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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
phosphatidylinositol glycan anchor biosynthesis class T
Summary
- Gene Symbol
-
- PIGT
- Aliases
-
- GPI transamidase component PIG-T
- GPI transamidase subunit
- PIG-T
- Organism
- Homo sapiens (human)
Annotation
- Keyword
-
- 3D-structure
- Alternative splicing
- Direct protein sequencing
- Disease variant
- Disulfide bond
- Endoplasmic reticulum
- Epilepsy
- GPI-anchor biosynthesis
- Glycoprotein
- Reference proteome
- Signal
- Transmembrane helix
- Proteins
| UniProt | Protein Name |
|---|---|
| Q969N2 |
|
Gene Ontology (GO)
| GO Term | Evidence Code | PMID |
|---|---|---|
| neuron differentiation | ||
| attachment of GPI anchor to protein | ||
| neuron apoptotic process |
GO Hierarchy
GO Hierarchy
GO Hierarchy
OrthoDB (Group)
- Group level
- Eukaryota
- Group Name
- uncharacterized protein
- Functional Category
-
- M: Cell wall/membrane/envelope biogenesis
- O: Posttranslational modification, protein turnover, chaperones
- T: Signal transduction mechanisms
| Gene Ontology |
|---|
| attachment of GPI anchor to protein |
| InterPro |
|---|
| GPI transamidase component PIG-T |
GlycoGene Database (GGDB)
- GGDB ID
- gg233
- Gene Symbol
-
- PIGT
Disease
- Disease Ontology
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0060284 | paroxysmal nocturnal hemoglobinuria | |
| DOID:0080140 | multiple congenital anomalies-hypotonia-seizures syndrome 3 |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0000006 | Autosomal dominant inheritance |
| HP:0000007 | Autosomal recessive inheritance |
| HP:0000071 | Ureteral stenosis |
| HP:0000072 | Hydroureter |
| HP:0000079 | Abnormality of the urinary system |
| HP:0000107 | Renal cyst |
| HP:0000110 | Renal dysplasia |
| HP:0000121 | Nephrocalcinosis |
| HP:0000164 | Abnormality of the dentition |
| HP:0000194 | Open mouth |
| Disease ID | Disease Name |
|---|---|
| ORPHA:369837 |
|
| OMIM:615398 |
|
| OMIM:615399 |
|
PubChem Disease
- GHR Health Conditions
- MedGen Diseases
- OMIM Phenotypes
- KEGG Diseases
LIPID MAPS Gene / Proteome Database
- LMPD ID
- LMP001664
- Gene Name
- phosphatidylinositol glycan anchor biosynthesis, class T
Ortholog
| Species | Gene ID | OrthoDB | Alliance of Genome Resources | Orthologous MAtrix |
|---|---|---|---|---|
| 31772 | FB:FBgn0030035 | |||
| 78928 | MGI:1926178 | MOUSE33788 | ||
| 179519 | WB:WBGene00008918 | |||
| 296360 | RGD:1307156 | RATNO27030 | ||
| 458282 | 9598_0:0051bb | PANTR24952 | ||
| 477244 | CANLF09586 | |||
| 494735 | Xenbase:XB-GENE-1014756 | |||
| 504724 | BOVIN05330 | |||
| 549869 | Xenbase:XB-GENE-1014749 | |||
| 556667 | ZFIN:ZDB-GENE-090313-46 | DANRE50251 |
