Solute carrier family 16 (monocarboxylic acid transporter), member 1

Preferred Label : Solute carrier family 16 (monocarboxylic acid transporter), member 1;

Symbol : SLC16A1;

CISMeF acronym : SLC16A1;

Type : Gene;

Alternative titles and symbols : Monocarboxylate transporter 1; MCT1;

Ensembl ID : ENSG00000155380;

Prefixed ID : *600682;

Details

Origin ID

600682;

UMLS CUI

C1420102;

Automatic exact mappings (from CISMeF team)
- CMA1 wt Allele [NCIt concept]
- MCTS1 wt Allele [NCIt concept]
- Malignant T Cell Amplified Sequence 1 [NCIt concept]
- Monocarboxylate Transporter 1 [NCIt concept]
- SLC16A1 Gene [NCIt concept]
- SLC16A1 wt Allele [NCIt concept]
- solute carrier family 16 member 1 [ORDO Gene]
- solute carrier family 16 member 1 [HGNC gene]
HGNC gene
- solute carrier family 16 member 1 [HGNC gene]
NCIt concept(s)
- Monocarboxylate Transporter 1 [NCIt concept]
- SLC16A1 Gene [NCIt concept]
- SLC16A1 wt Allele [NCIt concept]
ORDO concept(s)
- solute carrier family 16 member 1 [ORDO Gene]
Phenotypes related
- Erythrocyte lactate transporter defect [OMIM Phenotype]
- Hyperinsulinemic hypoglycemia, familial, 7 [OMIM Phenotype]
- Monocarboxylate transporter 1 deficiency [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- SLC16A1 Gene [NCIt concept]
- solute carrier family 16 member 1 [HGNC gene]

Keyword's position in hierarchy(ies) :

You can consult :

recommendations
documents concerning education
documents for patients