Solute carrier family 2, facilitated glucose transporter member 1
| GO Term | Evidence Code | Reference |
|---|---|---|
| response to hypoxia | ||
| central nervous system development | ||
| female pregnancy | ||
| long-chain fatty acid import across plasma membrane | ||
| L-ascorbic acid metabolic process |
| GO Term | Evidence Code | Reference |
|---|---|---|
| Golgi membrane | ||
| Golgi membrane | ||
| female germ cell nucleus |
|
|
| photoreceptor inner segment | ||
| photoreceptor inner segment |
| GO Term | Evidence Code | Reference |
|---|---|---|
| long-chain fatty acid transmembrane transporter activity | ||
| fucose transmembrane transporter activity | ||
| kinase binding | ||
| dehydroascorbic acid transmembrane transporter activity | ||
| dehydroascorbic acid transmembrane transporter activity |
| Position | Description |
|---|---|
| 411 | Not glycosylated |
| Position | Description | PubMed ID | GlyTouCan ID | Source |
|---|---|---|---|---|
| 45 |
|
|||
| 465 |
|
|||
| unknown |
|
| Pathway Name | Organism |
|---|---|
| Cellular hexose transport | Homo sapiens |
| Defective SLC2A1 causes GLUT1 deficiency syndrome 1 (GLUT1DS1) | Homo sapiens |
| Lactose synthesis | Homo sapiens |
| Regulation of insulin secretion | Homo sapiens |
| Vitamin C (ascorbate) metabolism | Homo sapiens |
Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0070560 | glucose transporter type 1 deficiency syndrome | |
| DOID:9970 | obesity | |
| DOID:1825 | childhood absence epilepsy | |
| DOID:0090044 | dystonia 9 | |
| DOID:9352 | type 2 diabetes mellitus | |
| DOID:0060326 | myelomeningocele | |
| DOID:0070561 | glucose transporter type 1 deficiency syndrome 1 | |
| DOID:0090045 | glucose transporter type 1 deficiency syndrome 2 | |
| DOID:0111313 | obsolete idiopathic generalized epilepsy 12 |
GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.
Supported by JST NBDC Grant Number JPMJND2204
Partly supported by NIH Common Fund Grant #1U01GM125267-01
This work is licensed under Creative Commons Attribution 4.0 International
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Last updated: April 6, 2026