Submissions
GlyTouCan
Glycan Structure Repository
GlyComb
Glycoconjugate Repository
GlycoPOST
Glycomics MS raw data Repository
UniCarb-DR
Glycomics MS Repository for glycan annotations from GlycoWorkbench
LM-GlycoRepo
Repository for lectin-assisted multimodality data
All Resources
Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / OrganismsTools
SugarDrawer
GlycanBuilder
Glycan Converters
GlycoMaple
GlycomeAtlas
LM-GlycomeAtlas
GALAXY
MCAW
GlycoSim
GRable
Guidelines
MIRAGE
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 apoptotic process |
GO Hierarchy
biological process
metabolic process [inference]
cellular process [inference]
| GO Term | Evidence Code | PMID |
|---|---|---|
| endoplasmic reticulum membrane | ||
| endoplasmic reticulum membrane | ||
| membrane | ||
| cytoplasmic vesicle | ||
| GPI-anchor transamidase complex |
GO Hierarchy
GO Hierarchy
OrthoDB (Group)
- Group level
- Eukaryota
- Group Name
- GPI transamidase
- 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:0000218 | High palate |
| HP:0000248 | Brachycephaly |
| HP:0000256 | Macrocephaly |
| HP:0000272 | Malar flattening |
| HP:0000341 | Narrow forehead |
| HP:0000343 | Long philtrum |
| HP:0000347 | Micrognathia |
| HP:0000348 | High forehead |
| HP:0000365 | Hearing impairment |
| HP:0000369 | Low-set ears |
| Disease ID | Disease Name |
|---|---|
| OMIM:615399 |
|
| OMIM:615398 |
|
| ORPHA:369837 |
|
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 |
|---|---|---|---|
| 102793327 | NEOBR05529 | ||
| 103138938 | POEFO06567 | ||
| 103245365 | CHLSB07647 | ||
| 103259847 | CARSF23640 | ||
| 103384972 | CYNSE01870 | ||
| 103481160 | POERE14098 | ||
| 103669872 | URSMA14596 | ||
| 103736141 | NANGA25405 | ||
| 104678844 | RHIRO03891 | ||
| 105013799 | ESOLU34437 |
