PIGP Chromosome 21
Phosphatidylinositol glycan anchor biosynthesis class P
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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
RS1399528026
Conflicting classifications of pathogenicity
Inborn genetic diseases, Inborn genetic diseases
Health Risk
RS759209452
Conflicting classifications of pathogenicity
Health Risk
RS768633670
Pathogenic/Likely pathogenic
Developmental and epileptic encephalopathy, 55, See cases
Health Risk
RS778481061
Pathogenic/Likely pathogenic
Developmental and epileptic encephalopathy, 55, Developmental and epileptic encephalopathy
Health Risk
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 |