solute carrier family 2 member 2
| GO Term | Evidence Code | PMID |
|---|---|---|
| carbohydrate metabolic process |
|
|
| fructose transmembrane transport |
|
|
| galactose transmembrane transport |
|
|
| positive regulation of insulin secretion involved in cellular response to glucose stimulus |
|
|
| obsolete D-glucose import |
|
|
| GO Term | Evidence Code | PMID |
|---|---|---|
| cytoplasm |
|
|
| plasma membrane |
|
|
| plasma membrane |
|
|
| plasma membrane |
|
|
| plasma membrane |
|
| GO Term | Evidence Code | PMID |
|---|---|---|
| fructose transmembrane transporter activity |
|
|
| fructose transmembrane transporter activity |
|
|
| galactose transmembrane transporter activity |
|
|
| hexose transmembrane transporter activity |
|
|
| transmembrane transporter activity |
|
| Gene Ontology |
|---|
| hexose transmembrane transporter activity |
Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0070562 | Fanconi-Bickel syndrome | |
| DOID:2747 | glycogen storage disease | |
| DOID:9352 | type 2 diabetes mellitus |
| HPO ID | HPO Term |
|---|---|
| HP:0000006 | Autosomal dominant inheritance |
| HP:0000007 | Autosomal recessive inheritance |
| HP:0000093 | Proteinuria |
| HP:0000112 | Nephropathy |
| HP:0000121 | Nephrocalcinosis |
| HP:0000124 | Renal tubular dysfunction |
| HP:0000295 | Doll-like facies |
| HP:0000819 | Diabetes mellitus |
| HP:0000855 | Insulin resistance |
| HP:0000938 | Osteopenia |
| Disease ID | Disease Name |
|---|---|
| OMIM:125853 |
|
| ORPHA:2088 |
|
| OMIM:227810 |
|
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