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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:1324 | lung cancer | |
| DOID:1325 | bronchus cancer | |
| DOID:13976 | peptic esophagitis | |
| DOID:14004 | thoracic aortic aneurysm | |
| DOID:14203 | childhood type dermatomyositis | |
| DOID:14415 | Legg-Calve-Perthes disease | |
| DOID:1612 | breast cancer | |
| DOID:162 | cancer | |
| DOID:1712 | aortic valve stenosis | |
| DOID:178 | vascular disease |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0000776 | Congenital diaphragmatic hernia |
| HP:0000822 | Hypertension |
| HP:0000963 | Thin skin |
| HP:0000973 | Cutis laxa |
| HP:0000974 | Hyperextensible skin |
| HP:0000977 | Soft skin |
| HP:0000978 | Bruising susceptibility |
| HP:0001027 | Soft, doughy skin |
| HP:0001119 | Keratoglobus |
| HP:0001166 | Arachnodactyly |
| 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 |
|---|---|---|---|
| 103186264 | CALMI34221 | ||
| 102364983 | LATCH10365 | ||
| 560546 | ZFIN:ZDB-GENE-080204-6 | DANRE03179 | |
| 103042379 | ASTMX05310 | ||
| 108255251 | ICTPU16406 | ||
| 106565264 | SALSA24493 | ||
| 115208344 | SALTR34707 | ||
| 115542397 | GADMO27705 | ||
| 100710582 | ORENI59894 | ||
| 115583513 | SPAAU42212 |
