MYO3A

GENERAL INFORMATION

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Gene name

MYO3A

Gene description

Myosin IIIA

Protein class

Disease related genes
Enzymes
Plasma proteins
Potential drug targets
Predicted intracellular proteins

Predicted localization

Intracellular

Number of transcripts

5
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HUMAN PROTEIN ATLAS INFORMATION

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RNA tissue category

HPA:Tissue enriched (testis)
GTEx:Tissue enriched (testis)

Protein evidence

Evidence at protein level

Protein localization

External data suggests expression in retina

ANTIBODY RELIABILITY

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Data reliability
description

Presumed off target binding observed and disregarded. Additional tissue shows expression in retina

Data reliability

Uncertain based on 1 antibody.
HPA048951
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RNA AND PROTEIN EXPRESSION SUMMARY

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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

Pancreas

Colon

Kidney

Testis



PROTEIN EXPRESSION OVERVIEW

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Organ

Expression



RNA EXPRESSION OVERVIEW

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HPA dataset
RNA tissue category:  Tissue enriched (testis)

Organ

Expression

GTEx dataset
RNA tissue category:  Tissue enriched (testis)

Organ

Expression



GENE INFORMATION

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Gene name

MYO3A (HGNC Symbol)

Synonyms

DFNB30

Description

Myosin IIIA (HGNC Symbol)

Entrez gene summary

The protein encoded by this gene belongs to the myosin superfamily. Myosins are actin-dependent motor proteins and are categorized into conventional myosins (class II) and unconventional myosins (classes I and III through XV) based on their variable C-terminal cargo-binding domains. Class III myosins, such as this one, have a kinase domain N-terminal to the conserved N-terminal motor domains and are expressed in photoreceptors. The protein encoded by this gene plays an important role in hearing in humans. Three different recessive, loss of function mutations in the encoded protein have been shown to cause nonsyndromic progressive hearing loss. Expression of this gene is highly restricted, with the strongest expression in retina and cochlea. [provided by RefSeq, Jul 2008]

Chromosome

10

Cytoband

p12.1

Chromosome location (bp)

25934267 - 26212527

Protein evidence

Evidence at protein level (all genes)

Ensembl

ENSG00000095777 (version 78.38)

Entrez gene

53904

UniProt

Q8NEV4 (UniProt - Evidence at transcript level)

neXtProt

NX_Q8NEV4

Antibodypedia

MYO3A antibodies


PROTEIN BROWSER

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ENST00000265944
 
ENST00000376301
 
ENST00000376302
 
ENST00000543632
 
ENST00000619592
 
 
 
 


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)

MYO3A-001 ENSP00000265944
ENST00000265944
Q8NEV4
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Show » Show » 1616 186.2 No 0
MYO3A-003 ENSP00000365479
ENST00000376302
Q8NEV4
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Show » Show » 247 27.7 No 0
MYO3A-004 ENSP00000365478
ENST00000376301
B1ANA3
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Show » Show » 197 22.2 No 0
MYO3A-201 ENSP00000445909
ENST00000543632
F5H0U9
Show all »
Show » Show » 664 74.6 No 0
MYO3A-202 ENSP00000481939
ENST00000619592
Show » Show » 1615 186.1 No 0