Jia et al., 2020 - Multiple Developmental Defects in sox11a Mutant Zebrafish with Features of Coffin-Siris Syndrome. International journal of biological sciences   16:3039-3049 Full text @ Int. J. Biol. Sci.
25 Genes / Markers
Marker Type Symbol Name
Gene akt2 v-akt murine thymoma viral oncogene homolog 2
Gene aldh7a1 aldehyde dehydrogenase 7 family, member A1
Gene and1 actinodin1
Gene atp6v1h ATPase H+ transporting V1 subunit H
Gene bglap bone gamma-carboxyglutamate (gla) protein
Gene calhm2.1 calcium homeostasis modulator family member 2, tandem duplicate 1
Gene chrm2a cholinergic receptor, muscarinic 2a
Gene col1a1a collagen, type I, alpha 1a
Gene crtap cartilage associated protein
Gene ctsk cathepsin K
Gene dlx4a distal-less homeobox 4a
Gene entpd5a ectonucleoside triphosphate diphosphohydrolase 5a
Gene matn1 matrilin 1
Gene mctp2b multiple C2 domains, transmembrane 2b
Gene p2rx4b purinergic receptor P2X, ligand-gated ion channel, 4b
Gene rcn3 reticulocalbin 3, EF-hand calcium binding domain
Gene runx2a RUNX family transcription factor 2a
Gene runx2b RUNX family transcription factor 2b
Gene s100a11 S100 calcium binding protein A11
Gene sec23a Sec23 homolog A, coat complex II component
Gene slc8a4a solute carrier family 8 member 4a
Gene sox11a SRY-box transcription factor 11a
Gene sox11b SRY-box transcription factor 11b
Gene twist1a twist family bHLH transcription factor 1a
Gene twist1b twist family bHLH transcription factor 1b