MYO1A

GENE INFORMATION

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Gene name

MYO1A (HGNC Symbol)

Synonyms

DFNA48, MYHL

Description

Myosin IA (HGNC Symbol)

Entrez gene summary

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]

Chromosome

12

Cytoband

q13.3

Chromosome location (bp)

57028517 - 57051198

Protein evidence

Evidence at protein level (all genes)

Ensembl

ENSG00000166866 (version 78.38)

Entrez gene

4640

UniProt

Q9UBC5 (UniProt - Evidence at protein level)

neXtProt

NX_Q9UBC5

Antibodypedia

MYO1A antibodies
 

PROTEIN VIEW

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MYO1A-001
 
MYO1A-002
 
MYO1A-003
 
MYO1A-004
 
 
 
 
 

PROTEIN INFORMATION

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Splice variant

Ensembl

UniProt

Protein class

Gene ontology

Length
(aa)

Molecular mass
(kDa)

Signal peptide
(predicted)

Transmembrane regions
(predicted)

MYO1A-001 ENSP00000300119
ENST00000300119
Q9UBC5
Show all »
Show » Show » 1043 118.4 No 0
MYO1A-002 ENSP00000400991
ENST00000433964
C9JU63
Show all »
Show » Show » 96 11.2 No 0
MYO1A-003 ENSP00000452229
ENST00000492945
G3V587
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Show » Show » 74 8.3 No 0
MYO1A-004 ENSP00000393392
ENST00000442789
Q9UBC5
Show all »
Show » Show » 1043 118.4 No 0