MYO1A
Sign in to saveAlso known as BBMI, DFNA48, MIHC, MYHL, myosin IA
protein-coding gene in the species Homo sapiens
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