Gene: CLCN4 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 1183
Gene Symbol: CLCN4
CLCN4 		0.300 Biomarker disease CLINGEN De novo and inherited mutations in the X-linked gene CLCN4 are associated with syndromic intellectual disability and behavior and seizure disorders in males and females. 27550844 2018
Entrez Id: 1183
Gene Symbol: CLCN4
CLCN4 		0.300 Biomarker disease CLINGEN X-exome sequencing of 405 unresolved families identifies seven novel intellectual disability genes. 25644381 2016
Entrez Id: 1183
Gene Symbol: CLCN4
CLCN4 		0.300 Biomarker disease CLINGEN Exome sequencing reveals new causal mutations in children with epileptic encephalopathies. 23647072 2013