MYO1A

GENERAL INFORMATION

? »

Gene name

MYO1A

Gene description

Myosin IA

Protein class

Disease related genes
Plasma proteins
Predicted intracellular proteins

Predicted localization

Intracellular

Number of transcripts

4
SHOW MORE

HUMAN PROTEIN ATLAS INFORMATION

? »

RNA tissue category

HPA:Group enriched (colon, duodenum, rectum, small intestine)
GTEx:Group enriched (colon, small intestine)

Protein evidence

Evidence at protein level

Protein localization

Most normal cells displayed moderate to strong cytoplasmic staining with a granular pattern. Lymphoid tissue were mainly negative.

ANTIBODY RELIABILITY

? »

Data reliability
description

Pending RNA-based expert annotation.

Data reliability

Uncertain based on 1 antibody.
HPA041633
SHOW MORE

RNA AND PROTEIN EXPRESSION SUMMARY

? »
RNA expression (FPKM) Protein expression (score)
Brain
Endocrine tissues
Bone marrow & immune system
Muscle tissues
Lung
Liver & gallbladder
Pancreas
Gastrointestinal tract
Kidney & urinary bladder
Male tissues
Female tissues
Adipose & soft tissue
Skin
Cerebral cortex

Lymph node

Liver

Colon

Rectum

Kidney

Testis



PROTEIN EXPRESSION OVERVIEW

? »

Organ

Expression



RNA EXPRESSION OVERVIEW

? »
HPA dataset
RNA tissue category:  Group enriched (colon, duodenum, rectum, small intestine)

Organ

Expression

GTEx dataset
RNA tissue category:  Group enriched (colon, small intestine)

Organ

Expression



GENE INFORMATION

? »

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 BROWSER

? »
 
 
 
ENST00000300119
 
ENST00000433964
 
ENST00000442789
 
ENST00000492945
 
 
 
 


PROTEIN INFORMATION

? »

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
Show all »
Show » Show » 74 8.3 No 0
MYO1A-004 ENSP00000393392
ENST00000442789
Q9UBC5
Show all »
Show » Show » 1043 118.4 No 0