SLC12A3

Also known as NCC, NCCT, TSC, solute carrier family 12 member 3, Sodium-chloride symporter

protein-coding gene in the species Homo sapiens

Gene data

SLC12A3

Name: solute carrier family 12 member 3
Type: protein-coding
Aliases: NCC, NCCT, TSC

This gene encodes a renal thiazide-sensitive sodium-chloride cotransporter that is important for electrolyte homeostasis. This cotransporter mediates sodium and chloride reabsorption in the distal convoluted tubule. Mutations in this gene cause Gitelman syndrome, a disease similar to Bartter's syndrome, that is characterized by hypokalemic alkalosis combined with hypomagnesemia, low urinary calcium, and increased renin activity associated with normal blood pressure. This cotransporter is the target for thiazide diuretics that are used for treating high blood pressure. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008].

via MyGene.info