MYH11

GENERAL INFORMATION

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Gene name

MYH11

Gene description

Myosin, heavy chain 11, smooth muscle

Protein class

Cancer-related genes
Candidate cardiovascular disease genes
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 enhanced (esophagus, smooth muscle)
GTEx:Expressed in all

Protein evidence

Evidence at protein level

Protein localization

Distinct expression was observed in myoepithelial cells and smooth muscle.

ANTIBODY RELIABILITY

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Data reliability
description

Pending RNA-based expert annotation.

Data reliability

Supportive based on 3 antibodies.
HPA014539 , HPA015310 , CAB002302
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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

Smooth muscle

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 enhanced (esophagus, smooth muscle)

Organ

Expression

GTEx dataset
RNA tissue category:  Expressed in all

Organ

Expression



GENE INFORMATION

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Gene name

MYH11 (HGNC Symbol)

Synonyms

SMHC, SMMHC

Description

Myosin, heavy chain 11, smooth muscle (HGNC Symbol)

Entrez gene summary

The protein encoded by this gene is a smooth muscle myosin belonging to the myosin heavy chain family. The gene product is a subunit of a hexameric protein that consists of two heavy chain subunits and two pairs of non-identical light chain subunits. It functions as a major contractile protein, converting chemical energy into mechanical energy through the hydrolysis of ATP. The gene encoding a human ortholog of rat NUDE1 is transcribed from the reverse strand of this gene, and its 3' end overlaps with that of the latter. The pericentric inversion of chromosome 16 [inv(16)(p13q22)] produces a chimeric transcript that encodes a protein consisting of the first 165 residues from the N terminus of core-binding factor beta in a fusion with the C-terminal portion of the smooth muscle myosin heavy chain. This chromosomal rearrangement is associated with acute myeloid leukemia of the M4Eo subtype. Alternative splicing generates isoforms that are differentially expressed, with ratios changing during muscle cell maturation. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2008]

Chromosome

16

Cytoband

p13.11

Chromosome location (bp)

15703135 - 15857033

Protein evidence

Evidence at protein level (all genes)

Ensembl

ENSG00000133392 (version 78.38)

Entrez gene

4629

UniProt

P35749 (UniProt - Evidence at protein level)

neXtProt

NX_P35749

Antibodypedia

MYH11 antibodies


PROTEIN BROWSER

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ENST00000300036
 
ENST00000396324
 
ENST00000452625
 
ENST00000576790
 
ENST00000611087
 
ENST00000616439
 
 
 
 


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)

MYH11-001 ENSP00000300036
ENST00000300036
P35749
Show all »
Show » Show » 1972 227.3 No 0
MYH11-003 ENSP00000458731
ENST00000576790
P35749
Show all »
Show » Show » 1938 223.6 No 0
MYH11-006 ENSP00000379616
ENST00000396324
P35749
Show all »
Show » Show » 1979 228.1 No 0
MYH11-013 ENSP00000407821
ENST00000452625
P35749
Show all »
Show » Show » 1945 224.3 No 0
MYH11-201 ENSP00000483524
ENST00000611087
B1PS43
Show all »
Show » Show » 2029 234.2 No 0
MYH11-202 ENSP00000484924
ENST00000616439
B1PS43
Show all »
Show » Show » 2029 234.2 No 0