Gene: CLCNKB ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 1188
Gene Symbol: CLCNKB
CLCNKB 		0.010 Biomarker phenotype BEFREE Mutations in CLCNKB, the gene encoding the renal chloride channel hClC-Kb, cause Bartter syndrome type III, a human genetic condition characterized by polyuria, hypokalemia, and alkalosis. 26453302 2015