CLCNKB (Chloride Voltage-Gated Channel Kb) is a Protein Coding gene. Diseases associated with CLCNKB include Bartter Syndrome, Type 3 and Bartter Syndrome, Type 4B, Digenic. Among its related pathways are Hepatic ABC Transporters and Transport of glucose and other sugars, bile salts and organic acids, metal ions and amine compounds.