Gene

myh9b

ID
ZDB-GENE-030131-998
Name
myosin, heavy chain 9b, non-muscle
Symbol
myh9b Nomenclature History
Previous Names
  • myh91
  • myh9l1
  • myhz9 (1)
  • fb55d12
  • myo2hc9 (1)
  • si:ch211-150d5.2
  • wu:fb30g06
  • wu:fb55d12
Type
protein_coding_gene
Location
Chr: 3 Mapping Details/Browsers
Description
Predicted to enable actin filament binding activity and microfilament motor activity. Acts upstream of or within several processes, including actin filament bundle distribution; cardiac ventricle development; and midbrain-hindbrain boundary morphogenesis. Predicted to be located in cell cortex and cortical granule. Predicted to be part of myosin II complex. Predicted to be active in cytoplasm and myosin filament. Is expressed in several structures, including brain; ectoderm; epidermis; eye; and pectoral fin. Human ortholog(s) of this gene implicated in several diseases, including auditory system disease (multiple); autosomal dominant Alport syndrome; blood platelet disease (multiple); end stage renal disease; and orofacial cleft. Orthologous to human MYH9 (myosin heavy chain 9).
Genome Resources
Note
None
Comparative Information
Expression
All Expression Data
3 figures from 3 publications
Cross-Species Comparison
High Throughput Data
Thisse Expression Data
No data available
Wild Type Expression Summary
Phenotype
All Phenotype Data
1 Figure from Gutzman et al., 2015
Cross-Species Comparison
Alliance
Phenotype Summary
Mutations
Mutants
Allele Type Localization Consequence Mutagen Supplier
sa18627Allele with one point mutationUnknownMissense, Splice SiteENU
sa33082Allele with one point mutationUnknownMissenseENU
sa39978Allele with one point mutationUnknownSplice SiteENU
zf3748Allele with one deletionUnknownUnknownCRISPR
1 - 4 of 4
Show
Sequence Targeting Reagents
1 - 6 of 6
Show
Human Disease
Associated With myh9b Human Ortholog
Disease Ontology Term Multi-Species Data OMIM Term OMIM Phenotype ID
autosomal dominant nonsyndromic deafness 17 Alliance Deafness, autosomal dominant 17 603622
MYH-9 related disease Alliance Macrothrombocytopenia and granulocyte inclusions with or without nephritis or sensorineural hearing loss 155100
Associated With myh9b Via Experimental Models
No data available
Gene Ontology
Protein Domains
Domain, Family, and Site Summary
Type InterPro ID Name
Binding_site IPR000048 IQ motif, EF-hand binding site
Domain IPR001609 Myosin head, motor domain-like
Domain IPR002928 Myosin tail
Domain IPR004009 Myosin, N-terminal, SH3-like
Homologous_superfamily IPR008989 Myosin S1 fragment, N-terminal
Homologous_superfamily IPR027417 P-loop containing nucleoside triphosphate hydrolase
Homologous_superfamily IPR036961 Kinesin motor domain superfamily
Domain Details Per Protein
Protein Additional Resources Length IQ motif, EF-hand binding site Kinesin motor domain superfamily Myosin head, motor domain-like Myosin, N-terminal, SH3-like Myosin S1 fragment, N-terminal Myosin tail P-loop containing nucleoside triphosphate hydrolase
UniProtKB:A0A8M2BB06 InterPro 1691
UniProtKB:A0A8M1QUS6 InterPro 1698
Transcripts
Genome Browsers
Genome Build: GRCz11Chromosome: 3
Type Name Annotation Method Has Havana Data Length (nt) Analysis
mRNA myh9b-201 (1) Ensembl 9,625 nt
mRNA myh9b-202 (1) Ensembl 5,253 nt
mRNA myh9b-203 (1) Ensembl 9,604 nt
Interactions and Pathways
No data available
Antibodies
No data available
Plasmids
No data available
Constructs
No data available
Marker Relationships
Relationship Marker Type Marker Accession Numbers Citations
Contained inBACCH211-150D5ZFIN Curated Data
Contained inFosmidCH1073-309B2ZFIN Curated Data
ContainsSNPrs3727673
    ZFIN Curated Data
    ContainsSNPrs3727674
      ZFIN Curated Data
      EncodesESTfb30g06ZFIN Curated Data
      EncodesESTfb55d12
      1 - 6 of 6
      Show
      Sequences
      Orthology
      Comparative Orthology
      Alliance
      Gene Tree
      Ensembl
      Species Symbol Chromosome Accession # Evidence
      HumanMYH922
      Conserved genome location (synteny) (1)
      Functional complementation (1)
      Amino acid sequence comparison (2)
      MouseMyh915
      Amino acid sequence comparison (1)
      Conserved genome location (synteny) (1)
      Citations
      1 - 10 of 12
      Show