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.
A synthesized peptide derived from human PYGO2, corresponding to a region within N-terminal amino acids.
A synthesized peptide derived from human PYK2, corresponding to a region within the internal amino acids.
A synthesized peptide derived from human PYM1.
A synthesized peptide derived from human Pyrin, corresponding to a region within N-terminal amino acids.
A synthesized peptide derived from Human PYROXD1.
The protein encoded by this gene is proteolytically processed to release a peptide that inhibits pancreatic secretion and mobility in the gut. Rare variations in this gene could increase susceptibility to obesity.
Inserisci la tua e-mail e seleziona le aree di interesse per ricevere le ultime novità, approfondimenti e promozioni.
Seleziona uno o più ambiti di interesse per ricevere comunicazioni più utili e mirate.
2025 TEMA Ricerca - All Rights Reserved.
