PIGQ Chromosome 16

Phosphatidylinositol glycan anchor biosynthesis class Q
56 variants 56 Health Risk

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What This Gene Does
This gene is involved in the first step in glycosylphosphatidylinositol (GPI)-anchor biosynthesis. The GPI-anchor is a glycolipid found on many blood cells and serves to anchor proteins to the cell surface. This gene encodes a N-acetylglucosaminyl transferase component that is part of the complex that catalyzes transfer of N-acetylglucosamine (GlcNAc) from UDP-GlcNAc to phosphatidylinositol (PI). Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jun 2012]
Gene Info
Gene Group
"Phosphatidylinositol glycan anchor biosynthesis|Glycosylphosphatidylinositol-N-acetylglucosaminyltransferase complex"
Locus Type
gene with protein product
Location
16p13.3
Ensembl
ENSG00000007541
Associated Conditions (8)
Epilepsy
Inborn genetic diseases
Developmental and epileptic encephalopathy
77
PIGQ-related disorder
Optic atrophy
Global developmental delay
Intractable seizure
Key Variants
All Variants (56)
RSID Category Clinical Significance Conditions
RS1283058431 Health Risk Conflicting classifications of pathogenicity Epilepsy, Inborn genetic diseases, Epilepsy
RS137907943 Health Risk Conflicting classifications of pathogenicity Epilepsy, Inborn genetic diseases, Epilepsy
RS1385011604 Health Risk Conflicting classifications of pathogenicity Epilepsy, Inborn genetic diseases, Epilepsy
RS139256741 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS142961139 Health Risk Conflicting classifications of pathogenicity Epilepsy, Inborn genetic diseases, Developmental and epileptic encephalopathy
RS146122020 Health Risk Conflicting classifications of pathogenicity Epilepsy, Inborn genetic diseases, Epilepsy
RS148151840 Health Risk Conflicting classifications of pathogenicity Epilepsy, Inborn genetic diseases, Epilepsy
RS149108761 Health Risk Conflicting classifications of pathogenicity PIGQ-related disorder, Developmental and epileptic encephalopathy, 77
RS149175905 Health Risk Conflicting classifications of pathogenicity Epilepsy, PIGQ-related disorder, Epilepsy
RS150887807 Health Risk Conflicting classifications of pathogenicity Epilepsy, Inborn genetic diseases, Developmental and epileptic encephalopathy
RS182739177 Health Risk Conflicting classifications of pathogenicity Epilepsy, Epilepsy
RS2035837216 Health Risk Conflicting classifications of pathogenicity Epilepsy, Inborn genetic diseases, Epilepsy
RS368941189 Health Risk Conflicting classifications of pathogenicity Epilepsy, Inborn genetic diseases, Epilepsy
RS370004325 Health Risk Conflicting classifications of pathogenicity Epilepsy, Inborn genetic diseases, Epilepsy
RS372069327 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Epilepsy, Inborn genetic diseases
RS372383821 Health Risk Conflicting classifications of pathogenicity Epilepsy, Inborn genetic diseases, Epilepsy
RS374896268 Health Risk Conflicting classifications of pathogenicity Epilepsy, Epilepsy
RS377584268 Health Risk Conflicting classifications of pathogenicity Epilepsy, Inborn genetic diseases, Epilepsy
RS767785877 Health Risk Conflicting classifications of pathogenicity Epilepsy, Developmental and epileptic encephalopathy, 77
RS768063812 Health Risk Conflicting classifications of pathogenicity Epilepsy, Epilepsy
RS773722943 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS774945335 Health Risk Conflicting classifications of pathogenicity Epilepsy, Developmental and epileptic encephalopathy, 77
RS779225248 Health Risk Conflicting classifications of pathogenicity Epilepsy, Inborn genetic diseases, Epilepsy
RS1300851687 Health Risk Likely pathogenic Epilepsy, Epilepsy
RS1361495767 Health Risk Likely pathogenic Developmental and epileptic encephalopathy, 77, Developmental and epileptic encephalopathy
RS2035766325 Health Risk Likely pathogenic PIGQ-related disorder, PIGQ-related disorder
RS2151047692 Health Risk Likely pathogenic Epilepsy, Epilepsy
RS1206309859 Health Risk Pathogenic Epilepsy, Epilepsy
RS1229740428 Health Risk Pathogenic Epilepsy, Epilepsy
RS1341033162 Health Risk Pathogenic Epilepsy, Epilepsy
RS1567174597 Health Risk Pathogenic Epilepsy, Epilepsy
RS1596385588 Health Risk Pathogenic Epilepsy, Epilepsy
RS200661329 Health Risk Pathogenic Epilepsy, PIGQ-related disorder, Developmental and epileptic encephalopathy
RS2035826930 Health Risk Pathogenic Developmental and epileptic encephalopathy, 77, Developmental and epileptic encephalopathy
RS2151044127 Health Risk Pathogenic Epilepsy, Epilepsy
RS2151044473 Health Risk Pathogenic Epilepsy, Epilepsy
RS2151047073 Health Risk Pathogenic Epilepsy, Epilepsy
RS2505931024 Health Risk Pathogenic Epilepsy, Epilepsy
RS2505931126 Health Risk Pathogenic Epilepsy, Epilepsy
RS2505931142 Health Risk Pathogenic Epilepsy, Epilepsy
RS2505933639 Health Risk Pathogenic Epilepsy, Epilepsy
RS2505936870 Health Risk Pathogenic PIGQ-related disorder, Epilepsy, PIGQ-related disorder
RS587777543 Health Risk Pathogenic Developmental and epileptic encephalopathy, 77, Developmental and epileptic encephalopathy
RS730882240 Health Risk Pathogenic Optic atrophy, Global developmental delay, Intractable seizure
RS747661902 Health Risk Pathogenic Inborn genetic diseases, Epilepsy, Developmental and epileptic encephalopathy
RS750315914 Health Risk Pathogenic Epilepsy, Epilepsy
RS758325986 Health Risk Pathogenic Inborn genetic diseases, Inborn genetic diseases
RS759540917 Health Risk Pathogenic Epilepsy, Epilepsy
RS762696210 Health Risk Pathogenic Epilepsy, Epilepsy
RS767373792 Health Risk Pathogenic Epilepsy, Epilepsy
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