MYO1A
Sign in to saveAlso known as BBMI, DFNA48, MIHC, MYHL, myosin IA
protein-coding gene in the species Homo sapiens
In the Vinony graph
Within Vinony's link graph, MYO1A is referenced by 273 other articles, and connects out to hair keratin, PubMed and human chromosome 12.
It is catalogued under the topic Genes on human chromosome 12.
Its subject is documented across 7 Wikipedia language editions.
Gene data
MYO1A- Name
- myosin IA
- Type
- protein-coding
- Position
- 57,025,262–57,051,198 (−)
- Aliases
- BBMI, DFNA48, DIAR15, MIHC, MYHL
- Ensembl
- ENSG00000166866
- RefSeq RNA
- NM_001256041.2, NM_005379.4, XM_011538373.3, XM_047428876.1, XM_054372105.1
- RefSeq protein
- NP_001242970.1, NP_005370.1, XP_011536675.1, XP_047284832.1, XP_054228080.1
This gene encodes a member of the myosin superfamily. The protein represents an unconventional myosin; it should not be confused with the conventional skeletal muscle myosin-1 (MYH1). Unconventional myosins contain the basic domains characteristic of conventional myosins and are further distinguished from class members by their tail domains. They function as actin-based molecular motors. Mutations in this gene have been associated with autosomal dominant deafness. Alternatively spliced variants have been found for this gene. [provided by RefSeq, Dec 2011].
Gene Ontology
Biological process
Molecular function
via MyGene.info
Gene · Ensembl
myosin IA
- Symbol
- MYO1A
- Biotype
- Protein coding
- Organism
- Homo sapiens
- Location
- 12:57,025,262-57,051,198
- Strand
- Reverse (−)
- Assembly
- GRCh38
via Ensembl · EMBL-EBI
Wikidata facts
- Instance of
- gene
Show 8 more facts
- found in taxon
- Homo sapiens
- exact match
- identifiers.org/ncbigene/4640
- HomoloGene ID
- 21113
- genomic end
- 57444982
- genomic start
- 57422301
- chromosome
- human chromosome 12
- cytogenetic location
- 12q13.3
- expressed in
- testicle
Sources (4)
via Wikidata · CC0