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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:10772 | thrombotic thrombocytopenic purpura | |
| DOID:1098 | fetal erythroblastosis | |
| DOID:11832 | visual epilepsy | |
| DOID:11847 | coronary thrombosis | |
| DOID:11963 | esophagitis | |
| DOID:12449 | aplastic anemia | |
| DOID:1247 | blood coagulation disease | |
| DOID:12554 | hemolytic-uremic syndrome | |
| DOID:13003 | vertebrobasilar insufficiency | |
| DOID:13515 | tuberous sclerosis |
- 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 |
|---|---|---|---|
| 100600234 | NOMLE39064 | ||
| 107555234 | SINGR77488 | ||
| 107600385 | SINGR40666 | ||
| 106841579 | EQUAS27507 | ||
| 116820947 | CHEAB28057 | ||
| 105293997 | PTEVA12981 | ||
| 115403658 | SALFA51573 | ||
| 115403813 | SALFA50512 | ||
| 115403817 | SALFA50593 | ||
| 113481627 | ATHCN02736 |
