Gene: KCNT2 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 343450
Gene Symbol: KCNT2
KCNT2 		0.120 GeneticVariation disease BEFREE De novo gain-of-function variants in KCNT2 as a novel cause of developmental and epileptic encephalopathy. 29740868 2018
Entrez Id: 343450
Gene Symbol: KCNT2
KCNT2 		0.120 Biomarker disease BEFREE A De Novo Mutation in the Sodium-Activated Potassium Channel KCNT2 Alters Ion Selectivity and Causes Epileptic Encephalopathy. 29069600 2017
Entrez Id: 343450
Gene Symbol: KCNT2
KCNT2 		0.120 Biomarker disease HPO