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Please note: We are reviewing Western blot images included in the antibody testing data in our catalog, including those provided by third parties. Unless expressly labeled or annotated as “raw-unedited”, Western blot images included in the antibody testing data in our catalog may have been edited, optimized or otherwise adjusted for presentation.
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 muscle; GPMM; muscle (McArdle syndrome); muscle glycogen phosphorylase; myophosphorylase; Phosphorylase glycogen; phosphorylase, glycogen, muscle; Phosphorylase, glycogen; muscle (McArdle syndrome); unnamed protein product
Gene Aliases: GSD5; Muscpho; PG
UniProt ID: (Human) P11217, (Mouse) Q9WUB3
Entrez Gene ID: (Human) 5837, (Mouse) 19309, (Rat) 24701
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