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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
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)
Annotation
- Keyword
-
- Alternative splicing
- Disease variant
- Endoplasmic reticulum
- Epilepsy
- GPI-anchor biosynthesis
- Glycoprotein
- Glycosyltransferase
- Intellectual disability
- Lipid metabolism
- Phosphoprotein
- Reference proteome
- Transmembrane helix
- Proteins
| UniProt | Protein Name |
|---|---|
| P37287 |
|
| A0A2K4ZA02 |
|
Gene Ontology (GO)
| GO Term | Evidence Code | PMID |
|---|---|---|
| GPI anchor biosynthetic process | ||
| preassembly of GPI anchor in ER membrane | ||
| cellular response to leukemia inhibitory factor |
GO Hierarchy
biological process
metabolic process [inference]
cellular process [inference]
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| phosphatidylinositol N-acetylglucosaminyltransferase activity | ||
| UDP-glycosyltransferase activity | ||
| protein binding |
GO Hierarchy
GlycoGene Database (GGDB)
- GGDB ID
- gg215
- Gene Symbol
-
- PIGA
KEGG BRITE Database
Rhea
Disease
- Disease Ontology
| 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
| HPO ID | HPO Term |
|---|---|
| HP:0003273 | Hip contracture |
| HP:0003487 | Babinski sign |
| HP:0003517 | Birth length greater than 97th percentile |
| HP:0003581 | Adult onset |
| HP:0003593 | Infantile onset |
| HP:0003641 | Hemoglobinuria |
| HP:0003700 | Generalized amyotrophy |
| HP:0004302 | Functional motor deficit |
| HP:0004322 | Short stature |
| HP:0004420 | Arterial thrombosis |
| Disease ID | Disease Name |
|---|---|
| ORPHA:293181 |
|
| OMIM:300868 |
|
| OMIM:301072 |
|
| OMIM:300818 |
|
| ORPHA:447 |
|
| ORPHA:3451 |
|
PubChem Disease
- GHR Health Conditions
- MedGen Diseases
- OMIM Phenotypes
- KEGG Diseases
LIPID MAPS Gene / Proteome Database
- LMPD ID
- LMP001689
- Gene Name
- phosphatidylinositol glycan anchor biosynthesis, class A
Ortholog
| Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
|---|---|---|---|
| 100156880 | PIGXX36954 | ||
| 102187116 | CAPHI31039 | ||
| 101102455 | SHEEP19526 | ||
| 103351771 | RABIT13307 | ||
| 105997667 | DIPOR16340 | ||
| 103164275 | CRIGR20701 | ||
| 103164276 | CRIGR20701 | ||
| 18700 | MGI:99461 | MOUSE66170 | |
| 363464 | RGD:1589723 | RATNO45598 | |
| 100713611 | CAVPO22590 |
