Solute carrier family 5 (choline transporter), member 7

Preferred Label : Solute carrier family 5 (choline transporter), member 7;

Symbol : SLC5A7;

CISMeF acronym : SLC5A7;

Type : Gene;

Alternative titles and symbols : Choline transporter; CHT; CHT1;

Ensembl ID : ENSG00000115665;

Prefixed ID : *608761;

Details

Origin ID

608761;

UMLS CUI

C1422359;

Automatic exact mappings (from CISMeF team)
- choline transport [GO term]
- choline transporter [MeSH concept]
- choline transporter [MeSH Supplementary Concept]
- solute carrier family 5 member 7 [ORDO Gene]
- solute carrier family 5 member 7 [HGNC gene]
HGNC gene
- solute carrier family 5 member 7 [HGNC gene]
ORDO concept(s)
- solute carrier family 5 member 7 [ORDO Gene]
Phenotypes related
- Myasthenic syndrome, congenital, 20, presynaptic [OMIM Phenotype]
- Neuronopathy, distal hereditary motor, autosomal dominant 7 [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- solute carrier family 5 member 7 [HGNC gene]

Keyword's position in hierarchy(ies) :

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