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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:341 | peripheral vascular disease | |
| DOID:3459 | breast carcinoma | |
| DOID:3526 | cerebral infarction | |
| DOID:3627 | aortic aneurysm | |
| DOID:3669 | intermittent claudication | |
| DOID:3683 | lung benign neoplasm | |
| DOID:3827 | congenital diaphragmatic hernia | |
| DOID:3904 | bronchus carcinoma | |
| DOID:3905 | lung carcinoma | |
| DOID:3910 | lung adenocarcinoma |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0001249 | Intellectual disability |
| HP:0001252 | Hypotonia |
| HP:0001263 | Global developmental delay |
| HP:0001290 | Generalized hypotonia |
| HP:0001328 | Specific learning disability |
| HP:0001363 | Craniosynostosis |
| HP:0001371 | Flexion contracture |
| HP:0001382 | Joint hypermobility |
| HP:0001385 | Hip dysplasia |
| HP:0001537 | Umbilical hernia |
| 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 |
