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General Information
ZIRC
ZFIN ID: ZDB-GENE-100921-1
Gene Name: myosin, heavy chain 14, non-muscle
Gene Symbol: myh14    Nomenclature History

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Previous Names: si:ch211-120k19.2, si:ch211-120k19.3

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(Including Attributions)
Gene Type: protein_coding_gene
Location: Chr: 16 Mapping Details/Browsers
Description: Predicted to have ATP binding activity; actin filament binding activity; and motor activity. Predicted to localize to the myosin complex. Human ortholog(s) of this gene implicated in autosomal dominant nonsyndromic deafness 4A and sensorineural hearing loss. Orthologous to human MYH14 (myosin heavy chain 14).
Genome Resources: Alliance (1),  Gene:563011 (1),  Ensembl(GRCz11):ENSDARG00000073732 (2)
GENE EXPRESSION No data available
PHENOTYPE No data available
DISEASE ASSOCIATED WITH myh14 HUMAN ORTHOLOG
Disease Ontology Term Multi-Species Data OMIM Term OMIM Phenotype ID
autosomal dominant nonsyndromic deafness 4A Alliance Deafness, autosomal dominant 4A 600652
?Peripheral neuropathy, myopathy, hoarseness, and hearing loss 614369
DISEASE ASSOCIATED WITH myh14 VIA EXPERIMENTAL MODELS No data available
GENE ONTOLOGY
Ontology GO Term
Cellular Component myosin complex (more)
Molecular Function actin binding (more)
GO Terms (all 6)
TRANSCRIPTS
Type Name Length (nt) Analysis
mRNA myh14-203 (1)    Ensembl 12826
myh14-204 (1)    Ensembl 446
ncRNA myh14-002 (1)    Ensembl 529
Browsers: NCBIEnsemblZFIN
INTERACTIONS AND PATHWAYS
ANTIBODIES No data available
PLASMIDS No data available
CONSTRUCTS WITH SEQUENCES FROM myh14 No data available
MARKER RELATIONSHIPS
myh14 Contained in: [BAC] CH211-120K19 (1) (order this)
SEQUENCE INFORMATION
Type Accession # Length (bp/aa) Analysis
RNA RefSeq:XM_005157931 (1) 7884 bp
Genomic GenBank:AL929505 (1) 178839 bp
Select Tool
Polypeptide UniProtKB:E9QFE1 (1) 2020 aa
Sequence Information (all 17)
ORTHOLOGY for myh14 ( Chr: 16 )
CITATIONS (13)