PIGA Products

Description

PIGA, also known as Phosphatidylinositol N-acetylglucosaminyltransferase subunit A, has three isoforms that are produced by alternative splicing. Isoform 1, the canonical sequence, is 484 amino acids long and 54 kDa. Isoform 2 and 3 are both shorter isoforms, at 315 and 250 amino acids, respectively. PIGA is a critical player in the synthesis of N-acetylglucosaminyl-phosphatidylinositol, which is the first intermediate in the biosynthesis of GPI anchors. Current research on PIGA is being conducted in relation to several diseases and disorders including Paroxysmal nocturnal hemoglobinuria, which may be caused by mutations in the PIGA gene. Other diseases and disorders related to PIGA include multiple congenital anomalies-hypotonia-seizures syndrome type 2, anemia, Burkitt's lymphoma, hepatic vein thrombosis and Myelodysplastic syndrome. PIGA has been shown to have interactions with DPM2, PIGQ, PIGH, PYURF and PIGP in pathways such as GPI anchor biosynthesis and metabolic pathways.

Bioinformatics

Entrez	5277 Human
Uniprot	B3KUV7 Human NP_002632 Human P37287 Human
Product By Gene ID	5277
Alternate Names	class A GlcNAc-inositol phospholipid assembly protein EC 2.4.1.198 GlcNAc-PI synthesis protein GPI anchor biosynthesis GPI3 phosphatidylinositol glycan anchor biosynthesis, class A phosphatidylinositol glycan, class A (paroxysmal nocturnal hemoglobinuria) phosphatidylinositol N-acetylglucosaminyltransferase subunit A Phosphatidylinositol-glycan biosynthesis class A protein phosphatidylinositol-glycan biosynthesis, class A protein PIG-A