081 mab21l1 ZFA:0001683 corneal epithelium PATO:0000646 malformed abnormal ZDB-GENE-020516-1 246091 4081 mab21l1 ZFA:0001685 corneal stroma PATO:0000592 decreased thickness abnormal ZDB-GENE-020516-1 246091 4081 mab21l1 ZFA:0005567 posterior segment eye PATO:0002002 has extra parts of type abnormal ZFA:0005046 hyaloid vessel ZDB-GENE-020516-1 246091 4081 mab21l1 ZFA:0005876 anterior chamber eye PATO:0000586 increased size abnormal ZDB-GENE-020516-1 246091 4081 mab21l1 ZFA:0009094 goblet cell PATO:0002261 located in abnormal BSPO:0000075 central region BFO:0000050 part_of ZFA:0001683 corneal epithelium ZDB-GENE-020530-1 246226 5742 ptgs1 GO:0001947 heart looping PATO:0001236 process quality abnormal ZDB-GENE-020530-1 246226 5742 ptgs1 GO:0055113 epiboly involved in gastrulation with mouth forming second PATO:0000502 delayed abnormal ZDB-GENE-020530-1 246226 5742 ptgs1 GO:0060271 cilium assembly PATO:0002302 decreased process quality abnormal ZDB-GENE-020530-1 246226 5742 ptgs1 GO:0031514 motile cilium BFO:0000050 part_of ZFA:0000001 Kupffer's vesicle PATO:0000574 decreased length abnormal ZDB-GENE-020530-1 246226 5742 ptgs1 ZFA:0000001 Kupffer's vesicle PATO:0002001 has fewer parts of type abnormal GO:0031514 motile cilium BFO:0000050 part_of ZFA:0000001 Kupffer's vesicle ZDB-GENE-020530-1 246226 5742 ptgs1 ZFA:0001261 ventricular system BFO:0000050 part_of ZFA:0000008 brain PATO:0001450 edematous abnormal ZDB-GENE-020530-1 246226 5742 ptgs1 ZFA:0000008 brain PATO:0001853 hydrocephalic abnormal ZDB-GENE-020530-1 246226 5742 ptgs1 ZFA:0000051 otic vesicle PATO:0002002 has extra parts of type abnormal ZFA:0001617 otolith ZDB-GENE-020530-1 246226 5742 ptgs1 ZFA:0000054 pericardium PATO:0001450 edematous abnormal ZDB-GENE-020530-1 246226 5742 ptgs1 ZFA:0000114 heart PATO:0001324 bilateral symmetry abnormal ZDB-GENE-020530-1 246226 5742 ptgs1 ZFA:0000123 liver PATO:0000587 decreased size abnormal ZDB-GENE-020530-1 246226 5742 ptgs1 ZFA:0005242 multi-ciliated epithelial cell BFO:0000050 part_of ZFA:0000150 pronephric duct PATO:0002001 has fewer parts of type abnormal GO:0005929 cilium BFO:0000050 part_of ZFA:0005242 multi-ciliated epithelial cell ZDB-GENE-020530-1 246226 5742 ptgs1 ZFA:0005242 multi-ciliated epithelial cell BFO:0000050 part_of ZFA:0000150 pronephric duct PATO:0001997 decreased amount abnormal ZDB-GENE-020530-1 246226 5742 ptgs1 ZFA:0000151 pronephros PATO:0002001 has fewer parts of type abnormal ZFA:0005242 multi-ciliated epithelial cell BFO:0000050 part_of ZFA:0000151 pronephros ZDB-GENE-020530-1 246226 5742 ptgs1 ZFA:0000166 lateral crista PATO:0002001 has fewer parts of type abnormal GO:0060091 kinocilium BFO:0000050 part_of ZFA:0000166 lateral crista ZDB-GENE-020530-1 246226 5742 ptgs1 ZFA:0001094 whole organism PATO:0000169 viability abnormal ZDB-GENE-020530-1 246226 5742 ptgs1 ZFA:0001115 trunk PATO:0001469 curved ventral abnormal ZDB-GENE-020530-1 246226 5742 ptgs1 ZFA:0001117 post-vent region PATO:0001469 curved ventral abnormal ZDB-GENE-020530-1 246226 5742 ptgs1 ZFA:0001249 exocrine pancreas PATO:0000587 decreased size abnormal ZDB-GENE-020530-1 246226 5742 ptgs1 ZFA:0005242 multi-ciliated epithelial cell BFO:0000050 part_of ZFA:0001620 pronephric proximal convoluted tubule PATO:0001997 decreased amount abnormal ZDB-GENE-020530-1 246226 5742 ptgs1 ZFA:0001622 pronephric distal early tubule PATO:0000586 increased size abnormal ZDB-GENE-020530-1 246226 5742 ptgs1 ZFA:0001624 pronephric distal late tubule PATO:0000587 decreased size abnormal ZDB-GENE-020530-1 246226 5742 ptgs1 ZFA:0009014 hematopoietic stem cell PATO:0001997 decreased amount abnormal ZDB-GENE-020530-2 246227 5743 ptgs2a GO:0060271 cilium assembly PATO:0002302 decreased process quality abnormal ZDB-GENE-020530-2 246227 5743 ptgs2a ZFA:0001261 ventricular system BFO:0000050 part_of ZFA:0000008 brain PATO:0001450 edematous abnormal ZDB-GENE-020530-2 246227 5743 ptgs2a ZFA:0000008 brain PATO:0001853 hydrocephalic abnormal ZDB-GENE-020530-2 246227 5743 ptgs2a ZFA:0000054 pericardium PATO:0001450 edematous abnormal ZDB-GENE-020530-2 246227 5743 ptgs2a ZFA:0000123 liver PATO:0000587 decreased size abnormal ZDB-GENE-020530-2 246227 5743 ptgs2a ZFA:0005242 multi-ciliated epithelial cell BFO:0000050 part_of ZFA:0000150 pronephric duct PATO:0002001 has fewer parts of type abnormal GO:0005929 cilium BFO:0000050 part_of ZFA:0005242 multi-ciliated epithelial cell ZDB-GENE-020530-2 246227 5743 ptgs2a ZFA:0005242 multi-ciliated epithelial cell BFO:0000050 part_of ZFA:0000150 pronephric duct PATO:0001997 decreased amount abnormal ZDB-GENE-020530-2 246227 5743 ptgs2a ZFA:0000166 lateral crista PATO:0002001 has fewer parts of type abnormal GO:0060091 kinocilium BFO:0000050 part_of ZFA:0000166 lateral crista ZDB-GENE-020530-2 246227 5743 ptgs2a ZFA:0001249 exocrine pancreas PATO:0000587 decreased size abnormal ZDB-GENE-020530-2 246227 5743 ptgs2a ZFA:0005242 multi-ciliated epithelial cell BFO:0000050 part_of ZFA:0001620 pronephric proximal convoluted tubule PATO:0001997 decreased amount abnormal ZDB-GENE-020530-2 246227 5743 ptgs2a ZFA:0009014 hematopoietic stem cell PATO:0001997 decreased amount abnormal ZDB-GENE-020604-1 246275 4622 myhz2 ZFA:0000135 notochord PATO:0001617 deformed abnormal ZDB-GENE-020604-1 246275 4622 myhz2 GO:0030017 sarcomere BFO:0000050 part_of ZFA:0000628 caudal fin musculature PATO:0000937 disorganized abnormal ZDB-GENE-020604-1 246275 4622 myhz2 ZFA:0009114 muscle cell BFO:0000050 part_of ZFA:0001058 caudal fin PATO:0000646 malformed abnormal ZDB-GENE-020604-1 246275 4622 myhz2 ZFA:0009114 muscle cell BFO:0000050 part_of ZFA:0001058 caudal fin PATO:0001617 deformed abnormal ZDB-GENE-020604-1 246275 4622 myhz2 ZFA:0001094 whole organism PATO:0000574 decreased length abnormal ZDB-GENE-020604-1 246275 4622 myhz2 GO:0030017 sarcomere BFO:0000050 part_of ZFA:0009114 muscle cell PATO:0000937 disorganized abnormal ZDB-GENE-020604-1 246275 4622 myhz2 ZFA:0009114 muscle cell PATO:0000646 malformed abnormal ZDB-GENE-020604-1 246275 4622 myhz2 ZFA:0009114 muscle cell PATO:0001617 deformed abnormal ZDB-GENE-020708-4 252850 7060 thbs4b GO:0005927 muscle tendon junction BFO:0000050 part_of ZFA:0001462 somite border PATO:0000051 morphology abnormal ZDB-GENE-020708-4 252850 7060 thbs4b ZFA:0005145 muscle PATO:0001453 detached from abnormal ZFA:0005647 tendon ZDB-GENE-020709-1 252846 4647 myo7aa GO:0001964 startle response PATO:0002052 decreased occurrence abnormal ZDB-GENE-020709-1 252846 4647 myo7aa GO:0001966 thigmotaxis PATO:0001507 disrupted abnormal ZDB-GENE-020709-1 252846 4647 myo7aa GO:0007610 behavior PATO:0000001 quality abnormal ZDB-GENE-020709-1 252846 4647 myo7aa GO:0008345 larval locomotory behavior PATO:0001236 process quality abnormal ZDB-GENE-020709-1 252846 4647 myo7aa GO:0009605 response to external stimulus PATO:0000001 quality abnormal ZDB-GENE-020709-1 252846 4647 myo7aa GO:0010996 response to auditory stimulus PATO:0002052 decreased occurrence abnormal ZDB-GENE-020709-1 252846 4647 myo7aa GO:0036372 opsin transport PATO:0002302 decreased process quality abnormal ZDB-GENE-020709-1 252846 4647 myo7aa GO:0050881 musculoskeletal movement PATO:0000001 quality abnormal ZDB-GENE-020709-1 252846 4647 myo7aa GO:0050885 neuromuscular process controlling balance PATO:0000001 quality abnormal ZDB-GENE-020709-1 252846 4647 myo7aa GO:0050908 detection of light stimulus involved in visual perception PATO:0001236 process quality abnormal ZDB-GENE-020709-1 252846 4647 myo7aa GO:0051602 response to electrical stimulus PATO:0001507 disrupted abnormal ZDB-GENE-020709-1 252846 4647 myo7aa GO:0060088 auditory receptor cell stereocilium organization PATO:0001507 disrupted abnormal ZDB-GENE-020709-1 252846 4647 myo7aa GO:0060122 inner ear receptor cell stereocilium organization PATO:0001507 disrupted abnormal ZDB-GENE-020709-1 252846 4647 myo7aa ZFA:0000076 swim bladder PATO:0002377 uninflated abnormal ZDB-GENE-020709-1 252846 4647 myo7aa GO:0032421 stereocilium bundle BFO:0000050 part_of ZFA:0000168 anterior macula PATO:0000617 bent abnormal ZDB-GENE-020709-1 252846 4647 myo7aa GO:0032421 stereocilium bundle BFO:0000050 part_of ZFA:0000168 anterior macula PATO:0001785 splayed abnormal ZDB-GENE-020709-1 252846 4647 myo7aa GO:0032420 stereocilium BFO:0000050 part_of ZFA:0000678 hair cell anterior macula PATO:0001997 decreased amount abnormal ZDB-GENE-020709-1 252846 4647 myo7aa ZFA:0001094 whole organism PATO:0000052 shape abnormal ZDB-GENE-020709-1 252846 4647 myo7aa ZFA:0001094 whole organism PATO:0000758 unbalanced abnormal ZDB-GENE-020709-1 252846 4647 myo7aa ZFA:0001094 whole organism PATO:0000761 decreased behavioural activity abnormal ZDB-GENE-020709-1 252846 4647 myo7aa ZFA:0001094 whole organism PATO:0001911 circling abnormal ZDB-GENE-020709-1 252846 4647 myo7aa GO:0006915 apoptotic process BFO:0000066 occurs_in ZFA:0001464 retinal outer nuclear layer PATO:0002304 increased process quality abnormal ZDB-GENE-020709-1 252846 4647 myo7aa GO:0008219 cell death BFO:0000066 occurs_in ZFA:0001464 retinal outer nuclear layer PATO:0002304 increased process quality abnormal ZDB-GENE-020709-1 252846 4647 myo7aa GO:0008021 synaptic vesicle BFO:0000050 part_of ZFA:0001469 lateral line PATO:0001997 decreased amount abnormal ZDB-GENE-020709-1 252846 4647 myo7aa GO:0014069 postsynaptic density BFO:0000050 part_of ZFA:0001469 lateral line PATO:0001997 decreased amount abnormal ZDB-GENE-020709-1 252846 4647 myo7aa GO:0032420 stereocilium BFO:0000050 part_of ZFA:0001469 lateral line PATO:0000937 disorganized abnormal ZDB-GENE-020709-1 252846 4647 myo7aa GO:0032420 stereocilium BFO:0000050 part_of ZFA:0001469 lateral line PATO:0001785 splayed abnormal ZDB-GENE-020709-1 252846 4647 myo7aa GO:0097470 ribbon synapse BFO:0000050 part_of ZFA:0001469 lateral line PATO:0001997 decreased amount abnormal ZDB-GENE-020709-1 252846 4647 myo7aa GO:0097470 ribbon synapse BFO:0000050 part_of ZFA:0001469 lateral line PATO:0002058 decreased area abnormal ZDB-GENE-020709-1 252846 4647 myo7aa GO:0032421 stereocilium bundle BFO:0000050 part_of ZFA:0009121 auditory receptor cell PATO:0000052 shape abnormal ZDB-GENE-020709-1 252846 4647 myo7aa GO:0032421 stereocilium bundle BFO:0000050 part_of ZFA:0009121 auditory receptor cell PATO:0001785 splayed abnormal ZDB-GENE-020709-1 252846 4647 myo7aa ZFA:0009367 neuromast hair cell PATO:0001997 decreased amount abnormal ZDB-GENE-020712-1 252845 64398 pals1a GO:0001841 neural tube formation PATO:0001507 disrupted abnormal ZDB-GENE-020712-1 252845 64398 pals1a GO:0002088 lens development in camera-type eye PATO:0000502 delayed abnormal ZDB-GENE-020712-1 252845 64398 pals1a GO:0003007 heart morphogenesis PATO:0001236 process quality abnormal ZDB-GENE-020712-1 252845 64398 pals1a GO:0003007 heart morphogenesis PATO:0001507 disrupted abnormal ZDB-GENE-020712-1 252845 64398 pals1a GO:0007420 brain development PATO:0001507 disrupted abnormal ZDB-GENE-020712-1 252845 64398 pals1a GO:0008015 blood circulation PATO:0001507 disrupted abnormal ZDB-GENE-020712-1 252845 64398 pals1a GO:0010458 exit from mitosis PATO:0001507 disrupted abnormal ZDB-GENE-020712-1 252845 64398 pals1a GO:0010842 retina layer formation PATO:0001507 disrupted abnormal ZDB-GENE-020712-1 252845 64398 pals1a GO:0021555 midbrain-hindbrain boundary morphogenesis PATO:0001507 disrupted abnormal ZDB-GENE-020712-1 252845 64398 pals1a GO:0021744 dorsal motor nucleus of vagus nerve development PATO:0001507 disrupted abnormal ZDB-GENE-020712-1 252845 64398 pals1a GO:0030318 melanocyte differentiation PATO:0000502 delayed abnormal ZDB-GENE-020712-1 252845 64398 pals1a GO:0035088 establishment or maintenance of apical/basal cell polarity PATO:0001507 disrupted abnormal ZDB-GENE-020712-1 252845 64398 pals1a GO:0035765 motor neuron precursor migration involved in dorsal motor nucleus of vagus nerve formation PATO:0001507 disrupted abnormal ZDB-GENE-020712-1 252845 64398 pals1a GO:0039021 pronephric glomerulus development PATO:0001236 process quality abnormal ZDB-GENE-020712-1 252845 64398 pals1a GO:0043297 apical junction assembly PATO:0001507 disrupted abnormal ZDB-GENE-020712-1 252845 64398 pals1a GO:0045197 establishment or maintenance of epithelial cell apical/basal polarity PATO:0001236 process quality abnormal ZDB-GENE-020712-1 252845 64398 pals1a GO:0048069 eye pigmentation PATO:0001507 disrupted abnormal ZDB-GENE-020712-1 252845 64398 pals1a GO:0048793 pronephros development PATO:0001236 process quality abnormal ZDB-GENE-020712-1 252845 64398 pals1a GO:0060059 embryonic retina morphogenesis in camera-type eye PATO:0001236 process quality abnormal ZDB-GENE-020712-1 252845 64398 pals1a ZFA:0000008 brain PATO:0000001 quality abnormal ZDB-GENE-020712-1 252845 64398 pals1a ZFA:0000008 brain PATO:0000051 morphology abnormal ZDB-GENE-020712-1 252845 64398 pals1a ZFA:0000008 brain PATO:0000052 shape abnormal ZDB-GENE-020712-1 252845 64398 pals1a ZFA:0000008 brain PATO:0001925 surface feature shape abnormal ZDB-GENE-020712-1 252845 64398 pals1a ZFA:0000014 dorsal aorta PATO:0001571 dilated abnormal ZDB-GENE-020712-1 252845 64398 pals1a ZFA:0000029 hindbrain PATO:0000001 quality abnormal ZDB-GENE-020712-1 252845 64398 pals1a GO:0005912 adherens junction BFO:0000050 part_of ZFA:0000035 lens PATO:0000462 absent abnormal ZDB-GENE-020712-1 252845 64398 pals1a ZFA:0009034 epithelial cell BFO:0000050 part_of ZFA:0000035 lens PATO:0000628 mislocalised abnormal ZDB-GENE-020712-1 252845 64398 pals1a ZFA:0009034 epithelial cell BFO:0000050 part_of ZFA:0000035 lens PATO:0001997 decreased amount abnormal ZDB-GENE-020712-1 252845 64398 pals1a ZFA:0000035 lens PATO:0000141 structure abnormal ZDB-GENE-020712-1 252845 64398 pals1a ZFA:0000035 lens PATO:0002112 perforate abnormal ZDB-GENE-020712-1 252845 64398 pals1a ZFA:0000042 midbrain hindbrain boundary PATO:0000051 morphology abnormal ZDB-GENE-020712-1 252845 64398 pals1a GO:0043296 apical junction complex BFO:0000050 part_of ZFA:0000046 retinal neural layer PATO:0000628 mislocalised abnormal ZDB-GENE-020712-1 252845 64398 pals1a ZFA:0000046 retinal neural layer PATO:0000937 disorganized abnormal ZDB-GENE-020712-1 252845 64398 pals1a ZFA:0000046 retinal neural layer PATO:0001769 positional polarity abnormal ZDB-GENE-020712-1 252845 64398 pals1a ZFA:0000054 pericardium PATO:0001450 edematous abnormal ZDB-GENE-020712-1 252845 64398 pals1a ZFA:0009075 astrocyte BFO:0000050 part_of ZFA:0000059 postoptic commissure PATO:0000628 mislocalised abnormal ZDB-GENE-020712-1 252845 64398 pals1a ZFA:0000059 postoptic commissure PATO:0000051 morphology abnormal ZDB-GENE-020712-1 252845 64398 pals1a ZFA:0000059 postoptic commissure PATO:0001959 defasciculated abnormal ZDB-GENE-020712-1 252845 64398 pals1a ZFA:0000098 proliferative region BFO:0000050 part_of ZFA:0000107 eye PATO:0000586 increased size abnormal ZDB-GENE-020712-1 252845 64398 pals1a ZFA:0000098 proliferative region BFO:0000050 part_of ZFA:0000107 eye PATO:0000628 mislocalised abnormal ZDB-GENE-020712-1 252845 64398 pals1a ZFA:0000107 eye PATO:0000001 quality abnormal ZDB-GENE-020712-1 252845 64398 pals1a GO:0071679 commissural neuron axon guidance BFO:0000066 occurs_in ZFA:0000109 forebrain PATO:0001507 disrupted abnormal ZDB-GENE-020712-1 252845 64398 pals1a ZFA:0000110 fourth ventricle PATO:0000596 decreased volume abnormal ZDB-GENE-020712-1 252845 64398 pals1a ZFA:0000110 fourth ventricle PATO:0001715 decreased diameter abnormal ZDB-GENE-020712-1 252845 64398 pals1a ZFA:0000112 gut PATO:0000587 decreased size abnormal ZDB-GENE-020712-1 252845 64398 pals1a ZFA:0000114 heart PATO:0000001 quality abnormal ZDB-GENE-020712-1 252845 64398 pals1a ZFA:0000114 heart PATO:0001450 edematous abnormal ZDB-GENE-020712-1 252845 64398 pals1a ZFA:0000114 heart PATO:0001501 immature abnormal ZDB-GENE-020712-1 252845 64398 pals1a ZFA:0000144 retinal pigmented epithelium PATO:0000001 quality abnormal ZDB-GENE-020712-1 252845 64398 pals1a ZFA:0000144 retinal pigmented epithelium PATO:0001608 patchy abnormal ZDB-GENE-020712-1 252845 64398 pals1a ZFA:0000144 retinal pigmented epithelium PATO:0002106 poorly differentiated abnormal ZDB-GENE-020712-1 252845 64398 pals1a ZFA:0000144 retinal pigmented epithelium PATO:0002112 perforate abnormal ZDB-GENE-020712-1 252845 64398 pals1a ZFA:0000152 retina PATO:0000001 quality abnormal ZDB-GENE-020712-1 252845 64398 pals1a ZFA:0000152 retina PATO:0000638 apoptotic abnormal ZDB-GENE-020712-1 252845 64398 pals1a ZFA:0000152 retina PATO:0000937 disorganized abnormal ZDB-GENE-020712-1 252845 64398 pals1a ZFA:0000152 retina PATO:0001501 immature abnormal ZDB-GENE-020712-1 252845 64398 pals1a ZFA:0000282 sensory system PATO:0000001 quality abnormal ZDB-GENE-020712-1 252845 64398 pals1a ZFA:0009316 cardiac muscle cell BFO:0000050 part_of ZFA:0000360 heart tube PATO:0000117 size abnormal ZDB-GENE-020712-1 252845 64398 pals1a ZFA:0009316 cardiac muscle cell BFO:0000050 part_of ZFA:0000360 heart tube PATO:0000141 structure abnormal ZDB-GENE-020712-1 252845 64398 pals1a ZFA:0000360 heart tube PATO:0000051 morphology abnormal ZDB-GENE-020712-1 252845 64398 pals1a ZFA:0000360 heart tube PATO:0000574 decreased length abnormal ZDB-GENE-020712-1 252845 64398 pals1a ZFA:0000396 nervous system PATO:0000001 quality abnormal ZDB-GENE-020712-1 252845 64398 pals1a ZFA:0000435 cranial nerve II PATO:0001959 defasciculated abnormal ZDB-GENE-020712-1 252845 64398 pals1a BSPO:0000005 anatomical surface BFO:0000050 part_of ZFA:0000640 cornea PATO:0000141 structure abnormal ZDB-GENE-020712-1 252845 64398 pals1a ZFA:0000640 cornea PATO:0000141 structure abnormal ZDB-GENE-020712-1 252845 64398 pals1a ZFA:0000938 central canal PATO:0000646 malformed abnormal ZDB-GENE-020712-1 252845 64398 pals1a ZFA:0001094 whole organism PATO:0000052 shape abnormal ZDB-GENE-020712-1 252845 64398 pals1a ZFA:0001094 whole organism PATO:0000406 curved abnormal ZDB-GENE-020712-1 252845 64398 pals1a ZFA:0001094 whole organism PATO:0000617 bent abnormal ZDB-GENE-020712-1 252845 64398 pals1a ZFA:0001094 whole organism PATO:0001450 edematous abnormal ZDB-GENE-020712-1 252845 64398 pals1a ZFA:0001094 whole organism PATO:0001469 curved ventral abnormal ZDB-GENE-020712-1 252845 64398 pals1a ZFA:0009075 astrocyte BFO:0000050 part_of ZFA:0001108 anterior commissure PATO:0000628 mislocalised abnormal ZDB-GENE-020712-1 252845 64398 pals1a ZFA:0001108 anterior commissure PATO:0000051 morphology abnormal ZDB-GENE-020712-1 252845 64398 pals1a ZFA:0001108 anterior commissure PATO:0001959 defasciculated abnormal ZDB-GENE-020712-1 252845 64398 pals1a ZFA:0001114 head PATO:0000587 decreased size abnormal ZDB-GENE-020712-1 252845 64398 pals1a ZFA:0001114 head PATO:0001925 surface feature shape abnormal ZDB-GENE-020712-1 252845 64398 pals1a ZFA:0001115 trunk PATO:0001468 curved dorsal abnormal ZDB-GENE-020712-1 252845 64398 pals1a ZFA:0001115 trunk PATO:0001469 curved ventral abnormal ZDB-GENE-020712-1 252845 64398 pals1a ZFA:0001117 post-vent region PATO:0000405 curled abnormal ZDB-GENE-020712-1 252845 64398 pals1a ZFA:0001135 neural tube PATO:0000646 malformed abnormal ZDB-GENE-020712-1 252845 64398 pals1a ZFA:0009248 neuron BFO:0000050 part_of ZFA:0001202 optic cup PATO:0001997 decreased amount abnormal ZDB-GENE-020712-1 252845 64398 pals1a ZFA:0001261 ventricular system PATO:0000587 decreased size abnormal ZDB-GENE-020712-1 252845 64398 pals1a GO:0005912 adherens junction BFO:0000050 part_of ZFA:0001326 lens epithelium PATO:0000628 mislocalised abnormal ZDB-GENE-020712-1 252845 64398 pals1a ZFA:0001329 retinal inner plexiform layer PATO:0001608 patchy abnormal ZDB-GENE-020712-1 252845 64398 pals1a ZFA:0001330 retinal outer plexiform layer PATO:0001608 patchy abnormal ZDB-GENE-020712-1 252845 64398 pals1a ZFA:0001439 anatomical system PATO:0000001 quality abnormal ZDB-GENE-020712-1 252845 64398 pals1a ZFA:0001557 pronephric glomerulus PATO:0000651 unfused from abnormal ZFA:0001557 pronephric glomerulus ZDB-GENE-020712-1 252845 64398 pals1a ZFA:0001557 pronephric glomerulus PATO:0002000 lacks all parts of type abnormal ZFA:0005309 pronephric glomerular capillary ZDB-GENE-020712-1 252845 64398 pals1a ZFA:0001557 pronephric glomerulus PATO:0000051 morphology abnormal ZDB-GENE-020712-1 252845 64398 pals1a ZFA:0001557 pronephric glomerulus PATO:0000645 hypoplastic abnormal ZDB-GENE-020712-1 252845 64398 pals1a ZFA:0001557 pronephric glomerulus PATO:0000937 disorganized abnormal ZDB-GENE-020712-1 252845 64398 pals1a ZFA:0001655 pericardial cavity PATO:0000586 increased size abnormal ZDB-GENE-020712-1 252845 64398 pals1a ZFA:0001673 pronephric podocyte PATO:0001241 physical object quality abnormal ZDB-GENE-020712-1 252845 64398 pals1a GO:0030057 desmosome BFO:0000050 part_of ZFA:0001683 corneal epithelium PATO:0001997 decreased amount abnormal ZDB-GENE-020712-1 252845 64398 pals1a ZFA:0001683 corneal epithelium PATO:0001987 saccular abnormal ZDB-GENE-020712-1 252845 64398 pals1a ZFA:0001685 corneal stroma PATO:0000937 disorganized abnormal ZDB-GENE-020712-1 252845 64398 pals1a ZFA:0001695 dorsolateral motor nucleus of vagal nerve PATO:0000646 malformed abnormal ZDB-GENE-020712-1 252845 64398 pals1a ZFA:0007067 vagal ganglion PATO:0000642 fused with abnormal ZFA:0007067 vagal ganglion ZDB-GENE-020712-1 252845 64398 pals1a ZFA:0009090 pigment cell PATO:0000001 quality abnormal ZDB-GENE-020712-1 252845 64398 pals1a ZFA:0009091 melanocyte PATO:0000001 quality abnormal ZDB-GENE-020712-1 252845 64398 pals1a ZFA:0009264 corneal epithelial cell PATO:0001531 cellular adhesivity abnormal ZFA:0009264 corneal epithelial cell ZDB-GENE-020712-1 252845 64398 pals1a GO:0045177 apical part of cell BFO:0000050 part_of ZFA:0009306 neuroepithelial cell PATO:0000599 decreased width abnormal ZDB-GENE-020712-1 252845 64398 pals1a ZFA:0009306 neuroepithelial cell PATO:0001769 positional polarity abnormal ZDB-GENE-020712-1 252845 64398 pals1a GO:0043296 apical junction complex BFO:0000050 part_of ZFA:0009316 cardiac muscle cell PATO:0000141 structure abnormal ZDB-GENE-020712-1 252845 64398 pals1a ZFA:0009401 lens fiber cell PATO:0000470 increased amount abnormal ZDB-GENE-020717-1 252913 94239 h2az2a GO:0043473 pigmentation PATO:0002052 decreased occurrence abnormal ZDB-GENE-020717-1 252913 94239 h2az2a ZFA:0009067 CNS neuron (sensu Vertebrata) BFO:0000050 part_of ZFA:0000075 spinal cord PATO:0000628 mislocalised abnormal ZDB-GENE-020717-1 252913 94239 h2az2a ZFA:0009091 melanocyte BFO:0000050 part_of ZFA:0001114 head PATO:0001997 decreased amount abnormal ZDB-GENE-020717-1 252913 94239 h2az2a ZFA:0009091 melanocyte BFO:0000050 part_of ZFA:0001469 lateral line PATO:0001997 decreased amount abnormal ZDB-GENE-020717-1 252913 94239 h2az2a ZFA:0009135 myelinating Schwann cell BFO:0000050 part_of ZFA:0001469 lateral line PATO:0001997 decreased amount abnormal ZDB-GENE-020717-1 252913 94239 h2az2a ZFA:0009091 melanocyte PATO:0001997 decreased amount abnormal ZDB-GENE-020717-1 252913 94239 h2az2a ZFA:0009165 neural crest cell PATO:0001997 decreased amount abnormal ZDB-GENE-020717-1 252913 94239 h2az2a ZFA:0009249 melanoblast PATO:0001997 decreased amount abnormal ZDB-GENE-020731-1 259186 57575 pcdh10a ZFA:0009091 melanocyte BFO:0000050 part_of ZFA:0001463 melanophore stripe PATO:0001997 decreased amount abnormal ZDB-GENE-020731-1 259186 57575 pcdh10a ZFA:0001463 melanophore stripe PATO:0000051 morphology abnormal ZDB-GENE-020731-1 259186 57575 pcdh10a ZFA:0007086 migratory neural crest cell PATO:0000628 mislocalised abnormal ZDB-GENE-020731-1 259186 57575 pcdh10a ZFA:0007086 migratory neural crest cell PATO:0001629 aggregated abnormal ZDB-GENE-020731-1 259186 57575 pcdh10a ZFA:0009091 melanocyte PATO:0000628 mislocalised abnormal ZDB-GENE-020731-1 259186 57575 pcdh10a ZFA:0009249 melanoblast PATO:0000628 mislocalised abnormal ZDB-GENE-020731-6 259191 2332 fmr1 GO:0006950 response to stress PATO:0001236 process quality abnormal ZDB-GENE-020731-6 259191 2332 fmr1 GO:0007411 axon guidance PATO:0001507 disrupted abnormal ZDB-GENE-020731-6 259191 2332 fmr1 GO:0007414 axonal defasciculation PATO:0001236 process quality abnormal ZDB-GENE-020731-6 259191 2332 fmr1 GO:0007611 learning or memory PATO:0001236 process quality abnormal ZDB-GENE-020731-6 259191 2332 fmr1 GO:0007626 locomotory behavior PATO:0000912 increased rate abnormal ZDB-GENE-020731-6 259191 2332 fmr1 GO:0031987 locomotion involved in locomotory behavior PATO:0002051 increased occurrence abnormal ZDB-GENE-020731-6 259191 2332 fmr1 GO:0035176 social behavior PATO:0001236 process quality abnormal ZDB-GENE-020731-6 259191 2332 fmr1 GO:0035178 turning behavior PATO:0001236 process quality abnormal ZDB-GENE-020731-6 259191 2332 fmr1 GO:0035640 exploration behavior PATO:0001236 process quality abnormal ZDB-GENE-020731-6 259191 2332 fmr1 GO:0035641 locomotory exploration behavior PATO:0001236 process quality abnormal ZDB-GENE-020731-6 259191 2332 fmr1 GO:0036268 swimming PATO:0040032 increased linear velocity abnormal ZDB-GENE-020731-6 259191 2332 fmr1 GO:0036268 swimming PATO:0055002 increased spatial extent of a process abnormal ZDB-GENE-020731-6 259191 2332 fmr1 GO:0060291 long-term synaptic potentiation PATO:0002018 decreased magnitude abnormal ZDB-GENE-020731-6 259191 2332 fmr1 GO:0060384 innervation PATO:0002052 decreased occurrence abnormal ZDB-GENE-020731-6 259191 2332 fmr1 GO:0016556 mRNA modification BFO:0000066 occurs_in ZFA:0000008 brain PATO:0002051 increased occurrence abnormal ZDB-GENE-020731-6 259191 2332 fmr1 ZFA:0000008 brain PATO:0000937 disorganized abnormal ZDB-GENE-020731-6 259191 2332 fmr1 ZFA:0000008 brain PATO:0001853 hydrocephalic abnormal ZDB-GENE-020731-6 259191 2332 fmr1 ZFA:0000042 midbrain hindbrain boundary PATO:0000051 morphology abnormal ZDB-GENE-020731-6 259191 2332 fmr1 ZFA:0000054 pericardium PATO:0001450 edematous abnormal ZDB-GENE-020731-6 259191 2332 fmr1 GO:0050910 detection of mechanical stimulus involved in sensory perception of sound BFO:0000066 occurs_in ZFA:0000079 telencephalon PATO:0015003 decreased efficacy abnormal ZDB-GENE-020731-6 259191 2332 fmr1 BSPO:0000084 ventral region BFO:0000050 part_of ZFA:0000101 diencephalon PATO:0000051 morphology abnormal ZDB-GENE-020731-6 259191 2332 fmr1 ZFA:0000106 extension PATO:0000587 decreased size abnormal ZDB-GENE-020731-6 259191 2332 fmr1 ZFA:0000110 fourth ventricle PATO:0000051 morphology abnormal ZDB-GENE-020731-6 259191 2332 fmr1 ZFA:0000135 notochord PATO:0000967 undulate abnormal ZDB-GENE-020731-6 259191 2332 fmr1 GO:0030424 axon BFO:0000050 part_of ZFA:0000295 trigeminal ganglion PATO:0002285 increased branchiness abnormal ZDB-GENE-020731-6 259191 2332 fmr1 GO:0043679 axon terminus BFO:0000050 part_of ZFA:0000295 trigeminal ganglion PATO:0000470 increased amount abnormal ZDB-GENE-020731-6 259191 2332 fmr1 ZFA:0000295 trigeminal ganglion PATO:0002001 has fewer parts of type abnormal ZFA:0009053 sensory neuron ZDB-GENE-020731-6 259191 2332 fmr1 ZFA:0000304 ventral telencephalon PATO:0000051 morphology abnormal ZDB-GENE-020731-6 259191 2332 fmr1 GO:0030424 axon BFO:0000050 part_of ZFA:0000534 lateral longitudinal fasciculus PATO:0001959 defasciculated abnormal ZDB-GENE-020731-6 259191 2332 fmr1 ZFA:0000534 lateral longitudinal fasciculus PATO:0000574 decreased length abnormal ZDB-GENE-020731-6 259191 2332 fmr1 GO:0060402 calcium ion transport into cytosol BFO:0000066 occurs_in ZFA:0000599 torus semicircularis PATO:0002051 increased occurrence abnormal ZDB-GENE-020731-6 259191 2332 fmr1 ZFA:0000641 cranial nerve PATO:0000140 position abnormal ZDB-GENE-020731-6 259191 2332 fmr1 ZFA:0000737 cranium PATO:0000599 decreased width abnormal ZDB-GENE-020731-6 259191 2332 fmr1 GO:0016556 mRNA modification BFO:0000066 occurs_in ZFA:0001094 whole organism PATO:0002051 increased occurrence abnormal ZDB-GENE-020731-6 259191 2332 fmr1 ZFA:0001094 whole organism PATO:0000760 increased behavioural activity abnormal ZDB-GENE-020731-6 259191 2332 fmr1 BSPO:0000036 anterior-most region BFO:0000050 part_of ZFA:0001114 head PATO:0000936 truncated abnormal ZDB-GENE-020731-6 259191 2332 fmr1 BSPO:0000036 anterior-most region BFO:0000050 part_of ZFA:0001114 head PATO:0002254 flattened abnormal ZDB-GENE-020731-6 259191 2332 fmr1 ZFA:0001205 Meckel's cartilage PATO:0002327 increased angle to abnormal BSPO:0000013 anterior-posterior axis BFO:0000050 part_of ZFA:0001094 whole organism ZDB-GENE-020731-6 259191 2332 fmr1 ZFA:0001205 Meckel's cartilage PATO:0000574 decreased length abnormal ZDB-GENE-020731-6 259191 2332 fmr1 ZFA:0001205 Meckel's cartilage PATO:0000600 increased width abnormal ZDB-GENE-020731-6 259191 2332 fmr1 GO:0060402 calcium ion transport into cytosol BFO:0000066 occurs_in ZFA:0001215 thalamus PATO:0002051 increased occurrence abnormal ZDB-GENE-020731-6 259191 2332 fmr1 ZFA:0001259 forebrain ventricle PATO:0000051 morphology abnormal ZDB-GENE-020731-6 259191 2332 fmr1 ZFA:0001261 ventricular system PATO:0001602 distended abnormal ZDB-GENE-020731-6 259191 2332 fmr1 ZFA:0001273 ventral mandibular arch PATO:0000574 decreased length abnormal ZDB-GENE-020731-6 259191 2332 fmr1 ZFA:0001400 ceratohyal cartilage PATO:0002327 increased angle to abnormal ZFA:0001510 basihyal cartilage ZDB-GENE-020731-6 259191 2332 fmr1 ZFA:0001400 ceratohyal cartilage PATO:0000574 decreased length abnormal ZDB-GENE-020731-6 259191 2332 fmr1 GO:0007416 synapse assembly BFO:0000066 occurs_in ZFA:0005778 hypocretin-secreting neuron PATO:0002051 increased occurrence abnormal ZDB-GENE-020731-6 259191 2332 fmr1 GO:0007416 synapse assembly BFO:0000066 occurs_in ZFA:0009052 motor neuron PATO:0002051 increased occurrence abnormal ZDB-GENE-020731-6 259191 2332 fmr1 GO:0048668 collateral sprouting BFO:0000066 occurs_in ZFA:0009052 motor neuron PATO:0002051 increased occurrence abnormal ZDB-GENE-020731-6 259191 2332 fmr1 GO:0007416 synapse assembly BFO:0000066 occurs_in ZFA:0009060 cholinergic neuron PATO:0002051 increased occurrence abnormal ZDB-GENE-020731-6 259191 2332 fmr1 GO:0030424 axon BFO:0000050 part_of ZFA:0009150 Rohon-Beard neuron PATO:0002285 increased branchiness abnormal ZDB-GENE-020731-6 259191 2332 fmr1 GO:0043679 axon terminus BFO:0000050 part_of ZFA:0009150 Rohon-Beard neuron PATO:0000470 increased amount abnormal ZDB-GENE-020801-1 259187 583 bbs2 GO:0007369 gastrulation PATO:0001507 disrupted abnormal ZDB-GENE-020801-1 259187 583 bbs2 GO:0007634 optokinetic behavior PATO:0002302 decreased process quality abnormal ZDB-GENE-020801-1 259187 583 bbs2 GO:0042074 cell migration involved in gastrulation PATO:0001507 disrupted abnormal ZDB-GENE-020801-1 259187 583 bbs2 GO:0048793 pronephros development PATO:0001507 disrupted abnormal ZDB-GENE-020801-1 259187 583 bbs2 GO:0060026 convergent extension PATO:0001236 process quality abnormal ZDB-GENE-020801-1 259187 583 bbs2 ZFA:0000135 notochord PATO:0000600 increased width abnormal ZDB-GENE-020801-1 259187 583 bbs2 ZFA:0000135 notochord PATO:0001798 kinked abnormal ZDB-GENE-020801-1 259187 583 bbs2 ZFA:0009077 microglial cell BFO:0000050 part_of ZFA:0000144 retinal pigmented epithelium PATO:0000470 increased amount abnormal ZDB-GENE-020801-1 259187 583 bbs2 GO:0008283 cell population proliferation BFO:0000066 occurs_in ZFA:0000152 retina PATO:0002304 increased process quality abnormal ZDB-GENE-020801-1 259187 583 bbs2 ZFA:0001466 photoreceptor outer segment layer BFO:0000050 part_of ZFA:0000152 retina PATO:0000574 decreased length abnormal ZDB-GENE-020801-1 259187 583 bbs2 ZFA:0001466 photoreceptor outer segment layer BFO:0000050 part_of ZFA:0000152 retina PATO:0000592 decreased thickness abnormal ZDB-GENE-020801-1 259187 583 bbs2 ZFA:0001466 photoreceptor outer segment layer BFO:0000050 part_of ZFA:0000152 retina PATO:0000937 disorganized abnormal ZDB-GENE-020801-1 259187 583 bbs2 ZFA:0009262 retinal cone cell BFO:0000050 part_of ZFA:0000152 retina PATO:0001997 decreased amount abnormal ZDB-GENE-020801-1 259187 583 bbs2 ZFA:0000155 somite PATO:0000600 increased width abnormal ZDB-GENE-020801-1 259187 583 bbs2 BSPO:0000013 anterior-posterior axis BFO:0000050 part_of ZFA:0001094 whole organism PATO:0000574 decreased length abnormal ZDB-GENE-020801-1 259187 583 bbs2 ZFA:0001094 whole organism PATO:0000574 decreased length abnormal ZDB-GENE-020801-1 259187 583 bbs2 ZFA:0009077 microglial cell BFO:0000050 part_of ZFA:0001466 photoreceptor outer segment layer PATO:0000470 increased amount abnormal ZDB-GENE-020801-1 259187 583 bbs2 ZFA:0001559 vertebral column PATO:0000406 curved abnormal ZDB-GENE-020801-1 259187 583 bbs2 ZFA:0001559 vertebral column PATO:0001798 kinked abnormal ZDB-GENE-020801-1 259187 583 bbs2 ZFA:0001620 pronephric proximal convoluted tubule PATO:0000051 morphology abnormal ZDB-GENE-020801-1 259187 583 bbs2 ZFA:0009077 microglial cell BFO:0000050 part_of ZFA:0005229 optic choroid PATO:0000470 increased amount abnormal ZDB-GENE-020802-4 259195 8573 caska ZFA:0001708 cerebellar white matter BFO:0000050 part_of ZFA:0000100 cerebellum PATO:0001997 decreased amount abnormal ZDB-GENE-020802-4 259195 8573 caska ZFA:0000188 corpus cerebelli PATO:0000051 morphology abnormal ZDB-GENE-020802-4 259195 8573 caska ZFA:0000188 corpus cerebelli PATO:0000645 hypoplastic abnormal ZDB-GENE-020802-4 259195 8573 caska ZFA:0001114 head PATO:0000587 decreased size abnormal ZDB-GENE-020806-3 259260 4485 mst1 GO:0030282 bone mineralization PATO:0000502 delayed abnormal ZDB-GENE-020806-3 259260 4485 mst1 ZFA:0009048 granulocyte BFO:0000050 part_of ZFA:0001076 intestinal bulb PATO:0000470 increased amount abnormal ZDB-GENE-020806-3 259260 4485 mst1 ZFA:0009094 goblet cell BFO:0000050 part_of ZFA:0001338 intestine PATO:0000470 increased amount abnormal ZDB-GENE-020806-3 259260 4485 mst1 GO:0008283 cell population proliferation BFO:0000066 occurs_in ZFA:0009399 intestinal epithelial cell PATO:0000912 increased rate abnormal ZDB-GENE-020806-4 79381 2950 gstp1.2 GO:0004364 glutathione transferase activity PATO:0002018 decreased magnitude abnormal ZDB-GENE-020806-4 79381 2950 gstp1.2 CHEBI:16856 glutathione BFO:0000050 part_of ZFA:0001094 whole organism PATO:0000470 increased amount abnormal ZDB-GENE-020806-4 79381 2950 gstp1.2 CHEBI:17858 glutathione disulfide BFO:0000050 part_of ZFA:0001094 whole organism PATO:0001997 decreased amount abnormal ZDB-GENE-020806-4 79381 2950 gstp1.2 CHEBI:26523 reactive oxygen species BFO:0000050 part_of ZFA:0001094 whole organism PATO:0001997 decreased amount abnormal ZDB-GENE-020806-4 79381 2950 gstp1.2 ZFA:0001094 whole organism PATO:0001549 increased sensitivity toward abnormal CHEBI:29699 tunicamycin BFO:0000050 part_of ZFA:0001094 whole organism ZDB-GENE-020806-4 79381 2950 gstp1.2 ZFA:0001094 whole organism PATO:0001549 increased sensitivity toward abnormal CHEBI:9516 thapsigargin BFO:0000050 part_of ZFA:0001094 whole organism ZDB-GENE-020806-4 79381 2950 gstp1.2 ZFA:0001094 whole organism PATO:0000169 viability abnormal ZDB-GENE-020806-5 259252 2099 esr1 GO:0007530 sex determination PATO:0001236 process quality abnormal ZDB-GENE-020806-5 259252 2099 esr1 GO:0048920 posterior lateral line neuromast primordium migration PATO:0000911 decreased rate abnormal ZDB-GENE-020806-5 259252 2099 esr1 GO:0048920 posterior lateral line neuromast primordium migration PATO:0001236 process quality abnormal ZDB-GENE-020806-5 259252 2099 esr1 ZFA:0000242 male organism PATO:0001470 proportionality to abnormal ZFA:0000303 female organism ZDB-GENE-020806-5 259252 2099 esr1 ZFA:0000242 male organism PATO:0000470 increased amount abnormal ZDB-GENE-020806-5 259252 2099 esr1 CHEBI:23965 estradiol BFO:0000050 part_of ZFA:0000303 female organism PATO:0000470 increased amount abnormal ZDB-GENE-020806-5 259252 2099 esr1 CHEBI:23965 estradiol BFO:0000050 part_of ZFA:0000303 female organism PATO:0001997 decreased amount abnormal ZDB-GENE-020806-5 259252 2099 esr1 CHEBI:34133 11-oxotestosterone BFO:0000050 part_of ZFA:0000303 female organism PATO:0001997 decreased amount abnormal ZDB-GENE-020806-5 259252 2099 esr1 ZFA:0000303 female organism PATO:0000117 size abnormal ZDB-GENE-020806-5 259252 2099 esr1 ZFA:0000303 female organism PATO:0000582 increased weight abnormal ZDB-GENE-020806-5 259252 2099 esr1 ZFA:0000303 female organism PATO:0000956 sterile abnormal ZDB-GENE-020806-5 259252 2099 esr1 ZFA:0000303 female organism PATO:0001834 decreased fertility abnormal ZDB-GENE-020806-5 259252 2099 esr1 ZFA:0000303 female organism PATO:0001997 decreased amount abnormal ZDB-GENE-020806-5 259252 2099 esr1 ZFA:0000403 ovary PATO:0000639 degenerate abnormal ZDB-GENE-020806-5 259252 2099 esr1 GO:0007296 vitellogenesis BFO:0000066 occurs_in ZFA:0001110 ovarian follicle PATO:0002052 decreased occurrence abnormal ZDB-GENE-020806-5 259252 2099 esr1 ZFA:0001110 ovarian follicle PATO:0015001 absence due to degeneration abnormal ZDB-GENE-020806-5 259252 2099 esr1 ZFA:0001157 posterior lateral line primordium PATO:0000304 decreased speed abnormal ZDB-GENE-020806-5 259252 2099 esr1 ZFA:0001157 posterior lateral line primordium PATO:0000628 mislocalised abnormal ZDB-GENE-020806-5 259252 2099 esr1 ZFA:0001157 posterior lateral line primordium PATO:0001241 physical object quality abnormal ZDB-GENE-020806-5 259252 2099 esr1 ZFA:0001264 ovarian follicle stage IV PATO:0015001 absence due to degeneration abnormal ZDB-GENE-020809-1 560765 54538 robo4 GO:0003260 cardioblast migration PATO:0002302 decreased process quality abnormal ZDB-GENE-020809-1 560765 54538 robo4 GO:0008015 blood circulation PATO:0001236 process quality abnormal ZDB-GENE-020809-1 560765 54538 robo4 ZFA:0000173 bulbus arteriosus PATO:0001624 decreased functionality abnormal ZDB-GENE-020809-1 560765 54538 robo4 ZFA:0009000 cell BFO:0000050 part_of ZFA:0001319 myocardium PATO:0000646 malformed abnormal ZDB-GENE-020809-1 560765 54538 robo4 ZFA:0009000 cell BFO:0000050 part_of ZFA:0001320 endocardium PATO:0000646 malformed abnormal ZDB-GENE-020809-4 259257 116 adcyap1a GO:0007420 brain development PATO:0001507 disrupted abnormal ZDB-GENE-020809-4 259257 116 adcyap1a GO:0043010 camera-type eye development PATO:0001507 disrupted abnormal ZDB-GENE-020809-4 259257 116 adcyap1a ZFA:0000042 midbrain hindbrain boundary PATO:0000141 structure abnormal ZDB-GENE-020809-4 259257 116 adcyap1a ZFA:0000042 midbrain hindbrain boundary PATO:0001617 deformed abnormal ZDB-GENE-020809-4 259257 116 adcyap1a ZFA:0000107 eye PATO:0000587 decreased size abnormal ZDB-GENE-020809-4 259257 116 adcyap1a ZFA:0000109 forebrain PATO:0000141 structure abnormal ZDB-GENE-020809-4 259257 116 adcyap1a ZFA:0000109 forebrain PATO:0001617 deformed abnormal ZDB-GENE-020812-3 259304 57045 twsg1b GO:0002040 sprouting angiogenesis PATO:0001236 process quality abnormal ZDB-GENE-020812-3 259304 57045 twsg1b ZFA:0001057 intersegmental vein PATO:0000646 malformed abnormal ZDB-GENE-020812-3 259304 57045 twsg1b ZFA:0001063 posterior caudal vein PATO:0000646 malformed abnormal ZDB-GENE-020812-3 259304 57045 twsg1b ZFA:0001286 caudal vein plexus PATO:0001571 dilated abnormal ZDB-GENE-020812-3 259304 57045 twsg1b ZFA:0005025 dorsal longitudinal anastomotic vessel PATO:0000646 malformed abnormal ZDB-GENE-020814-2 791793 1525 cxadr GO:0004035 alkaline phosphatase activity PATO:0002052 decreased occurrence abnormal ZDB-GENE-020814-2 791793 1525 cxadr ZFA:0000114 heart PATO:0001450 edematous abnormal ZDB-GENE-020814-2 791793 1525 cxadr ZFA:0000151 pronephros PATO:0001673 cystic abnormal ZDB-GENE-020814-2 791793 1525 cxadr ZFA:0000155 somite PATO:0000051 morphology abnormal ZDB-GENE-020814-2 791793 1525 cxadr ZFA:0000330 cloacal chamber PATO:0001617 deformed abnormal ZDB-GENE-020814-2 791793 1525 cxadr ZFA:0001094 whole organism PATO:0001450 edematous abnormal ZDB-GENE-020814-2 791793 1525 cxadr ZFA:0001117 post-vent region PATO:0001591 curvature abnormal ZDB-GENE-020814-2 791793 1525 cxadr ZFA:0001557 pronephric glomerulus PATO:0000051 morphology abnormal ZDB-GENE-020814-2 791793 1525 cxadr GO:0005886 plasma membrane BFO:0000050 part_of ZFA:0001558 pronephric tubule PATO:0000374 increased distance abnormal GO:0005886 plasma membrane BFO:0000050 part_of ZFA:0001558 pronephric tubule ZDB-GENE-020814-2 791793 1525 cxadr GO:0005902 microvillus BFO:0000050 part_of ZFA:0001558 pronephric tubule PATO:0001997 decreased amount abnormal ZDB-GENE-020814-2 791793 1525 cxadr ZFA:0001486 epithelium BFO:0000050 part_of ZFA:0001558 pronephric tubule PATO:0000141 structure abnormal ZDB-GENE-020814-2 791793 1525 cxadr ZFA:0009143 brush border epithelial cell BFO:0000050 part_of ZFA:0001558 pronephric tubule PATO:0000937 disorganized abnormal ZDB-GENE-020814-2 791793 1525 cxadr GO:0005886 plasma membrane BFO:0000050 part_of ZFA:0005123 gut epithelium PATO:0000374 increased distance abnormal GO:0005886 plasma membrane BFO:0000050 part_of ZFA:0005123 gut epithelium ZDB-GENE-020814-2 791793 1525 cxadr ZFA:0005123 gut epithelium PATO:0000141 structure abnormal ZDB-GENE-020814-2 791793 1525 cxadr ZFA:0009285 podocyte PATO:0000051 morphology abnormal ZDB-GENE-020822-1 260303 5649 reln GO:0021692 cerebellar Purkinje cell layer morphogenesis PATO:0002052 decreased occurrence abnormal ZDB-GENE-020822-1 260303 5649 reln GO:0035176 social behavior PATO:0001236 process quality abnormal ZDB-GENE-020822-1 260303 5649 reln CHEBI:28790 serotonin BFO:0000050 part_of ZFA:0000029 hindbrain PATO:0000470 increased amount abnormal ZDB-GENE-020822-1 260303 5649 reln ZFA:0000358 granular layer corpus cerebelli PATO:0002002 has extra parts of type abnormal ZFA:0009071 Purkinje cell ZDB-GENE-020822-1 260303 5649 reln ZFA:0000358 granular layer corpus cerebelli PATO:0002002 has extra parts of type abnormal ZFA:0009153 eurydendroid cell ZDB-GENE-020822-1 260303 5649 reln ZFA:0000358 granular layer corpus cerebelli PATO:0002002 has extra parts of type abnormal ZFA:0009282 Bergmann glial cell ZDB-GENE-020822-1 260303 5649 reln ZFA:0009248 neuron BFO:0000050 part_of ZFA:0000445 optic tectum PATO:0002178 mislocalised radially abnormal ZDB-GENE-020822-1 260303 5649 reln ZFA:0001706 Purkinje cell layer corpus cerebelli PATO:0002001 has fewer parts of type abnormal ZFA:0009071 Purkinje cell ZDB-GENE-020822-1 260303 5649 reln ZFA:0001706 Purkinje cell layer corpus cerebelli PATO:0002001 has fewer parts of type abnormal ZFA:0009153 eurydendroid cell ZDB-GENE-020822-1 260303 5649 reln GO:0043005 neuron projection BFO:0000050 part_of ZFA:0009071 Purkinje cell PATO:0000613 disoriented abnormal ZDB-GENE-020822-1 260303 5649 reln ZFA:0009071 Purkinje cell PATO:0000624 inserted into abnormal ZFA:0000358 granular layer corpus cerebelli ZDB-GENE-020822-1 260303 5649 reln ZFA:0009153 eurydendroid cell PATO:0000624 inserted into abnormal ZFA:0000358 granular layer corpus cerebelli ZDB-GENE-020822-1 260303 5649 reln ZFA:0009282 Bergmann glial cell PATO:0000624 inserted into abnormal ZFA:0000358 granular layer corpus cerebelli ZDB-GENE-020822-1 260303 5649 reln GO:0043005 neuron projection BFO:0000050 part_of ZFA:0009310 retinal ganglion cell PATO:0000628 mislocalised abnormal ZDB-GENE-020828-1 260350 3037 has2 GO:0001947 heart looping PATO:0001507 disrupted abnormal ZDB-GENE-020828-1 260350 3037 has2 GO:0003146 heart jogging PATO:0002302 decreased process quality abnormal ZDB-GENE-020828-1 260350 3037 has2 GO:0003190 atrioventricular valve formation PATO:0002302 decreased process quality abnormal ZDB-GENE-020828-1 260350 3037 has2 GO:0007368 determination of left/right symmetry PATO:0001507 disrupted abnormal ZDB-GENE-020828-1 260350 3037 has2 GO:0021535 cell migration in hindbrain PATO:0001507 disrupted abnormal ZDB-GENE-020828-1 260350 3037 has2 GO:0060030 dorsal convergence PATO:0001507 disrupted abnormal ZDB-GENE-020828-1 260350 3037 has2 GO:0060956 endocardial cell differentiation PATO:0002302 decreased process quality abnormal ZDB-GENE-020828-1 260350 3037 has2 ZFA:0000082 vein PATO:0001646 protruding out of abnormal ZFA:0001057 intersegmental vein BFO:0000050 part_of ZFA:0001058 caudal fin ZDB-GENE-020828-1 260350 3037 has2 ZFA:0000082 vein PATO:0001646 protruding out of abnormal ZFA:0005035 subintestinal vein BFO:0000050 part_of ZFA:0001058 caudal fin ZDB-GENE-020828-1 260350 3037 has2 ZFA:0000115 heart rudiment PATO:0000628 mislocalised abnormal ZDB-GENE-020828-1 260350 3037 has2 ZFA:0000115 heart rudiment PATO:0001324 bilateral symmetry abnormal ZDB-GENE-020828-1 260350 3037 has2 ZFA:0000115 heart rudiment PATO:0001599 rotated abnormal ZDB-GENE-020828-1 260350 3037 has2 ZFA:0000131 neural keel PATO:0000600 increased width abnormal ZDB-GENE-020828-1 260350 3037 has2 ZFA:0000082 vein BFO:0000050 part_of ZFA:0001058 caudal fin PATO:0001846 tangled abnormal ZDB-GENE-020828-1 260350 3037 has2 ZFA:0001057 intersegmental vein BFO:0000050 part_of ZFA:0001058 caudal fin PATO:0000051 morphology abnormal ZDB-GENE-020828-1 260350 3037 has2 ZFA:0001057 intersegmental vein BFO:0000050 part_of ZFA:0001058 caudal fin PATO:0001571 dilated abnormal ZDB-GENE-020828-1 260350 3037 has2 ZFA:0005035 subintestinal vein BFO:0000050 part_of ZFA:0001058 caudal fin PATO:0000051 morphology abnormal ZDB-GENE-020828-1 260350 3037 has2 ZFA:0005035 subintestinal vein BFO:0000050 part_of ZFA:0001058 caudal fin PATO:0001571 dilated abnormal ZDB-GENE-020828-1 260350 3037 has2 ZFA:0001058 caudal fin PATO:0000051 morphology abnormal ZDB-GENE-020828-1 260350 3037 has2 ZFA:0001486 epithelium BFO:0000050 part_of ZFA:0001135 neural tube PATO:0001473 duplicated abnormal ZDB-GENE-020828-1 260350 3037 has2 ZFA:0001286 caudal vein plexus PATO:0001571 dilated abnormal ZDB-GENE-020828-1 260350 3037 has2 ZFA:0001320 endocardium BFO:0000050 part_of ZFA:0001315 atrioventricular canal PATO:0000574 decreased length abnormal ZDB-GENE-020828-1 260350 3037 has2 ZFA:0001315 atrioventricular canal PATO:0000600 increased width abnormal ZDB-GENE-020828-1 260350 3037 has2 ZFA:0001318 cardiac jelly PATO:0000596 decreased volume abnormal ZDB-GENE-020828-1 260350 3037 has2 ZFA:0009065 endothelial cell BFO:0000050 part_of ZFA:0001616 atrioventricular canal endocardium PATO:0001804 scaly abnormal ZDB-GENE-020829-1 260351 6492 sim1a GO:0009790 embryo development PATO:0000502 delayed abnormal ZDB-GENE-020829-1 260351 6492 sim1a GO:0021979 hypothalamus cell differentiation PATO:0001236 process quality abnormal ZDB-GENE-020829-1 260351 6492 sim1a GO:0035776 pronephric proximal tubule development PATO:0002302 decreased process quality abnormal ZDB-GENE-020829-1 260351 6492 sim1a GO:0039011 pronephric proximal tubule morphogenesis PATO:0001236 process quality abnormal ZDB-GENE-020829-1 260351 6492 sim1a GO:0039011 pronephric proximal tubule morphogenesis PATO:0002302 decreased process quality abnormal ZDB-GENE-020829-1 260351 6492 sim1a GO:0039020 pronephric nephron tubule development PATO:0001236 process quality abnormal ZDB-GENE-020829-1 260351 6492 sim1a GO:0071542 dopaminergic neuron differentiation PATO:0001236 process quality abnormal ZDB-GENE-020829-1 260351 6492 sim1a GO:0097205 renal filtration PATO:0002302 decreased process quality abnormal ZDB-GENE-020829-1 260351 6492 sim1a ZFA:0009186 neurosecretory neuron BFO:0000050 part_of ZFA:0000032 hypothalamus PATO:0001997 decreased amount abnormal ZDB-GENE-020829-1 260351 6492 sim1a ZFA:0009301 dopaminergic neuron BFO:0000050 part_of ZFA:0000032 hypothalamus PATO:0001997 decreased amount abnormal ZDB-GENE-020829-1 260351 6492 sim1a ZFA:0009186 neurosecretory neuron BFO:0000050 part_of ZFA:0000101 diencephalon PATO:0000628 mislocalised abnormal ZDB-GENE-020829-1 260351 6492 sim1a ZFA:0000107 eye PATO:0000587 decreased size abnormal ZDB-GENE-020829-1 260351 6492 sim1a ZFA:0000114 heart PATO:0001450 edematous abnormal ZDB-GENE-020829-1 260351 6492 sim1a ZFA:0000151 pronephros PATO:0002000 lacks all parts of type abnormal ZFA:0001200 corpuscles of Stannius ZDB-GENE-020829-1 260351 6492 sim1a ZFA:0000151 pronephros PATO:0002000 lacks all parts of type abnormal ZFA:0001621 pronephric proximal straight tubule ZDB-GENE-020829-1 260351 6492 sim1a ZFA:0009186 neurosecretory neuron BFO:0000050 part_of ZFA:0000470 preoptic area PATO:0001997 decreased amount abnormal ZDB-GENE-020829-1 260351 6492 sim1a ZFA:0000470 preoptic area PATO:0000051 morphology abnormal ZDB-GENE-020829-1 260351 6492 sim1a ZFA:0009186 neurosecretory neuron BFO:0000050 part_of ZFA:0000633 caudal tuberculum PATO:0001997 decreased amount abnormal ZDB-GENE-020829-1 260351 6492 sim1a ZFA:0009301 dopaminergic neuron BFO:0000050 part_of ZFA:0000633 caudal tuberculum PATO:0001997 decreased amount abnormal ZDB-GENE-020829-1 260351 6492 sim1a ZFA:0001114 head PATO:0000587 decreased size abnormal ZDB-GENE-020829-1 260351 6492 sim1a ZFA:0001114 head PATO:0000638 apoptotic abnormal ZDB-GENE-020829-1 260351 6492 sim1a ZFA:0001620 pronephric proximal convoluted tubule PATO:0001602 distended abnormal ZDB-GENE-020829-1 260351 6492 sim1a ZFA:0001620 pronephric proximal convoluted tubule PATO:0001922 mislocalised posteriorly abnormal ZDB-GENE-020829-1 260351 6492 sim1a ZFA:0001620 pronephric proximal convoluted tubule PATO:0002180 straight abnormal ZDB-GENE-020829-1 260351 6492 sim1a ZFA:0001621 pronephric proximal straight tubule PATO:0000462 absent abnormal ZDB-GENE-020829-1 260351 6492 sim1a ZFA:0001621 pronephric proximal straight tubule PATO:0000587 decreased size abnormal ZDB-GENE-020829-1 260351 6492 sim1a GO:0030424 axon BFO:0000050 part_of ZFA:0001659 diencephalic nucleus PATO:0002168 displaced to abnormal BSPO:0000083 medial region BFO:0000050 part_of ZFA:0000029 hindbrain ZDB-GENE-020829-1 260351 6492 sim1a ZFA:0009098 neuroendocrine cell PATO:0001997 decreased amount abnormal ZDB-GENE-020829-1 260351 6492 sim1a GO:0030424 axon BFO:0000050 part_of ZFA:0009301 dopaminergic neuron PATO:0002168 displaced to abnormal BSPO:0000083 medial region BFO:0000050 part_of ZFA:0000029 hindbrain ZDB-GENE-020829-1 260351 6492 sim1a ZFA:0009301 dopaminergic neuron PATO:0001997 decreased amount abnormal ZDB-GENE-020905-1 260440 487 atp2a1 GO:0001966 thigmotaxis PATO:0001558 lacking processual parts abnormal GO:0014724 regulation of twitch skeletal muscle contraction ZDB-GENE-020905-1 260440 487 atp2a1 GO:0001966 thigmotaxis PATO:0001570 having decreased processual parts abnormal GO:0090076 relaxation of skeletal muscle ZDB-GENE-020905-1 260440 487 atp2a1 GO:0001966 thigmotaxis PATO:0001507 disrupted abnormal ZDB-GENE-020905-1 260440 487 atp2a1 GO:0003009 skeletal muscle contraction PATO:0001507 disrupted abnormal ZDB-GENE-020905-1 260440 487 atp2a1 GO:0007638 mechanosensory behavior PATO:0001236 process quality abnormal ZDB-GENE-020905-1 260440 487 atp2a1 GO:0009605 response to external stimulus PATO:0000001 quality abnormal ZDB-GENE-020905-1 260440 487 atp2a1 GO:0036269 swimming behavior PATO:0002302 decreased process quality abnormal ZDB-GENE-020905-1 260440 487 atp2a1 GO:0040011 locomotion PATO:0001530 behavioral quality of a process abnormal ZDB-GENE-020905-1 260440 487 atp2a1 GO:0050881 musculoskeletal movement PATO:0001507 disrupted abnormal ZDB-GENE-020905-1 260440 487 atp2a1 GO:0050885 neuromuscular process controlling balance PATO:0000001 quality abnormal ZDB-GENE-020905-1 260440 487 atp2a1 GO:0050885 neuromuscular process controlling balance PATO:0001507 disrupted abnormal ZDB-GENE-020905-1 260440 487 atp2a1 ZFA:0000135 notochord PATO:0000639 degenerate abnormal ZDB-GENE-020905-1 260440 487 atp2a1 ZFA:0000135 notochord PATO:0001167 damaged abnormal ZDB-GENE-020905-1 260440 487 atp2a1 ZFA:0000135 notochord PATO:0001485 condensed abnormal ZDB-GENE-020905-1 260440 487 atp2a1 ZFA:0000473 trunk musculature PATO:0000001 quality abnormal ZDB-GENE-020905-1 260440 487 atp2a1 ZFA:0000473 trunk musculature PATO:0001579 contractility abnormal ZDB-GENE-020905-1 260440 487 atp2a1 ZFA:0001094 whole organism PATO:0000052 shape abnormal ZDB-GENE-020905-1 260440 487 atp2a1 ZFA:0001094 whole organism PATO:0000169 viability abnormal ZDB-GENE-020905-1 260440 487 atp2a1 ZFA:0001094 whole organism PATO:0000617 bent abnormal ZDB-GENE-020905-1 260440 487 atp2a1 ZFA:0001094 whole organism PATO:0000718 lethal (sensu genetics) abnormal ZDB-GENE-020905-1 260440 487 atp2a1 ZFA:0001094 whole organism PATO:0002076 movement behavioral quality abnormal ZDB-GENE-020905-1 260440 487 atp2a1 ZFA:0001115 trunk PATO:0000617 bent abnormal ZDB-GENE-020905-1 260440 487 atp2a1 GO:0098723 skeletal muscle myofibril BFO:0000050 part_of ZFA:0009117 fast muscle cell PATO:0000937 disorganized abnormal ZDB-GENE-020905-2 260439 1314 copa GO:0030903 notochord development PATO:0000001 quality abnormal ZDB-GENE-020905-2 260439 1314 copa GO:0048066 developmental pigmentation PATO:0001507 disrupted abnormal ZDB-GENE-020905-2 260439 1314 copa ZFA:0000008 brain PATO:0000001 quality abnormal ZDB-GENE-020905-2 260439 1314 copa ZFA:0000084 yolk PATO:0000001 quality abnormal ZDB-GENE-020905-2 260439 1314 copa ZFA:0000084 yolk PATO:0000051 morphology abnormal ZDB-GENE-020905-2 260439 1314 copa GO:0005604 basement membrane BFO:0000050 part_of ZFA:0000135 notochord PATO:0000462 absent abnormal ZDB-GENE-020905-2 260439 1314 copa GO:0005604 basement membrane BFO:0000050 part_of ZFA:0000135 notochord PATO:0000592 decreased thickness abnormal ZDB-GENE-020905-2 260439 1314 copa GO:0005604 basement membrane BFO:0000050 part_of ZFA:0000135 notochord PATO:0000937 disorganized abnormal ZDB-GENE-020905-2 260439 1314 copa GO:0005783 endoplasmic reticulum BFO:0000050 part_of ZFA:0000135 notochord PATO:0001851 swollen abnormal ZDB-GENE-020905-2 260439 1314 copa GO:0005794 Golgi apparatus BFO:0000050 part_of ZFA:0000135 notochord PATO:0000141 structure abnormal ZDB-GENE-020905-2 260439 1314 copa ZFA:0009000 cell BFO:0000050 part_of ZFA:0000135 notochord PATO:0000141 structure abnormal ZDB-GENE-020905-2 260439 1314 copa ZFA:0000135 notochord PATO:0000001 quality abnormal ZDB-GENE-020905-2 260439 1314 copa ZFA:0000135 notochord PATO:0000574 decreased length abnormal ZDB-GENE-020905-2 260439 1314 copa ZFA:0000135 notochord PATO:0000638 apoptotic abnormal ZDB-GENE-020905-2 260439 1314 copa ZFA:0000135 notochord PATO:0000967 undulate abnormal ZDB-GENE-020905-2 260439 1314 copa ZFA:0000135 notochord PATO:0002100 undifferentiated abnormal ZDB-GENE-020905-2 260439 1314 copa ZFA:0000135 notochord PATO:0002106 poorly differentiated abnormal ZDB-GENE-020905-2 260439 1314 copa ZFA:0000155 somite PATO:0000001 quality abnormal ZDB-GENE-020905-2 260439 1314 copa ZFA:0000155 somite PATO:0000051 morphology abnormal ZDB-GENE-020905-2 260439 1314 copa ZFA:0000155 somite PATO:0000117 size abnormal ZDB-GENE-020905-2 260439 1314 copa ZFA:0000155 somite PATO:0001485 condensed abnormal ZDB-GENE-020905-2 260439 1314 copa ZFA:0000292 surface structure PATO:0000001 quality abnormal ZDB-GENE-020905-2 260439 1314 copa ZFA:0000435 cranial nerve II PATO:0001959 defasciculated abnormal ZDB-GENE-020905-2 260439 1314 copa ZFA:0001094 whole organism PATO:0000169 viability abnormal ZDB-GENE-020905-2 260439 1314 copa ZFA:0001094 whole organism PATO:0000574 decreased length abnormal ZDB-GENE-020905-2 260439 1314 copa ZFA:0001094 whole organism PATO:0000639 degenerate abnormal ZDB-GENE-020905-2 260439 1314 copa ZFA:0001094 whole organism PATO:0000647 necrotic abnormal ZDB-GENE-020905-2 260439 1314 copa ZFA:0001094 whole organism PATO:0000718 lethal (sensu genetics) abnormal ZDB-GENE-020905-2 260439 1314 copa ZFA:0001114 head PATO:0000051 morphology abnormal ZDB-GENE-020905-2 260439 1314 copa ZFA:0001114 head PATO:0001872 cuboid abnormal ZDB-GENE-020905-2 260439 1314 copa GO:0042470 melanosome BFO:0000050 part_of ZFA:0001115 trunk PATO:0000462 absent abnormal ZDB-GENE-020905-2 260439 1314 copa ZFA:0001115 trunk PATO:0000574 decreased length abnormal ZDB-GENE-020905-2 260439 1314 copa GO:0042470 melanosome BFO:0000050 part_of ZFA:0001117 post-vent region PATO:0000462 absent abnormal ZDB-GENE-020905-2 260439 1314 copa ZFA:0009147 glial cell (sensu Vertebrata) BFO:0000050 part_of ZFA:0007009 nerve PATO:0000402 branched abnormal ZDB-GENE-020905-2 260439 1314 copa GO:0042470 melanosome BFO:0000050 part_of ZFA:0009091 melanocyte PATO:0000462 absent abnormal ZDB-GENE-020905-2 260439 1314 copa GO:0005783 endoplasmic reticulum BFO:0000050 part_of ZFA:0009114 muscle cell PATO:0001851 swollen abnormal ZDB-GENE-020905-2 260439 1314 copa GO:0005794 Golgi apparatus BFO:0000050 part_of ZFA:0009114 muscle cell PATO:0000141 structure abnormal ZDB-GENE-020905-3 260437 2956 msh6 GO:0042127 regulation of cell population proliferation PATO:0001507 disrupted abnormal ZDB-GENE-020905-3 260437 2956 msh6 GO:0043570 maintenance of DNA repeat elements PATO:0001507 disrupted abnormal ZDB-GENE-020905-3 260437 2956 msh6 ZFA:0001094 whole organism PATO:0002011 neoplastic abnormal ZDB-GENE-020905-5 406431 5396 prrx1a GO:0001947 heart looping PATO:0001507 disrupted abnormal ZDB-GENE-020905-5 406431 5396 prrx1a GO:0003146 heart jogging PATO:0001236 process quality abnormal ZDB-GENE-020905-5 406431 5396 prrx1a GO:0007507 heart development PATO:0001507 disrupted abnormal ZDB-GENE-020905-5 406431 5396 prrx1a GO:0060973 cell migration involved in heart development PATO:0001236 process quality abnormal ZDB-GENE-020905-5 406431 5396 prrx1a GO:0061371 determination of heart left/right asymmetry PATO:0001507 disrupted abnormal ZDB-GENE-020905-5 406431 5396 prrx1a GO:0086014 atrial cardiac muscle cell action potential PATO:0000499 decreased duration abnormal ZDB-GENE-020905-5 406431 5396 prrx1a GO:0086014 atrial cardiac muscle cell action potential PATO:0001236 process quality abnormal ZDB-GENE-020905-5 406431 5396 prrx1a ZFA:0000114 heart PATO:0001199 linear abnormal ZDB-GENE-020905-5 406431 5396 prrx1a GO:0016477 cell migration BFO:0000066 occurs_in ZFA:0000121 lateral plate mesoderm PATO:0002052 decreased occurrence abnormal ZDB-GENE-020905-5 406431 5396 prrx1a ZFA:0000154 sinus venosus PATO:0000462 absent abnormal ZDB-GENE-020905-5 406431 5396 prrx1a ZFA:0000360 heart tube PATO:0000140 position abnormal ZDB-GENE-020905-5 406431 5396 prrx1a ZFA:0000471 atrium PATO:0000587 decreased size abnormal ZDB-GENE-020910-1 266599 3398 id2a GO:0001754 eye photoreceptor cell differentiation PATO:0002302 decreased process quality abnormal ZDB-GENE-020910-1 266599 3398 id2a GO:0010842 retina layer formation PATO:0001507 disrupted abnormal ZDB-GENE-020910-1 266599 3398 id2a GO:0035881 amacrine cell differentiation PATO:0000297 arrested abnormal ZDB-GENE-020910-1 266599 3398 id2a GO:0042670 retinal cone cell differentiation PATO:0000297 arrested abnormal ZDB-GENE-020910-1 266599 3398 id2a GO:0051320 S phase PATO:0000502 delayed abnormal ZDB-GENE-020910-1 266599 3398 id2a GO:0060040 retinal bipolar neuron differentiation PATO:0001507 disrupted abnormal ZDB-GENE-020910-1 266599 3398 id2a GO:0060059 embryonic retina morphogenesis in camera-type eye PATO:0000502 delayed abnormal ZDB-GENE-020910-1 266599 3398 id2a GO:0060219 camera-type eye photoreceptor cell differentiation PATO:0001507 disrupted abnormal ZDB-GENE-020910-1 266599 3398 id2a GO:0061074 regulation of neural retina development PATO:0001507 disrupted abnormal ZDB-GENE-020910-1 266599 3398 id2a ZFA:0000008 brain PATO:0000587 decreased size abnormal ZDB-GENE-020910-1 266599 3398 id2a ZFA:0009000 cell BFO:0000050 part_of ZFA:0000107 eye PATO:0001997 decreased amount abnormal ZDB-GENE-020910-1 266599 3398 id2a ZFA:0000107 eye PATO:0000587 decreased size abnormal ZDB-GENE-020910-1 266599 3398 id2a ZFA:0009000 cell BFO:0000050 part_of ZFA:0000119 retinal inner nuclear layer PATO:0002100 undifferentiated abnormal ZDB-GENE-020910-1 266599 3398 id2a ZFA:0000119 retinal inner nuclear layer PATO:0001412 unstructured abnormal ZDB-GENE-020910-1 266599 3398 id2a GO:0006915 apoptotic process BFO:0000066 occurs_in ZFA:0000123 liver PATO:0002051 increased occurrence abnormal ZDB-GENE-020910-1 266599 3398 id2a GO:0008283 cell population proliferation BFO:0000066 occurs_in ZFA:0000123 liver PATO:0002052 decreased occurrence abnormal ZDB-GENE-020910-1 266599 3398 id2a ZFA:0000123 liver PATO:0000587 decreased size abnormal ZDB-GENE-020910-1 266599 3398 id2a GO:0008283 cell population proliferation BFO:0000066 occurs_in ZFA:0000152 retina PATO:0001236 process quality abnormal ZDB-GENE-020910-1 266599 3398 id2a ZFA:0009000 cell BFO:0000050 part_of ZFA:0000152 retina PATO:0001997 decreased amount abnormal ZDB-GENE-020910-1 266599 3398 id2a ZFA:0001076 intestinal bulb PATO:0000587 decreased size abnormal ZDB-GENE-020910-1 266599 3398 id2a ZFA:0009000 cell BFO:0000050 part_of ZFA:0001464 retinal outer nuclear layer PATO:0002100 undifferentiated abnormal ZDB-GENE-020910-1 266599 3398 id2a ZFA:0001464 retinal outer nuclear layer PATO:0001412 unstructured abnormal ZDB-GENE-020910-1 266599 3398 id2a ZFA:0005169 intrahepatic bile duct PATO:0001629 aggregated abnormal ZDB-GENE-020910-1 266599 3398 id2a ZFA:0005169 intrahepatic bile duct PATO:0002286 decreased branchiness abnormal ZDB-GENE-020910-1 266599 3398 id2a ZFA:0009255 amacrine cell PATO:0000462 absent abnormal ZDB-GENE-020910-1 266599 3398 id2a ZFA:0009262 retinal cone cell PATO:0000462 absent abnormal ZDB-GENE-020910-1 266599 3398 id2a ZFA:0009275 retinal rod cell PATO:0001997 decreased amount abnormal ZDB-GENE-020910-1 266599 3398 id2a ZFA:0009280 Muller cell PATO:0001997 decreased amount abnormal ZDB-GENE-020910-1 266599 3398 id2a ZFA:0009318 retinal bipolar neuron PATO:0000462 absent abnormal ZDB-GENE-020919-2 266638 22872 sec31a GO:0055123 digestive system development PATO:0001507 disrupted abnormal ZDB-GENE-020919-2 266638 22872 sec31a ZFA:0000123 liver PATO:0000462 absent abnormal ZDB-GENE-020919-2 266638 22872 sec31a ZFA:0000123 liver PATO:0000587 decreased size abnormal ZDB-GENE-020919-2 266638 22872 sec31a ZFA:0001249 exocrine pancreas PATO:0000587 decreased size abnormal ZDB-GENE-020919-2 266638 22872 sec31a ZFA:0001338 intestine PATO:0000587 decreased size abnormal ZDB-GENE-020919-2 266638 22872 sec31a ZFA:0001460 pharyngeal arch cartilage PATO:0000646 malformed abnormal ZDB-GENE-020919-2 266638 22872 sec31a GO:0005783 endoplasmic reticulum BFO:0000050 part_of ZFA:0009084 chondrocyte PATO:0000051 morphology abnormal ZDB-GENE-020919-2 266638 22872 sec31a ZFA:0009139 endodermal cell PATO:0001997 decreased amount abnormal ZDB-GENE-020919-3 266640 146862 unc45b GO:0001947 heart looping PATO:0000297 arrested abnormal ZDB-GENE-020919-3 266640 146862 unc45b GO:0002088 lens development in camera-type eye PATO:0001236 process quality abnormal ZDB-GENE-020919-3 266640 146862 unc45b GO:0008015 blood circulation PATO:0000297 arrested abnormal ZDB-GENE-020919-3 266640 146862 unc45b GO:0008015 blood circulation PATO:0000462 absent abnormal ZDB-GENE-020919-3 266640 146862 unc45b GO:0008345 larval locomotory behavior PATO:0000297 arrested abnormal ZDB-GENE-020919-3 266640 146862 unc45b GO:0008345 larval locomotory behavior PATO:0001507 disrupted abnormal ZDB-GENE-020919-3 266640 146862 unc45b GO:0016203 muscle attachment PATO:0002052 decreased occurrence abnormal ZDB-GENE-020919-3 266640 146862 unc45b GO:0030239 myofibril assembly PATO:0000502 delayed abnormal ZDB-GENE-020919-3 266640 146862 unc45b GO:0030239 myofibril assembly PATO:0001507 disrupted abnormal ZDB-GENE-020919-3 266640 146862 unc45b GO:0055001 muscle cell development PATO:0001507 disrupted abnormal ZDB-GENE-020919-3 266640 146862 unc45b GO:0055002 striated muscle cell development PATO:0001236 process quality abnormal ZDB-GENE-020919-3 266640 146862 unc45b GO:0060047 heart contraction PATO:0000297 arrested abnormal ZDB-GENE-020919-3 266640 146862 unc45b GO:0060538 skeletal muscle organ development PATO:0001236 process quality abnormal ZDB-GENE-020919-3 266640 146862 unc45b ZFA:0000009 cardiac ventricle PATO:0001511 non-functional abnormal ZDB-GENE-020919-3 266640 146862 unc45b GO:0005634 nucleus BFO:0000050 part_of ZFA:0000035 lens PATO:0001851 swollen abnormal ZDB-GENE-020919-3 266640 146862 unc45b GO:0090601 enucleation BFO:0000066 occurs_in ZFA:0000035 lens PATO:0001236 process quality abnormal ZDB-GENE-020919-3 266640 146862 unc45b ZFA:0000035 lens PATO:0000141 structure abnormal ZDB-GENE-020919-3 266640 146862 unc45b ZFA:0000035 lens PATO:0000587 decreased size abnormal ZDB-GENE-020919-3 266640 146862 unc45b ZFA:0000035 lens PATO:0001297 reflectivity abnormal ZDB-GENE-020919-3 266640 146862 unc45b ZFA:0000035 lens PATO:0002505 nucleated abnormal ZDB-GENE-020919-3 266640 146862 unc45b ZFA:0000054 pericardium PATO:0001450 edematous abnormal ZDB-GENE-020919-3 266640 146862 unc45b ZFA:0000076 swim bladder PATO:0001483 aplastic abnormal ZDB-GENE-020919-3 266640 146862 unc45b ZFA:0000084 yolk PATO:0001450 edematous abnormal ZDB-GENE-020919-3 266640 146862 unc45b ZFA:0000107 eye PATO:0000587 decreased size abnormal ZDB-GENE-020919-3 266640 146862 unc45b ZFA:0000107 eye PATO:0002058 decreased area abnormal ZDB-GENE-020919-3 266640 146862 unc45b ZFA:0000114 heart PATO:0000141 structure abnormal ZDB-GENE-020919-3 266640 146862 unc45b ZFA:0000114 heart PATO:0001450 edematous abnormal ZDB-GENE-020919-3 266640 146862 unc45b GO:0030016 myofibril BFO:0000050 part_of ZFA:0000155 somite PATO:0000051 morphology abnormal ZDB-GENE-020919-3 266640 146862 unc45b GO:0030016 myofibril BFO:0000050 part_of ZFA:0000155 somite PATO:0001802 loose abnormal ZDB-GENE-020919-3 266640 146862 unc45b ZFA:0000170 basibranchial PATO:0000141 structure abnormal ZDB-GENE-020919-3 266640 146862 unc45b ZFA:0000170 basibranchial PATO:0001920 mislocalised ventrally abnormal ZDB-GENE-020919-3 266640 146862 unc45b ZFA:0000316 basihyal bone PATO:0000574 decreased length abnormal ZDB-GENE-020919-3 266640 146862 unc45b ZFA:0000316 basihyal bone PATO:0001920 mislocalised ventrally abnormal ZDB-GENE-020919-3 266640 146862 unc45b ZFA:0000407 pectoral girdle PATO:0002290 aplastic/hypoplastic abnormal ZDB-GENE-020919-3 266640 146862 unc45b ZFA:0000473 trunk musculature PATO:0000141 structure abnormal ZDB-GENE-020919-3 266640 146862 unc45b ZFA:0000473 trunk musculature PATO:0000937 disorganized abnormal ZDB-GENE-020919-3 266640 146862 unc45b ZFA:0000488 ceratobranchial bone PATO:0000141 structure abnormal ZDB-GENE-020919-3 266640 146862 unc45b ZFA:0000488 ceratobranchial bone PATO:0001920 mislocalised ventrally abnormal ZDB-GENE-020919-3 266640 146862 unc45b ZFA:0000610 vertical myoseptum PATO:0000646 malformed abnormal ZDB-GENE-020919-3 266640 146862 unc45b ZFA:0001056 myotome PATO:0000646 malformed abnormal ZDB-GENE-020919-3 266640 146862 unc45b ZFA:0001094 whole organism PATO:0000763 paralysed abnormal ZDB-GENE-020919-3 266640 146862 unc45b ZFA:0001114 head PATO:0000587 decreased size abnormal ZDB-GENE-020919-3 266640 146862 unc45b ZFA:0001205 Meckel's cartilage PATO:0000574 decreased length abnormal ZDB-GENE-020919-3 266640 146862 unc45b ZFA:0001205 Meckel's cartilage PATO:0002181 displaced abnormal ZDB-GENE-020919-3 266640 146862 unc45b ZFA:0001205 Meckel's cartilage PATO:0002364 shortened abnormal ZDB-GENE-020919-3 266640 146862 unc45b ZFA:0001283 pupil PATO:0001715 decreased diameter abnormal ZDB-GENE-020919-3 266640 146862 unc45b GO:0014704 intercalated disc BFO:0000050 part_of ZFA:0001319 myocardium PATO:0000937 disorganized abnormal ZDB-GENE-020919-3 266640 146862 unc45b ZFA:0001399 palatoquadrate cartilage PATO:0000574 decreased length abnormal ZDB-GENE-020919-3 266640 146862 unc45b ZFA:0001399 palatoquadrate cartilage PATO:0000628 mislocalised abnormal ZDB-GENE-020919-3 266640 146862 unc45b ZFA:0001399 palatoquadrate cartilage PATO:0002364 shortened abnormal ZDB-GENE-020919-3 266640 146862 unc45b ZFA:0001400 ceratohyal cartilage PATO:0000133 orientation abnormal ZFA:0001400 ceratohyal cartilage ZDB-GENE-020919-3 266640 146862 unc45b ZFA:0001400 ceratohyal cartilage PATO:0000141 structure abnormal ZDB-GENE-020919-3 266640 146862 unc45b ZFA:0001400 ceratohyal cartilage PATO:0001920 mislocalised ventrally abnormal ZDB-GENE-020919-3 266640 146862 unc45b ZFA:0001651 sternohyoid PATO:0002181 displaced abnormal ZDB-GENE-020919-3 266640 146862 unc45b GO:0030016 myofibril BFO:0000050 part_of ZFA:0009115 skeletal muscle cell PATO:0000937 disorganized abnormal ZDB-GENE-020919-3 266640 146862 unc45b GO:0030017 sarcomere BFO:0000050 part_of ZFA:0009115 skeletal muscle cell PATO:0000141 structure abnormal ZDB-GENE-020919-3 266640 146862 unc45b GO:0005884 actin filament BFO:0000050 part_of ZFA:0009116 slow muscle cell PATO:0000937 disorganized abnormal ZDB-GENE-020919-3 266640 146862 unc45b GO:0032982 myosin filament BFO:0000050 part_of ZFA:0009116 slow muscle cell PATO:0000937 disorganized abnormal ZDB-GENE-020919-3 266640 146862 unc45b GO:0030016 myofibril BFO:0000050 part_of ZFA:0009117 fast muscle cell PATO:0000937 disorganized abnormal ZDB-GENE-020919-3 266640 146862 unc45b GO:0030016 myofibril BFO:0000050 part_of ZFA:0009316 cardiac muscle cell PATO:0000462 absent abnormal ZDB-GENE-020919-3 266640 146862 unc45b ZFA:0009401 lens fiber cell PATO:0000937 disorganized abnormal ZDB-GENE-020919-4 555134 8128 st8sia2 GO:0007411 axon guidance PATO:0001507 disrupted abnormal ZDB-GENE-020919-4 555134 8128 st8sia2 ZFA:0000320 caudal commissure PATO:0001959 defasciculated abnormal ZDB-GENE-020919-4 555134 8128 st8sia2 ZFA:0000338 diencephalic white matter PATO:0001786 split abnormal ZDB-GENE-020919-4 555134 8128 st8sia2 ZFA:0000338 diencephalic white matter PATO:0001997 decreased amount abnormal ZDB-GENE-021003-1 266753 94 acvrl1 GO:0001944 vasculature development PATO:0001236 process quality abnormal ZDB-GENE-021003-1 266753 94 acvrl1 GO:0001974 blood vessel remodeling PATO:0002052 decreased occurrence abnormal ZDB-GENE-021003-1 266753 94 acvrl1 GO:0008015 blood circulation PATO:0001507 disrupted abnormal ZDB-GENE-021003-1 266753 94 acvrl1 GO:0008015 blood circulation PATO:0002052 decreased occurrence abnormal ZDB-GENE-021003-1 266753 94 acvrl1 GO:0043534 blood vessel endothelial cell migration PATO:0001236 process quality abnormal ZDB-GENE-021003-1 266753 94 acvrl1 GO:0060973 cell migration involved in heart development PATO:0002052 decreased occurrence abnormal ZDB-GENE-021003-1 266753 94 acvrl1 ZFA:0000006 ball PATO:0001450 edematous abnormal ZDB-GENE-021003-1 266753 94 acvrl1 ZFA:0000054 pericardium PATO:0001450 edematous abnormal ZDB-GENE-021003-1 266753 94 acvrl1 ZFA:0000099 brain vasculature PATO:0000646 malformed abnormal ZDB-GENE-021003-1 266753 94 acvrl1 ZFA:0000170 basibranchial PATO:0001485 condensed abnormal ZDB-GENE-021003-1 266753 94 acvrl1 GO:0001568 blood vessel development BFO:0000066 occurs_in ZFA:0001051 caudal division of the internal carotid artery PATO:0001236 process quality abnormal ZDB-GENE-021003-1 266753 94 acvrl1 GO:0043534 blood vessel endothelial cell migration BFO:0000066 occurs_in ZFA:0001051 caudal division of the internal carotid artery PATO:0001236 process quality abnormal ZDB-GENE-021003-1 266753 94 acvrl1 GO:0043534 blood vessel endothelial cell migration BFO:0000066 occurs_in ZFA:0001051 caudal division of the internal carotid artery PATO:0002051 increased occurrence abnormal ZDB-GENE-021003-1 266753 94 acvrl1 ZFA:0009065 endothelial cell BFO:0000050 part_of ZFA:0001051 caudal division of the internal carotid artery PATO:0000470 increased amount abnormal ZDB-GENE-021003-1 266753 94 acvrl1 ZFA:0001051 caudal division of the internal carotid artery PATO:0000586 increased size abnormal ZDB-GENE-021003-1 266753 94 acvrl1 ZFA:0001051 caudal division of the internal carotid artery PATO:0000600 increased width abnormal ZDB-GENE-021003-1 266753 94 acvrl1 ZFA:0001052 primordial hindbrain channel PATO:0000586 increased size abnormal ZDB-GENE-021003-1 266753 94 acvrl1 ZFA:0001079 blood vasculature PATO:0000001 quality abnormal ZDB-GENE-021003-1 266753 94 acvrl1 ZFA:0001094 whole organism PATO:0000051 morphology abnormal ZDB-GENE-021003-1 266753 94 acvrl1 ZFA:0001094 whole organism PATO:0000169 viability abnormal ZDB-GENE-021003-1 266753 94 acvrl1 ZFA:0005314 blood vessel BFO:0000050 part_of ZFA:0001114 head PATO:0002105 hemorrhagic abnormal ZDB-GENE-021003-1 266753 94 acvrl1 ZFA:0001114 head PATO:0001450 edematous abnormal ZDB-GENE-021003-1 266753 94 acvrl1 ZFA:0001267 cranial vasculature PATO:0000646 malformed abnormal ZDB-GENE-021003-1 266753 94 acvrl1 ZFA:0001272 palatoquadrate arch PATO:0000574 decreased length abnormal ZDB-GENE-021003-1 266753 94 acvrl1 ZFA:0001400 ceratohyal cartilage PATO:0000133 orientation abnormal ZFA:0001400 ceratohyal cartilage ZDB-GENE-021003-1 266753 94 acvrl1 ZFA:0001516 ceratobranchial cartilage PATO:0000133 orientation abnormal ZFA:0001516 ceratobranchial cartilage ZDB-GENE-021003-1 266753 94 acvrl1 ZFA:0009036 blood vessel endothelial cell BFO:0000050 part_of ZFA:0005000 basal communicating artery PATO:0000470 increased amount abnormal ZDB-GENE-021003-1 266753 94 acvrl1 ZFA:0009065 endothelial cell BFO:0000050 part_of ZFA:0005000 basal communicating artery PATO:0000470 increased amount abnormal ZDB-GENE-021003-1 266753 94 acvrl1 ZFA:0009065 endothelial cell BFO:0000050 part_of ZFA:0005000 basal communicating artery PATO:0001997 decreased amount abnormal ZDB-GENE-021003-1 266753 94 acvrl1 ZFA:0005000 basal communicating artery PATO:0001453 detached from abnormal ZFA:0005017 primordial midbrain channel ZDB-GENE-021003-1 266753 94 acvrl1 ZFA:0005000 basal communicating artery PATO:0001667 attached to abnormal ZFA:0005017 primordial midbrain channel ZDB-GENE-021003-1 266753 94 acvrl1 ZFA:0005000 basal communicating artery PATO:0000586 increased size abnormal ZDB-GENE-021003-1 266753 94 acvrl1 ZFA:0009036 blood vessel endothelial cell BFO:0000050 part_of ZFA:0005001 posterior communicating artery PATO:0000470 increased amount abnormal ZDB-GENE-021003-1 266753 94 acvrl1 ZFA:0009065 endothelial cell BFO:0000050 part_of ZFA:0005001 posterior communicating artery PATO:0000470 increased amount abnormal ZDB-GENE-021003-1 266753 94 acvrl1 ZFA:0005001 posterior communicating artery PATO:0000586 increased size abnormal ZDB-GENE-021003-1 266753 94 acvrl1 ZFA:0005002 basilar artery PATO:0001667 attached to abnormal ZFA:0001052 primordial hindbrain channel ZDB-GENE-021003-1 266753 94 acvrl1 ZFA:0005002 basilar artery PATO:0001667 attached to abnormal ZFA:0005017 primordial midbrain channel ZDB-GENE-021003-1 266753 94 acvrl1 ZFA:0005002 basilar artery PATO:0000586 increased size abnormal ZDB-GENE-021003-1 266753 94 acvrl1 GO:0001568 blood vessel development BFO:0000066 occurs_in ZFA:0005005 aortic arch 1 PATO:0001236 process quality abnormal ZDB-GENE-021003-1 266753 94 acvrl1 GO:0043534 blood vessel endothelial cell migration BFO:0000066 occurs_in ZFA:0005005 aortic arch 1 PATO:0001236 process quality abnormal ZDB-GENE-021003-1 266753 94 acvrl1 GO:0043534 blood vessel endothelial cell migration BFO:0000066 occurs_in ZFA:0005005 aortic arch 1 PATO:0002302 decreased process quality abnormal ZDB-GENE-021003-1 266753 94 acvrl1 GO:0060973 cell migration involved in heart development BFO:0000066 occurs_in ZFA:0005005 aortic arch 1 PATO:0002052 decreased occurrence abnormal ZDB-GENE-021003-1 266753 94 acvrl1 ZFA:0009065 endothelial cell BFO:0000050 part_of ZFA:0005005 aortic arch 1 PATO:0001997 decreased amount abnormal ZDB-GENE-021003-1 266753 94 acvrl1 ZFA:0005005 aortic arch 1 PATO:0000051 morphology abnormal ZDB-GENE-021003-1 266753 94 acvrl1 ZFA:0005005 aortic arch 1 PATO:0001847 constricted abnormal ZDB-GENE-021003-1 266753 94 acvrl1 ZFA:0005017 primordial midbrain channel PATO:0000586 increased size abnormal ZDB-GENE-021003-1 266753 94 acvrl1 ZFA:0005017 primordial midbrain channel PATO:0001571 dilated abnormal ZDB-GENE-021003-1 266753 94 acvrl1 ZFA:0005020 central artery PATO:0001819 atretic abnormal ZDB-GENE-021003-1 266753 94 acvrl1 GO:0001568 blood vessel development BFO:0000066 occurs_in ZFA:0005081 internal carotid artery PATO:0001236 process quality abnormal ZDB-GENE-021003-1 266753 94 acvrl1 GO:0043534 blood vessel endothelial cell migration BFO:0000066 occurs_in ZFA:0005081 internal carotid artery PATO:0001236 process quality abnormal ZDB-GENE-021003-1 266753 94 acvrl1 ZFA:0009065 endothelial cell BFO:0000050 part_of ZFA:0005081 internal carotid artery PATO:0000470 increased amount abnormal ZDB-GENE-021003-1 266753 94 acvrl1 ZFA:0005081 internal carotid artery PATO:0000600 increased width abnormal ZDB-GENE-021003-1 266753 94 acvrl1 GO:0048844 artery morphogenesis BFO:0000066 occurs_in ZFA:0005297 cranial blood vessel PATO:0001236 process quality abnormal ZDB-GENE-021003-1 266753 94 acvrl1 ZFA:0005297 cranial blood vessel PATO:0001571 dilated abnormal ZDB-GENE-021003-1 266753 94 acvrl1 ZFA:0009065 endothelial cell PATO:0000470 increased amount abnormal ZDB-GENE-021008-1 266748 8456 foxn1 GO:0048538 thymus development PATO:0001507 disrupted abnormal ZDB-GENE-021008-1 266748 8456 foxn1 ZFA:0009250 lymphocyte BFO:0000050 part_of ZFA:0000669 head kidney PATO:0001997 decreased amount abnormal ZDB-GENE-021008-1 266748 8456 foxn1 GO:0008283 cell population proliferation BFO:0000066 occurs_in ZFA:0001078 thymus PATO:0002052 decreased occurrence abnormal ZDB-GENE-021008-1 266748 8456 foxn1 ZFA:0009034 epithelial cell BFO:0000050 part_of ZFA:0001078 thymus PATO:0001997 decreased amount abnormal ZDB-GENE-021008-1 266748 8456 foxn1 ZFA:0001078 thymus PATO:0000587 decreased size abnormal ZDB-GENE-021008-1 266748 8456 foxn1 ZFA:0001078 thymus PATO:0001623 atrophied abnormal ZDB-GENE-021011-1 266757 23471 tram1 GO:0061371 determination of heart left/right asymmetry PATO:0001507 disrupted abnormal ZDB-GENE-021011-1 266757 23471 tram1 ZFA:0000009 cardiac ventricle PATO:0000625 inverted abnormal ZDB-GENE-021011-1 266757 23471 tram1 ZFA:0000114 heart PATO:0000051 morphology abnormal ZDB-GENE-021011-1 266757 23471 tram1 ZFA:0000114 heart PATO:0001450 edematous abnormal ZDB-GENE-021011-1 266757 23471 tram1 ZFA:0000471 atrium PATO:0000625 inverted abnormal ZDB-GENE-021011-1 266757 23471 tram1 ZFA:0005024 trunk vasculature PATO:0000646 malformed abnormal ZDB-GENE-021011-2 266749 5062 pak2a ZFA:0000008 brain PATO:0002105 hemorrhagic abnormal ZDB-GENE-021011-2 266749 5062 pak2a ZFA:0000099 brain vasculature PATO:0001362 fragile abnormal ZDB-GENE-021011-2 266749 5062 pak2a ZFA:0001267 cranial vasculature PATO:0001362 fragile abnormal ZDB-GENE-021011-2 266749 5062 pak2a ZFA:0001267 cranial vasculature PATO:0002105 hemorrhagic abnormal ZDB-GENE-021016-2 266796 29927 sec61a1b ZFA:0001558 pronephric tubule PATO:0000052 shape abnormal ZDB-GENE-021016-2 266796 29927 sec61a1b ZFA:0001558 pronephric tubule PATO:0001623 atrophied abnormal ZDB-GENE-021021-2 266964 3195 tlx1 ZFA:0000436 spleen PATO:0000462 absent abnormal ZDB-GENE-021022-3 266966 7994 kat6a GO:0048703 embryonic viscerocranium morphogenesis PATO:0001236 process quality abnormal ZDB-GENE-021022-3 266966 7994 kat6a GO:0051216 cartilage development PATO:0001507 disrupted abnormal ZDB-GENE-021022-3 266966 7994 kat6a ZFA:0000095 pharyngeal arch 3-7 skeleton PATO:0000001 quality abnormal ZDB-GENE-021022-3 266966 7994 kat6a ZFA:0001227 mandibular arch skeleton PATO:0001473 duplicated abnormal ZDB-GENE-021022-3 266966 7994 kat6a ZFA:0001276 pharyngeal arch 2 skeleton PATO:0001483 aplastic abnormal ZDB-GENE-021022-3 266966 7994 kat6a ZFA:0001400 ceratohyal cartilage PATO:0000646 malformed abnormal ZDB-GENE-021022-3 266966 7994 kat6a ZFA:0001422 hyosymplectic cartilage PATO:0000646 malformed abnormal ZDB-GENE-021022-3 266966 7994 kat6a ZFA:0001520 ceratobranchial 1 cartilage PATO:0000646 malformed abnormal ZDB-GENE-021022-3 266966 7994 kat6a ZFA:0001611 pharyngeal arch 2 PATO:0001241 physical object quality abnormal ZDB-GENE-021028-1 266985 4869 npm1a ZFA:0009324 myeloid cell PATO:0001997 decreased amount abnormal ZDB-GENE-021029-1 266989 2107 etf1b GO:0048884 neuromast development PATO:0001507 disrupted abnormal ZDB-GENE-021029-1 266989 2107 etf1b ZFA:0000008 brain PATO:0000587 decreased size abnormal ZDB-GENE-021029-1 266989 2107 etf1b ZFA:0000012 central nervous system PATO:0000592 decreased thickness abnormal ZDB-GENE-021029-1 266989 2107 etf1b ZFA:0000054 pericardium PATO:0001450 edematous abnormal ZDB-GENE-021029-1 266989 2107 etf1b ZFA:0000076 swim bladder PATO:0002377 uninflated abnormal ZDB-GENE-021029-1 266989 2107 etf1b ZFA:0000107 eye PATO:0000587 decreased size abnormal ZDB-GENE-021029-1 266989 2107 etf1b ZFA:0000135 notochord PATO:0000617 bent abnormal ZDB-GENE-021029-1 266989 2107 etf1b ZFA:0000940 posterior lateral line neuromast PATO:0002001 has fewer parts of type abnormal ZFA:0009367 neuromast hair cell ZDB-GENE-021029-1 266989 2107 etf1b ZFA:0001094 whole organism PATO:0000051 morphology abnormal ZDB-GENE-021029-1 266989 2107 etf1b ZFA:0001094 whole organism PATO:0000587 decreased size abnormal ZDB-GENE-021029-1 266989 2107 etf1b ZFA:0001114 head PATO:0000587 decreased size abnormal ZDB-GENE-021029-1 266989 2107 etf1b ZFA:0001115 trunk PATO:0001469 curved ventral abnormal ZDB-GENE-021030-1 406625 5641 lgmn GO:0030282 bone mineralization BFO:0000066 occurs_in ZFA:0001189 vertebra PATO:0002051 increased occurrence abnormal ZDB-GENE-021030-3 266987 875 cbsb GO:0003401 axis elongation PATO:0001507 disrupted abnormal ZDB-GENE-021030-3 266987 875 cbsb CHEBI:17230 homocysteine BFO:0000050 part_of ZFA:0000008 brain PATO:0000470 increased amount abnormal ZDB-GENE-021030-3 266987 875 cbsb BSPO:0000013 anterior-posterior axis BFO:0000050 part_of ZFA:0001094 whole organism PATO:0000617 bent abnormal ZDB-GENE-021030-3 266987 875 cbsb BSPO:0000013 anterior-posterior axis BFO:0000050 part_of ZFA:0001094 whole organism PATO:0002364 shortened abnormal ZDB-GENE-021030-3 266987 875 cbsb ZFA:0001094 whole organism PATO:0001422 dead abnormal ZDB-GENE-021030-3 266987 875 cbsb ZFA:0001094 whole organism PATO:0001604 decreased life span abnormal ZDB-GENE-021030-3 266987 875 cbsb ZFA:0001114 head PATO:0001450 edematous abnormal ZDB-GENE-021030-3 266987 875 cbsb ZFA:0001115 trunk PATO:0000617 bent abnormal ZDB-GENE-021030-4 266992 790 cad GO:0007219 Notch signaling pathway PATO:0001783 decreased intensity abnormal ZDB-GENE-021030-4 266992 790 cad GO:0000278 mitotic cell cycle BFO:0000066 occurs_in ZFA:0000029 hindbrain PATO:0002302 decreased process quality abnormal ZDB-GENE-021030-4 266992 790 cad ZFA:0000054 pericardium PATO:0001450 edematous abnormal ZDB-GENE-021030-4 266992 790 cad ZFA:0000084 yolk PATO:0000001 quality abnormal ZDB-GENE-021030-4 266992 790 cad ZFA:0000084 yolk PATO:0000411 circular abnormal ZDB-GENE-021030-4 266992 790 cad ZFA:0000100 cerebellum PATO:0000141 structure abnormal ZDB-GENE-021030-4 266992 790 cad ZFA:0000100 cerebellum PATO:0000587 decreased size abnormal ZDB-GENE-021030-4 266992 790 cad ZFA:0000106 extension PATO:0000592 decreased thickness abnormal ZDB-GENE-021030-4 266992 790 cad GO:0008219 cell death BFO:0000066 occurs_in ZFA:0000107 eye PATO:0002304 increased process quality abnormal ZDB-GENE-021030-4 266992 790 cad ZFA:0000107 eye PATO:0000587 decreased size abnormal ZDB-GENE-021030-4 266992 790 cad GO:0008219 cell death BFO:0000066 occurs_in ZFA:0000109 forebrain PATO:0002304 increased process quality abnormal ZDB-GENE-021030-4 266992 790 cad ZFA:0000112 gut PATO:0000001 quality abnormal ZDB-GENE-021030-4 266992 790 cad ZFA:0000112 gut PATO:0000645 hypoplastic abnormal ZDB-GENE-021030-4 266992 790 cad ZFA:0000114 heart PATO:0000001 quality abnormal ZDB-GENE-021030-4 266992 790 cad ZFA:0000123 liver PATO:0000001 quality abnormal ZDB-GENE-021030-4 266992 790 cad ZFA:0000123 liver PATO:0000645 hypoplastic abnormal ZDB-GENE-021030-4 266992 790 cad BSPO:0000672 posterior margin BFO:0000050 part_of ZFA:0000128 midbrain PATO:0000600 increased width abnormal ZDB-GENE-021030-4 266992 790 cad GO:0008219 cell death BFO:0000066 occurs_in ZFA:0000128 midbrain PATO:0002304 increased process quality abnormal ZDB-GENE-021030-4 266992 790 cad BSPO:0000075 central region BFO:0000050 part_of ZFA:0000445 optic tectum PATO:0002102 proliferative abnormal ZDB-GENE-021030-4 266992 790 cad GO:0006915 apoptotic process BFO:0000066 occurs_in ZFA:0000445 optic tectum PATO:0002051 increased occurrence abnormal ZDB-GENE-021030-4 266992 790 cad GO:0033278 cell proliferation in midbrain BFO:0000066 occurs_in ZFA:0000445 optic tectum PATO:0002051 increased occurrence abnormal ZDB-GENE-021030-4 266992 790 cad GO:0050767 regulation of neurogenesis BFO:0000066 occurs_in ZFA:0000445 optic tectum PATO:0001236 process quality abnormal ZDB-GENE-021030-4 266992 790 cad ZFA:0000445 optic tectum PATO:0000141 structure abnormal ZDB-GENE-021030-4 266992 790 cad ZFA:0000445 optic tectum PATO:0000587 decreased size abnormal ZDB-GENE-021030-4 266992 790 cad ZFA:0001061 intersegmental artery PATO:0002285 increased branchiness abnormal ZDB-GENE-021030-4 266992 790 cad ZFA:0001094 whole organism PATO:0000587 decreased size abnormal ZDB-GENE-021030-4 266992 790 cad ZFA:0001114 head PATO:0000587 decreased size abnormal ZDB-GENE-021030-4 266992 790 cad ZFA:0001205 Meckel's cartilage PATO:0002364 shortened abnormal ZDB-GENE-021030-4 266992 790 cad ZFA:0001273 ventral mandibular arch PATO:0001623 atrophied abnormal ZDB-GENE-021030-4 266992 790 cad GO:0030424 axon BFO:0000050 part_of ZFA:0001291 facial ganglion PATO:0000646 malformed abnormal ZDB-GENE-021030-4 266992 790 cad ZFA:0001291 facial ganglion PATO:0000587 decreased size abnormal ZDB-GENE-021030-4 266992 790 cad GO:0030424 axon BFO:0000050 part_of ZFA:0001301 glossopharyngeal ganglion PATO:0000646 malformed abnormal ZDB-GENE-021030-4 266992 790 cad ZFA:0001301 glossopharyngeal ganglion PATO:0001999 lacks parts or has fewer parts of type abnormal GO:0030424 axon BFO:0000050 part_of ZFA:0001301 glossopharyngeal ganglion ZDB-GENE-021030-4 266992 790 cad ZFA:0001301 glossopharyngeal ganglion PATO:0000587 decreased size abnormal ZDB-GENE-021030-4 266992 790 cad ZFA:0001400 ceratohyal cartilage PATO:0001617 deformed abnormal ZDB-GENE-021030-4 266992 790 cad ZFA:0001516 ceratobranchial cartilage PATO:0000462 absent abnormal ZDB-GENE-021030-4 266992 790 cad GO:0030424 axon BFO:0000050 part_of ZFA:0001555 epibranchial ganglion PATO:0000051 morphology abnormal ZDB-GENE-021030-4 266992 790 cad GO:0061564 axon development BFO:0000066 occurs_in ZFA:0001555 epibranchial ganglion PATO:0001236 process quality abnormal ZDB-GENE-021030-4 266992 790 cad GO:0030424 axon BFO:0000050 part_of ZFA:0007067 vagal ganglion PATO:0000646 malformed abnormal ZDB-GENE-021030-4 266992 790 cad GO:0097155 fasciculation of sensory neuron axon BFO:0000066 occurs_in ZFA:0007067 vagal ganglion PATO:0002302 decreased process quality abnormal ZDB-GENE-021030-4 266992 790 cad ZFA:0007067 vagal ganglion PATO:0000587 decreased size abnormal ZDB-GENE-021030-4 266992 790 cad ZFA:0009036 blood vessel endothelial cell PATO:0000470 increased amount abnormal ZDB-GENE-021030-5 558976 10048 ranbp9 GO:0010842 retina layer formation PATO:0001507 disrupted abnormal ZDB-GENE-021030-5 558976 10048 ranbp9 ZFA:0000008 brain PATO:0000587 decreased size abnormal ZDB-GENE-021030-5 558976 10048 ranbp9 ZFA:0000076 swim bladder PATO:0002377 uninflated abnormal ZDB-GENE-021030-5 558976 10048 ranbp9 ZFA:0009000 cell BFO:0000050 part_of ZFA:0000152 retina PATO:0001997 decreased amount abnormal ZDB-GENE-021030-5 558976 10048 ranbp9 GO:0006915 apoptotic process BFO:0000066 occurs_in ZFA:0000445 optic tectum PATO:0002051 increased occurrence abnormal ZDB-GENE-021030-5 558976 10048 ranbp9 ZFA:0001115 trunk PATO:0000587 decreased size abnormal ZDB-GENE-021030-5 558976 10048 ranbp9 ZFA:0009280 Muller cell PATO:0000462 absent abnormal ZDB-GENE-021031-1 266983 4756 neo1a GO:0001756 somitogenesis PATO:0001507 disrupted abnormal ZDB-GENE-021031-1 266983 4756 neo1a GO:0007275 multicellular organism development PATO:0001507 disrupted abnormal ZDB-GENE-021031-1 266983 4756 neo1a GO:0007399 nervous system development PATO:0001507 disrupted abnormal ZDB-GENE-021031-1 266983 4756 neo1a GO:0021915 neural tube development PATO:0001507 disrupted abnormal ZDB-GENE-021031-1 266983 4756 neo1a BSPO:0000013 anterior-posterior axis BFO:0000050 part_of ZFA:0000008 brain PATO:0000587 decreased size abnormal ZDB-GENE-021031-1 266983 4756 neo1a ZFA:0000008 brain PATO:0000051 morphology abnormal ZDB-GENE-021031-1 266983 4756 neo1a ZFA:0000008 brain PATO:0000141 structure abnormal ZDB-GENE-021031-1 266983 4756 neo1a ZFA:0009248 neuron BFO:0000050 part_of ZFA:0000029 hindbrain PATO:0001997 decreased amount abnormal ZDB-GENE-021031-1 266983 4756 neo1a ZFA:0000029 hindbrain PATO:0000051 morphology abnormal ZDB-GENE-021031-1 266983 4756 neo1a ZFA:0000054 pericardium PATO:0001450 edematous abnormal ZDB-GENE-021031-1 266983 4756 neo1a ZFA:0000100 cerebellum PATO:0000051 morphology abnormal ZDB-GENE-021031-1 266983 4756 neo1a ZFA:0000101 diencephalon PATO:0002000 lacks all parts of type abnormal ZFA:0000161 third ventricle ZDB-GENE-021031-1 266983 4756 neo1a ZFA:0000101 diencephalon PATO:0000051 morphology abnormal ZDB-GENE-021031-1 266983 4756 neo1a ZFA:0000107 eye PATO:0000587 decreased size abnormal ZDB-GENE-021031-1 266983 4756 neo1a ZFA:0000132 neural plate PATO:0000600 increased width abnormal ZDB-GENE-021031-1 266983 4756 neo1a ZFA:0000155 somite PATO:0000051 morphology abnormal ZDB-GENE-021031-1 266983 4756 neo1a ZFA:0000155 somite PATO:0000592 decreased thickness abnormal ZDB-GENE-021031-1 266983 4756 neo1a ZFA:0000155 somite PATO:0000600 increased width abnormal ZDB-GENE-021031-1 266983 4756 neo1a ZFA:0000155 somite PATO:0001154 elongated abnormal ZDB-GENE-021031-1 266983 4756 neo1a ZFA:0000155 somite PATO:0001879 U-shaped abnormal ZDB-GENE-021031-1 266983 4756 neo1a ZFA:0000155 somite PATO:0002254 flattened abnormal ZDB-GENE-021031-1 266983 4756 neo1a ZFA:0000160 tegmentum PATO:0000051 morphology abnormal ZDB-GENE-021031-1 266983 4756 neo1a ZFA:0009248 neuron BFO:0000050 part_of ZFA:0000295 trigeminal ganglion PATO:0001997 decreased amount abnormal ZDB-GENE-021031-1 266983 4756 neo1a GO:0030424 axon BFO:0000050 part_of ZFA:0000318 brainstem and spinal white matter PATO:0001997 decreased amount abnormal ZDB-GENE-021031-1 266983 4756 neo1a ZFA:0000543 medial longitudinal fasciculus PATO:0000592 decreased thickness abnormal ZDB-GENE-021031-1 266983 4756 neo1a BSPO:0000013 anterior-posterior axis BFO:0000050 part_of ZFA:0001094 whole organism PATO:0000574 decreased length abnormal ZDB-GENE-021031-1 266983 4756 neo1a BSPO:0000013 anterior-posterior axis BFO:0000050 part_of ZFA:0001094 whole organism PATO:0002364 shortened abnormal ZDB-GENE-021031-1 266983 4756 neo1a ZFA:0001094 whole organism PATO:0000169 viability abnormal ZDB-GENE-021031-1 266983 4756 neo1a ZFA:0001094 whole organism PATO:0000574 decreased length abnormal ZDB-GENE-021031-1 266983 4756 neo1a ZFA:0001094 whole organism PATO:0000647 necrotic abnormal ZDB-GENE-021031-1 266983 4756 neo1a ZFA:0001094 whole organism PATO:0002251 decreased pigmentation abnormal ZDB-GENE-021031-1 266983 4756 neo1a ZFA:0001114 head PATO:0002254 flattened abnormal ZDB-GENE-021031-1 266983 4756 neo1a ZFA:0001117 post-vent region PATO:0001592 increased curvature abnormal ZDB-GENE-021031-1 266983 4756 neo1a ZFA:0001135 neural tube PATO:0001473 duplicated abnormal ZDB-GENE-021031-1 266983 4756 neo1a ZFA:0001135 neural tube PATO:0001896 unlumenized abnormal ZDB-GENE-021031-1 266983 4756 neo1a ZFA:0005209 hindbrain interneuron PATO:0001997 decreased amount abnormal ZDB-GENE-021031-1 266983 4756 neo1a ZFA:0005266 dorsal longitudinal fasciculus PATO:0000592 decreased thickness abnormal ZDB-GENE-021031-1 266983 4756 neo1a ZFA:0009248 neuron BFO:0000050 part_of ZFA:0007001 dorso-rostral cluster PATO:0001997 decreased amount abnormal ZDB-GENE-021031-1 266983 4756 neo1a GO:0000902 cell morphogenesis BFO:0000066 occurs_in ZFA:0007029 hindbrain neural keel PATO:0001236 process quality abnormal ZDB-GENE-021031-1 266983 4756 neo1a GO:0005874 microtubule BFO:0000050 part_of ZFA:0007029 hindbrain neural keel PATO:0000628 mislocalised abnormal ZDB-GENE-021031-1 266983 4756 neo1a GO:0005874 microtubule BFO:0000050 part_of ZFA:0007029 hindbrain neural keel PATO:0000937 disorganized abnormal ZDB-GENE-021031-1 266983 4756 neo1a GO:0005874 microtubule BFO:0000050 part_of ZFA:0007029 hindbrain neural keel PATO:0002364 shortened abnormal ZDB-GENE-021031-1 266983 4756 neo1a ZFA:0009306 neuroepithelial cell BFO:0000050 part_of ZFA:0007029 hindbrain neural keel PATO:0000052 shape abnormal ZDB-GENE-021031-1 266983 4756 neo1a ZFA:0009306 neuroepithelial cell BFO:0000050 part_of ZFA:0007029 hindbrain neural keel PATO:0000411 circular abnormal ZDB-GENE-021031-1 266983 4756 neo1a ZFA:0009150 Rohon-Beard neuron PATO:0001997 decreased amount abnormal ZDB-GENE-021031-1 266983 4756 neo1a GO:0030424 axon BFO:0000050 part_of ZFA:0009243 CaP motoneuron PATO:0001997 decreased amount abnormal ZDB-GENE-021031-1 266983 4756 neo1a ZFA:0009244 primary motor neuron PATO:0001997 decreased amount abnormal ZDB-GENE-021031-1 266983 4756 neo1a GO:0000902 cell morphogenesis BFO:0000066 occurs_in ZFA:0009306 neuroepithelial cell PATO:0001236 process quality abnormal ZDB-GENE-021031-1 266983 4756 neo1a ZFA:0009306 neuroepithelial cell PATO:0000628 mislocalised abnormal ZDB-GENE-021031-1 266983 4756 neo1a ZFA:0009306 neuroepithelial cell PATO:0001997 decreased amount abnormal ZDB-GENE-021031-3 266990 5822 pwp2h GO:0000028 ribosomal small subunit assembly PATO:0001507 disrupted abnormal ZDB-GENE-021031-3 266990 5822 pwp2h GO:0008283 cell population proliferation PATO:0001236 process quality abnormal ZDB-GENE-021031-3 266990 5822 pwp2h GO:0042254 ribosome biogenesis PATO:0001507 disrupted abnormal ZDB-GENE-021031-3 266990 5822 pwp2h ZFA:0000076 swim bladder PATO:0002377 uninflated abnormal ZDB-GENE-021031-3 266990 5822 pwp2h ZFA:0000107 eye PATO:0000587 decreased size abnormal ZDB-GENE-021031-3 266990 5822 pwp2h ZFA:0000123 liver PATO:0000587 decreased size abnormal ZDB-GENE-021031-3 266990 5822 pwp2h ZFA:0000140 pancreas PATO:0000587 decreased size abnormal ZDB-GENE-021031-3 266990 5822 pwp2h ZFA:0001076 intestinal bulb PATO:0000587 decreased size abnormal ZDB-GENE-021031-3 266990 5822 pwp2h ZFA:0001094 whole organism PATO:0001422 dead abnormal ZDB-GENE-021031-3 266990 5822 pwp2h ZFA:0001114 head PATO:0000646 malformed abnormal ZDB-GENE-021031-3 266990 5822 pwp2h ZFA:0009034 epithelial cell BFO:0000050 part_of ZFA:0001338 intestine PATO:0001872 cuboid abnormal ZDB-GENE-021031-3 266990 5822 pwp2h GO:0044754 autolysosome BFO:0000050 part_of ZFA:0005124 intestinal epithelium PATO:0000470 increased amount abnormal ZDB-GENE-021031-3 266990 5822 pwp2h ZFA:0005124 intestinal epithelium PATO:0000052 shape abnormal ZDB-GENE-021031-3 266990 5822 pwp2h ZFA:0005124 intestinal epithelium PATO:0000587 decreased size abnormal ZDB-GENE-021031-3 266990 5822 pwp2h ZFA:0005124 intestinal epithelium PATO:0000592 decreased thickness abnormal ZDB-GENE-021031-3 266990 5822 pwp2h ZFA:0005125 intestinal villus PATO:0001609 sparse abnormal ZDB-GENE-021031-3 266990 5822 pwp2h BSPO:0000014 apical-basal axis relative to substrate BFO:0000050 part_of ZFA:0005126 intestinal bulb epithelium PATO:0000574 decreased length abnormal ZDB-GENE-021031-4 556077 8985 plod3 GO:0001755 neural crest cell migration PATO:0001236 process quality abnormal ZDB-GENE-021031-4 556077 8985 plod3 GO:0001966 thigmotaxis PATO:0001507 disrupted abnormal ZDB-GENE-021031-4 556077 8985 plod3 GO:0002089 lens morphogenesis in camera-type eye PATO:0002302 decreased process quality abnormal ZDB-GENE-021031-4 556077 8985 plod3 GO:0003009 skeletal muscle contraction PATO:0001507 disrupted abnormal ZDB-GENE-021031-4 556077 8985 plod3 GO:0008045 motor neuron axon guidance PATO:0001236 process quality abnormal ZDB-GENE-021031-4 556077 8985 plod3 GO:0021522 spinal cord motor neuron differentiation PATO:0001236 process quality abnormal ZDB-GENE-021031-4 556077 8985 plod3 GO:0040011 locomotion PATO:0001530 behavioral quality of a process abnormal ZDB-GENE-021031-4 556077 8985 plod3 GO:0050881 musculoskeletal movement PATO:0000001 quality abnormal ZDB-GENE-021031-4 556077 8985 plod3 ZFA:0000008 brain PATO:0000001 quality abnormal ZDB-GENE-021031-4 556077 8985 plod3 ZFA:0000029 hindbrain PATO:0000001 quality abnormal ZDB-GENE-021031-4 556077 8985 plod3 ZFA:0000029 hindbrain PATO:0000051 morphology abnormal ZDB-GENE-021031-4 556077 8985 plod3 ZFA:0000029 hindbrain PATO:0001450 edematous abnormal ZDB-GENE-021031-4 556077 8985 plod3 ZFA:0000035 lens PATO:0000052 shape abnormal ZDB-GENE-021031-4 556077 8985 plod3 ZFA:0000035 lens PATO:0000587 decreased size abnormal ZDB-GENE-021031-4 556077 8985 plod3 ZFA:0000035 lens PATO:0001852 dislocated abnormal ZDB-GENE-021031-4 556077 8985 plod3 ZFA:0000135 notochord PATO:0000639 degenerate abnormal ZDB-GENE-021031-4 556077 8985 plod3 ZFA:0000135 notochord PATO:0000967 undulate abnormal ZDB-GENE-021031-4 556077 8985 plod3 ZFA:0000155 somite PATO:0000001 quality abnormal ZDB-GENE-021031-4 556077 8985 plod3 ZFA:0000155 somite PATO:0000051 morphology abnormal ZDB-GENE-021031-4 556077 8985 plod3 ZFA:0000217 inner ear PATO:0002210 bulbous abnormal ZDB-GENE-021031-4 556077 8985 plod3 ZFA:0000396 nervous system PATO:0000001 quality abnormal ZDB-GENE-021031-4 556077 8985 plod3 ZFA:0000473 trunk musculature PATO:0001579 contractility abnormal ZDB-GENE-021031-4 556077 8985 plod3 ZFA:0001094 whole organism PATO:0000169 viability abnormal ZDB-GENE-021031-4 556077 8985 plod3 ZFA:0001094 whole organism PATO:0000574 decreased length abnormal ZDB-GENE-021031-4 556077 8985 plod3 ZFA:0001094 whole organism PATO:0000718 lethal (sensu genetics) abnormal ZDB-GENE-021031-4 556077 8985 plod3 ZFA:0001094 whole organism PATO:0002076 movement behavioral quality abnormal ZDB-GENE-021031-4 556077 8985 plod3 GO:0008045 motor neuron axon guidance BFO:0000066 occurs_in ZFA:0001115 trunk PATO:0001236 process quality abnormal ZDB-GENE-021031-4 556077 8985 plod3 ZFA:0001227 mandibular arch skeleton PATO:0000646 malformed abnormal ZDB-GENE-021031-4 556077 8985 plod3 BSPO:0000071 anterior region BFO:0000050 part_of ZFA:0001326 lens epithelium PATO:0000584 hypertrophic abnormal ZDB-GENE-021031-4 556077 8985 plod3 GO:0007179 transforming growth factor beta receptor signaling pathway BFO:0000066 occurs_in ZFA:0001326 lens epithelium PATO:0002051 increased occurrence abnormal ZDB-GENE-021031-4 556077 8985 plod3 GO:0008219 cell death BFO:0000066 occurs_in ZFA:0001326 lens epithelium PATO:0002051 increased occurrence abnormal ZDB-GENE-021031-4 556077 8985 plod3 GO:0070306 lens fiber cell differentiation BFO:0000066 occurs_in ZFA:0001326 lens epithelium PATO:0000057 occurrence abnormal ZDB-GENE-021031-4 556077 8985 plod3 GO:0097166 lens epithelial cell proliferation BFO:0000066 occurs_in ZFA:0001326 lens epithelium PATO:0002051 increased occurrence abnormal ZDB-GENE-021031-4 556077 8985 plod3 ZFA:0001326 lens epithelium PATO:0000584 hypertrophic abnormal ZDB-GENE-021031-4 556077 8985 plod3 ZFA:0001326 lens epithelium PATO:0000646 malformed abnormal ZDB-GENE-021031-4 556077 8985 plod3 ZFA:0001326 lens epithelium PATO:0040026 structurally discontinuous abnormal ZDB-GENE-021031-4 556077 8985 plod3 GO:0030424 axon BFO:0000050 part_of ZFA:0005179 MiP motor neuron PATO:0000462 absent abnormal ZDB-GENE-021031-4 556077 8985 plod3 GO:0030424 axon BFO:0000050 part_of ZFA:0005179 MiP motor neuron PATO:0000628 mislocalised abnormal ZDB-GENE-021031-4 556077 8985 plod3 GO:0030424 axon BFO:0000050 part_of ZFA:0005180 RoP motor neuron PATO:0000628 mislocalised abnormal ZDB-GENE-021031-4 556077 8985 plod3 GO:0031012 extracellular matrix BFO:0000050 part_of ZFA:0005574 lens capsule PATO:0001608 patchy abnormal ZDB-GENE-021031-4 556077 8985 plod3 ZFA:0005574 lens capsule PATO:0000646 malformed abnormal ZDB-GENE-021031-4 556077 8985 plod3 ZFA:0009165 neural crest cell PATO:0001999 lacks parts or has fewer parts of type abnormal GO:0030175 filopodium BFO:0000050 part_of ZFA:0009165 neural crest cell ZDB-GENE-021031-4 556077 8985 plod3 GO:0030424 axon BFO:0000050 part_of ZFA:0009243 CaP motoneuron PATO:0000574 decreased length abnormal ZDB-GENE-021031-4 556077 8985 plod3 GO:0030424 axon BFO:0000050 part_of ZFA:0009243 CaP motoneuron PATO:0000628 mislocalised abnormal ZDB-GENE-021031-5 266988 64094 smoc2 GO:0008015 blood circulation PATO:0000502 delayed abnormal ZDB-GENE-021031-5 266988 64094 smoc2 GO:0030097 hemopoiesis PATO:0001236 process quality abnormal ZDB-GENE-021031-5 266988 64094 smoc2 GO:0030282 bone mineralization PATO:0001507 disrupted abnormal ZDB-GENE-021031-5 266988 64094 smoc2 GO:0030509 BMP signaling pathway PATO:0002302 decreased process quality abnormal ZDB-GENE-021031-5 266988 64094 smoc2 GO:0061515 myeloid cell development PATO:0001236 process quality abnormal ZDB-GENE-021031-5 266988 64094 smoc2 ZFA:0000094 blood island PATO:0000586 increased size abnormal ZDB-GENE-021031-5 266988 64094 smoc2 ZFA:0000106 extension PATO:0000574 decreased length abnormal ZDB-GENE-021031-5 266988 64094 smoc2 ZFA:0000107 eye PATO:0000462 absent abnormal ZDB-GENE-021031-5 266988 64094 smoc2 ZFA:0000155 somite PATO:0000052 shape abnormal ZDB-GENE-021031-5 266988 64094 smoc2 ZFA:0000694 ceratobranchial 5 tooth PATO:0000462 absent abnormal ZDB-GENE-021031-5 266988 64094 smoc2 ZFA:0000694 ceratobranchial 5 tooth PATO:0000587 decreased size abnormal ZDB-GENE-021031-5 266988 64094 smoc2 ZFA:0001058 caudal fin PATO:0001469 curved ventral abnormal ZDB-GENE-021031-5 266988 64094 smoc2 BSPO:0000013 anterior-posterior axis BFO:0000050 part_of ZFA:0001094 whole organism PATO:0000574 decreased length abnormal ZDB-GENE-021031-5 266988 64094 smoc2 ZFA:0001114 head PATO:0000587 decreased size abnormal ZDB-GENE-021031-5 266988 64094 smoc2 ZFA:0001114 head PATO:0000645 hypoplastic abnormal ZDB-GENE-021031-5 266988 64094 smoc2 ZFA:0001400 ceratohyal cartilage PATO:0000625 inverted abnormal ZDB-GENE-021031-5 266988 64094 smoc2 ZFA:0001400 ceratohyal cartilage PATO:0002254 flattened abnormal ZDB-GENE-021031-5 266988 64094 smoc2 ZFA:0001458 cranial cartilage PATO:0000051 morphology abnormal ZDB-GENE-021031-5 266988 64094 smoc2 ZFA:0001458 cranial cartilage PATO:0000462 absent abnormal ZDB-GENE-021031-5 266988 64094 smoc2 ZFA:0001516 ceratobranchial cartilage PATO:0000587 decreased size abnormal ZDB-GENE-021031-5 266988 64094 smoc2 ZFA:0001516 ceratobranchial cartilage PATO:0001997 decreased amount abnormal ZDB-GENE-021031-5 266988 64094 smoc2 ZFA:0009327 neutrophil PATO:0001997 decreased amount abnormal ZDB-GENE-021115-1 678623 4891 slc11a2 ZFA:0000007 blood PATO:0000001 quality abnormal ZDB-GENE-021115-1 678623 4891 slc11a2 ZFA:0001439 anatomical system PATO:0000001 quality abnormal ZDB-GENE-021115-1 678623 4891 slc11a2 ZFA:0009256 nucleate erythrocyte PATO:0000328 low saturation abnormal ZDB-GENE-021115-1 678623 4891 slc11a2 ZFA:0009256 nucleate erythrocyte PATO:0001997 decreased amount abnormal ZDB-GENE-021115-1 678623 4891 slc11a2 ZFA:0009325 erythroid lineage cell PATO:0001997 decreased amount abnormal ZDB-GENE-021115-2 280653 54822 trpm7 GO:0000278 mitotic cell cycle PATO:0001507 disrupted abnormal ZDB-GENE-021115-2 280653 54822 trpm7 GO:0001957 intramembranous ossification PATO:0001750 postdisplaced growth abnormal ZDB-GENE-021115-2 280653 54822 trpm7 GO:0001958 endochondral ossification PATO:0001754 predisplaced growth abnormal ZDB-GENE-021115-2 280653 54822 trpm7 GO:0001966 thigmotaxis PATO:0000297 arrested abnormal ZDB-GENE-021115-2 280653 54822 trpm7 GO:0001966 thigmotaxis PATO:0001507 disrupted abnormal ZDB-GENE-021115-2 280653 54822 trpm7 GO:0003014 renal system process PATO:0002302 decreased process quality abnormal ZDB-GENE-021115-2 280653 54822 trpm7 GO:0008344 adult locomotory behavior PATO:0001530 behavioral quality of a process abnormal ZDB-GENE-021115-2 280653 54822 trpm7 GO:0009605 response to external stimulus PATO:0000001 quality abnormal ZDB-GENE-021115-2 280653 54822 trpm7 GO:0010960 magnesium ion homeostasis PATO:0002302 decreased process quality abnormal ZDB-GENE-021115-2 280653 54822 trpm7 GO:0030318 melanocyte differentiation PATO:0000502 delayed abnormal ZDB-GENE-021115-2 280653 54822 trpm7 GO:0030318 melanocyte differentiation PATO:0001507 disrupted abnormal ZDB-GENE-021115-2 280653 54822 trpm7 GO:0036269 swimming behavior PATO:0001309 duration abnormal ZDB-GENE-021115-2 280653 54822 trpm7 GO:0036269 swimming behavior PATO:0002302 decreased process quality abnormal ZDB-GENE-021115-2 280653 54822 trpm7 GO:0040007 growth PATO:0002018 decreased magnitude abnormal ZDB-GENE-021115-2 280653 54822 trpm7 GO:0042438 melanin biosynthetic process PATO:0000502 delayed abnormal ZDB-GENE-021115-2 280653 54822 trpm7 GO:0042438 melanin biosynthetic process PATO:0001507 disrupted abnormal ZDB-GENE-021115-2 280653 54822 trpm7 GO:0050673 epithelial cell proliferation PATO:0002052 decreased occurrence abnormal ZDB-GENE-021115-2 280653 54822 trpm7 GO:0050881 musculoskeletal movement PATO:0000001 quality abnormal ZDB-GENE-021115-2 280653 54822 trpm7 GO:0055074 calcium ion homeostasis PATO:0002302 decreased process quality abnormal ZDB-GENE-021115-2 280653 54822 trpm7 GO:0060047 heart contraction PATO:0000911 decreased rate abnormal ZDB-GENE-021115-2 280653 54822 trpm7 ZFA:0000107 eye PATO:0000587 decreased size abnormal ZDB-GENE-021115-2 280653 54822 trpm7 ZFA:0000114 heart PATO:0001624 decreased functionality abnormal ZDB-GENE-021115-2 280653 54822 trpm7 ZFA:0000126 centrum PATO:0000025 composition abnormal ZDB-GENE-021115-2 280653 54822 trpm7 ZFA:0000150 pronephric duct PATO:0000648 obstructed abnormal ZDB-GENE-021115-2 280653 54822 trpm7 ZFA:0000158 urostyle PATO:0000025 composition abnormal ZDB-GENE-021115-2 280653 54822 trpm7 ZFA:0000240 metapterygoid PATO:0001448 ossified abnormal ZDB-GENE-021115-2 280653 54822 trpm7 ZFA:0000270 maxilla PATO:0000025 composition abnormal ZDB-GENE-021115-2 280653 54822 trpm7 ZFA:0000282 sensory system PATO:0000001 quality abnormal ZDB-GENE-021115-2 280653 54822 trpm7 ZFA:0000316 basihyal bone PATO:0001448 ossified abnormal ZDB-GENE-021115-2 280653 54822 trpm7 ZFA:0000326 caudal vertebra PATO:0001485 condensed abnormal ZDB-GENE-021115-2 280653 54822 trpm7 ZFA:0000364 hypural PATO:0000025 composition abnormal ZDB-GENE-021115-2 280653 54822 trpm7 ZFA:0000368 integument PATO:0002251 decreased pigmentation abnormal ZDB-GENE-021115-2 280653 54822 trpm7 ZFA:0009361 serotonergic neuron BFO:0000050 part_of ZFA:0000418 pretectum PATO:0000470 increased amount abnormal ZDB-GENE-021115-2 280653 54822 trpm7 ZFA:0000434 skeletal system PATO:0000001 quality abnormal ZDB-GENE-021115-2 280653 54822 trpm7 ZFA:0000514 frontal bone PATO:0000025 composition abnormal ZDB-GENE-021115-2 280653 54822 trpm7 ZFA:0000519 hemal arch PATO:0000025 composition abnormal ZDB-GENE-021115-2 280653 54822 trpm7 ZFA:0000529 kidney PATO:0001447 calcified abnormal ZDB-GENE-021115-2 280653 54822 trpm7 ZFA:0000529 kidney PATO:0001624 decreased functionality abnormal ZDB-GENE-021115-2 280653 54822 trpm7 ZFA:0000561 parasphenoid PATO:0000025 composition abnormal ZDB-GENE-021115-2 280653 54822 trpm7 ZFA:0000567 premaxilla PATO:0000025 composition abnormal ZDB-GENE-021115-2 280653 54822 trpm7 ZFA:0000578 ceratohyal bone PATO:0001448 ossified abnormal ZDB-GENE-021115-2 280653 54822 trpm7 ZFA:0000621 quadrate PATO:0001448 ossified abnormal ZDB-GENE-021115-2 280653 54822 trpm7 ZFA:0000627 epihyal PATO:0001448 ossified abnormal ZDB-GENE-021115-2 280653 54822 trpm7 ZFA:0000656 ectopterygoid PATO:0000025 composition abnormal ZDB-GENE-021115-2 280653 54822 trpm7 ZFA:0000657 entopterygoid PATO:0000025 composition abnormal ZDB-GENE-021115-2 280653 54822 trpm7 ZFA:0000660 epural PATO:0000025 composition abnormal ZDB-GENE-021115-2 280653 54822 trpm7 ZFA:0000672 hyomandibula PATO:0001448 ossified abnormal ZDB-GENE-021115-2 280653 54822 trpm7 ZFA:0000692 symplectic PATO:0001448 ossified abnormal ZDB-GENE-021115-2 280653 54822 trpm7 ZFA:0001066 neural arch PATO:0000025 composition abnormal ZDB-GENE-021115-2 280653 54822 trpm7 ZFA:0001094 whole organism PATO:0000052 shape abnormal ZDB-GENE-021115-2 280653 54822 trpm7 ZFA:0001094 whole organism PATO:0000587 decreased size abnormal ZDB-GENE-021115-2 280653 54822 trpm7 ZFA:0001094 whole organism PATO:0001906 movement quality abnormal ZDB-GENE-021115-2 280653 54822 trpm7 ZFA:0001094 whole organism PATO:0002076 movement behavioral quality abnormal ZDB-GENE-021115-2 280653 54822 trpm7 ZFA:0001094 whole organism PATO:0002251 decreased pigmentation abnormal ZDB-GENE-021115-2 280653 54822 trpm7 ZFA:0001115 trunk PATO:0002000 lacks all parts of type abnormal ZFA:0009091 melanocyte ZDB-GENE-021115-2 280653 54822 trpm7 ZFA:0001188 Weberian apparatus PATO:0000646 malformed abnormal ZDB-GENE-021115-2 280653 54822 trpm7 ZFA:0001188 Weberian apparatus PATO:0001485 condensed abnormal ZDB-GENE-021115-2 280653 54822 trpm7 ZFA:0001190 Weberian vertebra PATO:0001485 condensed abnormal ZDB-GENE-021115-2 280653 54822 trpm7 ZFA:0001200 corpuscles of Stannius PATO:0001241 physical object quality abnormal ZDB-GENE-021115-2 280653 54822 trpm7 ZFA:0001237 ceratobranchial 1 bone PATO:0001448 ossified abnormal ZDB-GENE-021115-2 280653 54822 trpm7 ZFA:0001240 ceratobranchial 4 bone PATO:0001448 ossified abnormal ZDB-GENE-021115-2 280653 54822 trpm7 ZFA:0001241 ceratobranchial 3 bone PATO:0001448 ossified abnormal ZDB-GENE-021115-2 280653 54822 trpm7 ZFA:0001242 ceratobranchial 2 bone PATO:0001448 ossified abnormal ZDB-GENE-021115-2 280653 54822 trpm7 ZFA:0001249 exocrine pancreas PATO:0000645 hypoplastic abnormal ZDB-GENE-021115-2 280653 54822 trpm7 ZFA:0001287 renal tubule PATO:0001447 calcified abnormal ZDB-GENE-021115-2 280653 54822 trpm7 ZFA:0001396 parapophysis/rib PATO:0000646 malformed abnormal ZDB-GENE-021115-2 280653 54822 trpm7 ZFA:0001550 caudal fin lepidotrichium PATO:0000025 composition abnormal ZDB-GENE-021115-2 280653 54822 trpm7 ZFA:0001559 vertebral column PATO:0001798 kinked abnormal ZDB-GENE-021115-2 280653 54822 trpm7 ZFA:0009045 epithelial cell of pancreas PATO:0002058 decreased area abnormal ZDB-GENE-021115-2 280653 54822 trpm7 ZFA:0009090 pigment cell PATO:0000001 quality abnormal ZDB-GENE-021115-2 280653 54822 trpm7 GO:0042391 regulation of membrane potential BFO:0000066 occurs_in ZFA:0009091 melanocyte PATO:0001507 disrupted abnormal ZDB-GENE-021115-2 280653 54822 trpm7 GO:0042470 melanosome BFO:0000050 part_of ZFA:0009091 melanocyte PATO:0000646 malformed abnormal ZDB-GENE-021115-2 280653 54822 trpm7 GO:0042470 melanosome BFO:0000050 part_of ZFA:0009091 melanocyte PATO:0001629 aggregated abnormal ZDB-GENE-021115-2 280653 54822 trpm7 ZFA:0009091 melanocyte PATO:0000001 quality abnormal ZDB-GENE-021115-2 280653 54822 trpm7 ZFA:0009091 melanocyte PATO:0000049 intensity abnormal ZDB-GENE-021115-2 280653 54822 trpm7 ZFA:0009091 melanocyte PATO:0000051 morphology abnormal ZDB-GENE-021115-2 280653 54822 trpm7 ZFA:0009091 melanocyte PATO:0000060 spatial pattern abnormal ZDB-GENE-021115-2 280653 54822 trpm7 ZFA:0009091 melanocyte PATO:0000328 low saturation abnormal ZDB-GENE-021115-2 280653 54822 trpm7 ZFA:0009091 melanocyte PATO:0000330 irregular spatial pattern abnormal ZDB-GENE-021115-2 280653 54822 trpm7 ZFA:0009091 melanocyte PATO:0000337 colorless abnormal ZDB-GENE-021115-2 280653 54822 trpm7 ZFA:0009091 melanocyte PATO:0000587 decreased size abnormal ZDB-GENE-021115-2 280653 54822 trpm7 ZFA:0009091 melanocyte PATO:0000646 malformed abnormal ZDB-GENE-021115-2 280653 54822 trpm7 ZFA:0009091 melanocyte PATO:0000647 necrotic abnormal ZDB-GENE-021115-2 280653 54822 trpm7 ZFA:0009091 melanocyte PATO:0001997 decreased amount abnormal ZDB-GENE-021115-2 280653 54822 trpm7 ZFA:0009091 melanocyte PATO:0002251 decreased pigmentation abnormal ZDB-GENE-021115-2 280653 54822 trpm7 ZFA:0009249 melanoblast PATO:0002251 decreased pigmentation abnormal ZDB-GENE-021115-2 280653 54822 trpm7 ZFA:0009277 acinar cell PATO:0000587 decreased size abnormal ZDB-GENE-021115-2 280653 54822 trpm7 ZFA:0009301 dopaminergic neuron PATO:0001997 decreased amount abnormal ZDB-GENE-021115-4 280652 50937 cdon ZFA:0001284 optic fissure PATO:0000609 closure incomplete abnormal ZDB-GENE-021115-5 280651 2113 ets1 GO:0006915 apoptotic process BFO:0000066 occurs_in ZFA:0009036 blood vessel endothelial cell PATO:0002304 increased process quality abnormal ZDB-GENE-021115-7 280649 5347 plk1 GO:0000236 mitotic prometaphase PATO:0000297 arrested abnormal ZDB-GENE-021115-7 280649 5347 plk1 GO:0002088 lens development in camera-type eye PATO:0002302 decreased process quality abnormal ZDB-GENE-021115-7 280649 5347 plk1 GO:0006915 apoptotic process PATO:0002304 increased process quality abnormal ZDB-GENE-021115-7 280649 5347 plk1 GO:0007080 mitotic metaphase chromosome alignment PATO:0001507 disrupted abnormal ZDB-GENE-021115-7 280649 5347 plk1 GO:0007100 mitotic centrosome separation PATO:0001507 disrupted abnormal ZDB-GENE-021115-7 280649 5347 plk1 GO:0030261 chromosome condensation PATO:0002051 increased occurrence abnormal ZDB-GENE-021115-7 280649 5347 plk1 GO:0040016 embryonic cleavage PATO:0000688 asynchronous abnormal ZDB-GENE-021115-7 280649 5347 plk1 GO:0045448 mitotic cell cycle, embryonic PATO:0001507 disrupted abnormal ZDB-GENE-021115-7 280649 5347 plk1 GO:0051306 mitotic sister chromatid separation PATO:0001507 disrupted abnormal ZDB-GENE-021115-7 280649 5347 plk1 GO:0090307 mitotic spindle assembly PATO:0001507 disrupted abnormal ZDB-GENE-021115-7 280649 5347 plk1 ZFA:0000008 brain PATO:0000141 structure abnormal ZDB-GENE-021115-7 280649 5347 plk1 ZFA:0000008 brain PATO:0000647 necrotic abnormal ZDB-GENE-021115-7 280649 5347 plk1 ZFA:0000012 central nervous system PATO:0000647 necrotic abnormal ZDB-GENE-021115-7 280649 5347 plk1 ZFA:0000035 lens PATO:0000587 decreased size abnormal ZDB-GENE-021115-7 280649 5347 plk1 ZFA:0000040 median fin fold PATO:0000638 apoptotic abnormal ZDB-GENE-021115-7 280649 5347 plk1 ZFA:0000054 pericardium PATO:0001450 edematous abnormal ZDB-GENE-021115-7 280649 5347 plk1 ZFA:0000075 spinal cord PATO:0000638 apoptotic abnormal ZDB-GENE-021115-7 280649 5347 plk1 ZFA:0000077 tail bud PATO:0000638 apoptotic abnormal ZDB-GENE-021115-7 280649 5347 plk1 ZFA:0000107 eye PATO:0000587 decreased size abnormal ZDB-GENE-021115-7 280649 5347 plk1 ZFA:0000114 heart PATO:0000001 quality abnormal ZDB-GENE-021115-7 280649 5347 plk1 ZFA:0000152 retina PATO:0000051 morphology abnormal ZDB-GENE-021115-7 280649 5347 plk1 ZFA:0000152 retina PATO:0000937 disorganized abnormal ZDB-GENE-021115-7 280649 5347 plk1 ZFA:0000368 integument PATO:0001362 fragile abnormal ZDB-GENE-021115-7 280649 5347 plk1 GO:0043005 neuron projection BFO:0000050 part_of ZFA:0000641 cranial nerve PATO:0001241 physical object quality abnormal ZDB-GENE-021115-7 280649 5347 plk1 ZFA:0001058 caudal fin PATO:0000647 necrotic abnormal ZDB-GENE-021115-7 280649 5347 plk1 GO:0032502 developmental process BFO:0000066 occurs_in ZFA:0001094 whole organism PATO:0002052 decreased occurrence abnormal ZDB-GENE-021115-7 280649 5347 plk1 ZFA:0001094 whole organism PATO:0000574 decreased length abnormal ZDB-GENE-021115-7 280649 5347 plk1 ZFA:0001094 whole organism PATO:0000587 decreased size abnormal ZDB-GENE-021115-7 280649 5347 plk1 ZFA:0001114 head PATO:0000587 decreased size abnormal ZDB-GENE-021115-7 280649 5347 plk1 ZFA:0001114 head PATO:0001617 deformed abnormal ZDB-GENE-021115-7 280649 5347 plk1 ZFA:0001115 trunk PATO:0000592 decreased thickness abnormal ZDB-GENE-021115-7 280649 5347 plk1 ZFA:0001115 trunk PATO:0000639 degenerate abnormal ZDB-GENE-021115-7 280649 5347 plk1 GO:0005929 cilium BFO:0000050 part_of ZFA:0001135 neural tube PATO:0001997 decreased amount abnormal ZDB-GENE-021115-7 280649 5347 plk1 GO:0060271 cilium assembly BFO:0000066 occurs_in ZFA:0001135 neural tube PATO:0002052 decreased occurrence abnormal ZDB-GENE-021115-7 280649 5347 plk1 ZFA:0001216 splanchnocranium PATO:0000645 hypoplastic abnormal ZDB-GENE-021115-7 280649 5347 plk1 ZFA:0001580 neurocranium PATO:0000646 malformed abnormal ZDB-GENE-021115-7 280649 5347 plk1 GO:0005813 centrosome BFO:0000050 part_of ZFA:0009000 cell PATO:0000140 position abnormal ZDB-GENE-021115-7 280649 5347 plk1 GO:0005813 centrosome BFO:0000050 part_of ZFA:0009000 cell PATO:0001956 variability of size abnormal ZDB-GENE-021115-7 280649 5347 plk1 GO:0072686 mitotic spindle BFO:0000050 part_of ZFA:0009000 cell PATO:0000937 disorganized abnormal ZDB-GENE-021115-7 280649 5347 plk1 ZFA:0009248 neuron PATO:0001997 decreased amount abnormal ZDB-GENE-021115-8 280647 3735 kars1 GO:0001964 startle response PATO:0000297 arrested abnormal ZDB-GENE-021115-8 280647 3735 kars1 GO:0001966 thigmotaxis PATO:0000297 arrested abnormal ZDB-GENE-021115-8 280647 3735 kars1 GO:0010842 retina layer formation PATO:0001507 disrupted abnormal ZDB-GENE-021115-8 280647 3735 kars1 GO:0035284 brain segmentation PATO:0001507 disrupted abnormal ZDB-GENE-021115-8 280647 3735 kars1 GO:0006915 apoptotic process BFO:0000066 occurs_in ZFA:0000008 brain PATO:0002051 increased occurrence abnormal ZDB-GENE-021115-8 280647 3735 kars1 ZFA:0000008 brain PATO:0002001 has fewer parts of type abnormal ZFA:0009248 neuron ZDB-GENE-021115-8 280647 3735 kars1 ZFA:0000008 brain PATO:0000941 vacuolated abnormal ZDB-GENE-021115-8 280647 3735 kars1 ZFA:0000008 brain PATO:0001480 spongy abnormal ZDB-GENE-021115-8 280647 3735 kars1 ZFA:0000051 otic vesicle PATO:0000587 decreased size abnormal ZDB-GENE-021115-8 280647 3735 kars1 ZFA:0000054 pericardium PATO:0001450 edematous abnormal ZDB-GENE-021115-8 280647 3735 kars1 ZFA:0000076 swim bladder PATO:0002377 uninflated abnormal ZDB-GENE-021115-8 280647 3735 kars1 GO:0006915 apoptotic process BFO:0000066 occurs_in ZFA:0000107 eye PATO:0002051 increased occurrence abnormal ZDB-GENE-021115-8 280647 3735 kars1 ZFA:0000107 eye PATO:0000587 decreased size abnormal ZDB-GENE-021115-8 280647 3735 kars1 ZFA:0000107 eye PATO:0000596 decreased volume abnormal ZDB-GENE-021115-8 280647 3735 kars1 ZFA:0000112 gut PATO:0000001 quality abnormal ZDB-GENE-021115-8 280647 3735 kars1 ZFA:0000112 gut PATO:0000645 hypoplastic abnormal ZDB-GENE-021115-8 280647 3735 kars1 ZFA:0000114 heart PATO:0000001 quality abnormal ZDB-GENE-021115-8 280647 3735 kars1 ZFA:0000123 liver PATO:0000001 quality abnormal ZDB-GENE-021115-8 280647 3735 kars1 ZFA:0000123 liver PATO:0000645 hypoplastic abnormal ZDB-GENE-021115-8 280647 3735 kars1 ZFA:0000152 retina PATO:0000051 morphology abnormal ZDB-GENE-021115-8 280647 3735 kars1 GO:0006915 apoptotic process BFO:0000066 occurs_in ZFA:0000217 inner ear PATO:0002051 increased occurrence abnormal ZDB-GENE-021115-8 280647 3735 kars1 ZFA:0000217 inner ear PATO:0002001 has fewer parts of type abnormal GO:0032420 stereocilium BFO:0000050 part_of ZFA:0000217 inner ear ZDB-GENE-021115-8 280647 3735 kars1 ZFA:0009114 muscle cell BFO:0000050 part_of ZFA:0000473 trunk musculature PATO:0000051 morphology abnormal ZDB-GENE-021115-8 280647 3735 kars1 ZFA:0000940 posterior lateral line neuromast PATO:0002001 has fewer parts of type abnormal ZFA:0009367 neuromast hair cell ZDB-GENE-021115-8 280647 3735 kars1 ZFA:0001094 whole organism PATO:0000169 viability abnormal ZDB-GENE-021115-8 280647 3735 kars1 ZFA:0001094 whole organism PATO:0001422 dead abnormal ZDB-GENE-021115-8 280647 3735 kars1 ZFA:0001096 immature anterior macula PATO:0002254 flattened abnormal ZDB-GENE-021115-8 280647 3735 kars1 ZFA:0001097 immature posterior macula PATO:0002254 flattened abnormal ZDB-GENE-021115-8 280647 3735 kars1 ZFA:0001114 head PATO:0000587 decreased size abnormal ZDB-GENE-021115-8 280647 3735 kars1 GO:0006915 apoptotic process BFO:0000066 occurs_in ZFA:0001115 trunk PATO:0002051 increased occurrence abnormal ZDB-GENE-021115-8 280647 3735 kars1 ZFA:0001115 trunk PATO:0000639 degenerate abnormal ZDB-GENE-021115-8 280647 3735 kars1 ZFA:0001617 otolith PATO:0000587 decreased size abnormal ZDB-GENE-021115-8 280647 3735 kars1 GO:0043005 neuron projection BFO:0000050 part_of ZFA:0009052 motor neuron PATO:0000587 decreased size abnormal ZDB-GENE-021115-8 280647 3735 kars1 GO:0043679 axon terminus BFO:0000050 part_of ZFA:0009052 motor neuron PATO:0002286 decreased branchiness abnormal ZDB-GENE-021115-8 280647 3735 kars1 GO:0030424 axon BFO:0000050 part_of ZFA:0009244 primary motor neuron PATO:0001715 decreased diameter abnormal ZDB-GENE-021115-9 280650 1316 klf6a GO:0001889 liver development PATO:0001507 disrupted abnormal ZDB-GENE-021115-9 280650 1316 klf6a GO:0008015 blood circulation PATO:0001507 disrupted abnormal ZDB-GENE-021115-9 280650 1316 klf6a GO:0008219 cell death PATO:0002051 increased occurrence abnormal ZDB-GENE-021115-9 280650 1316 klf6a GO:0008283 cell population proliferation PATO:0002052 decreased occurrence abnormal ZDB-GENE-021115-9 280650 1316 klf6a GO:0035701 hematopoietic stem cell migration PATO:0002052 decreased occurrence abnormal ZDB-GENE-021115-9 280650 1316 klf6a GO:0043249 erythrocyte maturation PATO:0000297 arrested abnormal ZDB-GENE-021115-9 280650 1316 klf6a GO:0060319 primitive erythrocyte differentiation PATO:0000297 arrested abnormal ZDB-GENE-021115-9 280650 1316 klf6a ZFA:0000054 pericardium PATO:0001450 edematous abnormal ZDB-GENE-021115-9 280650 1316 klf6a ZFA:0000084 yolk PATO:0001450 edematous abnormal ZDB-GENE-021115-9 280650 1316 klf6a GO:0007049 cell cycle BFO:0000066 occurs_in ZFA:0000094 blood island PATO:0001236 process quality abnormal ZDB-GENE-021115-9 280650 1316 klf6a GO:0008283 cell population proliferation BFO:0000066 occurs_in ZFA:0000094 blood island PATO:0002302 decreased process quality abnormal ZDB-GENE-021115-9 280650 1316 klf6a ZFA:0000099 brain vasculature PATO:0002105 hemorrhagic abnormal ZDB-GENE-021115-9 280650 1316 klf6a ZFA:0000107 eye PATO:0000587 decreased size abnormal ZDB-GENE-021115-9 280650 1316 klf6a ZFA:0000112 gut PATO:0000587 decreased size abnormal ZDB-GENE-021115-9 280650 1316 klf6a ZFA:0000123 liver PATO:0000587 decreased size abnormal ZDB-GENE-021115-9 280650 1316 klf6a ZFA:0001094 whole organism PATO:0000587 decreased size abnormal ZDB-GENE-021115-9 280650 1316 klf6a ZFA:0001114 head PATO:0000587 decreased size abnormal ZDB-GENE-021115-9 280650 1316 klf6a ZFA:0001114 head PATO:0001450 edematous abnormal ZDB-GENE-021115-9 280650 1316 klf6a ZFA:0001227 mandibular arch skeleton PATO:0000587 decreased size abnormal ZDB-GENE-021115-9 280650 1316 klf6a ZFA:0001249 exocrine pancreas PATO:0000587 decreased size abnormal ZDB-GENE-021115-9 280650 1316 klf6a GO:0043534 blood vessel endothelial cell migration BFO:0000066 occurs_in ZFA:0001286 caudal vein plexus PATO:0002302 decreased process quality abnormal ZDB-GENE-021115-9 280650 1316 klf6a GO:0048845 venous blood vessel morphogenesis BFO:0000066 occurs_in ZFA:0001286 caudal vein plexus PATO:0002302 decreased process quality abnormal ZDB-GENE-021115-9 280650 1316 klf6a ZFA:0009014 hematopoietic stem cell BFO:0000050 part_of ZFA:0001286 caudal vein plexus PATO:0001997 decreased amount abnormal ZDB-GENE-021115-9 280650 1316 klf6a ZFA:0001286 caudal vein plexus PATO:0000592 decreased thickness abnormal ZDB-GENE-021115-9 280650 1316 klf6a ZFA:0001286 caudal vein plexus PATO:0000596 decreased volume abnormal ZDB-GENE-021115-9 280650 1316 klf6a ZFA:0001286 caudal vein plexus PATO:0000937 disorganized abnormal ZDB-GENE-021115-9 280650 1316 klf6a ZFA:0001338 intestine PATO:0000587 decreased size abnormal ZDB-GENE-021115-9 280650 1316 klf6a ZFA:0005125 intestinal villus PATO:0000462 absent abnormal ZDB-GENE-021115-9 280650 1316 klf6a GO:0071425 hematopoietic stem cell proliferation BFO:0000066 occurs_in ZFA:0005898 caudal hematopoietic tissue PATO:0002052 decreased occurrence abnormal ZDB-GENE-021115-9 280650 1316 klf6a ZFA:0009014 hematopoietic stem cell BFO:0000050 part_of ZFA:0005898 caudal hematopoietic tissue PATO:0001997 decreased amount abnormal ZDB-GENE-021115-9 280650 1316 klf6a ZFA:0009354 hematopoietic multipotent progenitor cell BFO:0000050 part_of ZFA:0005898 caudal hematopoietic tissue PATO:0001997 decreased amount abnormal ZDB-GENE-021115-9 280650 1316 klf6a ZFA:0009256 nucleate erythrocyte PATO:0001997 decreased amount abnormal ZDB-GENE-021118-1 282555 3038 has3 ZFA:0001094 whole organism PATO:0000051 morphology abnormal ZDB-GENE-021119-2 282557 1813 drd2a GO:0048266 behavioral response to pain PATO:0002304 increased process quality abnormal ZDB-GENE-021119-2 282557 1813 drd2a GO:1904057 negative regulation of sensory perception of pain PATO:0001236 process quality abnormal ZDB-GENE-021119-2 282557 1813 drd2a ZFA:0000008 brain PATO:0000587 decreased size abnormal ZDB-GENE-021119-2 282557 1813 drd2a ZFA:0000114 heart PATO:0001836 congested abnormal ZDB-GENE-021119-2 282557 1813 drd2a ZFA:0001094 whole organism PATO:0000574 decreased length abnormal ZDB-GENE-021120-2 565450 2916 grm6b GO:0050908 detection of light stimulus involved in visual perception PATO:0002302 decreased process quality abnormal ZDB-GENE-021120-2 565450 2916 grm6b ZFA:0000152 retina PATO:0001624 decreased functionality abnormal ZDB-GENE-021125-1 282615 8467 smarca5 GO:0010842 retina layer formation PATO:0000297 arrested abnormal ZDB-GENE-021125-1 282615 8467 smarca5 ZFA:0000008 brain PATO:0000647 necrotic abnormal ZDB-GENE-021125-1 282615 8467 smarca5 ZFA:0000009 cardiac ventricle PATO:0000587 decreased size abnormal ZDB-GENE-021125-1 282615 8467 smarca5 ZFA:0000012 central nervous system PATO:0000647 necrotic abnormal ZDB-GENE-021125-1 282615 8467 smarca5 ZFA:0000107 eye PATO:0000587 decreased size abnormal ZDB-GENE-021125-1 282615 8467 smarca5 ZFA:0000112 gut PATO:0000001 quality abnormal ZDB-GENE-021125-1 282615 8467 smarca5 ZFA:0000112 gut PATO:0000645 hypoplastic abnormal ZDB-GENE-021125-1 282615 8467 smarca5 ZFA:0000123 liver PATO:0000001 quality abnormal ZDB-GENE-021125-1 282615 8467 smarca5 ZFA:0000123 liver PATO:0000645 hypoplastic abnormal ZDB-GENE-021125-1 282615 8467 smarca5 ZFA:0000152 retina PATO:0000001 quality abnormal ZDB-GENE-021125-1 282615 8467 smarca5 ZFA:0001094 whole organism PATO:0000587 decreased size abnormal ZDB-GENE-021125-1 282615 8467 smarca5 ZFA:0001114 head PATO:0000587 decreased size abnormal ZDB-GENE-021205-1 567779 89795 nav3 GO:0001889 liver development PATO:0001507 disrupted abnormal ZDB-GENE-021205-1 567779 89795 nav3 GO:0016477 cell migration PATO:0001507 disrupted abnormal ZDB-GENE-021205-1 567779 89795 nav3 GO:0031016 pancreas development PATO:0001507 disrupted abnormal ZDB-GENE-021205-1 567779 89795 nav3 GO:0048794 swim bladder development PATO:0001507 disrupted abnormal ZDB-GENE-021205-1 567779 89795 nav3 ZFA:0000123 liver PATO:0000052 shape abnormal ZDB-GENE-021205-1 567779 89795 nav3 ZFA:0000123 liver PATO:0000587 decreased size abnormal ZDB-GENE-021205-1 567779 89795 nav3 ZFA:0000123 liver PATO:0001483 aplastic abnormal ZDB-GENE-021205-1 567779 89795 nav3 ZFA:0000124 liver primordium PATO:0000587 decreased size abnormal ZDB-GENE-021206-1 282676 3329 hspd1 GO:0048798 swim bladder inflation PATO:0002052 decreased occurrence abnormal ZDB-GENE-021206-1 282676 3329 hspd1 GO:0086067 AV node cell to bundle of His cell communication PATO:0002302 decreased process quality abnormal ZDB-GENE-021206-1 282676 3329 hspd1 CHEBI:26523 reactive oxygen species BFO:0000050 part_of ZFA:0000009 cardiac ventricle PATO:0000470 increased amount abnormal ZDB-GENE-021206-1 282676 3329 hspd1 CHEBI:3815 Collagen BFO:0000050 part_of ZFA:0000009 cardiac ventricle PATO:0000470 increased amount abnormal ZDB-GENE-021206-1 282676 3329 hspd1 GO:0005739 mitochondrion BFO:0000050 part_of ZFA:0000009 cardiac ventricle PATO:0000470 increased amount abnormal ZDB-GENE-021206-1 282676 3329 hspd1 GO:0005739 mitochondrion BFO:0000050 part_of ZFA:0000009 cardiac ventricle PATO:0000587 decreased size abnormal ZDB-GENE-021206-1 282676 3329 hspd1 GO:0005776 autophagosome BFO:0000050 part_of ZFA:0000009 cardiac ventricle PATO:0000470 increased amount abnormal ZDB-GENE-021206-1 282676 3329 hspd1 GO:0030017 sarcomere BFO:0000050 part_of ZFA:0000009 cardiac ventricle PATO:0000592 decreased thickness abnormal ZDB-GENE-021206-1 282676 3329 hspd1 GO:0030017 sarcomere BFO:0000050 part_of ZFA:0000009 cardiac ventricle PATO:0040044 ruptured abnormal ZDB-GENE-021206-1 282676 3329 hspd1 ZFA:0000009 cardiac ventricle PATO:0001571 dilated abnormal ZDB-GENE-021206-1 282676 3329 hspd1 ZFA:0001632 portion of connective tissue BFO:0000050 part_of ZFA:0000114 heart PATO:0000470 increased amount abnormal ZDB-GENE-021206-1 282676 3329 hspd1 GO:0036269 swimming behavior BFO:0000066 occurs_in ZFA:0001094 whole organism PATO:0002302 decreased process quality abnormal ZDB-GENE-021206-1 282676 3329 hspd1 ZFA:0001094 whole organism PATO:0001604 decreased life span abnormal ZDB-GENE-021206-1 282676 3329 hspd1 ZFA:0001270 blastema PATO:0000001 quality abnormal ZDB-GENE-021206-1 282676 3329 hspd1 ZFA:0005061 ventricular myocardium PATO:0000592 decreased thickness abnormal ZDB-GENE-021206-12 266961 6927 hnf1a GO:0042593 glucose homeostasis PATO:0001507 disrupted abnormal ZDB-GENE-021206-12 266961 6927 hnf1a ZFA:0009102 pancreatic B cell PATO:0001997 decreased amount abnormal ZDB-GENE-021206-12 266961 6927 hnf1a ZFA:0009102 pancreatic B cell PATO:0002058 decreased area abnormal ZDB-GENE-021206-13 282673 10577 npc2.1 GO:0008015 blood circulation PATO:0001507 disrupted abnormal ZDB-GENE-021206-13 282673 10577 npc2.1 GO:0006954 inflammatory response BFO:0000066 occurs_in ZFA:0000008 brain PATO:0002304 increased process quality abnormal ZDB-GENE-021206-13 282673 10577 npc2.1 GO:0042552 myelination BFO:0000066 occurs_in ZFA:0000008 brain PATO:0002302 decreased process quality abnormal ZDB-GENE-021206-13 282673 10577 npc2.1 GO:0055074 calcium ion homeostasis BFO:0000066 occurs_in ZFA:0000008 brain PATO:0001236 process quality abnormal ZDB-GENE-021206-13 282673 10577 npc2.1 ZFA:0000008 brain PATO:0000587 decreased size abnormal ZDB-GENE-021206-13 282673 10577 npc2.1 GO:0005771 multivesicular body BFO:0000050 part_of ZFA:0000029 hindbrain PATO:0000470 increased amount abnormal ZDB-GENE-021206-13 282673 10577 npc2.1 ZFA:0000029 hindbrain PATO:0000587 decreased size abnormal ZDB-GENE-021206-13 282673 10577 npc2.1 ZFA:0000029 hindbrain PATO:0002037 degeneration abnormal ZDB-GENE-021206-13 282673 10577 npc2.1 GO:0005764 lysosome BFO:0000050 part_of ZFA:0000047 peripheral olfactory organ PATO:0000470 increased amount abnormal ZDB-GENE-021206-13 282673 10577 npc2.1 ZFA:0000047 peripheral olfactory organ PATO:0002270 increased accumulation abnormal CHEBI:52163 nile blue A BFO:0000050 part_of ZFA:0000047 peripheral olfactory organ ZDB-GENE-021206-13 282673 10577 npc2.1 GO:0005737 cytoplasm BFO:0000050 part_of ZFA:0000051 otic vesicle PATO:0000596 decreased volume abnormal ZDB-GENE-021206-13 282673 10577 npc2.1 ZFA:0000051 otic vesicle PATO:0000937 disorganized abnormal ZDB-GENE-021206-13 282673 10577 npc2.1 ZFA:0000076 swim bladder PATO:0002377 uninflated abnormal ZDB-GENE-021206-13 282673 10577 npc2.1 ZFA:0000079 telencephalon PATO:0000941 vacuolated abnormal ZDB-GENE-021206-13 282673 10577 npc2.1 CHEBI:16113 cholesterol BFO:0000050 part_of ZFA:0000088 yolk syncytial layer PATO:0000470 increased amount abnormal ZDB-GENE-021206-13 282673 10577 npc2.1 ZFA:0009071 Purkinje cell BFO:0000050 part_of ZFA:0000100 cerebellum PATO:0000141 structure abnormal ZDB-GENE-021206-13 282673 10577 npc2.1 ZFA:0009071 Purkinje cell BFO:0000050 part_of ZFA:0000100 cerebellum PATO:0001566 distributed abnormal ZDB-GENE-021206-13 282673 10577 npc2.1 GO:0006954 inflammatory response BFO:0000066 occurs_in ZFA:0000123 liver PATO:0002304 increased process quality abnormal ZDB-GENE-021206-13 282673 10577 npc2.1 GO:0055074 calcium ion homeostasis BFO:0000066 occurs_in ZFA:0000123 liver PATO:0001236 process quality abnormal ZDB-GENE-021206-13 282673 10577 npc2.1 GO:0042552 myelination BFO:0000066 occurs_in ZFA:0000128 midbrain PATO:0002302 decreased process quality abnormal ZDB-GENE-021206-13 282673 10577 npc2.1 ZFA:0000128 midbrain PATO:0000941 vacuolated abnormal ZDB-GENE-021206-13 282673 10577 npc2.1 ZFA:0000213 habenula PATO:0000141 structure abnormal ZDB-GENE-021206-13 282673 10577 npc2.1 ZFA:0000213 habenula PATO:0000941 vacuolated abnormal ZDB-GENE-021206-13 282673 10577 npc2.1 GO:0005764 lysosome BFO:0000050 part_of ZFA:0000243 neuromast PATO:0000470 increased amount abnormal ZDB-GENE-021206-13 282673 10577 npc2.1 ZFA:0000249 cranial nerve I PATO:0002037 degeneration abnormal ZDB-GENE-021206-13 282673 10577 npc2.1 ZFA:0000353 fasciculus retroflexus PATO:0000941 vacuolated abnormal ZDB-GENE-021206-13 282673 10577 npc2.1 GO:0042552 myelination BFO:0000066 occurs_in ZFA:0000359 habenular commissure PATO:0002302 decreased process quality abnormal ZDB-GENE-021206-13 282673 10577 npc2.1 ZFA:0000402 olfactory bulb PATO:0000941 vacuolated abnormal ZDB-GENE-021206-13 282673 10577 npc2.1 ZFA:0000435 cranial nerve II PATO:0000941 vacuolated abnormal ZDB-GENE-021206-13 282673 10577 npc2.1 ZFA:0000445 optic tectum PATO:0000941 vacuolated abnormal ZDB-GENE-021206-13 282673 10577 npc2.1 ZFA:0000534 lateral longitudinal fasciculus PATO:0002037 degeneration abnormal ZDB-GENE-021206-13 282673 10577 npc2.1 ZFA:0000543 medial longitudinal fasciculus PATO:0002037 degeneration abnormal ZDB-GENE-021206-13 282673 10577 npc2.1 ZFA:0000903 interpeduncular nucleus tegmentum PATO:0000941 vacuolated abnormal ZDB-GENE-021206-13 282673 10577 npc2.1 GO:0001966 thigmotaxis BFO:0000066 occurs_in ZFA:0001094 whole organism PATO:0002304 increased process quality abnormal ZDB-GENE-021206-13 282673 10577 npc2.1 GO:0007626 locomotory behavior BFO:0000066 occurs_in ZFA:0001094 whole organism PATO:0002302 decreased process quality abnormal ZDB-GENE-021206-13 282673 10577 npc2.1 GO:0042552 myelination BFO:0000066 occurs_in ZFA:0001094 whole organism PATO:0002302 decreased process quality abnormal ZDB-GENE-021206-13 282673 10577 npc2.1 ZFA:0001094 whole organism PATO:0000574 decreased length abnormal ZDB-GENE-021206-13 282673 10577 npc2.1 ZFA:0001094 whole organism PATO:0000583 decreased weight abnormal ZDB-GENE-021206-13 282673 10577 npc2.1 ZFA:0001114 head PATO:0000587 decreased size abnormal ZDB-GENE-021206-13 282673 10577 npc2.1 CHEBI:16113 cholesterol BFO:0000050 part_of ZFA:0001115 trunk PATO:0000470 increased amount abnormal ZDB-GENE-021206-13 282673 10577 npc2.1 ZFA:0001117 post-vent region PATO:0001468 curved dorsal abnormal ZDB-GENE-021206-13 282673 10577 npc2.1 ZFA:0001117 post-vent region PATO:0001469 curved ventral abnormal ZDB-GENE-021206-13 282673 10577 npc2.1 ZFA:0001117 post-vent region PATO:0001649 curved lateral abnormal ZDB-GENE-021206-13 282673 10577 npc2.1 ZFA:0001117 post-vent region PATO:0001798 kinked abnormal ZDB-GENE-021206-13 282673 10577 npc2.1 ZFA:0001429 raphe nucleus PATO:0000941 vacuolated abnormal ZDB-GENE-021206-13 282673 10577 npc2.1 ZFA:0001559 vertebral column PATO:0001592 increased curvature abnormal ZDB-GENE-021206-13 282673 10577 npc2.1 ZFA:0001559 vertebral column PATO:0001798 kinked abnormal ZDB-GENE-021206-13 282673 10577 npc2.1 ZFA:0001617 otolith PATO:0000462 absent abnormal ZDB-GENE-021206-13 282673 10577 npc2.1 CHEBI:16113 cholesterol BFO:0000050 part_of ZFA:0005739 pancreatic acinar cell PATO:0000470 increased amount abnormal ZDB-GENE-021206-13 282673 10577 npc2.1 GO:0016234 inclusion body BFO:0000050 part_of ZFA:0005739 pancreatic acinar cell PATO:0000470 increased amount abnormal ZDB-GENE-021206-13 282673 10577 npc2.1 GO:0042588 zymogen granule BFO:0000050 part_of ZFA:0005739 pancreatic acinar cell PATO:0000462 absent abnormal ZDB-GENE-021206-13 282673 10577 npc2.1 GO:0005634 nucleus BFO:0000050 part_of ZFA:0009111 hepatocyte PATO:0000586 increased size abnormal ZDB-GENE-021206-13 282673 10577 npc2.1 ZFA:0009111 hepatocyte PATO:0002270 increased accumulation abnormal GO:0005811 lipid droplet BFO:0000050 part_of ZFA:0009111 hepatocyte ZDB-GENE-021206-13 282673 10577 npc2.1 GO:0030424 axon BFO:0000050 part_of ZFA:0009150 Rohon-Beard neuron PATO:0001997 decreased amount abnormal ZDB-GENE-021206-13 282673 10577 npc2.1 ZFA:0009389 kidney cell PATO:0002037 degeneration abnormal ZDB-GENE-021206-3 282667 6383 sdc2 GO:0001947 heart looping PATO:0001236 process quality abnormal ZDB-GENE-021206-3 282667 6383 sdc2 GO:0003140 determination of left/right asymmetry in lateral mesoderm PATO:0001236 process quality abnormal ZDB-GENE-021206-3 282667 6383 sdc2 GO:0007507 heart development PATO:0001507 disrupted abnormal ZDB-GENE-021206-3 282667 6383 sdc2 GO:0040036 regulation of fibroblast growth factor receptor signaling pathway PATO:0001236 process quality abnormal ZDB-GENE-021206-3 282667 6383 sdc2 GO:0043473 pigmentation PATO:0002052 decreased occurrence abnormal ZDB-GENE-021206-3 282667 6383 sdc2 GO:0045176 apical protein localization PATO:0001507 disrupted abnormal ZDB-GENE-021206-3 282667 6383 sdc2 GO:0048565 digestive tract development PATO:0001507 disrupted abnormal ZDB-GENE-021206-3 282667 6383 sdc2 GO:0055113 epiboly involved in gastrulation with mouth forming second PATO:0001507 disrupted abnormal ZDB-GENE-021206-3 282667 6383 sdc2 GO:0060287 epithelial cilium movement involved in determination of left/right asymmetry PATO:0001236 process quality abnormal ZDB-GENE-021206-3 282667 6383 sdc2 GO:0060973 cell migration involved in heart development PATO:0001507 disrupted abnormal ZDB-GENE-021206-3 282667 6383 sdc2 GO:0070121 Kupffer's vesicle development PATO:0001236 process quality abnormal ZDB-GENE-021206-3 282667 6383 sdc2 GO:0071711 basement membrane organization PATO:0001507 disrupted abnormal ZDB-GENE-021206-3 282667 6383 sdc2 GO:0097435 supramolecular fiber organization PATO:0001507 disrupted abnormal ZDB-GENE-021206-3 282667 6383 sdc2 GO:0031514 motile cilium BFO:0000050 part_of ZFA:0000001 Kupffer's vesicle PATO:0000574 decreased length abnormal ZDB-GENE-021206-3 282667 6383 sdc2 GO:0031514 motile cilium BFO:0000050 part_of ZFA:0000001 Kupffer's vesicle PATO:0001997 decreased amount abnormal ZDB-GENE-021206-3 282667 6383 sdc2 ZFA:0000001 Kupffer's vesicle PATO:0000587 decreased size abnormal ZDB-GENE-021206-3 282667 6383 sdc2 ZFA:0000001 Kupffer's vesicle PATO:0000646 malformed abnormal ZDB-GENE-021206-3 282667 6383 sdc2 ZFA:0000001 Kupffer's vesicle PATO:0001241 physical object quality abnormal ZDB-GENE-021206-3 282667 6383 sdc2 ZFA:0000023 forerunner cell group PATO:0000587 decreased size abnormal ZDB-GENE-021206-3 282667 6383 sdc2 ZFA:0000023 forerunner cell group PATO:0001241 physical object quality abnormal ZDB-GENE-021206-3 282667 6383 sdc2 ZFA:0000054 pericardium PATO:0001450 edematous abnormal ZDB-GENE-021206-3 282667 6383 sdc2 ZFA:0000084 yolk PATO:0000586 increased size abnormal ZDB-GENE-021206-3 282667 6383 sdc2 ZFA:0000106 extension PATO:0000051 morphology abnormal ZDB-GENE-021206-3 282667 6383 sdc2 ZFA:0000114 heart PATO:0000965 symmetry abnormal ZDB-GENE-021206-3 282667 6383 sdc2 ZFA:0000121 lateral plate mesoderm PATO:0000965 symmetry abnormal ZDB-GENE-021206-3 282667 6383 sdc2 ZFA:0001094 whole organism PATO:0000587 decreased size abnormal ZDB-GENE-021206-7 798918 10768 ahcyl1 GO:0007420 brain development PATO:0001507 disrupted abnormal ZDB-GENE-021206-7 798918 10768 ahcyl1 ZFA:0000008 brain PATO:0000051 morphology abnormal ZDB-GENE-021206-7 798918 10768 ahcyl1 ZFA:0000008 brain PATO:0000647 necrotic abnormal ZDB-GENE-021206-7 798918 10768 ahcyl1 ZFA:0001094 whole organism PATO:0000636 wholly ventralized abnormal ZDB-GENE-021206-7 798918 10768 ahcyl1 ZFA:0001094 whole organism PATO:0001592 increased curvature abnormal ZDB-GENE-021206-7 798918 10768 ahcyl1 ZFA:0001117 post-vent region PATO:0001602 distended abnormal ZDB-GENE-021206-9 282670 2159 f10 GO:0007599 hemostasis PATO:0000502 delayed abnormal ZDB-GENE-021206-9 282670 2159 f10 GO:0007599 hemostasis PATO:0001507 disrupted abnormal ZDB-GENE-021206-9 282670 2159 f10 ZFA:0000008 brain PATO:0002105 hemorrhagic abnormal ZDB-GENE-021206-9 282670 2159 f10 ZFA:0000029 hindbrain PATO:0002105 hemorrhagic abnormal ZDB-GENE-021206-9 282670 2159 f10 ZFA:0000112 gut PATO:0002105 hemorrhagic abnormal ZDB-GENE-021206-9 282670 2159 f10 ZFA:0000128 midbrain PATO:0002105 hemorrhagic abnormal ZDB-GENE-021206-9 282670 2159 f10 ZFA:0000667 gill filament PATO:0002105 hemorrhagic abnormal ZDB-GENE-021206-9 282670 2159 f10 ZFA:0001094 whole organism PATO:0001422 dead abnormal ZDB-GENE-021206-9 282670 2159 f10 ZFA:0001094 whole organism PATO:0001604 decreased life span abnormal ZDB-GENE-021206-9 282670 2159 f10 ZFA:0005145 muscle PATO:0002105 hemorrhagic abnormal ZDB-GENE-021209-1 286747 4174 mcm5 GO:0001702 gastrulation with mouth forming second PATO:0001507 disrupted abnormal ZDB-GENE-021209-1 286747 4174 mcm5 GO:0006915 apoptotic process PATO:0002051 increased occurrence abnormal ZDB-GENE-021209-1 286747 4174 mcm5 GO:0009790 embryo development PATO:0001507 disrupted abnormal ZDB-GENE-021209-1 286747 4174 mcm5 GO:0009794 regulation of mitotic cell cycle, embryonic PATO:0001507 disrupted abnormal ZDB-GENE-021209-1 286747 4174 mcm5 GO:0006915 apoptotic process BFO:0000066 occurs_in ZFA:0000029 hindbrain PATO:0002304 increased process quality abnormal ZDB-GENE-021209-1 286747 4174 mcm5 GO:0008283 cell population proliferation BFO:0000066 occurs_in ZFA:0000029 hindbrain PATO:0002302 decreased process quality abnormal ZDB-GENE-021209-1 286747 4174 mcm5 ZFA:0005730 cranial motor neuron BFO:0000050 part_of ZFA:0000029 hindbrain PATO:0001997 decreased amount abnormal ZDB-GENE-021209-1 286747 4174 mcm5 ZFA:0000042 midbrain hindbrain boundary PATO:0001518 blurry abnormal ZDB-GENE-021209-1 286747 4174 mcm5 ZFA:0005730 cranial motor neuron BFO:0000050 part_of ZFA:0000069 rhombomere 6 PATO:0000470 increased amount abnormal ZDB-GENE-021209-1 286747 4174 mcm5 ZFA:0000095 pharyngeal arch 3-7 skeleton PATO:0000001 quality abnormal ZDB-GENE-021209-1 286747 4174 mcm5 ZFA:0000107 eye PATO:0000587 decreased size abnormal ZDB-GENE-021209-1 286747 4174 mcm5 ZFA:0000110 fourth ventricle PATO:0000587 decreased size abnormal ZDB-GENE-021209-1 286747 4174 mcm5 ZFA:0000117 hypoblast PATO:0000638 apoptotic abnormal ZDB-GENE-021209-1 286747 4174 mcm5 ZFA:0005730 cranial motor neuron BFO:0000050 part_of ZFA:0000823 rhombomere 5 PATO:0000470 increased amount abnormal ZDB-GENE-021209-1 286747 4174 mcm5 ZFA:0005730 cranial motor neuron BFO:0000050 part_of ZFA:0000949 rhombomere 7 PATO:0001997 decreased amount abnormal ZDB-GENE-021209-1 286747 4174 mcm5 ZFA:0005730 cranial motor neuron BFO:0000050 part_of ZFA:0000949 rhombomere 7 PATO:0040060 absence of anatomical entity abnormal ZDB-GENE-021209-1 286747 4174 mcm5 BSPO:0000005 anatomical surface BFO:0000050 part_of ZFA:0001094 whole organism PATO:0002058 decreased area abnormal ZDB-GENE-021209-1 286747 4174 mcm5 ZFA:0001094 whole organism PATO:0000969 dwarf-like abnormal ZDB-GENE-021209-1 286747 4174 mcm5 ZFA:0001114 head PATO:0000587 decreased size abnormal ZDB-GENE-021211-2 286739 4478 msna GO:0034332 adherens junction organization PATO:0001236 process quality abnormal ZDB-GENE-021211-2 286739 4478 msna GO:0072554 blood vessel lumenization PATO:0001236 process quality abnormal ZDB-GENE-021211-2 286739 4478 msna ZFA:0000054 pericardium PATO:0001450 edematous abnormal ZDB-GENE-021211-2 286739 4478 msna ZFA:0001285 intersegmental vessel PATO:0001896 unlumenized abnormal ZDB-GENE-021211-2 286739 4478 msna GO:0005912 adherens junction BFO:0000050 part_of ZFA:0009036 blood vessel endothelial cell PATO:0001241 physical object quality abnormal ZDB-GENE-021212-1 286745 57696 ddx55 ZFA:0000012 central nervous system PATO:0000647 necrotic abnormal ZDB-GENE-021212-1 286745 57696 ddx55 ZFA:0000042 midbrain hindbrain boundary PATO:0001485 condensed abnormal ZDB-GENE-021212-1 286745 57696 ddx55 ZFA:0000054 pericardium PATO:0001450 edematous abnormal ZDB-GENE-021212-1 286745 57696 ddx55 ZFA:0000084 yolk PATO:0000411 circular abnormal ZDB-GENE-021212-1 286745 57696 ddx55 ZFA:0000084 yolk PATO:0000950 grey abnormal ZDB-GENE-021212-1 286745 57696 ddx55 ZFA:0000095 pharyngeal arch 3-7 skeleton PATO:0000001 quality abnormal ZDB-GENE-021212-1 286745 57696 ddx55 ZFA:0000106 extension PATO:0000592 decreased thickness abnormal ZDB-GENE-021212-1 286745 57696 ddx55 ZFA:0000107 eye PATO:0000587 decreased size abnormal ZDB-GENE-021212-1 286745 57696 ddx55 ZFA:0000112 gut PATO:0000645 hypoplastic abnormal ZDB-GENE-021212-1 286745 57696 ddx55 ZFA:0001094 whole organism PATO:0001623 atrophied abnormal ZDB-GENE-021212-1 286745 57696 ddx55 ZFA:0001114 head PATO:0000587 decreased size abnormal ZDB-GENE-021212-1 286745 57696 ddx55 ZFA:0001115 trunk PATO:0000592 decreased thickness abnormal ZDB-GENE-021212-1 286745 57696 ddx55 ZFA:0001400 ceratohyal cartilage PATO:0000617 bent abnormal ZDB-GENE-021213-1 286746 55153 sdad1 ZFA:0000054 pericardium PATO:0001450 edematous abnormal ZDB-GENE-021213-1 286746 55153 sdad1 ZFA:0000084 yolk PATO:0000411 circular abnormal ZDB-GENE-021213-1 286746 55153 sdad1 ZFA:0000084 yolk PATO:0000950 grey abnormal ZDB-GENE-021213-1 286746 55153 sdad1 ZFA:0000107 eye PATO:0000587 decreased size abnormal ZDB-GENE-021213-1 286746 55153 sdad1 ZFA:0000112 gut PATO:0000001 quality abnormal ZDB-GENE-021213-1 286746 55153 sdad1 ZFA:0000112 gut PATO:0000645 hypoplastic abnormal ZDB-GENE-021213-1 286746 55153 sdad1 ZFA:0000114 heart PATO:0000001 quality abnormal ZDB-GENE-021213-1 286746 55153 sdad1 ZFA:0000123 liver PATO:0000001 quality abnormal ZDB-GENE-021213-1 286746 55153 sdad1 ZFA:0000123 liver PATO:0000645 hypoplastic abnormal ZDB-GENE-021213-1 286746 55153 sdad1 ZFA:0001114 head PATO:0000587 decreased size abnormal ZDB-GENE-021213-1 286746 55153 sdad1 ZFA:0001227 mandibular arch skeleton PATO:0001483 aplastic abnormal ZDB-GENE-021217-1 797134 55588 med29 GO:0008015 blood circulation PATO:0001507 disrupted abnormal ZDB-GENE-021217-1 797134 55588 med29 ZFA:0000054 pericardium PATO:0001450 edematous abnormal ZDB-GENE-021217-1 797134 55588 med29 ZFA:0000084 yolk PATO:0000950 grey abnormal ZDB-GENE-021217-1 797134 55588 med29 ZFA:0000107 eye PATO:0000001 quality abnormal ZDB-GENE-021217-1 797134 55588 med29 ZFA:0000112 gut PATO:0000645 hypoplastic abnormal ZDB-GENE-021217-1 797134 55588 med29 ZFA:0000143 retinal photoreceptor layer PATO:0000001 quality abnormal ZDB-GENE-021217-1 797134 55588 med29 ZFA:0000548 musculature system PATO:0000001 quality abnormal ZDB-GENE-021217-1 797134 55588 med29 ZFA:0001114 head PATO:0000411 circular abnormal ZDB-GENE-021217-1 797134 55588 med29 ZFA:0001114 head PATO:0000587 decreased size abnormal ZDB-GENE-021217-1 797134 55588 med29 ZFA:0001114 head PATO:0000647 necrotic abnormal ZDB-GENE-021217-1 797134 55588 med29 ZFA:0005145 muscle PATO:0000639 degenerate abnormal ZDB-GENE-021217-1 797134 55588 med29 ZFA:0005145 muscle PATO:0000937 disorganized abnormal ZDB-GENE-021217-2 286787 27042 utp25 GO:0000462 maturation of SSU-rRNA from tricistronic rRNA transcript (SSU-rRNA, 5.8S rRNA, LSU-rRNA) PATO:0001507 disrupted abnormal ZDB-GENE-021217-2 286787 27042 utp25 GO:0001889 liver development PATO:0001507 disrupted abnormal ZDB-GENE-021217-2 286787 27042 utp25 GO:0031017 exocrine pancreas development PATO:0001507 disrupted abnormal ZDB-GENE-021217-2 286787 27042 utp25 GO:0042254 ribosome biogenesis PATO:0001507 disrupted abnormal ZDB-GENE-021217-2 286787 27042 utp25 GO:0048485 sympathetic nervous system development PATO:0001507 disrupted abnormal ZDB-GENE-021217-2 286787 27042 utp25 GO:0048565 digestive tract development PATO:0001507 disrupted abnormal ZDB-GENE-021217-2 286787 27042 utp25 ZFA:0000107 eye PATO:0000587 decreased size abnormal ZDB-GENE-021217-2 286787 27042 utp25 ZFA:0000112 gut PATO:0000001 quality abnormal ZDB-GENE-021217-2 286787 27042 utp25 ZFA:0000112 gut PATO:0000645 hypoplastic abnormal ZDB-GENE-021217-2 286787 27042 utp25 ZFA:0000123 liver PATO:0000001 quality abnormal ZDB-GENE-021217-2 286787 27042 utp25 ZFA:0000123 liver PATO:0000587 decreased size abnormal ZDB-GENE-021217-2 286787 27042 utp25 ZFA:0000339 digestive system PATO:0000645 hypoplastic abnormal ZDB-GENE-021217-2 286787 27042 utp25 ZFA:0001094 whole organism PATO:0000169 viability abnormal ZDB-GENE-021217-2 286787 27042 utp25 ZFA:0001094 whole organism PATO:0001604 decreased life span abnormal ZDB-GENE-021217-2 286787 27042 utp25 ZFA:0001114 head PATO:0000587 decreased size abnormal ZDB-GENE-021217-2 286787 27042 utp25 ZFA:0001249 exocrine pancreas PATO:0000645 hypoplastic abnormal ZDB-GENE-021217-2 286787 27042 utp25 ZFA:0001338 intestine PATO:0000645 hypoplastic abnormal ZDB-GENE-021217-2 286787 27042 utp25 ZFA:0001439 anatomical system PATO:0000001 quality abnormal ZDB-GENE-021217-2 286787 27042 utp25 ZFA:0001572 superior cervical ganglion PATO:0000587 decreased size abnormal ZDB-GENE-021217-2 286787 27042 utp25 ZFA:0001572 superior cervical ganglion PATO:0000645 hypoplastic abnormal ZDB-GENE-021217-2 286787 27042 utp25 ZFA:0005123 gut epithelium PATO:0000051 morphology abnormal ZDB-GENE-021217-3 286784 200894 arl13b GO:0003140 determination of left/right asymmetry in lateral mesoderm PATO:0001236 process quality abnormal ZDB-GENE-021217-3 286784 200894 arl13b GO:0003351 epithelial cilium movement involved in extracellular fluid movement PATO:0000911 decreased rate abnormal ZDB-GENE-021217-3 286784 200894 arl13b GO:0007368 determination of left/right symmetry PATO:0001236 process quality abnormal ZDB-GENE-021217-3 286784 200894 arl13b GO:0007634 optokinetic behavior PATO:0002302 decreased process quality abnormal ZDB-GENE-021217-3 286784 200894 arl13b GO:0021587 cerebellum morphogenesis PATO:0002302 decreased process quality abnormal ZDB-GENE-021217-3 286784 200894 arl13b GO:0021702 cerebellar Purkinje cell differentiation PATO:0002052 decreased occurrence abnormal ZDB-GENE-021217-3 286784 200894 arl13b GO:0021707 cerebellar granule cell differentiation PATO:0002052 decreased occurrence abnormal ZDB-GENE-021217-3 286784 200894 arl13b GO:0036268 swimming PATO:0002302 decreased process quality abnormal ZDB-GENE-021217-3 286784 200894 arl13b GO:0060027 convergent extension involved in gastrulation PATO:0001236 process quality abnormal ZDB-GENE-021217-3 286784 200894 arl13b GO:0060271 cilium assembly PATO:0001236 process quality abnormal ZDB-GENE-021217-3 286784 200894 arl13b GO:0060271 cilium assembly PATO:0001507 disrupted abnormal ZDB-GENE-021217-3 286784 200894 arl13b ZFA:0000092 axis PATO:0000574 decreased length abnormal ZDB-GENE-021217-3 286784 200894 arl13b ZFA:0000114 heart PATO:0001324 bilateral symmetry abnormal ZDB-GENE-021217-3 286784 200894 arl13b ZFA:0000121 lateral plate mesoderm PATO:0001324 bilateral symmetry abnormal ZDB-GENE-021217-3 286784 200894 arl13b GO:0005929 cilium BFO:0000050 part_of ZFA:0000150 pronephric duct PATO:0000574 decreased length abnormal ZDB-GENE-021217-3 286784 200894 arl13b GO:0005929 cilium BFO:0000050 part_of ZFA:0000150 pronephric duct PATO:0000613 disoriented abnormal ZDB-GENE-021217-3 286784 200894 arl13b GO:0005929 cilium BFO:0000050 part_of ZFA:0000150 pronephric duct PATO:0001997 decreased amount abnormal ZDB-GENE-021217-3 286784 200894 arl13b GO:0031514 motile cilium BFO:0000050 part_of ZFA:0000150 pronephric duct PATO:0000574 decreased length abnormal ZDB-GENE-021217-3 286784 200894 arl13b ZFA:0000150 pronephric duct PATO:0002000 lacks all parts of type abnormal GO:0031514 motile cilium BFO:0000050 part_of ZFA:0000150 pronephric duct ZDB-GENE-021217-3 286784 200894 arl13b ZFA:0000150 pronephric duct PATO:0001714 increased diameter abnormal ZDB-GENE-021217-3 286784 200894 arl13b GO:0031514 motile cilium BFO:0000050 part_of ZFA:0000151 pronephros PATO:0000406 curved abnormal ZDB-GENE-021217-3 286784 200894 arl13b ZFA:0000151 pronephros PATO:0001673 cystic abnormal ZDB-GENE-021217-3 286784 200894 arl13b ZFA:0000155 somite PATO:0000600 increased width abnormal ZDB-GENE-021217-3 286784 200894 arl13b ZFA:0000358 granular layer corpus cerebelli PATO:0002001 has fewer parts of type abnormal ZFA:0001691 cerebellar granule cell ZDB-GENE-021217-3 286784 200894 arl13b ZFA:0001713 parallel fiber BFO:0000050 part_of ZFA:0000394 molecular layer corpus cerebelli PATO:0000937 disorganized abnormal ZDB-GENE-021217-3 286784 200894 arl13b ZFA:0000529 kidney PATO:0001673 cystic abnormal ZDB-GENE-021217-3 286784 200894 arl13b ZFA:0001094 whole organism PATO:0000052 shape abnormal ZDB-GENE-021217-3 286784 200894 arl13b ZFA:0001094 whole organism PATO:0000406 curved abnormal ZDB-GENE-021217-3 286784 200894 arl13b ZFA:0001094 whole organism PATO:0001469 curved ventral abnormal ZDB-GENE-021217-3 286784 200894 arl13b ZFA:0001115 trunk PATO:0000600 increased width abnormal ZDB-GENE-021217-3 286784 200894 arl13b ZFA:0001115 trunk PATO:0001469 curved ventral abnormal ZDB-GENE-021217-3 286784 200894 arl13b ZFA:0001117 post-vent region PATO:0000406 curved abnormal ZDB-GENE-021217-3 286784 200894 arl13b ZFA:0001117 post-vent region PATO:0001469 curved ventral abnormal ZDB-GENE-021217-3 286784 200894 arl13b ZFA:0001117 post-vent region PATO:0001592 increased curvature abnormal ZDB-GENE-021217-3 286784 200894 arl13b ZFA:0001557 pronephric glomerulus PATO:0001673 cystic abnormal ZDB-GENE-021217-3 286784 200894 arl13b ZFA:0001558 pronephric tubule PATO:0001673 cystic abnormal ZDB-GENE-021217-3 286784 200894 arl13b BSPO:0000069 dorso-medial region BFO:0000050 part_of ZFA:0001706 Purkinje cell layer corpus cerebelli PATO:0002001 has fewer parts of type abnormal ZFA:0009071 Purkinje cell ZDB-GENE-021217-3 286784 200894 arl13b ZFA:0001706 Purkinje cell layer corpus cerebelli PATO:0002001 has fewer parts of type abnormal ZFA:0009071 Purkinje cell ZDB-GENE-021217-3 286784 200894 arl13b GO:0061564 axon development BFO:0000066 occurs_in ZFA:0001713 parallel fiber PATO:0002302 decreased process quality abnormal ZDB-GENE-021217-3 286784 200894 arl13b GO:0097733 photoreceptor cell cilium BFO:0000050 part_of ZFA:0009127 photoreceptor cell PATO:0000574 decreased length abnormal ZDB-GENE-021217-3 286784 200894 arl13b GO:0001750 photoreceptor outer segment BFO:0000050 part_of ZFA:0009275 retinal rod cell PATO:0000574 decreased length abnormal ZDB-GENE-021217-3 286784 200894 arl13b GO:0060091 kinocilium BFO:0000050 part_of ZFA:0009367 neuromast hair cell PATO:0000574 decreased length abnormal ZDB-GENE-021219-1 286778 54955 airim ZFA:0000095 pharyngeal arch 3-7 skeleton PATO:0000001 quality abnormal ZDB-GENE-021219-1 286778 54955 airim ZFA:0000095 pharyngeal arch 3-7 skeleton PATO:0000587 decreased size abnormal ZDB-GENE-021219-1 286778 54955 airim ZFA:0000107 eye PATO:0000587 decreased size abnormal ZDB-GENE-021219-1 286778 54955 airim ZFA:0000112 gut PATO:0000001 quality abnormal ZDB-GENE-021219-1 286778 54955 airim ZFA:0000112 gut PATO:0000645 hypoplastic abnormal ZDB-GENE-021219-1 286778 54955 airim ZFA:0000123 liver PATO:0000001 quality abnormal ZDB-GENE-021219-1 286778 54955 airim ZFA:0000123 liver PATO:0000645 hypoplastic abnormal ZDB-GENE-021219-1 286778 54955 airim ZFA:0001114 head PATO:0000411 circular abnormal ZDB-GENE-021219-1 286778 54955 airim ZFA:0001114 head PATO:0000587 decreased size abnormal ZDB-GENE-021219-1 286778 54955 airim ZFA:0001400 ceratohyal cartilage PATO:0000617 bent abnormal ZDB-GENE-021219-1 286778 54955 airim ZFA:0001400 ceratohyal cartilage PATO:0001922 mislocalised posteriorly abnormal ZDB-GENE-021219-1 286778 54955 airim ZFA:0001613 pharyngeal arch 3-7 PATO:0000574 decreased length abnormal ZDB-GENE-021219-2 286779 51606 atp6v1h GO:0030282 bone mineralization PATO:0001507 disrupted abnormal ZDB-GENE-021219-2 286779 51606 atp6v1h GO:0030282 bone mineralization PATO:0002052 decreased occurrence abnormal ZDB-GENE-021219-2 286779 51606 atp6v1h GO:0043473 pigmentation PATO:0001507 disrupted abnormal ZDB-GENE-021219-2 286779 51606 atp6v1h GO:0043473 pigmentation PATO:0002052 decreased occurrence abnormal ZDB-GENE-021219-2 286779 51606 atp6v1h GO:0048069 eye pigmentation PATO:0001507 disrupted abnormal ZDB-GENE-021219-2 286779 51606 atp6v1h GO:0060042 retina morphogenesis in camera-type eye PATO:0001236 process quality abnormal ZDB-GENE-021219-2 286779 51606 atp6v1h GO:0090398 cellular senescence PATO:0002017 increased magnitude abnormal ZDB-GENE-021219-2 286779 51606 atp6v1h ZFA:0000008 brain PATO:0000647 necrotic abnormal ZDB-GENE-021219-2 286779 51606 atp6v1h ZFA:0000054 pericardium PATO:0001450 edematous abnormal ZDB-GENE-021219-2 286779 51606 atp6v1h ZFA:0000076 swim bladder PATO:0002377 uninflated abnormal ZDB-GENE-021219-2 286779 51606 atp6v1h ZFA:0000107 eye PATO:0000014 color abnormal ZDB-GENE-021219-2 286779 51606 atp6v1h ZFA:0000107 eye PATO:0000587 decreased size abnormal ZDB-GENE-021219-2 286779 51606 atp6v1h ZFA:0000112 gut PATO:0000587 decreased size abnormal ZDB-GENE-021219-2 286779 51606 atp6v1h ZFA:0000112 gut PATO:0000645 hypoplastic abnormal ZDB-GENE-021219-2 286779 51606 atp6v1h ZFA:0000123 liver PATO:0000587 decreased size abnormal ZDB-GENE-021219-2 286779 51606 atp6v1h ZFA:0000123 liver PATO:0000645 hypoplastic abnormal ZDB-GENE-021219-2 286779 51606 atp6v1h ZFA:0000126 centrum PATO:0002078 hollow abnormal ZDB-GENE-021219-2 286779 51606 atp6v1h ZFA:0000144 retinal pigmented epithelium PATO:0000001 quality abnormal ZDB-GENE-021219-2 286779 51606 atp6v1h ZFA:0000144 retinal pigmented epithelium PATO:0000646 malformed abnormal ZDB-GENE-021219-2 286779 51606 atp6v1h ZFA:0000144 retinal pigmented epithelium PATO:0001241 physical object quality abnormal ZDB-GENE-021219-2 286779 51606 atp6v1h ZFA:0000144 retinal pigmented epithelium PATO:0001354 translucent abnormal ZDB-GENE-021219-2 286779 51606 atp6v1h GO:0008219 cell death BFO:0000066 occurs_in ZFA:0000243 neuromast PATO:0002051 increased occurrence abnormal ZDB-GENE-021219-2 286779 51606 atp6v1h ZFA:0000396 nervous system PATO:0000001 quality abnormal ZDB-GENE-021219-2 286779 51606 atp6v1h ZFA:0001094 whole organism PATO:0000328 low saturation abnormal ZDB-GENE-021219-2 286779 51606 atp6v1h ZFA:0001094 whole organism PATO:0001422 dead abnormal ZDB-GENE-021219-2 286779 51606 atp6v1h ZFA:0001094 whole organism PATO:0001604 decreased life span abnormal ZDB-GENE-021219-2 286779 51606 atp6v1h ZFA:0001094 whole organism PATO:0002251 decreased pigmentation abnormal ZDB-GENE-021219-2 286779 51606 atp6v1h ZFA:0001114 head PATO:0000587 decreased size abnormal ZDB-GENE-021219-2 286779 51606 atp6v1h ZFA:0001114 head PATO:0002251 decreased pigmentation abnormal ZDB-GENE-021219-2 286779 51606 atp6v1h ZFA:0001115 trunk PATO:0000406 curved abnormal ZDB-GENE-021219-2 286779 51606 atp6v1h ZFA:0001189 vertebra PATO:0000051 morphology abnormal ZDB-GENE-021219-2 286779 51606 atp6v1h ZFA:0001189 vertebra PATO:0000587 decreased size abnormal ZDB-GENE-021219-2 286779 51606 atp6v1h ZFA:0001472 anterior lateral line neuromast PATO:0002001 has fewer parts of type abnormal GO:0060091 kinocilium BFO:0000050 part_of ZFA:0001472 anterior lateral line neuromast ZDB-GENE-021219-2 286779 51606 atp6v1h ZFA:0001472 anterior lateral line neuromast PATO:0002001 has fewer parts of type abnormal ZFA:0009367 neuromast hair cell ZDB-GENE-021219-2 286779 51606 atp6v1h ZFA:0001472 anterior lateral line neuromast PATO:0000646 malformed abnormal ZDB-GENE-021219-2 286779 51606 atp6v1h ZFA:0001472 anterior lateral line neuromast PATO:0002058 decreased area abnormal ZDB-GENE-021219-2 286779 51606 atp6v1h ZFA:0009091 melanocyte BFO:0000050 part_of ZFA:0005220 larval melanophore stripe PATO:0001354 translucent abnormal ZDB-GENE-021219-2 286779 51606 atp6v1h ZFA:0009090 pigment cell PATO:0000001 quality abnormal ZDB-GENE-021219-2 286779 51606 atp6v1h ZFA:0009090 pigment cell PATO:0001997 decreased amount abnormal ZDB-GENE-021219-2 286779 51606 atp6v1h GO:0042470 melanosome BFO:0000050 part_of ZFA:0009091 melanocyte PATO:0000411 circular abnormal ZDB-GENE-021219-2 286779 51606 atp6v1h GO:0042470 melanosome BFO:0000050 part_of ZFA:0009091 melanocyte PATO:0000587 decreased size abnormal ZDB-GENE-021219-2 286779 51606 atp6v1h GO:0042470 melanosome BFO:0000050 part_of ZFA:0009091 melanocyte PATO:0002251 decreased pigmentation abnormal ZDB-GENE-021219-2 286779 51606 atp6v1h ZFA:0009091 melanocyte PATO:0000462 absent abnormal ZDB-GENE-021219-2 286779 51606 atp6v1h ZFA:0009091 melanocyte PATO:0000586 increased size abnormal ZDB-GENE-021219-2 286779 51606 atp6v1h ZFA:0009091 melanocyte PATO:0000587 decreased size abnormal ZDB-GENE-021219-2 286779 51606 atp6v1h ZFA:0009091 melanocyte PATO:0000646 malformed abnormal ZDB-GENE-021219-2 286779 51606 atp6v1h ZFA:0009091 melanocyte PATO:0001354 translucent abnormal ZDB-GENE-021219-3 286774 84844 phf5a ZFA:0000008 brain PATO:0000647 necrotic abnormal ZDB-GENE-021219-3 286774 84844 phf5a ZFA:0000012 central nervous system PATO:0000647 necrotic abnormal ZDB-GENE-021219-3 286774 84844 phf5a ZFA:0000054 pericardium PATO:0001450 edematous abnormal ZDB-GENE-021219-3 286774 84844 phf5a ZFA:0000106 extension PATO:0001847 constricted abnormal ZDB-GENE-021219-3 286774 84844 phf5a ZFA:0000107 eye PATO:0000587 decreased size abnormal ZDB-GENE-021219-3 286774 84844 phf5a ZFA:0000107 eye PATO:0000647 necrotic abnormal ZDB-GENE-021219-3 286774 84844 phf5a ZFA:0000112 gut PATO:0000645 hypoplastic abnormal ZDB-GENE-021219-3 286774 84844 phf5a ZFA:0000123 liver PATO:0000645 hypoplastic abnormal ZDB-GENE-021219-3 286774 84844 phf5a ZFA:0001094 whole organism PATO:0000406 curved abnormal ZDB-GENE-021219-3 286774 84844 phf5a ZFA:0001114 head PATO:0000587 decreased size abnormal ZDB-GENE-021219-3 286774 84844 phf5a ZFA:0001114 head PATO:0000647 necrotic abnormal ZDB-GENE-021219-3 286774 84844 phf5a ZFA:0001115 trunk PATO:0000592 decreased thickness abnormal ZDB-GENE-021219-3 286774 84844 phf5a ZFA:0001115 trunk PATO:0000617 bent abnormal ZDB-GENE-021219-3 286774 84844 phf5a ZFA:0001115 trunk PATO:0000647 necrotic abnormal ZDB-GENE-021219-3 286774 84844 phf5a ZFA:0001115 trunk PATO:0001468 curved dorsal abnormal ZDB-GENE-021220-2 286777 79039 ddx54 ZFA:0000008 brain PATO:0000647 necrotic abnormal ZDB-GENE-021220-2 286777 79039 ddx54 ZFA:0000012 central nervous system PATO:0000647 necrotic abnormal ZDB-GENE-021220-2 286777 79039 ddx54 ZFA:0000107 eye PATO:0000587 decreased size abnormal ZDB-GENE-021220-2 286777 79039 ddx54 ZFA:0000112 gut PATO:0000645 hypoplastic abnormal ZDB-GENE-021220-2 286777 79039 ddx54 ZFA:0000123 liver PATO:0000645 hypoplastic abnormal ZDB-GENE-021220-2 286777 79039 ddx54 ZFA:0001114 head PATO:0000587 decreased size abnormal ZDB-GENE-021220-3 450035 58524 dmrt3a GO:0036269 swimming behavior PATO:0000381 decreased frequency abnormal ZDB-GENE-021220-3 450035 58524 dmrt3a GO:0036269 swimming behavior PATO:0001507 disrupted abnormal ZDB-GENE-021220-3 450035 58524 dmrt3a GO:0043056 forward locomotion PATO:0040033 decreased linear velocity abnormal ZDB-GENE-021220-3 450035 58524 dmrt3a ZFA:0001058 caudal fin PATO:0002472 decreased velocity abnormal ZDB-GENE-021220-6 286776 25896 ints7 ZFA:0000035 lens PATO:0000001 quality abnormal ZDB-GENE-021220-6 286776 25896 ints7 ZFA:0000054 pericardium PATO:0001450 edematous abnormal ZDB-GENE-021220-6 286776 25896 ints7 ZFA:0000095 pharyngeal arch 3-7 skeleton PATO:0000001 quality abnormal ZDB-GENE-021220-6 286776 25896 ints7 ZFA:0001114 head PATO:0000599 decreased width abnormal ZDB-GENE-021220-6 286776 25896 ints7 ZFA:0001227 mandibular arch skeleton PATO:0000052 shape abnormal ZDB-GENE-021220-6 286776 25896 ints7 ZFA:0001580 neurocranium PATO:0000052 shape abnormal ZDB-GENE-021223-1 286829 1605 dag1 GO:0001966 thigmotaxis PATO:0001507 disrupted abnormal ZDB-GENE-021223-1 286829 1605 dag1 GO:0008345 larval locomotory behavior PATO:0001507 disrupted abnormal ZDB-GENE-021223-1 286829 1605 dag1 GO:0009790 embryo development PATO:0000502 delayed abnormal ZDB-GENE-021223-1 286829 1605 dag1 GO:0016203 muscle attachment PATO:0001507 disrupted abnormal ZDB-GENE-021223-1 286829 1605 dag1 GO:0031987 locomotion involved in locomotory behavior PATO:0000911 decreased rate abnormal ZDB-GENE-021223-1 286829 1605 dag1 GO:0031987 locomotion involved in locomotory behavior PATO:0001507 disrupted abnormal ZDB-GENE-021223-1 286829 1605 dag1 GO:0033292 T-tubule organization PATO:0001236 process quality abnormal ZDB-GENE-021223-1 286829 1605 dag1 GO:0048593 camera-type eye morphogenesis PATO:0001236 process quality abnormal ZDB-GENE-021223-1 286829 1605 dag1 GO:0048741 skeletal muscle fiber development PATO:0001236 process quality abnormal ZDB-GENE-021223-1 286829 1605 dag1 GO:0050881 musculoskeletal movement PATO:0001507 disrupted abnormal ZDB-GENE-021223-1 286829 1605 dag1 ZFA:0001285 intersegmental vessel BFO:0000050 part_of ZFA:0000014 dorsal aorta PATO:0001505 separated from abnormal ZFA:0005025 dorsal longitudinal anastomotic vessel ZDB-GENE-021223-1 286829 1605 dag1 ZFA:0000035 lens PATO:0000646 malformed abnormal ZDB-GENE-021223-1 286829 1605 dag1 ZFA:0000076 swim bladder PATO:0000462 absent abnormal ZDB-GENE-021223-1 286829 1605 dag1 ZFA:0000152 retina PATO:0000646 malformed abnormal ZDB-GENE-021223-1 286829 1605 dag1 ZFA:0001089 myoseptum BFO:0000050 part_of ZFA:0000155 somite PATO:0001617 deformed abnormal ZDB-GENE-021223-1 286829 1605 dag1 ZFA:0001285 intersegmental vessel BFO:0000050 part_of ZFA:0000155 somite PATO:0000462 absent abnormal ZDB-GENE-021223-1 286829 1605 dag1 ZFA:0001285 intersegmental vessel BFO:0000050 part_of ZFA:0000155 somite PATO:0000937 disorganized abnormal ZDB-GENE-021223-1 286829 1605 dag1 ZFA:0000358 granular layer corpus cerebelli PATO:0000937 disorganized abnormal ZDB-GENE-021223-1 286829 1605 dag1 ZFA:0000445 optic tectum PATO:0000937 disorganized abnormal ZDB-GENE-021223-1 286829 1605 dag1 ZFA:0009115 skeletal muscle cell BFO:0000050 part_of ZFA:0000473 trunk musculature PATO:0001477 retracted abnormal ZDB-GENE-021223-1 286829 1605 dag1 ZFA:0000473 trunk musculature PATO:0001780 dystrophic abnormal ZDB-GENE-021223-1 286829 1605 dag1 GO:0005604 basement membrane BFO:0000050 part_of ZFA:0000610 vertical myoseptum PATO:0000330 irregular spatial pattern abnormal ZDB-GENE-021223-1 286829 1605 dag1 ZFA:0000610 vertical myoseptum PATO:0000600 increased width abnormal ZDB-GENE-021223-1 286829 1605 dag1 ZFA:0000610 vertical myoseptum PATO:0000646 malformed abnormal ZDB-GENE-021223-1 286829 1605 dag1 ZFA:0000610 vertical myoseptum PATO:0001241 physical object quality abnormal ZDB-GENE-021223-1 286829 1605 dag1 ZFA:0000610 vertical myoseptum PATO:0001617 deformed abnormal ZDB-GENE-021223-1 286829 1605 dag1 ZFA:0000640 cornea PATO:0000462 absent abnormal ZDB-GENE-021223-1 286829 1605 dag1 GO:0005604 basement membrane BFO:0000050 part_of ZFA:0001056 myotome PATO:0000646 malformed abnormal ZDB-GENE-021223-1 286829 1605 dag1 GO:0005927 muscle tendon junction BFO:0000050 part_of ZFA:0001056 myotome PATO:0000646 malformed abnormal ZDB-GENE-021223-1 286829 1605 dag1 GO:0005927 muscle tendon junction BFO:0000050 part_of ZFA:0001056 myotome PATO:0000937 disorganized abnormal ZDB-GENE-021223-1 286829 1605 dag1 ZFA:0005277 skeletal muscle BFO:0000050 part_of ZFA:0001056 myotome PATO:0000639 degenerate abnormal ZDB-GENE-021223-1 286829 1605 dag1 ZFA:0009114 muscle cell BFO:0000050 part_of ZFA:0001056 myotome PATO:0001453 detached from abnormal GO:0005927 muscle tendon junction BFO:0000050 part_of ZFA:0001056 myotome ZDB-GENE-021223-1 286829 1605 dag1 ZFA:0009114 muscle cell BFO:0000050 part_of ZFA:0001056 myotome PATO:0002264 organization quality abnormal ZDB-GENE-021223-1 286829 1605 dag1 ZFA:0001056 myotome PATO:0001372 refractivity abnormal ZDB-GENE-021223-1 286829 1605 dag1 ZFA:0001058 caudal fin PATO:0001798 kinked abnormal ZDB-GENE-021223-1 286829 1605 dag1 ZFA:0001069 ventral fin fold PATO:0000587 decreased size abnormal ZDB-GENE-021223-1 286829 1605 dag1 CHEBI:5058 Fibronectin BFO:0000050 part_of ZFA:0001089 myoseptum PATO:0001997 decreased amount abnormal ZDB-GENE-021223-1 286829 1605 dag1 GO:0005604 basement membrane BFO:0000050 part_of ZFA:0001089 myoseptum PATO:0070044 anatomical structure quality abnormal ZDB-GENE-021223-1 286829 1605 dag1 ZFA:0001089 myoseptum PATO:0001444 broken abnormal ZDB-GENE-021223-1 286829 1605 dag1 ZFA:0001094 whole organism PATO:0000304 decreased speed abnormal ZDB-GENE-021223-1 286829 1605 dag1 ZFA:0001094 whole organism PATO:0001422 dead abnormal ZDB-GENE-021223-1 286829 1605 dag1 ZFA:0001094 whole organism PATO:0001780 dystrophic abnormal ZDB-GENE-021223-1 286829 1605 dag1 ZFA:0009114 muscle cell BFO:0000050 part_of ZFA:0001117 post-vent region PATO:0000051 morphology abnormal ZDB-GENE-021223-1 286829 1605 dag1 ZFA:0001117 post-vent region PATO:0000574 decreased length abnormal ZDB-GENE-021223-1 286829 1605 dag1 ZFA:0001117 post-vent region PATO:0001592 increased curvature abnormal ZDB-GENE-021223-1 286829 1605 dag1 GO:0006936 muscle contraction BFO:0000066 occurs_in ZFA:0005145 muscle PATO:0002302 decreased process quality abnormal ZDB-GENE-021223-1 286829 1605 dag1 GO:0016529 sarcoplasmic reticulum BFO:0000050 part_of ZFA:0005145 muscle PATO:0001412 unstructured abnormal ZDB-GENE-021223-1 286829 1605 dag1 GO:0030017 sarcomere BFO:0000050 part_of ZFA:0005145 muscle PATO:0000051 morphology abnormal ZDB-GENE-021223-1 286829 1605 dag1 GO:0030017 sarcomere BFO:0000050 part_of ZFA:0005145 muscle PATO:0001997 decreased amount abnormal ZDB-GENE-021223-1 286829 1605 dag1 ZFA:0005145 muscle PATO:0000051 morphology abnormal ZDB-GENE-021223-1 286829 1605 dag1 ZFA:0005145 muscle PATO:0000647 necrotic abnormal ZDB-GENE-021223-1 286829 1605 dag1 ZFA:0005145 muscle PATO:0000937 disorganized abnormal ZDB-GENE-021223-1 286829 1605 dag1 ZFA:0005145 muscle PATO:0001167 damaged abnormal ZDB-GENE-021223-1 286829 1605 dag1 ZFA:0005145 muscle PATO:0001780 dystrophic abnormal ZDB-GENE-021223-1 286829 1605 dag1 ZFA:0005145 muscle PATO:0002246 decreased force abnormal ZDB-GENE-021223-1 286829 1605 dag1 ZFA:0005145 muscle PATO:0002284 tension abnormal ZDB-GENE-021223-1 286829 1605 dag1 GO:0031594 neuromuscular junction BFO:0000050 part_of ZFA:0005277 skeletal muscle PATO:0000051 morphology abnormal ZDB-GENE-021223-1 286829 1605 dag1 ZFA:0005277 skeletal muscle PATO:0001780 dystrophic abnormal ZDB-GENE-021223-1 286829 1605 dag1 ZFA:0009114 muscle cell PATO:0001453 detached from abnormal ZFA:0000610 vertical myoseptum ZDB-GENE-021223-1 286829 1605 dag1 ZFA:0009114 muscle cell PATO:0001453 detached from abnormal ZFA:0001089 myoseptum ZDB-GENE-021223-1 286829 1605 dag1 ZFA:0009114 muscle cell PATO:0001453 detached from abnormal ZFA:0009114 muscle cell ZDB-GENE-021223-1 286829 1605 dag1 GO:0014802 terminal cisterna BFO:0000050 part_of ZFA:0009115 skeletal muscle cell PATO:0000646 malformed abnormal ZDB-GENE-021223-1 286829 1605 dag1 GO:0030315 T-tubule BFO:0000050 part_of ZFA:0009115 skeletal muscle cell PATO:0000646 malformed abnormal ZDB-GENE-021223-1 286829 1605 dag1 GO:0042383 sarcolemma BFO:0000050 part_of ZFA:0009115 skeletal muscle cell PATO:0001505 separated from abnormal GO:0042383 sarcolemma BFO:0000050 part_of ZFA:0009115 skeletal muscle cell ZDB-GENE-021223-1 286829 1605 dag1 ZFA:0009115 skeletal muscle cell PATO:0001453 detached from abnormal ZFA:0001089 myoseptum ZDB-GENE-021223-1 286829 1605 dag1 ZFA:0009116 slow muscle cell PATO:0001453 detached from abnormal ZFA:0001089 myoseptum ZDB-GENE-021223-1 286829 1605 dag1 ZFA:0009117 fast muscle cell PATO:0001453 detached from abnormal ZFA:0001089 myoseptum ZDB-GENE-021223-2 286833 4160 mc4r GO:0007631 feeding behavior PATO:0002304 increased process quality abnormal ZDB-GENE-021223-2 286833 4160 mc4r GO:0042593 glucose homeostasis PATO:0015003 decreased efficacy abnormal ZDB-GENE-021223-2 286833 4160 mc4r ZFA:0001094 whole organism PATO:0000573 increased length abnormal ZDB-GENE-021226-1 286830 3912 lamb1a GO:0003140 determination of left/right asymmetry in lateral mesoderm PATO:0001507 disrupted abnormal ZDB-GENE-021226-1 286830 3912 lamb1a GO:0003140 determination of left/right asymmetry in lateral mesoderm PATO:0002302 decreased process quality abnormal ZDB-GENE-021226-1 286830 3912 lamb1a GO:0003266 regulation of secondary heart field cardioblast proliferation PATO:0002304 increased process quality abnormal ZDB-GENE-021226-1 286830 3912 lamb1a GO:0007411 axon guidance PATO:0001236 process quality abnormal ZDB-GENE-021226-1 286830 3912 lamb1a GO:0007634 optokinetic behavior PATO:0000911 decreased rate abnormal ZDB-GENE-021226-1 286830 3912 lamb1a GO:0008078 mesodermal cell migration PATO:0001507 disrupted abnormal ZDB-GENE-021226-1 286830 3912 lamb1a GO:0008104 protein localization PATO:0001507 disrupted abnormal ZDB-GENE-021226-1 286830 3912 lamb1a GO:0010842 retina layer formation PATO:0001507 disrupted abnormal ZDB-GENE-021226-1 286830 3912 lamb1a GO:0014028 notochord formation PATO:0001507 disrupted abnormal ZDB-GENE-021226-1 286830 3912 lamb1a GO:0014812 muscle cell migration PATO:0001507 disrupted abnormal ZDB-GENE-021226-1 286830 3912 lamb1a GO:0021555 midbrain-hindbrain boundary morphogenesis PATO:0001507 disrupted abnormal ZDB-GENE-021226-1 286830 3912 lamb1a GO:0030903 notochord development PATO:0000001 quality abnormal ZDB-GENE-021226-1 286830 3912 lamb1a GO:0033564 anterior/posterior axon guidance PATO:0001236 process quality abnormal ZDB-GENE-021226-1 286830 3912 lamb1a GO:0035469 determination of pancreatic left/right asymmetry PATO:0002302 decreased process quality abnormal ZDB-GENE-021226-1 286830 3912 lamb1a GO:0048369 lateral mesoderm morphogenesis PATO:0002302 decreased process quality abnormal ZDB-GENE-021226-1 286830 3912 lamb1a GO:0048565 digestive tract development PATO:0001507 disrupted abnormal ZDB-GENE-021226-1 286830 3912 lamb1a GO:0048570 notochord morphogenesis PATO:0001507 disrupted abnormal ZDB-GENE-021226-1 286830 3912 lamb1a GO:0048741 skeletal muscle fiber development PATO:0001507 disrupted abnormal ZDB-GENE-021226-1 286830 3912 lamb1a GO:0048798 swim bladder inflation PATO:0000297 arrested abnormal ZDB-GENE-021226-1 286830 3912 lamb1a GO:0050908 detection of light stimulus involved in visual perception PATO:0000297 arrested abnormal ZDB-GENE-021226-1 286830 3912 lamb1a GO:0060035 notochord cell development PATO:0002302 decreased process quality abnormal ZDB-GENE-021226-1 286830 3912 lamb1a GO:0060271 cilium assembly PATO:0002302 decreased process quality abnormal ZDB-GENE-021226-1 286830 3912 lamb1a GO:0060287 epithelial cilium movement involved in determination of left/right asymmetry PATO:0002302 decreased process quality abnormal ZDB-GENE-021226-1 286830 3912 lamb1a GO:0060537 muscle tissue development PATO:0001507 disrupted abnormal ZDB-GENE-021226-1 286830 3912 lamb1a GO:0061386 closure of optic fissure PATO:0002302 decreased process quality abnormal ZDB-GENE-021226-1 286830 3912 lamb1a GO:0070121 Kupffer's vesicle development PATO:0002302 decreased process quality abnormal ZDB-GENE-021226-1 286830 3912 lamb1a GO:0070831 basement membrane assembly PATO:0002302 decreased process quality abnormal ZDB-GENE-021226-1 286830 3912 lamb1a GO:0071907 determination of digestive tract left/right asymmetry PATO:0002302 decreased process quality abnormal ZDB-GENE-021226-1 286830 3912 lamb1a GO:0071910 determination of liver left/right asymmetry PATO:0002302 decreased process quality abnormal ZDB-GENE-021226-1 286830 3912 lamb1a GO:0031514 motile cilium BFO:0000050 part_of ZFA:0000001 Kupffer's vesicle PATO:0000574 decreased length abnormal ZDB-GENE-021226-1 286830 3912 lamb1a GO:0031514 motile cilium BFO:0000050 part_of ZFA:0000001 Kupffer's vesicle PATO:0001624 decreased functionality abnormal ZDB-GENE-021226-1 286830 3912 lamb1a ZFA:0000008 brain PATO:0000051 morphology abnormal ZDB-GENE-021226-1 286830 3912 lamb1a ZFA:0000008 brain PATO:0000052 shape abnormal ZDB-GENE-021226-1 286830 3912 lamb1a ZFA:0000008 brain PATO:0000647 necrotic abnormal ZDB-GENE-021226-1 286830 3912 lamb1a ZFA:0000008 brain PATO:0000937 disorganized abnormal ZDB-GENE-021226-1 286830 3912 lamb1a ZFA:0000008 brain PATO:0001925 surface feature shape abnormal ZDB-GENE-021226-1 286830 3912 lamb1a ZFA:0000017 endoderm PATO:0000600 increased width abnormal ZDB-GENE-021226-1 286830 3912 lamb1a ZFA:0000024 retinal ganglion cell layer PATO:0001630 dispersed abnormal ZDB-GENE-021226-1 286830 3912 lamb1a ZFA:0000029 hindbrain PATO:0000001 quality abnormal ZDB-GENE-021226-1 286830 3912 lamb1a ZFA:0000029 hindbrain PATO:0000051 morphology abnormal ZDB-GENE-021226-1 286830 3912 lamb1a ZFA:0000031 hypochord PATO:0000051 morphology abnormal ZDB-GENE-021226-1 286830 3912 lamb1a ZFA:0000035 lens PATO:0000141 structure abnormal ZDB-GENE-021226-1 286830 3912 lamb1a ZFA:0000035 lens PATO:0000587 decreased size abnormal ZDB-GENE-021226-1 286830 3912 lamb1a ZFA:0000035 lens PATO:0000628 mislocalised abnormal ZDB-GENE-021226-1 286830 3912 lamb1a ZFA:0000035 lens PATO:0000639 degenerate abnormal ZDB-GENE-021226-1 286830 3912 lamb1a ZFA:0000035 lens PATO:0000645 hypoplastic abnormal ZDB-GENE-021226-1 286830 3912 lamb1a ZFA:0000035 lens PATO:0000646 malformed abnormal ZDB-GENE-021226-1 286830 3912 lamb1a ZFA:0000035 lens PATO:0000937 disorganized abnormal ZDB-GENE-021226-1 286830 3912 lamb1a ZFA:0000035 lens PATO:0001483 aplastic abnormal ZDB-GENE-021226-1 286830 3912 lamb1a ZFA:0000035 lens PATO:0001598 protruding abnormal ZDB-GENE-021226-1 286830 3912 lamb1a ZFA:0000035 lens PATO:0002112 perforate abnormal ZDB-GENE-021226-1 286830 3912 lamb1a ZFA:0000035 lens PATO:0002181 displaced abnormal ZDB-GENE-021226-1 286830 3912 lamb1a ZFA:0000042 midbrain hindbrain boundary PATO:0000051 morphology abnormal ZDB-GENE-021226-1 286830 3912 lamb1a ZFA:0000042 midbrain hindbrain boundary PATO:0000052 shape abnormal ZDB-GENE-021226-1 286830 3912 lamb1a ZFA:0000054 pericardium PATO:0001450 edematous abnormal ZDB-GENE-021226-1 286830 3912 lamb1a GO:0071679 commissural neuron axon guidance BFO:0000066 occurs_in ZFA:0000059 postoptic commissure PATO:0001507 disrupted abnormal ZDB-GENE-021226-1 286830 3912 lamb1a ZFA:0009075 astrocyte BFO:0000050 part_of ZFA:0000059 postoptic commissure PATO:0000628 mislocalised abnormal ZDB-GENE-021226-1 286830 3912 lamb1a ZFA:0000059 postoptic commissure PATO:0002001 has fewer parts of type abnormal ZFA:0009075 astrocyte ZDB-GENE-021226-1 286830 3912 lamb1a ZFA:0000059 postoptic commissure PATO:0000587 decreased size abnormal ZDB-GENE-021226-1 286830 3912 lamb1a ZFA:0000059 postoptic commissure PATO:0001959 defasciculated abnormal ZDB-GENE-021226-1 286830 3912 lamb1a GO:0006915 apoptotic process BFO:0000066 occurs_in ZFA:0000107 eye PATO:0002051 increased occurrence abnormal ZDB-GENE-021226-1 286830 3912 lamb1a ZFA:0000107 eye PATO:0000001 quality abnormal ZDB-GENE-021226-1 286830 3912 lamb1a ZFA:0000107 eye PATO:0000051 morphology abnormal ZDB-GENE-021226-1 286830 3912 lamb1a ZFA:0000107 eye PATO:0000052 shape abnormal ZDB-GENE-021226-1 286830 3912 lamb1a ZFA:0000107 eye PATO:0000587 decreased size abnormal ZDB-GENE-021226-1 286830 3912 lamb1a ZFA:0000107 eye PATO:0001920 mislocalised ventrally abnormal ZDB-GENE-021226-1 286830 3912 lamb1a GO:0071679 commissural neuron axon guidance BFO:0000066 occurs_in ZFA:0000109 forebrain PATO:0001507 disrupted abnormal ZDB-GENE-021226-1 286830 3912 lamb1a ZFA:0000110 fourth ventricle PATO:0000586 increased size abnormal ZDB-GENE-021226-1 286830 3912 lamb1a ZFA:0000110 fourth ventricle PATO:0000587 decreased size abnormal ZDB-GENE-021226-1 286830 3912 lamb1a GO:0043256 laminin complex BFO:0000050 part_of ZFA:0000121 lateral plate mesoderm PATO:0001997 decreased amount abnormal ZDB-GENE-021226-1 286830 3912 lamb1a ZFA:0000121 lateral plate mesoderm PATO:0000628 mislocalised abnormal ZDB-GENE-021226-1 286830 3912 lamb1a ZFA:0000121 lateral plate mesoderm PATO:0000937 disorganized abnormal ZDB-GENE-021226-1 286830 3912 lamb1a ZFA:0000121 lateral plate mesoderm PATO:0001324 bilateral symmetry abnormal ZDB-GENE-021226-1 286830 3912 lamb1a ZFA:0000123 liver PATO:0001324 bilateral symmetry abnormal ZDB-GENE-021226-1 286830 3912 lamb1a ZFA:0000124 liver primordium PATO:0001324 bilateral symmetry abnormal ZDB-GENE-021226-1 286830 3912 lamb1a GO:0005604 basement membrane BFO:0000050 part_of ZFA:0000135 notochord PATO:0000937 disorganized abnormal ZDB-GENE-021226-1 286830 3912 lamb1a GO:0005773 vacuole BFO:0000050 part_of ZFA:0000135 notochord PATO:0000587 decreased size abnormal ZDB-GENE-021226-1 286830 3912 lamb1a GO:0005773 vacuole BFO:0000050 part_of ZFA:0000135 notochord PATO:0001997 decreased amount abnormal ZDB-GENE-021226-1 286830 3912 lamb1a ZFA:0009000 cell BFO:0000050 part_of ZFA:0000135 notochord PATO:0000141 structure abnormal ZDB-GENE-021226-1 286830 3912 lamb1a ZFA:0000135 notochord PATO:0000001 quality abnormal ZDB-GENE-021226-1 286830 3912 lamb1a ZFA:0000135 notochord PATO:0000051 morphology abnormal ZDB-GENE-021226-1 286830 3912 lamb1a ZFA:0000135 notochord PATO:0000141 structure abnormal ZDB-GENE-021226-1 286830 3912 lamb1a ZFA:0000135 notochord PATO:0000585 hypotrophic abnormal ZDB-GENE-021226-1 286830 3912 lamb1a ZFA:0000135 notochord PATO:0000592 decreased thickness abnormal ZDB-GENE-021226-1 286830 3912 lamb1a ZFA:0000135 notochord PATO:0000638 apoptotic abnormal ZDB-GENE-021226-1 286830 3912 lamb1a ZFA:0000135 notochord PATO:0000967 undulate abnormal ZDB-GENE-021226-1 286830 3912 lamb1a ZFA:0000135 notochord PATO:0001396 cellular quality abnormal ZDB-GENE-021226-1 286830 3912 lamb1a ZFA:0000135 notochord PATO:0002100 undifferentiated abnormal ZDB-GENE-021226-1 286830 3912 lamb1a ZFA:0000135 notochord PATO:0002106 poorly differentiated abnormal ZDB-GENE-021226-1 286830 3912 lamb1a ZFA:0000135 notochord PATO:0002111 moderately well differentiated abnormal ZDB-GENE-021226-1 286830 3912 lamb1a ZFA:0009096 endocrine cell BFO:0000050 part_of ZFA:0000140 pancreas PATO:0000628 mislocalised abnormal ZDB-GENE-021226-1 286830 3912 lamb1a ZFA:0000140 pancreas PATO:0001324 bilateral symmetry abnormal ZDB-GENE-021226-1 286830 3912 lamb1a ZFA:0000143 retinal photoreceptor layer PATO:0000592 decreased thickness abnormal ZDB-GENE-021226-1 286830 3912 lamb1a ZFA:0000152 retina PATO:0000001 quality abnormal ZDB-GENE-021226-1 286830 3912 lamb1a ZFA:0000152 retina PATO:0000587 decreased size abnormal ZDB-GENE-021226-1 286830 3912 lamb1a GO:0043256 laminin complex BFO:0000050 part_of ZFA:0000155 somite PATO:0001997 decreased amount abnormal ZDB-GENE-021226-1 286830 3912 lamb1a ZFA:0000155 somite PATO:0000001 quality abnormal ZDB-GENE-021226-1 286830 3912 lamb1a ZFA:0000155 somite PATO:0000051 morphology abnormal ZDB-GENE-021226-1 286830 3912 lamb1a ZFA:0000155 somite PATO:0000646 malformed abnormal ZDB-GENE-021226-1 286830 3912 lamb1a ZFA:0000155 somite PATO:0001485 condensed abnormal ZDB-GENE-021226-1 286830 3912 lamb1a ZFA:0000155 somite PATO:0002254 flattened abnormal ZDB-GENE-021226-1 286830 3912 lamb1a ZFA:0000159 tectal ventricle PATO:0000587 decreased size abnormal ZDB-GENE-021226-1 286830 3912 lamb1a ZFA:0000254 pancreas primordium PATO:0001324 bilateral symmetry abnormal ZDB-GENE-021226-1 286830 3912 lamb1a ZFA:0000282 sensory system PATO:0000001 quality abnormal ZDB-GENE-021226-1 286830 3912 lamb1a GO:0030424 axon BFO:0000050 part_of ZFA:0000318 brainstem and spinal white matter PATO:0001997 decreased amount abnormal ZDB-GENE-021226-1 286830 3912 lamb1a ZFA:0000396 nervous system PATO:0000001 quality abnormal ZDB-GENE-021226-1 286830 3912 lamb1a ZFA:0000435 cranial nerve II PATO:0000051 morphology abnormal ZDB-GENE-021226-1 286830 3912 lamb1a ZFA:0000435 cranial nerve II PATO:0000587 decreased size abnormal ZDB-GENE-021226-1 286830 3912 lamb1a ZFA:0000435 cranial nerve II PATO:0000592 decreased thickness abnormal ZDB-GENE-021226-1 286830 3912 lamb1a ZFA:0000435 cranial nerve II PATO:0001959 defasciculated abnormal ZDB-GENE-021226-1 286830 3912 lamb1a GO:0005927 muscle tendon junction BFO:0000050 part_of ZFA:0001056 myotome PATO:0000051 morphology abnormal ZDB-GENE-021226-1 286830 3912 lamb1a ZFA:0001056 myotome PATO:0000052 shape abnormal ZDB-GENE-021226-1 286830 3912 lamb1a ZFA:0001056 myotome PATO:0000592 decreased thickness abnormal ZDB-GENE-021226-1 286830 3912 lamb1a ZFA:0001056 myotome PATO:0001879 U-shaped abnormal ZDB-GENE-021226-1 286830 3912 lamb1a GO:0006915 apoptotic process BFO:0000066 occurs_in ZFA:0001094 whole organism PATO:0002051 increased occurrence abnormal ZDB-GENE-021226-1 286830 3912 lamb1a ZFA:0001094 whole organism PATO:0000169 viability abnormal ZDB-GENE-021226-1 286830 3912 lamb1a ZFA:0001094 whole organism PATO:0000574 decreased length abnormal ZDB-GENE-021226-1 286830 3912 lamb1a ZFA:0001094 whole organism PATO:0000617 bent abnormal ZDB-GENE-021226-1 286830 3912 lamb1a ZFA:0001094 whole organism PATO:0000718 lethal (sensu genetics) abnormal ZDB-GENE-021226-1 286830 3912 lamb1a ZFA:0001094 whole organism PATO:0001468 curved dorsal abnormal ZDB-GENE-021226-1 286830 3912 lamb1a ZFA:0001094 whole organism PATO:0001604 decreased life span abnormal ZDB-GENE-021226-1 286830 3912 lamb1a ZFA:0009075 astrocyte BFO:0000050 part_of ZFA:0001108 anterior commissure PATO:0000628 mislocalised abnormal ZDB-GENE-021226-1 286830 3912 lamb1a ZFA:0001108 anterior commissure PATO:0002001 has fewer parts of type abnormal ZFA:0009075 astrocyte ZDB-GENE-021226-1 286830 3912 lamb1a ZFA:0001114 head PATO:0000587 decreased size abnormal ZDB-GENE-021226-1 286830 3912 lamb1a ZFA:0001114 head PATO:0001872 cuboid abnormal ZDB-GENE-021226-1 286830 3912 lamb1a ZFA:0001115 trunk PATO:0000574 decreased length abnormal ZDB-GENE-021226-1 286830 3912 lamb1a ZFA:0001115 trunk PATO:0001468 curved dorsal abnormal ZDB-GENE-021226-1 286830 3912 lamb1a ZFA:0001117 post-vent region PATO:0002364 shortened abnormal ZDB-GENE-021226-1 286830 3912 lamb1a GO:0043256 laminin complex BFO:0000050 part_of ZFA:0001135 neural tube PATO:0001997 decreased amount abnormal ZDB-GENE-021226-1 286830 3912 lamb1a ZFA:0001259 forebrain ventricle PATO:0000587 decreased size abnormal ZDB-GENE-021226-1 286830 3912 lamb1a ZFA:0001284 optic fissure PATO:0000600 increased width abnormal ZDB-GENE-021226-1 286830 3912 lamb1a ZFA:0001284 optic fissure PATO:0000609 closure incomplete abnormal ZDB-GENE-021226-1 286830 3912 lamb1a ZFA:0001285 intersegmental vessel PATO:0001483 aplastic abnormal ZDB-GENE-021226-1 286830 3912 lamb1a ZFA:0001367 forebrain midbrain boundary PATO:0000600 increased width abnormal ZDB-GENE-021226-1 286830 3912 lamb1a ZFA:0005738 intestinal bulb primordium PATO:0001324 bilateral symmetry abnormal ZDB-GENE-021226-1 286830 3912 lamb1a GO:0032982 myosin filament BFO:0000050 part_of ZFA:0009116 slow muscle cell PATO:0000937 disorganized abnormal ZDB-GENE-021226-1 286830 3912 lamb1a GO:0032982 myosin filament BFO:0000050 part_of ZFA:0009117 fast muscle cell PATO:0000937 disorganized abnormal ZDB-GENE-021226-1 286830 3912 lamb1a GO:0042995 cell projection BFO:0000050 part_of ZFA:0009292 radial glial cell PATO:0000937 disorganized abnormal ZDB-GENE-021226-1 286830 3912 lamb1a GO:0030424 axon BFO:0000050 part_of ZFA:0009310 retinal ganglion cell PATO:0002035 ipsilateral to abnormal ZFA:0000107 eye ZDB-GENE-021226-1 286830 3912 lamb1a GO:0030424 axon BFO:0000050 part_of ZFA:0009310 retinal ganglion cell PATO:0000629 misrouted abnormal ZDB-GENE-021226-1 286830 3912 lamb1a ZFA:0009369 fast muscle myoblast PATO:0000574 decreased length abnormal ZDB-GENE-021226-2 286831 22798 lamb4 GO:0044297 cell body BFO:0000050 part_of ZFA:0009280 Muller cell PATO:0000060 spatial pattern abnormal ZDB-GENE-021226-2 286831 22798 lamb4 GO:0044297 cell body BFO:0000050 part_of ZFA:0009280 Muller cell PATO:0000140 position abnormal ZDB-GENE-021226-2 286831 22798 lamb4 GO:0044297 cell body BFO:0000050 part_of ZFA:0009280 Muller cell PATO:0002181 displaced abnormal ZDB-GENE-021226-2 286831 22798 lamb4 ZFA:0009280 Muller cell PATO:0001241 physical object quality abnormal ZDB-GENE-021226-3 286832 3915 lamc1 GO:0001947 heart looping PATO:0002302 decreased process quality abnormal ZDB-GENE-021226-3 286832 3915 lamc1 GO:0007015 actin filament organization PATO:0001507 disrupted abnormal ZDB-GENE-021226-3 286832 3915 lamc1 GO:0007283 spermatogenesis PATO:0001507 disrupted abnormal ZDB-GENE-021226-3 286832 3915 lamc1 GO:0007411 axon guidance PATO:0001236 process quality abnormal ZDB-GENE-021226-3 286832 3915 lamc1 GO:0007634 optokinetic behavior PATO:0000911 decreased rate abnormal ZDB-GENE-021226-3 286832 3915 lamc1 GO:0014028 notochord formation PATO:0001507 disrupted abnormal ZDB-GENE-021226-3 286832 3915 lamc1 GO:0014812 muscle cell migration PATO:0001507 disrupted abnormal ZDB-GENE-021226-3 286832 3915 lamc1 GO:0021555 midbrain-hindbrain boundary morphogenesis PATO:0001507 disrupted abnormal ZDB-GENE-021226-3 286832 3915 lamc1 GO:0030903 notochord development PATO:0000001 quality abnormal ZDB-GENE-021226-3 286832 3915 lamc1 GO:0030903 notochord development PATO:0001507 disrupted abnormal ZDB-GENE-021226-3 286832 3915 lamc1 GO:0033564 anterior/posterior axon guidance PATO:0001236 process quality abnormal ZDB-GENE-021226-3 286832 3915 lamc1 GO:0048570 notochord morphogenesis PATO:0001507 disrupted abnormal ZDB-GENE-021226-3 286832 3915 lamc1 GO:0048644 muscle organ morphogenesis PATO:0000502 delayed abnormal ZDB-GENE-021226-3 286832 3915 lamc1 GO:0048675 axon extension PATO:0001236 process quality abnormal ZDB-GENE-021226-3 286832 3915 lamc1 GO:0048741 skeletal muscle fiber development PATO:0001507 disrupted abnormal ZDB-GENE-021226-3 286832 3915 lamc1 GO:0050908 detection of light stimulus involved in visual perception PATO:0000297 arrested abnormal ZDB-GENE-021226-3 286832 3915 lamc1 GO:0060537 muscle tissue development PATO:0001507 disrupted abnormal ZDB-GENE-021226-3 286832 3915 lamc1 ZFA:0000008 brain PATO:0000001 quality abnormal ZDB-GENE-021226-3 286832 3915 lamc1 ZFA:0000008 brain PATO:0000051 morphology abnormal ZDB-GENE-021226-3 286832 3915 lamc1 ZFA:0000008 brain PATO:0000052 shape abnormal ZDB-GENE-021226-3 286832 3915 lamc1 ZFA:0000008 brain PATO:0000646 malformed abnormal ZDB-GENE-021226-3 286832 3915 lamc1 ZFA:0000008 brain PATO:0000937 disorganized abnormal ZDB-GENE-021226-3 286832 3915 lamc1 ZFA:0000008 brain PATO:0001925 surface feature shape abnormal ZDB-GENE-021226-3 286832 3915 lamc1 ZFA:0000024 retinal ganglion cell layer PATO:0001630 dispersed abnormal ZDB-GENE-021226-3 286832 3915 lamc1 ZFA:0000029 hindbrain PATO:0000001 quality abnormal ZDB-GENE-021226-3 286832 3915 lamc1 ZFA:0000029 hindbrain PATO:0000051 morphology abnormal ZDB-GENE-021226-3 286832 3915 lamc1 ZFA:0000035 lens PATO:0000141 structure abnormal ZDB-GENE-021226-3 286832 3915 lamc1 ZFA:0000035 lens PATO:0000587 decreased size abnormal ZDB-GENE-021226-3 286832 3915 lamc1 ZFA:0000035 lens PATO:0000628 mislocalised abnormal ZDB-GENE-021226-3 286832 3915 lamc1 ZFA:0000035 lens PATO:0000639 degenerate abnormal ZDB-GENE-021226-3 286832 3915 lamc1 ZFA:0000035 lens PATO:0000937 disorganized abnormal ZDB-GENE-021226-3 286832 3915 lamc1 ZFA:0000035 lens PATO:0001598 protruding abnormal ZDB-GENE-021226-3 286832 3915 lamc1 ZFA:0000035 lens PATO:0002112 perforate abnormal ZDB-GENE-021226-3 286832 3915 lamc1 ZFA:0000042 midbrain hindbrain boundary PATO:0000051 morphology abnormal ZDB-GENE-021226-3 286832 3915 lamc1 ZFA:0000042 midbrain hindbrain boundary PATO:0000052 shape abnormal ZDB-GENE-021226-3 286832 3915 lamc1 ZFA:0000054 pericardium PATO:0001450 edematous abnormal ZDB-GENE-021226-3 286832 3915 lamc1 ZFA:0000106 extension PATO:0000001 quality abnormal ZDB-GENE-021226-3 286832 3915 lamc1 ZFA:0000107 eye PATO:0000001 quality abnormal ZDB-GENE-021226-3 286832 3915 lamc1 ZFA:0000107 eye PATO:0000051 morphology abnormal ZDB-GENE-021226-3 286832 3915 lamc1 ZFA:0000107 eye PATO:0000587 decreased size abnormal ZDB-GENE-021226-3 286832 3915 lamc1 ZFA:0000107 eye PATO:0000646 malformed abnormal ZDB-GENE-021226-3 286832 3915 lamc1 ZFA:0000107 eye PATO:0001920 mislocalised ventrally abnormal ZDB-GENE-021226-3 286832 3915 lamc1 ZFA:0000110 fourth ventricle PATO:0000586 increased size abnormal ZDB-GENE-021226-3 286832 3915 lamc1 ZFA:0000110 fourth ventricle PATO:0000587 decreased size abnormal ZDB-GENE-021226-3 286832 3915 lamc1 ZFA:0000114 heart PATO:0000001 quality abnormal ZDB-GENE-021226-3 286832 3915 lamc1 ZFA:0000114 heart PATO:0000586 increased size abnormal ZDB-GENE-021226-3 286832 3915 lamc1 ZFA:0000114 heart PATO:0000587 decreased size abnormal ZDB-GENE-021226-3 286832 3915 lamc1 GO:0005587 collagen type IV trimer BFO:0000050 part_of ZFA:0000135 notochord PATO:0000462 absent abnormal ZDB-GENE-021226-3 286832 3915 lamc1 GO:0005604 basement membrane BFO:0000050 part_of ZFA:0000135 notochord PATO:0000937 disorganized abnormal ZDB-GENE-021226-3 286832 3915 lamc1 GO:0005773 vacuole BFO:0000050 part_of ZFA:0000135 notochord PATO:0000587 decreased size abnormal ZDB-GENE-021226-3 286832 3915 lamc1 GO:0005773 vacuole BFO:0000050 part_of ZFA:0000135 notochord PATO:0001997 decreased amount abnormal ZDB-GENE-021226-3 286832 3915 lamc1 ZFA:0009000 cell BFO:0000050 part_of ZFA:0000135 notochord PATO:0000141 structure abnormal ZDB-GENE-021226-3 286832 3915 lamc1 ZFA:0000135 notochord PATO:0001999 lacks parts or has fewer parts of type abnormal GO:0005791 rough endoplasmic reticulum BFO:0000050 part_of ZFA:0009000 cell ZDB-GENE-021226-3 286832 3915 lamc1 ZFA:0000135 notochord PATO:0000001 quality abnormal ZDB-GENE-021226-3 286832 3915 lamc1 ZFA:0000135 notochord PATO:0000051 morphology abnormal ZDB-GENE-021226-3 286832 3915 lamc1 ZFA:0000135 notochord PATO:0000141 structure abnormal ZDB-GENE-021226-3 286832 3915 lamc1 ZFA:0000135 notochord PATO:0000592 decreased thickness abnormal ZDB-GENE-021226-3 286832 3915 lamc1 ZFA:0000135 notochord PATO:0000638 apoptotic abnormal ZDB-GENE-021226-3 286832 3915 lamc1 ZFA:0000135 notochord PATO:0000967 undulate abnormal ZDB-GENE-021226-3 286832 3915 lamc1 ZFA:0000135 notochord PATO:0002014 structure, cavities abnormal ZDB-GENE-021226-3 286832 3915 lamc1 ZFA:0000135 notochord PATO:0002100 undifferentiated abnormal ZDB-GENE-021226-3 286832 3915 lamc1 ZFA:0000135 notochord PATO:0002106 poorly differentiated abnormal ZDB-GENE-021226-3 286832 3915 lamc1 ZFA:0000143 retinal photoreceptor layer PATO:0000592 decreased thickness abnormal ZDB-GENE-021226-3 286832 3915 lamc1 ZFA:0000152 retina PATO:0000001 quality abnormal ZDB-GENE-021226-3 286832 3915 lamc1 ZFA:0000152 retina PATO:0000587 decreased size abnormal ZDB-GENE-021226-3 286832 3915 lamc1 ZFA:0001086 muscle pioneer BFO:0000050 part_of ZFA:0000155 somite PATO:0000462 absent abnormal ZDB-GENE-021226-3 286832 3915 lamc1 ZFA:0000155 somite PATO:0000001 quality abnormal ZDB-GENE-021226-3 286832 3915 lamc1 ZFA:0000155 somite PATO:0000051 morphology abnormal ZDB-GENE-021226-3 286832 3915 lamc1 ZFA:0000155 somite PATO:0000052 shape abnormal ZDB-GENE-021226-3 286832 3915 lamc1 ZFA:0000155 somite PATO:0001485 condensed abnormal ZDB-GENE-021226-3 286832 3915 lamc1 ZFA:0000159 tectal ventricle PATO:0000587 decreased size abnormal ZDB-GENE-021226-3 286832 3915 lamc1 ZFA:0000282 sensory system PATO:0000001 quality abnormal ZDB-GENE-021226-3 286832 3915 lamc1 GO:0030424 axon BFO:0000050 part_of ZFA:0000318 brainstem and spinal white matter PATO:0001997 decreased amount abnormal ZDB-GENE-021226-3 286832 3915 lamc1 ZFA:0000396 nervous system PATO:0000001 quality abnormal ZDB-GENE-021226-3 286832 3915 lamc1 ZFA:0000435 cranial nerve II PATO:0000051 morphology abnormal ZDB-GENE-021226-3 286832 3915 lamc1 ZFA:0000598 testis PATO:0000141 structure abnormal ZDB-GENE-021226-3 286832 3915 lamc1 GO:0005927 muscle tendon junction BFO:0000050 part_of ZFA:0001056 myotome PATO:0000051 morphology abnormal ZDB-GENE-021226-3 286832 3915 lamc1 GO:0005927 muscle tendon junction BFO:0000050 part_of ZFA:0001056 myotome PATO:0000646 malformed abnormal ZDB-GENE-021226-3 286832 3915 lamc1 ZFA:0009114 muscle cell BFO:0000050 part_of ZFA:0001056 myotome PATO:0001453 detached from abnormal GO:0005927 muscle tendon junction BFO:0000050 part_of ZFA:0001056 myotome ZDB-GENE-021226-3 286832 3915 lamc1 ZFA:0001056 myotome PATO:0000052 shape abnormal ZDB-GENE-021226-3 286832 3915 lamc1 ZFA:0001056 myotome PATO:0001879 U-shaped abnormal ZDB-GENE-021226-3 286832 3915 lamc1 ZFA:0001094 whole organism PATO:0000052 shape abnormal ZDB-GENE-021226-3 286832 3915 lamc1 ZFA:0001094 whole organism PATO:0000169 viability abnormal ZDB-GENE-021226-3 286832 3915 lamc1 ZFA:0001094 whole organism PATO:0000574 decreased length abnormal ZDB-GENE-021226-3 286832 3915 lamc1 ZFA:0001094 whole organism PATO:0000718 lethal (sensu genetics) abnormal ZDB-GENE-021226-3 286832 3915 lamc1 ZFA:0001094 whole organism PATO:0001468 curved dorsal abnormal ZDB-GENE-021226-3 286832 3915 lamc1 ZFA:0001114 head PATO:0000407 flat abnormal ZDB-GENE-021226-3 286832 3915 lamc1 ZFA:0001114 head PATO:0001450 edematous abnormal ZDB-GENE-021226-3 286832 3915 lamc1 ZFA:0001114 head PATO:0001851 swollen abnormal ZDB-GENE-021226-3 286832 3915 lamc1 ZFA:0001115 trunk PATO:0000574 decreased length abnormal ZDB-GENE-021226-3 286832 3915 lamc1 ZFA:0001117 post-vent region PATO:0000574 decreased length abnormal ZDB-GENE-021226-3 286832 3915 lamc1 ZFA:0001227 mandibular arch skeleton PATO:0000587 decreased size abnormal ZDB-GENE-021226-3 286832 3915 lamc1 ZFA:0001259 forebrain ventricle PATO:0000587 decreased size abnormal ZDB-GENE-021226-3 286832 3915 lamc1 ZFA:0001285 intersegmental vessel PATO:0001483 aplastic abnormal ZDB-GENE-021226-3 286832 3915 lamc1 ZFA:0001367 forebrain midbrain boundary PATO:0000600 increased width abnormal ZDB-GENE-021226-3 286832 3915 lamc1 GO:0003382 epithelial cell morphogenesis BFO:0000066 occurs_in ZFA:0007125 midbrain hindbrain boundary constriction PATO:0001236 process quality abnormal ZDB-GENE-021226-3 286832 3915 lamc1 GO:0021555 midbrain-hindbrain boundary morphogenesis BFO:0000066 occurs_in ZFA:0007125 midbrain hindbrain boundary constriction PATO:0001236 process quality abnormal ZDB-GENE-021226-3 286832 3915 lamc1 GO:0032982 myosin filament BFO:0000050 part_of ZFA:0009116 slow muscle cell PATO:0000937 disorganized abnormal ZDB-GENE-021226-3 286832 3915 lamc1 ZFA:0009116 slow muscle cell PATO:0001453 detached from abnormal ZFA:0009116 slow muscle cell ZDB-GENE-021226-3 286832 3915 lamc1 ZFA:0009116 slow muscle cell PATO:0000639 degenerate abnormal ZDB-GENE-021226-3 286832 3915 lamc1 GO:0032982 myosin filament BFO:0000050 part_of ZFA:0009117 fast muscle cell PATO:0000937 disorganized abnormal ZDB-GENE-021226-3 286832 3915 lamc1 GO:0030424 axon BFO:0000050 part_of ZFA:0009149 Mauthner neuron PATO:0001924 mislocalised medially abnormal ZDB-GENE-021226-3 286832 3915 lamc1 GO:0045177 apical part of cell BFO:0000050 part_of ZFA:0009306 neuroepithelial cell PATO:0000599 decreased width abnormal ZDB-GENE-021226-3 286832 3915 lamc1 GO:0045178 basal part of cell BFO:0000050 part_of ZFA:0009306 neuroepithelial cell PATO:0000600 increased width abnormal ZDB-GENE-021226-3 286832 3915 lamc1 GO:0030424 axon BFO:0000050 part_of ZFA:0009310 retinal ganglion cell PATO:0002035 ipsilateral to abnormal ZFA:0000107 eye ZDB-GENE-021226-3 286832 3915 lamc1 GO:0030424 axon BFO:0000050 part_of ZFA:0009310 retinal ganglion cell PATO:0000629 misrouted abnormal ZDB-GENE-021226-3 286832 3915 lamc1 ZFA:0009369 fast muscle myoblast PATO:0000574 decreased length abnormal ZDB-GENE-021231-2 317639 90121 tsr2 ZFA:0000054 pericardium PATO:0001450 edematous abnormal ZDB-GENE-021231-2 317639 90121 tsr2 ZFA:0000107 eye PATO:0000587 decreased size abnormal ZDB-GENE-021231-2 317639 90121 tsr2 ZFA:0000112 gut PATO:0000001 quality abnormal ZDB-GENE-021231-2 317639 90121 tsr2 ZFA:0000112 gut PATO:0000645 hypoplastic abnormal ZDB-GENE-021231-2 317639 90121 tsr2 ZFA:0000114 heart PATO:0000001 quality abnormal ZDB-GENE-021231-2 317639 90121 tsr2 ZFA:0000123 liver PATO:0000001 quality abnormal ZDB-GENE-021231-2 317639 90121 tsr2 ZFA:0000123 liver PATO:0000645 hypoplastic abnormal ZDB-GENE-021231-2 317639 90121 tsr2 ZFA:0001114 head PATO:0000599 decreased width abnormal ZDB-GENE-021231-2 317639 90121 tsr2 ZFA:0001114 head PATO:0002258 pointed abnormal ZDB-GENE-021231-2 317639 90121 tsr2 ZFA:0001306 pharyngeal arch PATO:0000052 shape abnormal ZDB-GENE-021231-2 317639 90121 tsr2 ZFA:0001400 ceratohyal cartilage PATO:0000617 bent abnormal ZDB-GENE-021231-3 317637 23160 wdr43 GO:0001525 angiogenesis PATO:0001507 disrupted abnormal ZDB-GENE-021231-3 317637 23160 wdr43 GO:0001570 vasculogenesis PATO:0001507 disrupted abnormal ZDB-GENE-021231-3 317637 23160 wdr43 GO:0006364 rRNA processing PATO:0002302 decreased process quality abnormal ZDB-GENE-021231-3 317637 23160 wdr43 GO:0006915 apoptotic process PATO:0002051 increased occurrence abnormal ZDB-GENE-021231-3 317637 23160 wdr43 GO:0008283 cell population proliferation PATO:0002052 decreased occurrence abnormal ZDB-GENE-021231-3 317637 23160 wdr43 GO:0014033 neural crest cell differentiation PATO:0002302 decreased process quality abnormal ZDB-GENE-021231-3 317637 23160 wdr43 GO:0021551 central nervous system morphogenesis PATO:0002302 decreased process quality abnormal ZDB-GENE-021231-3 317637 23160 wdr43 GO:0048596 embryonic camera-type eye morphogenesis PATO:0002302 decreased process quality abnormal ZDB-GENE-021231-3 317637 23160 wdr43 GO:0048703 embryonic viscerocranium morphogenesis PATO:0002302 decreased process quality abnormal ZDB-GENE-021231-3 317637 23160 wdr43 GO:0060218 hematopoietic stem cell differentiation PATO:0001507 disrupted abnormal ZDB-GENE-021231-3 317637 23160 wdr43 GO:0072331 signal transduction by p53 class mediator PATO:0002304 increased process quality abnormal ZDB-GENE-021231-3 317637 23160 wdr43 ZFA:0000008 brain PATO:0000647 necrotic abnormal ZDB-GENE-021231-3 317637 23160 wdr43 ZFA:0000012 central nervous system PATO:0000647 necrotic abnormal ZDB-GENE-021231-3 317637 23160 wdr43 ZFA:0000014 dorsal aorta PATO:0000051 morphology abnormal ZDB-GENE-021231-3 317637 23160 wdr43 ZFA:0000045 neural crest PATO:0002106 poorly differentiated abnormal ZDB-GENE-021231-3 317637 23160 wdr43 ZFA:0000084 yolk PATO:0000411 circular abnormal ZDB-GENE-021231-3 317637 23160 wdr43 ZFA:0000107 eye PATO:0000051 morphology abnormal ZDB-GENE-021231-3 317637 23160 wdr43 ZFA:0000107 eye PATO:0000587 decreased size abnormal ZDB-GENE-021231-3 317637 23160 wdr43 ZFA:0000110 fourth ventricle PATO:0001853 hydrocephalic abnormal ZDB-GENE-021231-3 317637 23160 wdr43 ZFA:0001120 neuroectoderm BFO:0000050 part_of ZFA:0000152 retina PATO:0000647 necrotic abnormal ZDB-GENE-021231-3 317637 23160 wdr43 ZFA:0009023 common lymphoid progenitor BFO:0000050 part_of ZFA:0001077 thymus primordium PATO:0000462 absent abnormal ZDB-GENE-021231-3 317637 23160 wdr43 ZFA:0001094 whole organism PATO:0000169 viability abnormal ZDB-GENE-021231-3 317637 23160 wdr43 ZFA:0001114 head PATO:0001999 lacks parts or has fewer parts of type abnormal ZFA:0001460 pharyngeal arch cartilage ZDB-GENE-021231-3 317637 23160 wdr43 ZFA:0001115 trunk PATO:0000647 necrotic abnormal ZDB-GENE-021231-3 317637 23160 wdr43 ZFA:0001135 neural tube PATO:0000647 necrotic abnormal ZDB-GENE-021231-3 317637 23160 wdr43 ZFA:0001285 intersegmental vessel PATO:0001483 aplastic abnormal ZDB-GENE-021231-3 317637 23160 wdr43 ZFA:0001306 pharyngeal arch PATO:0000051 morphology abnormal ZDB-GENE-021231-3 317637 23160 wdr43 ZFA:0001306 pharyngeal arch PATO:0000647 necrotic abnormal ZDB-GENE-021231-3 317637 23160 wdr43 ZFA:0001306 pharyngeal arch PATO:0001241 physical object quality abnormal ZDB-GENE-021231-3 317637 23160 wdr43 ZFA:0009014 hematopoietic stem cell BFO:0000050 part_of ZFA:0005028 ventral wall of dorsal aorta PATO:0000462 absent abnormal ZDB-GENE-021231-4 317644 84365 nifk ZFA:0000008 brain PATO:0000647 necrotic abnormal ZDB-GENE-021231-4 317644 84365 nifk ZFA:0000012 central nervous system PATO:0000647 necrotic abnormal ZDB-GENE-021231-4 317644 84365 nifk ZFA:0000042 midbrain hindbrain boundary PATO:0001485 condensed abnormal ZDB-GENE-021231-4 317644 84365 nifk ZFA:0000107 eye PATO:0000587 decreased size abnormal ZDB-GENE-021231-4 317644 84365 nifk ZFA:0000110 fourth ventricle PATO:0001602 distended abnormal ZDB-GENE-021231-4 317644 84365 nifk ZFA:0000112 gut PATO:0000645 hypoplastic abnormal ZDB-GENE-021231-4 317644 84365 nifk ZFA:0000123 liver PATO:0000645 hypoplastic abnormal ZDB-GENE-021231-4 317644 84365 nifk ZFA:0001094 whole organism PATO:0000169 viability abnormal ZDB-GENE-021231-4 317644 84365 nifk ZFA:0001114 head PATO:0000587 decreased size abnormal ZDB-GENE-021231-4 317644 84365 nifk ZFA:0001115 trunk PATO:0000592 decreased thickness abnormal ZDB-GENE-021231-4 317644 84365 nifk ZFA:0001115 trunk PATO:0000647 necrotic abnormal ZDB-GENE-030102-1 317640 55622 ttc27 ZFA:0000054 pericardium PATO:0001450 edematous abnormal ZDB-GENE-030102-1 317640 55622 ttc27 ZFA:0000107 eye PATO:0000587 decreased size abnormal ZDB-GENE-030102-1 317640 55622 ttc27 ZFA:0000114 heart PATO:0000001 quality abnormal ZDB-GENE-030102-1 317640 55622 ttc27 ZFA:0001114 head PATO:0000599 decreased width abnormal ZDB-GENE-030102-1 317640 55622 ttc27 ZFA:0001114 head PATO:0002258 pointed abnormal ZDB-GENE-030102-2 317641 84186 zcchc7 ZFA:0000054 pericardium PATO:0001450 edematous abnormal ZDB-GENE-030102-2 317641 84186 zcchc7 ZFA:0000107 eye PATO:0000587 decreased size abnormal ZDB-GENE-030102-2 317641 84186 zcchc7 ZFA:0000112 gut PATO:0000001 quality abnormal ZDB-GENE-030102-2 317641 84186 zcchc7 ZFA:0000112 gut PATO:0000645 hypoplastic abnormal ZDB-GENE-030102-2 317641 84186 zcchc7 ZFA:0000114 heart PATO:0000001 quality abnormal ZDB-GENE-030102-2 317641 84186 zcchc7 ZFA:0000123 liver PATO:0000001 quality abnormal ZDB-GENE-030102-2 317641 84186 zcchc7 ZFA:0000123 liver PATO:0000645 hypoplastic abnormal ZDB-GENE-030102-2 317641 84186 zcchc7 ZFA:0001114 head PATO:0000587 decreased size abnormal ZDB-GENE-030102-2 317641 84186 zcchc7 ZFA:0001613 pharyngeal arch 3-7 PATO:0001483 aplastic abnormal ZDB-GENE-030109-1 317678 10856 ruvbl2 GO:0001889 liver development PATO:0001507 disrupted abnormal ZDB-GENE-030109-1 317678 10856 ruvbl2 GO:0003351 epithelial cilium movement involved in extracellular fluid movement PATO:0000297 arrested abnormal ZDB-GENE-030109-1 317678 10856 ruvbl2 GO:0007507 heart development PATO:0001507 disrupted abnormal ZDB-GENE-030109-1 317678 10856 ruvbl2 GO:0008015 blood circulation PATO:0000297 arrested abnormal ZDB-GENE-030109-1 317678 10856 ruvbl2 GO:0031017 exocrine pancreas development PATO:0001507 disrupted abnormal ZDB-GENE-030109-1 317678 10856 ruvbl2 GO:0036158 outer dynein arm assembly PATO:0002052 decreased occurrence abnormal ZDB-GENE-030109-1 317678 10856 ruvbl2 GO:0036159 inner dynein arm assembly PATO:0002052 decreased occurrence abnormal ZDB-GENE-030109-1 317678 10856 ruvbl2 GO:0048565 digestive tract development PATO:0001507 disrupted abnormal ZDB-GENE-030109-1 317678 10856 ruvbl2 GO:0060575 intestinal epithelial cell differentiation PATO:0001507 disrupted abnormal ZDB-GENE-030109-1 317678 10856 ruvbl2 GO:0006974 DNA damage response BFO:0000066 occurs_in ZFA:0000008 brain PATO:0002051 increased occurrence abnormal ZDB-GENE-030109-1 317678 10856 ruvbl2 ZFA:0000008 brain PATO:0000647 necrotic abnormal ZDB-GENE-030109-1 317678 10856 ruvbl2 ZFA:0000009 cardiac ventricle PATO:0000584 hypertrophic abnormal ZDB-GENE-030109-1 317678 10856 ruvbl2 ZFA:0000009 cardiac ventricle PATO:0000644 hyperplastic abnormal ZDB-GENE-030109-1 317678 10856 ruvbl2 ZFA:0000009 cardiac ventricle PATO:0001511 non-functional abnormal ZDB-GENE-030109-1 317678 10856 ruvbl2 ZFA:0000012 central nervous system PATO:0000647 necrotic abnormal ZDB-GENE-030109-1 317678 10856 ruvbl2 ZFA:0000054 pericardium PATO:0001450 edematous abnormal ZDB-GENE-030109-1 317678 10856 ruvbl2 ZFA:0000107 eye PATO:0000587 decreased size abnormal ZDB-GENE-030109-1 317678 10856 ruvbl2 ZFA:0000112 gut PATO:0000001 quality abnormal ZDB-GENE-030109-1 317678 10856 ruvbl2 ZFA:0000114 heart PATO:0000001 quality abnormal ZDB-GENE-030109-1 317678 10856 ruvbl2 ZFA:0000123 liver PATO:0000001 quality abnormal ZDB-GENE-030109-1 317678 10856 ruvbl2 GO:0031514 motile cilium BFO:0000050 part_of ZFA:0000150 pronephric duct PATO:0002001 has fewer parts of type abnormal GO:0036156 inner dynein arm BFO:0000050 part_of ZFA:0000150 pronephric duct ZDB-GENE-030109-1 317678 10856 ruvbl2 GO:0031514 motile cilium BFO:0000050 part_of ZFA:0000150 pronephric duct PATO:0002001 has fewer parts of type abnormal GO:0036157 outer dynein arm BFO:0000050 part_of ZFA:0000150 pronephric duct ZDB-GENE-030109-1 317678 10856 ruvbl2 ZFA:0000150 pronephric duct PATO:0001714 increased diameter abnormal ZDB-GENE-030109-1 317678 10856 ruvbl2 ZFA:0000151 pronephros PATO:0000001 quality abnormal ZDB-GENE-030109-1 317678 10856 ruvbl2 ZFA:0000151 pronephros PATO:0001673 cystic abnormal ZDB-GENE-030109-1 317678 10856 ruvbl2 ZFA:0000152 retina PATO:0000051 morphology abnormal ZDB-GENE-030109-1 317678 10856 ruvbl2 ZFA:0000529 kidney PATO:0001673 cystic abnormal ZDB-GENE-030109-1 317678 10856 ruvbl2 ZFA:0001094 whole organism PATO:0000617 bent abnormal ZDB-GENE-030109-1 317678 10856 ruvbl2 ZFA:0001094 whole organism PATO:0000647 necrotic abnormal ZDB-GENE-030109-1 317678 10856 ruvbl2 ZFA:0001094 whole organism PATO:0001469 curved ventral abnormal ZDB-GENE-030109-1 317678 10856 ruvbl2 ZFA:0001114 head PATO:0000587 decreased size abnormal ZDB-GENE-030109-1 317678 10856 ruvbl2 ZFA:0001115 trunk PATO:0001469 curved ventral abnormal ZDB-GENE-030109-1 317678 10856 ruvbl2 ZFA:0001117 post-vent region PATO:0001469 curved ventral abnormal ZDB-GENE-030109-1 317678 10856 ruvbl2 ZFA:0001227 mandibular arch skeleton PATO:0000587 decreased size abnormal ZDB-GENE-030109-1 317678 10856 ruvbl2 ZFA:0001249 exocrine pancreas PATO:0000587 decreased size abnormal ZDB-GENE-030109-1 317678 10856 ruvbl2 GO:0031514 motile cilium BFO:0000050 part_of ZFA:0001623 posterior pronephric duct PATO:0000300 immobile abnormal ZDB-GENE-030109-1 317678 10856 ruvbl2 GO:0030017 sarcomere BFO:0000050 part_of ZFA:0009316 cardiac muscle cell PATO:0000470 increased amount abnormal ZDB-GENE-030109-1 317678 10856 ruvbl2 ZFA:0009316 cardiac muscle cell PATO:0000470 increased amount abnormal ZDB-GENE-030109-2 317679 8607 ruvbl1 ZFA:0000008 brain PATO:0000647 necrotic abnormal ZDB-GENE-030109-2 317679 8607 ruvbl1 ZFA:0000009 cardiac ventricle PATO:0000584 hypertrophic abnormal ZDB-GENE-030109-2 317679 8607 ruvbl1 ZFA:0000009 cardiac ventricle PATO:0000644 hyperplastic abnormal ZDB-GENE-030109-2 317679 8607 ruvbl1 ZFA:0000012 central nervous system PATO:0000647 necrotic abnormal ZDB-GENE-030109-2 317679 8607 ruvbl1 GO:0031514 motile cilium BFO:0000050 part_of ZFA:0000047 peripheral olfactory organ PATO:0000300 immobile abnormal ZDB-GENE-030109-2 317679 8607 ruvbl1 ZFA:0000054 pericardium PATO:0001450 edematous abnormal ZDB-GENE-030109-2 317679 8607 ruvbl1 ZFA:0000114 heart PATO:0000001 quality abnormal ZDB-GENE-030109-2 317679 8607 ruvbl1 ZFA:0000151 pronephros PATO:0000001 quality abnormal ZDB-GENE-030109-2 317679 8607 ruvbl1 ZFA:0000151 pronephros PATO:0001673 cystic abnormal ZDB-GENE-030109-2 317679 8607 ruvbl1 ZFA:0001094 whole organism PATO:0000617 bent abnormal ZDB-GENE-030109-2 317679 8607 ruvbl1 ZFA:0001094 whole organism PATO:0000647 necrotic abnormal ZDB-GENE-030109-2 317679 8607 ruvbl1 ZFA:0001114 head PATO:0000587 decreased size abnormal ZDB-GENE-030109-2 317679 8607 ruvbl1 ZFA:0001115 trunk PATO:0001469 curved ventral abnormal ZDB-GENE-030109-2 317679 8607 ruvbl1 ZFA:0001117 post-vent region PATO:0001469 curved ventral abnormal ZDB-GENE-030109-2 317679 8607 ruvbl1 ZFA:0001117 post-vent region PATO:0001592 increased curvature abnormal ZDB-GENE-030109-2 317679 8607 ruvbl1 ZFA:0001557 pronephric glomerulus PATO:0001673 cystic abnormal ZDB-GENE-030109-2 317679 8607 ruvbl1 GO:0031514 motile cilium BFO:0000050 part_of ZFA:0001558 pronephric tubule PATO:0002001 has fewer parts of type abnormal GO:0036156 inner dynein arm BFO:0000050 part_of ZFA:0001558 pronephric tubule ZDB-GENE-030109-2 317679 8607 ruvbl1 GO:0031514 motile cilium BFO:0000050 part_of ZFA:0001558 pronephric tubule PATO:0002001 has fewer parts of type abnormal GO:0036157 outer dynein arm BFO:0000050 part_of ZFA:0001558 pronephric tubule ZDB-GENE-030109-2 317679 8607 ruvbl1 GO:0031514 motile cilium BFO:0000050 part_of ZFA:0001558 pronephric tubule PATO:0000300 immobile abnormal ZDB-GENE-030113-2 7273 ttn.2 GO:0006936 muscle contraction PATO:0001507 disrupted abnormal ZDB-GENE-030113-2 7273 ttn.2 GO:0007411 axon guidance PATO:0001507 disrupted abnormal ZDB-GENE-030113-2 7273 ttn.2 GO:0007519 skeletal muscle tissue development PATO:0001507 disrupted abnormal ZDB-GENE-030113-2 7273 ttn.2 GO:0007522 visceral muscle development PATO:0001507 disrupted abnormal ZDB-GENE-030113-2 7273 ttn.2 GO:0008015 blood circulation PATO:0002052 decreased occurrence abnormal ZDB-GENE-030113-2 7273 ttn.2 GO:0008217 regulation of blood pressure PATO:0001507 disrupted abnormal ZDB-GENE-030113-2 7273 ttn.2 GO:0008345 larval locomotory behavior PATO:0000462 absent abnormal ZDB-GENE-030113-2 7273 ttn.2 GO:0008345 larval locomotory behavior PATO:0001507 disrupted abnormal ZDB-GENE-030113-2 7273 ttn.2 GO:0014866 skeletal myofibr