PYGM, glycogen phosphorylase, muscle associated

PYGM, glycogen phosphorylase, muscle associated

• 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]

• Gene Synonyms (glycogen phosphorylase, muscle form, myophosphorylase, phosphorylase, glycogen, muscle, GSD5,)
• NCBI Gene ID: 5837
• Species: Homo sapiens (Human)
• UNIPROT ID#>>P11217
• View the NCBI Database for this Gene »

Gene products are often involved in multiple pathways and networks within a living cell. Learn more about other interacting partners.

glycogen phosphorylase, muscle associated interacts with:

• agrin
  coiled-coil domain containing 15
  delta 4-desaturase, sphingolipid 1
  DNA topoisomerase I
  glycogen phosphorylase, muscle associated
  N-terminal glutamine amidase 1
  pleckstrin homology domain containing A4
  protein kinase C and casein kinase substrate in neurons 3
  S100 calcium binding protein A1
  TLE family member 3, transcriptional corepressor
  tripartite motif containing 63

Paste a protein or nucleic acid sequence in the box below to confirm that it matches this gene’s reference sequence(s). Click on a link under RELATED ORF CLONES to see how a sequence matches to an experimentally-validated ORF clone.