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Solute carrier family 12 member 1 (SLC12A1), also known as NKCC2, is a membrane protein that functions as a sodium-potassium-chloride cotransporter. It is primarily expressed in the kidney, specifically on the luminal membrane of epithelial cells in the thick ascending limb of the loop of Henle. This transporter plays a critical role in renal salt reabsorption and overall fluid and electrolyte balance. Mutations in SLC12A1 are associated with Bartter syndrome type I.
Inhibition of Na+/K+/2Cl- cotransport
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