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General Information
ZIRC
ZFIN ID: ZDB-GENE-100921-1
Gene Name: myosin, heavy chain 14, non-muscle
Gene Symbol: myh14
Sequence Ontology ID : SO:0001217

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

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(Including Attributions)
Location: Chr: 16 Mapping Details/Browsers
Nomenclature History
AUTOMATED 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  ...
GENE EXPRESSION No data available
PHENOTYPE No data available
DISEASE ASSOCIATED WITH myh14 HUMAN ORTHOLOG
Disease Ontology Term OMIM Term OMIM Phenotype ID
autosomal dominant nonsyndromic deafness 4A 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 (bp) Analysis
ncRNA myh14-002 (1) 529
mRNA myh14-203 (1) 12826
myh14-204 (1) 446
 Withdrawn Transcriptsextinct
GENE PRODUCT DESCRIPTION
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)