Submissions
GlyTouCan
Glycan Structure Repository
GlyComb
Glycoconjugate Repository
GlycoPOST
Glycomics MS raw data Repository
UniCarb-DR
Glycomics MS Repository for glycan annotations from GlycoWorkbench
All Resources
Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
protein O-linked mannose N-acetylglucosaminyltransferase 1 (beta 1,2-) S homeolog
Summary
- Gene Symbol
-
- pomgnt1.S
- Organism
- Xenopus laevis (African clawed frog)
External Links
- NCBI Gene
- 495292
- KEGG Gene ID
- xla:495292
- PubChem
- 495292
- Alliance of Genome Resources
Annotation
- Keyword
-
- Glycosyltransferase
- Golgi apparatus
- Lectin
- Manganese
- Metal-binding
- Phosphoprotein
- Reference proteome
- Signal-anchor
- Transmembrane helix
- Proteins
| UniProt | Protein Name |
|---|---|
| Q5U5D7 |
|
Gene Ontology (GO)
| GO Term | Evidence Code | PMID |
|---|---|---|
| O-glycan processing | ||
| protein glycosylation |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| membrane | ||
| Golgi apparatus | ||
| Golgi membrane |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| glycosyltransferase activity | ||
| manganese ion binding | ||
| metal ion binding | ||
| carbohydrate binding | ||
| acetylglucosaminyltransferase activity |
GO Hierarchy
KEGG BRITE Database
G61491DK
G85856KC
Disease
- Disease Ontology
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0050453 | lissencephaly | |
| DOID:0050560 | Walker-Warburg syndrome | |
| DOID:0110292 | autosomal recessive limb-girdle muscular dystrophy type 2O | |
| DOID:0111236 | congenital muscular dystrophy-dystroglycanopathy type A3 | |
| DOID:0112378 | muscular dystrophy-dystroglycanopathy type B3 | |
| DOID:10584 | retinitis pigmentosa | |
| DOID:9884 | muscular dystrophy |
Ortholog
| Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
|---|---|---|---|
| 100158594 | Xenbase:XB-GENE-959856 | ||
| 55624 | HGNC:19139 |
