SLC16A1 wt Allele

Preferred Label : SLC16A1 wt Allele;

NCIt synonyms : MCT 1; HHF7; MCT1; MCT; Solute Carrier Family 16, Member 1 (Monocarboxylic Acid Transporter 1) Gene; Solute Carrier Family 16 (Monocarboxylate Transporter), Member 1 Gene; Solute Carrier Family 16 Member 1 wt Allele; Solute Carrier Family 16 (Monocarboxylic Acid Transporters), Member 1 Gene;

NCIt definition : Human SLC16A1 wild-type allele is located in the vicinity of 1p12 and is approximately 45 kb in length. This allele, which encodes monocarboxylate transporter 1 protein, plays a role in the transport of monocarboxylates across the plasma membrane. Mutations in this gene are associated with erythrocyte lactate transporter defect and hyperinsulinemic hypoglycemia, familial, 7.;

GenBank Accession Number : NM_003051;

Details

Origin ID

C107461;

UMLS CUI

C3811697;

Automatic exact mappings (from CISMeF team)
- Hyperinsulinemic hypoglycemia, familial, 7 [OMIM Phenotype]
- Malignant t-cell amplified sequence 1 [OMIM gene]
- Solute carrier family 16 (monocarboxylic acid transporter), member 1 [OMIM gene]
- brain injuries [MeSH Descriptor]
- familial hyperinsulinemic hypoglycemia 7 [DO Concept]
- malonyl-CoA-acyl carrier protein transacylase [ORDO Gene]
- medium-chain triglyceride [Artificial nutrition thesaurus concept]
- mucociliary clearance [GO term]
- solute carrier family 16 member 1 [ORDO Gene]
- tomography, X-ray computed [MeSH Descriptor]
OMIM relation
- Solute carrier family 16 (monocarboxylic acid transporter), member 1 [OMIM gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
concept_is_in_subset
- CTRP Biomarker Terminology [NCIt concept]
- CTRP Molecular Genetic Biomarker Terminology [NCIt concept]
- CTRP Terminology [NCIt concept]
gene_found_in_organism
- Human [NCIt concept]
gene_plays_role_in_process
- Ion Transport Process [NCIt concept]
- Ligand Binding [NCIt concept]
- Transmembrane Transport [NCIt concept]
- Transport Process [NCIt concept]

Keyword's position in hierarchy(ies) :

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