Solute carrier family 2 (facilitated glucose transporter), member 1

Preferred Label : Solute carrier family 2 (facilitated glucose transporter), member 1;

Symbol : SLC2A1;

CISMeF acronym : SLC2A1;

Type : Gene;

Alternative titles and symbols : Glucose transporter 1; Erythrocyte/hepatoma glucose transporter; Human t-cell leukemia virus receptor; Htlv-1 and htlv-2 receptor; GLUT; GLUT1; HTLVR;

Ensembl ID : ENSG00000117394;

Prefixed ID : *138140;

Details

Origin ID

138140;

UMLS CUI

C1335837;

Automatic exact mappings (from CISMeF team)
- SLC2A1 Gene [NCIt concept]
- SLC2A1 wt Allele [NCIt concept]
- Solute Carrier Family 2, Facilitated Glucose Transporter Member 1 [NCIt concept]
- solute carrier family 2 member 1 [HGNC gene]
- solute carrier family 2 member 1 [ORDO Gene]
HGNC gene
- solute carrier family 2 member 1 [HGNC gene]
NCIt concept(s)
- SLC2A1 Gene [NCIt concept]
- SLC2A1 wt Allele [NCIt concept]
- Solute Carrier Family 2, Facilitated Glucose Transporter Member 1 [NCIt concept]
ORDO concept(s)
- solute carrier family 2 member 1 [ORDO Gene]
Phenotypes related
- Dystonia 9 [OMIM Phenotype]
- Epilepsy, idiopathic generalized, susceptibility to, 12 [OMIM Phenotype]
- Glut1 deficiency syndrome 1 [OMIM Phenotype]
- Glut1 deficiency syndrome 2 [OMIM Phenotype]
- Stomatin-deficient cryohydrocytosis with neurologic defects [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- SLC2A1 Gene [NCIt concept]
- solute carrier family 2 member 1 [HGNC gene]

Keyword's position in hierarchy(ies) :

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