Gene: CLCN2 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 1181
Gene Symbol: CLCN2
CLCN2 		0.050 GeneticVariation disease LHGDN Mutations in the CLCN2 gene are a rare cause of idiopathic generalized epilepsy syndromes. 16932951 2006
Entrez Id: 1181
Gene Symbol: CLCN2
CLCN2 		0.050 Biomarker disease LHGDN CLCN2 and idiopathic generalized epilepsy. 15508929 2005
Entrez Id: 1181
Gene Symbol: CLCN2
CLCN2 		0.050 GeneticVariation disease LHGDN Functional evaluation of human ClC-2 chloride channel mutations associated with idiopathic generalized epilepsies. 15252188 2004
Entrez Id: 1181
Gene Symbol: CLCN2
CLCN2 		0.050 GeneticVariation disease BEFREE Functional evaluation of human ClC-2 chloride channel mutations associated with idiopathic generalized epilepsies. 15252188 2004
Entrez Id: 1181
Gene Symbol: CLCN2
CLCN2 		0.050 GeneticVariation disease BEFREE Mutations in the chloride channel gene CLCN2 have been associated with the most common forms of idiopathic generalized epilepsies. 15021241 2004
Entrez Id: 1181
Gene Symbol: CLCN2
CLCN2 		0.050 GeneticVariation disease BEFREE Mutations in CLCN2 encoding a voltage-gated chloride channel are associated with idiopathic generalized epilepsies. 12612585 2003
Entrez Id: 1181
Gene Symbol: CLCN2
CLCN2 		0.050 GeneticVariation disease LHGDN Mutations in CLCN2 encoding a voltage-gated chloride channel are associated with idiopathic generalized epilepsies. 12612585 2003