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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 | ||
| neuron apoptotic process | ||
| attachment of GPI anchor to protein |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| endoplasmic reticulum membrane | ||
| membrane | ||
| GPI-anchor transamidase complex | ||
| cytoplasmic vesicle |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| protein binding |
GO Hierarchy
GlycoGene Database (GGDB)
- GGDB ID
- gg233
- Gene Symbol
-
- PIGT
Disease
- Disease Ontology
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:13250 | diarrhea | |
| DOID:0060249 | scoliosis | |
| DOID:0060284 | paroxysmal nocturnal hemoglobinuria | |
| DOID:0080140 | multiple congenital anomalies-hypotonia-seizures syndrome 3 | |
| DOID:10293 | monocular esotropia | |
| DOID:10575 | calcium metabolism disease | |
| DOID:11476 | osteoporosis | |
| DOID:11771 | spontaneous ocular nystagmus | |
| DOID:11832 | visual epilepsy | |
| DOID:12678 | hypercalcemia |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0001263 | Global developmental delay |
| HP:0001272 | Cerebellar atrophy |
| HP:0001290 | Generalized hypotonia |
| HP:0001321 | Cerebellar hypoplasia |
| HP:0001363 | Craniosynostosis |
| HP:0001382 | Joint hypermobility |
| HP:0001442 | Typified by somatic mosaicism |
| HP:0001513 | Obesity |
| HP:0001520 | Large for gestational age |
| HP:0001627 | Abnormal heart morphology |
| Disease ID | Disease Name |
|---|---|
| OMIM:615398 |
|
| ORPHA:369837 |
|
| 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 | Alliance of Genome Resources | Orthologous MAtrix |
|---|---|---|---|
| 113013141 | ASTCA21461 | ||
| 115585201 | SPAAU52704 | ||
| 494735 | Xenbase:XB-GENE-1014756 | ||
| 549869 | Xenbase:XB-GENE-1014749 | ||
| 101931969 | CHRPI04858 | ||
| 113434409 | PSETE05116 | ||
| 100085380 | ORNAN25492 | ||
| 100930569 | SARHA01997 | ||
| 100408743 | CALJA32637 | ||
| 105588473 | CERAT30270 |
