ZFIN ID: ZDB-GENE-100921-1 |
Gene Name: | myosin, heavy chain 14, non-muscle | ||||||
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Gene Symbol: | myh14 Nomenclature History | ||||||
Previous Names: | si:ch211-120k19.2, si:ch211-120k19.3 | ||||||
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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) |
Disease Ontology Term | Multi-Species Data | OMIM Term | OMIM Phenotype ID |
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autosomal dominant nonsyndromic deafness 4A | Alliance | Deafness, autosomal dominant 4A | 600652 |
?Peripheral neuropathy, myopathy, hoarseness, and hearing loss | 614369 |
Ontology | GO Term |
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Cellular Component | myosin complex (more) |
Molecular Function | actin binding (more) |
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Type | Name | Length (nt) | Analysis | |
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mRNA |
myh14-203
(1)
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12826 |
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myh14-204
(1)
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446 |
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ncRNA |
myh14-002
(1)
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529 |
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Browsers: NCBI, Ensembl, ZFIN |
Type | Accession # | Length (bp/aa) | Analysis |
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RNA | RefSeq:XM_005157931 (1) | 7884 bp |
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Genomic | GenBank:AL929505 (1) | 178839 bp | |
Polypeptide | UniProtKB:E9QFE1 (1) | 2020 aa |
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