Gene: KCNQ2 ×
Source: INFERRED ×
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 3785
Gene Symbol: KCNQ2
KCNQ2 		0.500 CausalMutation phenotype CLINVAR Moderate loss of function of cyclic-AMP-modulated KCNQ2/KCNQ3 K+ channels causes epilepsy. 9872318 1998
Entrez Id: 3785
Gene Symbol: KCNQ2
KCNQ2 		0.500 CausalMutation phenotype CLINVAR Seizure characteristics in chromosome 20 benign familial neonatal convulsions. 8327138 1993
Entrez Id: 3785
Gene Symbol: KCNQ2
KCNQ2 		0.500 CausalMutation phenotype CLINVAR Familial neonatal and infantile seizures: an autosomal-dominant disorder. 6476007 1984
Entrez Id: 3785
Gene Symbol: KCNQ2
KCNQ2 		0.500 Biomarker phenotype HPO