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
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:0111040 | glycogen storage disease IXd | |
| DOID:0111041 | glycogen storage disease IXb | |
| DOID:0111042 | glycogen storage disease IXa | |
| DOID:0111043 | glycogen storage disease IXc | |
| DOID:10461 | dentin caries | |
| DOID:10486 | intestinal atresia | |
| DOID:10573 | osteomalacia | |
| DOID:10603 | glucose intolerance | |
| DOID:10607 | tropical sprue | |
| DOID:10609 | rickets |
- 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 |
|---|---|---|---|
| 173525 | WB:WBGene00019207 | ||
| 178634 | WB:WBGene00019979 | ||
| 186195 | WB:WBGene00018779 | ||
| 35520 | FB:FBgn0033047 | ||
| 35774 | FB:FBgn0028563 | ||
| 38109 | FB:FBgn0264574 | ||
| 322493 | ZFIN:ZDB-GENE-030131-1213 | DANRE29727 | |
| 108278343 | ICTPU09633 | ||
| 113576487 | ELEEL18604 | ||
| 106594064 | SALSA44807 |
