Peptide Sequence: DRIPELRQVI EQLSSGFFSP KQPDLFKDIV NMLMHHDRFK VFADYEDYIK CQEKVSALYK NPREWTRMVI RNIATSGKFS SDRTIAQYAR EIWGVEPSRQ RLPAPDEAI
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
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Protein Aliases: Glycogen phosphorylase, muscle form; muscle form; Myophosphorylase; PYGM
Gene Aliases: PYGM
UniProt ID: (Human) P11217
Entrez Gene ID: (Human) 5837