MYL3

GENE INFORMATION

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Gene name

MYL3 (HGNC Symbol)

Synonyms

CMH8, MLC1SB, MLC1V, VLC1

Description

Myosin, light chain 3, alkali; ventricular, skeletal, slow (HGNC Symbol)

Entrez gene summary

MYL3 encodes myosin light chain 3, an alkali light chain also referred to in the literature as both the ventricular isoform and the slow skeletal muscle isoform. Mutations in MYL3 have been identified as a cause of mid-left ventricular chamber type hypertrophic cardiomyopathy. [provided by RefSeq, Jul 2008]

Chromosome

3

Cytoband

p21.31

Chromosome location (bp)

46899362 - 46923659

Protein evidence

Evidence at protein level (all genes)

Ensembl

ENSG00000160808 (version 75.37)

Entrez gene

4634

UniProt

P08590 (UniProt - Evidence at protein level)

neXtProt

NX_P08590

Antibodypedia

MYL3 antibodies
 

PROTEIN VIEW

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MYL3-001
 
MYL3-002
 
MYL3-003
 
 
 
 
 

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)

MYL3-001 ENSP00000292327
ENST00000292327
P08590
Show all »
Show » Show » 195 21.9 No 0
MYL3-002 ENSP00000379210
ENST00000395869
P08590
Show all »
Show » Show » 195 21.9 No 0
MYL3-003 ENSP00000393455
ENST00000431168
E9PGV7
Show all »
Show » Show » 46 5 No 0