solute carrier family 2 member 1

Summary
Gene Symbol
  • SLC2A1
Organism
Homo sapiens (human)
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
OrthoDB (Group)
Group level
Eukaryota
Group Name
solute carrier family 2
Functional Category
  • E: Amino acid transport and metabolism
  • M: Cell wall/membrane/envelope biogenesis
  • T: Signal transduction mechanisms
Disease
Disease Ontology
Displaying entries 1 - 10 of 16 in total
DO ID Disease Name Source
DOID:0060326 myelomeningocele
DOID:0090044 dystonia 9
DOID:0090045 childhood onset GLUT1 deficiency syndrome 2
DOID:0111313 idiopathic generalized epilepsy 12
DOID:10487 Hirschsprung's disease
DOID:10591 pre-eclampsia
DOID:10652 Alzheimer's disease
DOID:10763 hypertension
DOID:1459 hypothyroidism
DOID:1825 childhood absence epilepsy

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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: December 9, 2024