PYGM

GENE INFORMATION

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Gene name

PYGM

Synonyms

Description

Phosphorylase, glycogen, muscle (HGNC Symbol)

Entrez gene summary

This gene encodes a muscle enzyme involved in glycogenolysis. Highly similar enzymes encoded by different genes are found in liver and brain. Mutations in this gene are associated with McArdle disease (myophosphorylase deficiency), a glycogen storage disease of muscle. Alternative splicing results in multiple transcript variants.[provided by RefSeq, Sep 2009]

Chromosome

11

Cytoband

q13.1

Chromosome location (bp)

64746389 - 64760297

Protein evidence

Evidence at protein level (all genes)

Ensembl

ENSG00000068976 (version 78.38)

Entrez gene

5837

UniProt

P11217 (UniProt - Evidence at protein level)

neXtProt

NX_P11217

Antibodypedia

PYGM antibodies
 

PROTEIN VIEW

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PYGM-001
 
PYGM-002
 
 
 
 
 

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)

PYGM-001 ENSP00000164139
ENST00000164139
P11217
Show all »
Show » Show » 842 97.1 No 0
PYGM-002 ENSP00000366650
ENST00000377432
P11217
Show all »
Show » Show » 754 87.3 No 0