This gene encodes a glycosylphosphatidylinositol (GPI)-specific phospholipase that primarily localizes to the Golgi apparatus. This ubiquitously expressed gene is predicted to encode a seven-transmembrane protein that removes unsaturated fatty acids from the sn-2 position of GPI. The remodeling of the constituent fatty acids on GPI is thought to be important for the proper association between GPI-anchored proteins and lipid rafts. The tethering of proteins to plasma membranes via posttranslational GPI-anchoring is thought to play a role in protein sorting and trafficking. Mutations in this gene cause an autosomal recessive form of neurologic hyperphosphatasia with cognitive disability (HPMRS4). Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Jul 2017]
SKU | Test Kits | Buffer | Dye Color | Order Now |
---|---|---|---|---|
PGAP3-20-RE | 20 (40 μL) | 200 μL | Request Pricing | |
PGAP3-20-OR | 20 (40 μL) | 200 μL | Request Pricing | |
PGAP3-20-GO | 20 (40 μL) | 200 μL | Request Pricing | |
PGAP3-20-GR | 20 (40 μL) | 200 μL | Request Pricing | |
PGAP3-20-AQ | 20 (40 μL) | 200 μL | Request Pricing |
This gene encodes a glycosylphosphatidylinositol (GPI)-specific phospholipase that primarily localizes to the Golgi apparatus. This ubiquitously expressed gene is predicted to encode a seven-transmembrane protein that removes unsaturated fatty acids from the sn-2 position of GPI. The remodeling of the constituent fatty acids on GPI is thought to be important for the proper association between GPI-anchored proteins and lipid rafts. The tethering of proteins to plasma membranes via posttranslational GPI-anchoring is thought to play a role in protein sorting and trafficking. Mutations in this gene cause an autosomal recessive form of neurologic hyperphosphatasia with cognitive disability (HPMRS4). Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Jul 2017]
Gene Symbol : PGAP3
Gene Name : Post-GPI attachment to proteins 3
Chromosome : CHR 17: 396,880,69-396,711,21
Locus : 17q12
Alt. Genes : FEM1B
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