MYH2

GENERAL INFORMATION

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Gene name

MYH2

Gene description

Myosin, heavy chain 2, skeletal muscle, adult

Protein class

Disease related genes
Plasma proteins
Predicted intracellular proteins

Predicted localization

Intracellular

Number of transcripts

6
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HUMAN PROTEIN ATLAS INFORMATION

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RNA tissue category

HPA:Tissue enriched (skeletal muscle)
GTEx:Tissue enriched (skeletal muscle)

Protein evidence

Evidence at protein level

Protein localization

Selective cytoplasmic expression mainly in skeletal muscle.

ANTIBODY RELIABILITY

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Data reliability
description

Caution, targets protein from more than one gene. Presumed off target binding observed and disregarded.

Data reliability

Supportive based on 2 antibodies.
HPA001349 , CAB010760
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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

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 (skeletal muscle)

Organ

Expression

GTEx dataset
RNA tissue category:  Tissue enriched (skeletal muscle)

Organ

Expression



GENE INFORMATION

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Gene name

MYH2 (HGNC Symbol)

Synonyms

IBM3, MYH2A, MYHas8, MyHC-2A, MyHC-IIa, MYHSA2

Description

Myosin, heavy chain 2, skeletal muscle, adult (HGNC Symbol)

Entrez gene summary

Myosins are actin-based motor proteins that function in the generation of mechanical force in eukaryotic cells. Muscle myosins are heterohexamers composed of 2 myosin heavy chains and 2 pairs of nonidentical myosin light chains. This gene encodes a member of the class II or conventional myosin heavy chains, and functions in skeletal muscle contraction. This gene is found in a cluster of myosin heavy chain genes on chromosome 17. A mutation in this gene results in inclusion body myopathy-3. Multiple alternatively spliced variants, encoding the same protein, have been identified. [provided by RefSeq, Sep 2009]

Chromosome

17

Cytoband

p13.1

Chromosome location (bp)

10521148 - 10549957

Protein evidence

Evidence at protein level (all genes)

Ensembl

ENSG00000125414 (version 78.38)

Entrez gene

4620

UniProt

Q9UKX2 (UniProt - Evidence at protein level)

neXtProt

NX_Q9UKX2

Antibodypedia

MYH2 antibodies


PROTEIN BROWSER

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ENST00000245503
 
ENST00000397183
 
ENST00000420805
 
ENST00000532183
 
ENST00000578017
 
ENST00000622564
 
 
 
 


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)

MYH2-001 ENSP00000245503
ENST00000245503
Q9UKX2
Show all »
Show » Show » 1941 223 No 0
MYH2-002 ENSP00000399348
ENST00000420805
E7EX84
Show all »
Show » Show » 182 20.7 No 0
MYH2-006 ENSP00000433944
ENST00000532183
Q9UKX2
Show all »
Show » Show » 708 79.9 No 0
MYH2-009 ENSP00000463668
ENST00000578017
J3QLR0
Show all »
Show » Show » 155 17.6 No 0
MYH2-201 ENSP00000380367
ENST00000397183
Q9UKX2
Show all »
Show » Show » 1941 223 No 0
MYH2-202 ENSP00000482463
ENST00000622564
Q9UKX2
Show all »
Show » Show » 708 79.9 No 0