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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
solute carrier family 2 member 10
Summary
- Gene Symbol
-
- SLC2A10
- Aliases
-
- GLUT-10
- GLUT10
- facilitative glucose transporter GLUT10
- Organism
- Homo sapiens (human)
Annotation
- Keyword
-
- Cytoplasm
- Disease variant
- Glycoprotein
- Reference proteome
- Sugar transport
- Transmembrane helix
- Proteins
| UniProt | Protein Name |
|---|---|
| O95528 |
|
Gene Ontology (GO)
| GO Term | Evidence Code | PMID |
|---|---|---|
| hexose transmembrane transport |
|
GO Hierarchy
biological process
localization [inference]
biological regulation [inference]
regulation of biological process [inference]
regulation of metabolic process [inference]
regulation of biosynthetic process [inference]
negative regulation of metabolic process [inference]
positive regulation of metabolic process [inference]
regulation of cellular metabolic process [inference]
regulation of nitrogen compound metabolic process [inference]
regulation of macromolecule metabolic process [inference]
regulation of signaling [inference]
positive regulation of biological process [inference]
negative regulation of biological process [inference]
regulation of response to stimulus [inference]
regulation of cellular process [inference]
| GO Term | Evidence Code | PMID |
|---|---|---|
| carbohydrate:proton symporter activity |
|
|
| symporter activity | ||
| D-glucose transmembrane transporter activity | ||
| dehydroascorbic acid 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:11847 | coronary thrombosis | |
| DOID:11963 | esophagitis | |
| DOID:11984 | hypertrophic cardiomyopathy | |
| DOID:1222 | cartilage disease | |
| DOID:12639 | pyloric stenosis | |
| DOID:12642 | hiatus hernia | |
| DOID:12716 | newborn respiratory distress syndrome | |
| DOID:12930 | dilated cardiomyopathy | |
| DOID:12932 | endomyocardial fibrosis | |
| DOID:13099 | Moyamoya disease |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0000007 | Autosomal recessive inheritance |
| HP:0000023 | Inguinal hernia |
| HP:0000193 | Bifid uvula |
| HP:0000218 | High palate |
| HP:0000256 | Macrocephaly |
| HP:0000272 | Malar flattening |
| HP:0000276 | Long face |
| HP:0000316 | Hypertelorism |
| HP:0000343 | Long philtrum |
| HP:0000347 | Micrognathia |
| Disease ID | Disease Name |
|---|---|
| OMIM:208050 |
|
| ORPHA:3342 |
|
PubChem Disease
- GHR Health Conditions
- MedGen Diseases
- OMIM Phenotypes
- KEGG Diseases
Ortholog
| Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
|---|---|---|---|
| 108533312 | RHIBE04020 | ||
| 104678800 | RHIRO03794 | ||
| 100595321 | NOMLE07491 | ||
| 114599603 | PODMU05469 | ||
| 107557529 | SINGR80363 | ||
| 106847628 | EQUAS06731 | ||
| 105807178 | PROCO13608 | ||
| 109098400 | CYPCA118751 | ||
| 103729388 | NANGA19576 | ||
| 103263512 | CARSF13183 |
