solute carrier family 2 member 1

Summary
Gene Symbol
  • SLC2A1
Organism
Homo sapiens (human)
External Links
NCBI Gene
6513
PubChem
6513
Alliance of Genome Resources
Annotation
Keyword
  • 3D-structure
  • Acetylation
  • Cataract
  • Cell membrane
  • Direct protein sequencing
  • Disease variant
  • Dystonia
  • Epilepsy
  • Glycoprotein
  • Hereditary hemolytic anemia
  • Intellectual disability
  • Phosphoprotein
  • Reference proteome
  • Sugar transport
  • Transmembrane helix
Proteins
Displaying all 2 entries
UniProt Protein Name
Q59GX2
  • Glucose transporter type 1, erythrocyte/brain
P11166
  • Glucose transporter type 1, erythrocyte/brain
  • HepG2 glucose transporter
Gene Ontology (GO)
GO Hierarchy
GO Hierarchy
Disease
Disease Ontology
Displaying entries 11 - 17 of 17 in total
DO ID Disease Name Source
DOID:2154 nephroblastoma
DOID:255 hemangioma
DOID:2978 carbohydrate metabolic disorder
DOID:3525 middle cerebral artery infarction
DOID:9351 diabetes mellitus
DOID:9352 type 2 diabetes mellitus
DOID:9970 obesity
Ortholog
Displaying entry 111 - 111 of 111 in total
Species Gene ID Alliance of Genome Resources Orthologous MAtrix
115617508 STRHB16377

About Release Notes Help Feedback

Click here to visit the beta site.


International Collaboration

GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


Logo License Policies Site Map

Contact: support@glycosmos.org

This work is licensed under Creative Commons Attribution 4.0 International


GlyCosmos Portal v4.0.0

Last updated: August 19, 2024