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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
GPI transamidase component PIG-T
Summary
- UniProt ID
- Q969N2
- Gene Symbol
-
- PIGT
- 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
- Gene Ontology (GO)
| GO Term |
|---|
| neuron differentiation |
| neuron apoptotic process |
| attachment of GPI anchor to protein |
| GO Term |
|---|
| membrane |
| cytoplasmic vesicle |
| GPI-anchor transamidase complex |
| endoplasmic reticulum membrane |
Sequence
MAAAMPLALLVLLLLGPGGWCLAEPPRDSLREELVITPLPSGDVAATFQFRTRWDSELQREGVSHYRLFPKALGQLISKYSLRELHLSFTQGFWRTRYWGPPFLQAPSGAELWVWFQDTVTDVDKSWKELSNVLSGIFCASLNFIDSTNTVTPTASFKPLGLANDTDHYFLRYAVLPREVVCTENLTPWKKLLPCSSKAGLSVLLKADRLFHTSYHSQAVHIRPVCRNARCTSISWELRQTLSVVFDAFITGQGKKDWSLFRMFSRTLTEPCPLASESRVYVDITTYNQDNETLEVHPPPTTTYQDVILGTRKTYAIYDLLDTAMINNSRNLNIQLKWKRPPENEAPPVPFLHAQRYVSGYGLQKGELSTLLYNTHPYRAFPVLLLDTVPWYLRLYVHTLTITSKGKENKPSYIHYQPAQDRLQPHLLEMLIQLPANSVTKVSIQFERALLKWTEYTPDPNHGFYVSPSVLSALVPSMVAAKPVDWEESPLFNSLFPVSDGSNYFVRLYTEPLLVNLPTPDFSMPYNVICLTCTVVAVCYGSFYNLLTRTFHIEEPRTGGLAKRLANLIRRARGVPPL
Glycosylation Sites
| Position | Description | PubMed ID | GlyTouCan ID | Source |
|---|---|---|---|---|
| 164 | N-linked (GlcNAc...) asparagine | |||
| 185 |
|
|||
| 291 | N-linked (GlcNAc...) asparagine | |||
| 327 | N-linked (GlcNAc...) asparagine | |||
| 328 |
|
|
||
|
|
G62765YT
G12795MA
G41247ZX
G46503DX
G80920RR
G31852PQ
G90575OW
G23719VF
G39446WN
G39188ZX
G36379GD
G02815KT
G06110VR
G92050GC
G28681TP
G49108TO
Feature
: Glycosylation Site from GlyGen
: Glycosylation Site from UniProt
Pathway
| Pathway Name | Organism |
|---|---|
| Attachment of GPI anchor to uPAR | Homo sapiens |
Disease
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:9834 | hyperopia | |
| DOID:9837 | hypertropia | |
| DOID:9840 | esotropia | |
| 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 |
