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solute carrier family 2 member 2
Summary
- Gene Symbol
-
- SLC2A2
- Aliases
-
- GLUT-2
- Organism
- Homo sapiens (human)
Annotation
Gene Ontology (GO)
| GO Term | Evidence Code | PMID |
|---|---|---|
| positive regulation of insulin secretion involved in cellular response to glucose stimulus | ||
| glucose import |
GO Hierarchy
biological process
biological regulation [inference]
regulation of biological process [inference]
regulation of signaling [inference]
regulation of localization [inference]
positive regulation of biological process [inference]
regulation of cellular process [inference]
| GO Term | Evidence Code | PMID |
|---|---|---|
| cytoplasm | ||
| cell-cell junction | ||
| plasma membrane | ||
| membrane | ||
| apical plasma membrane |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| galactose transmembrane transporter activity | ||
| glucose transmembrane transporter activity | ||
| D-glucose transmembrane transporter activity | ||
| hexose transmembrane transporter activity | ||
| fructose transmembrane transporter activity |
GO Hierarchy
Human Protein Atlas
Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.
KEGG BRITE Database
Disease
- Disease Ontology
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0014667 | disease of metabolism | |
| DOID:0050336 | hypophosphatemia | |
| DOID:0050424 | familial adenomatous polyposis | |
| DOID:0050445 | X-linked dominant hypophosphatemic rickets | |
| DOID:0050524 | maturity-onset diabetes of the young | |
| DOID:0050865 | tongue squamous cell carcinoma | |
| DOID:0060326 | myelomeningocele | |
| DOID:0060334 | transient neonatal diabetes mellitus | |
| DOID:0060639 | permanent neonatal diabetes mellitus | |
| DOID:0110741 | type 1 diabetes mellitus 2 |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0004396 | Poor appetite |
| HP:0004915 | Impairment of galactose metabolism |
| HP:0004919 | Galactose intolerance |
| HP:0005978 | Type II diabetes mellitus |
| HP:0006487 | Bowing of the long bones |
| HP:0006568 | Increased hepatic glycogen content |
| HP:0008897 | Postnatal growth retardation |
| HP:0011998 | Postprandial hyperglycemia |
| HP:0012024 | Hypergalactosemia |
| HP:0012202 | Increased serum bile acid concentration |
| Disease ID | Disease Name |
|---|---|
| ORPHA:2088 |
|
| OMIM:227810 |
|
| OMIM:125853 |
|
PubChem Disease
- MedGen Diseases
- OMIM Phenotypes
- KEGG Diseases
Ortholog
| Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
|---|---|---|---|
| 116826731 | CHEAB07296 | ||
| 115035490 | ECHNA39741 | ||
| 105806978 | PROCO04756 | ||
| 852543 | SGD:S000000445 | ||
| 116448479 | CORMO00630 | ||
| 103260645 | CARSF18016 | ||
| 115611833 | STRHB11601 |
