Phosphatidylinositol N-acetylglucosaminyltransferase subunit A

Summary
UniProt ID
P37287
Gene Symbol
PIGA
Gene ID
5277
Organism
Homo sapiens (human)
PubChem
P37287
The Human Metabolome Database
HMDBP00941
Re-Glyco
P37287
Annotation
Keyword
Alternative splicing Disease variant Endoplasmic reticulum Epilepsy GPI-anchor biosynthesis Glycoprotein Glycosyltransferase Intellectual disability Lipid metabolism Phosphoprotein Proteomics identification Reference proteome Transmembrane helix
Gene Ontology (GO)
GO Hierarchy
Sequence
MACRGGAGNGHRASATLSRVSPGSLYTCRTRTHNICMVSDFFYPNMGGVESHIYQLSQCLIERGHKVIIVTHAYGNRKGIRYLTSGLKVYYLPLKVMYNQSTATTLFHSLPLLRYIFVRERVTIIHSHSSFSAMAHDALFHAKTMGLQTVFTDHSLFGFADVSSVLTNKLLTVSLCDTNHIICVSYTSKENTVLRAALNPEIVSVIPNAVDPTDFTPDPFRRHDSITIVVVSRLVYRKGIDLLSGIIPELCQKYPDLNFIIGGEGPKRIILEEVRERYQLHDRVRLLGALEHKDVRNVLVQGHIFLNTSLTEAFCMAIVEAASCGLQVVSTRVGGIPEVLPENLIILCEPSVKSLCEGLEKAIFQLKSGTLPAPENIHNIVKTFYTWRNVAERTEKVYDRVSVEAVLPMDKRLDRLISHCGPVTGYIFALLAVFNFLFLIFLRWMTPDSIIDVAIDATGPRGAWTNNYSHSKRGGENNEISETR
Glycosylation Sites
Displaying 1 entry
Position Description PubMed ID GlyTouCan ID Source
467
  • N-linked (GlcNAc...) asparagine
Feature
  • ProtVista GlyGen : Glycosylation Site from GlyGen
  • ProtVista UniProt : Glycosylation Site from UniProt
Pathway
Displaying 1 entry
Pathway Name Organism
Synthesis of glycosylphosphatidylinositol (GPI) Homo sapiens
Disease
Displaying all 2 entries
DO ID Disease Name Source
DOID:0080139 multiple congenital anomalies-hypotonia-seizures syndrome 2
DOID:0060284 paroxysmal nocturnal hemoglobinuria

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International Collaboration

GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: April 6, 2026