SLC12A1 wt Allele
**Semantic type:** Gene or Genome
**Definition:** Human SLC12A1 wild-type allele is located in the vicinity of 15q21.1 and is approximately 126 kb in length. This allele, which encodes solute carrier family 12 member 1 protein, plays a role in ion transport and urine concentration in the kidney. Mutations in the gene are associated with Bartter syndrome 1.
**Synonyms:** - BSC - BSC-1 - BSC1 - Bumetanide-Sensitive Cotransporter Type 1 Gene - CCC2 - NKCC2 - Na-K-2Cl Cotransporter 2 Gene - Na-K-2Cl Cotransporter Gene - Sodium-Potassium-Chloride Transporter 2 Gene - Solute Carrier Family 12 (Sodium/Potassium/Chloride Transporter), Member 1 Gene - Solute Carrier Family 12 (Sodium/Potassium/Chloride Transporters), Member 1 Gene - Solute Carrier Family 12 Member 1 wt Allele
/api/v1/systems/nci_thesaurus/nodes/C207888Hierarchy Explorer
Cross-system equivalences0
No cross-system equivalences mapped for this node.