phosphatidylinositol glycan anchor biosynthesis class A

Summary
Gene Symbol
  • PIGA
Aliases
  • GPI3
  • GPI3 (SPT14) homolog (S. cerevisiae)
  • PIG-A
  • Phosphatidylinositol N-acetylglucosaminyltransferase subunit A
  • paroxysmal nocturnal hemoglobinuria
Organism
Homo sapiens (human)
External Links
NCBI Gene
5277
GGDB ID
HGNC
8957
mRNA
map
  • Xp22.1, Xp22.2 (OMIM)
Protein
OMIM
KEGG Gene ID
hsa:5277
PubChem
5277
Alliance of Genome Resources
Annotation
Keyword
  • Alternative splicing
  • Disease variant
  • Endoplasmic reticulum
  • Epilepsy
  • GPI-anchor biosynthesis
  • Glycoprotein
  • Glycosyltransferase
  • Intellectual disability
  • Lipid metabolism
  • Phosphoprotein
  • Reference proteome
  • Transmembrane helix
Proteins
Displaying all 2 entries
UniProt Protein Name
P37287
  • GlcNAc-PI synthesis protein
  • Phosphatidylinositol-glycan biosynthesis class A protein
A0A2K4ZA02
  • GlcNAc-PI synthesis protein
Gene Ontology (GO)
GO Hierarchy
GlycoGene Database (GGDB)
GGDB ID
gg215
Gene Symbol
  • PIGA
KEGG BRITE Database
Orthology
K03857
Name
phosphatidylinositol N-acetylglucosaminyltransferase subunit A [EC:2.4.1.198]
References
Disease
Disease Ontology
Displaying entries 71 - 80 of 88 in total
DO ID Disease Name Source
DOID:582 hemoglobinuria
DOID:583 hemolytic anemia
DOID:5844 myocardial infarction
DOID:5854 silent myocardial infarction
DOID:6536 plasma cell neoplasm
DOID:6688 autoimmune lymphoproliferative syndrome
DOID:74 hematopoietic system disease
DOID:758 situs inversus
DOID:8534 gastroesophageal reflux disease
DOID:8584 Burkitt lymphoma
The Human Phenotype Ontology
Displaying entries 141 - 150 of 168 in total
HPO ID HPO Term
HP:0007190 Neuronal loss in the cerebral cortex
HP:0007334 Bilateral tonic-clonic seizure with focal onset
HP:0007361 Abnormal pons morphology
HP:0008064 Ichthyosis
HP:0008282 Unconjugated hyperbilirubinemia
HP:0008936 Axial hypotonia
HP:0009085 Alveolar ridge overgrowth
HP:0010821 Focal emotional seizure with laughing
HP:0010841 Multifocal epileptiform discharges
HP:0011097 Epileptic spasm
Displaying all 6 entries
Disease ID Disease Name
ORPHA:293181
  • malignant migrating partial seizures of infancy
OMIM:300868
  • multiple congenital anomalies-hypotonia-seizures syndrome 2
OMIM:301072
  • ferro-cerebro-cutaneous syndrome
OMIM:300818
  • paroxysmal nocturnal hemoglobinuria 1
ORPHA:447
  • paroxysmal nocturnal hemoglobinuria
ORPHA:3451
  • West syndrome
LIPID MAPS Gene / Proteome Database
LMPD ID
LMP001689
Gene Name
phosphatidylinositol glycan anchor biosynthesis, class A

About Release Notes Help Feedback

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


Logo License Policies Site Map

Contact: support@glycosmos.org

This work is licensed under Creative Commons Attribution 4.0 International


GlyCosmos Portal v4.0.0

Last updated: August 19, 2024