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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
solute carrier family 2 member 1
Summary
- Gene Symbol
-
- SLC2A1
- Organism
- Homo sapiens (human)
Annotation
- Keyword
-
- 3D-structure
- Acetylation
- Cataract
- Cell membrane
- Direct protein sequencing
- Disease variant
- Dystonia
- Epilepsy
- Glycoprotein
- Hereditary hemolytic anemia
- Intellectual disability
- Phosphoprotein
- Reference proteome
- Sugar transport
- Transmembrane helix
- Proteins
Gene Ontology (GO)
| GO Term | Evidence Code | PMID |
|---|---|---|
| glucose import | ||
| cerebral cortex development | ||
| central nervous system development | ||
| response to insulin | ||
| xenobiotic transport |
GO Hierarchy
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| glucose transmembrane transporter activity | ||
| kinase binding | ||
| long-chain fatty acid transporter activity | ||
| D-glucose transmembrane transporter activity | ||
| protein self-association |
|
GO Hierarchy
Disease
- Disease Ontology
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0060326 | myelomeningocele | |
| DOID:0090044 | dystonia 9 | |
| DOID:0090045 | childhood onset GLUT1 deficiency syndrome 2 | |
| DOID:0111313 | idiopathic generalized epilepsy 12 | |
| DOID:10487 | Hirschsprung's disease | |
| DOID:10591 | pre-eclampsia | |
| DOID:10652 | Alzheimer's disease | |
| DOID:10763 | hypertension | |
| DOID:1459 | hypothyroidism | |
| DOID:1825 | childhood absence epilepsy |
Ortholog
| Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
|---|---|---|---|
| 113890035 | BOBOX07747 | ||
| 105862274 | MICMU04595 | ||
| 100959166 | OTOGA04242 | ||
| 101073552 | TAKRU21279 | ||
| 102796706 | NEOBR03079 | ||
| 102017914 | CHILA22929 | ||
| 108231650 | KRYMA05387 | ||
| 105705048 | AOTNA11696 | ||
| 110206215 | PHACI12884 | ||
| 101049410 | SAIBB27679 |
