PYGM Polyclonal Antibody

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.

Glycogen phosphorylase, Glycogen phosphorylase muscle form, muscle form, Muscpho, Myophosphorylase, Phosphorylase glycogen muscle (McArdle syndrome glycogen storage disease type V), Pygm, PYGM