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
Displaying entries 1 - 5 of 20 in total
GO Term Evidence Code PMID
cortical actin cytoskeleton
photoreceptor inner segment
melanosome
Z disc
cytosol
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

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

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


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Last updated: August 19, 2024