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 		0.210 GeneticVariation disease BEFREE Genetic evidence suggests their involvement in transepithelial transport of chloride in distal nephron segments; ClC-K1 gene deletion leads to nephrogenic diabetes insipidus in mice, and mutations of the hClC-Kb gene cause Bartter's syndrome type III in humans. 10831588 2000
Entrez Id: 1188
Gene Symbol: CLCNKB
CLCNKB 		0.210 Biomarker disease MGD Overt nephrogenic diabetes insipidus in mice lacking the CLC-K1 chloride channel. 9916798 1999