SLC16A1 wt Allele

**Semantic type:** Gene or Genome

**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.

**Synonyms:** - HHF7 - MCT - MCT 1 - MCT1 - Solute Carrier Family 16 (Monocarboxylate Transporter), Member 1 Gene - Solute Carrier Family 16 (Monocarboxylic Acid Transporters), Member 1 Gene - Solute Carrier Family 16 Member 1 wt Allele - Solute Carrier Family 16, Member 1 (Monocarboxylic Acid Transporter 1) Gene