PHKG2 phosphorylase kinase catalytic subunit gamma 2 [ Homo sapiens (human) ]
Source: NCBI Gene (ID 5261)
Source: NCBI Gene (ID 5261)
Symbol: PHKG2
Full name: phosphorylase kinase catalytic subunit gamma 2
Gene type: protein coding
RefSeq status: REVIEWED
Organism: Homo sapiens
Also known as: GSD9C
Summary: Phosphorylase kinase is a polymer of 16 subunits, four each of alpha, beta, gamma and delta. The alpha subunit includes the skeletal muscle and hepatic isoforms, encoded by two different genes. The beta subunit is the same in both the muscle and hepatic isoforms, and encoded by one gene. The gamma subunit also includes the skeletal muscle and hepatic isoforms, and the hepatic isoform is encoded by this gene. The delta subunit is a calmodulin and can be encoded by three different genes. The gamma subunits contain the active site of the enzyme, whereas the alpha and beta subunits have regulatory functions controlled by phosphorylation. The delta subunit mediates the dependence of the enzyme on calcium concentration. Mutations in this gene cause glycogen storage disease type 9C, also known as autosomal liver glycogenosis. Alternatively spliced transcript variants encoding different isoforms have been identified in this gene.[provided by RefSeq, Feb 2010]
Expression: Broad expression in testis (RPKM 22.8), bone marrow (RPKM 6.1) and 24 other tissues
Orthologs: mouse
Gene size: 12752bp
Exon count: 10