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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
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:0000006 | Autosomal dominant inheritance |
| HP:0000007 | Autosomal recessive inheritance |
| HP:0000093 | Proteinuria |
| HP:0000112 | Nephropathy |
| HP:0000121 | Nephrocalcinosis |
| HP:0000124 | Renal tubular dysfunction |
| HP:0000295 | Doll-like facies |
| HP:0000819 | Diabetes mellitus |
| HP:0000855 | Insulin resistance |
| HP:0000938 | Osteopenia |
| 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 |
|---|---|---|---|
| 101022043 | PAPAN23874 | ||
| 105552594 | MANLE29513 | ||
| 101126141 | GORGO28157 | ||
| 100983878 | PANPA29243 | ||
| 460848 | PANTR32639 | ||
| 100437366 | PONAB25746 | ||
| 488165 | CANLF13649 | ||
| 112926672 | VULVU21030 | ||
| 123786389 | URSAM11073 | ||
| 100475889 | AILME11147 |
