Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 1178
Gene Symbol: CLC
CLC
0.020 GeneticVariation disease BEFREE Human mutations in CLC channels are known to cause diseases as diverse as myotonia (muscle stiffness), Bartter syndrome (renal salt loss) with or without deafness, Dent's disease (proteinuria and kidney stones), osteopetrosis and neurodegeneration, and possibly epilepsy. 15709978 2005
Entrez Id: 1178
Gene Symbol: CLC
CLC
0.020 Biomarker disease BEFREE X-linked nephrolithiasis and engineered deficiencies in some other CLC Cl(-) channels are thought to represent defects of organellar acidification. 11826292 2002