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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:0050156 | idiopathic pulmonary fibrosis | |
| DOID:0050429 | Hailey-Hailey disease | |
| DOID:0050466 | Loeys-Dietz syndrome | |
| DOID:0050645 | arterial tortuosity syndrome | |
| DOID:0050700 | cardiomyopathy | |
| DOID:0050830 | peripheral artery disease | |
| DOID:0060249 | scoliosis | |
| DOID:0060305 | megalocornea | |
| DOID:0060319 | cardiac arrest | |
| DOID:0060320 | inguinal hernia |
- 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 |
|---|---|---|---|
| 716558 | MACMU02042 | ||
| 105496485 | MACNE14190 | ||
| 101026949 | PAPAN12883 | ||
| 105542281 | MANLE23194 | ||
| 101131480 | GORGO22074 | ||
| 100978426 | PANPA22482 | ||
| 469963 | PANTR25055 | ||
| 100445476 | PONAB20878 | ||
| 485911 | CANLF09627 | ||
| 112931897 | VULVU27512 |
