PIGP Chromosome 21

Phosphatidylinositol glycan anchor biosynthesis class P
4 variants 4 Health Risk

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What This Gene Does
This gene encodes an enzyme involved in the first step of glycosylphosphatidylinositol (GPI)-anchor biosynthesis. The GPI-anchor is a glycolipid found on many blood cells that serves to anchor proteins to the cell surface. The encoded protein is a component of the GPI-N-acetylglucosaminyltransferase complex that catalyzes the transfer of N-acetylglucosamine (GlcNAc) from UDP-GlcNAc to phosphatidylinositol (PI). This gene is located in the Down Syndrome critical region on chromosome 21 and is a candidate for the pathogenesis of Down syndrome. This gene has multiple pseudogenes and is a member of the phosphatidylinositol glycan anchor biosynthesis gene family. Alternatively spliced transcript variants encoding different isoforms have been described. [provided by RefSeq, Feb 2016]
Gene Info
Gene Group
"Phosphatidylinositol glycan anchor biosynthesis|Glycosylphosphatidylinositol-N-acetylglucosaminyltransferase complex"
Locus Type
gene with protein product
Location
21q22.13
Ensembl
ENSG00000185808
Associated Conditions (5)
Inborn genetic diseases
Developmental and epileptic encephalopathy
55
See cases
PIGP-related disorder
Key Variants
All Variants (4)
RSID Category Clinical Significance Conditions
RS1399528026 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS759209452 Health Risk Conflicting classifications of pathogenicity
RS768633670 Health Risk Pathogenic/Likely pathogenic Developmental and epileptic encephalopathy, 55, See cases
RS778481061 Health Risk Pathogenic/Likely pathogenic Developmental and epileptic encephalopathy, 55, Developmental and epileptic encephalopathy
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