Gene: KCNN3 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 3782
Gene Symbol: KCNN3
KCNN3 		0.310 GeneticVariation disease BEFREE Analogous experiments with the KCNN3 p.Val450Leu mutant previously identified in a family with portal hypertension indicated basal constitutive channel activity and thus a different gain-of-function mechanism compared to the ZLS-associated mutant channels. 31155282 2019
Entrez Id: 3782
Gene Symbol: KCNN3
KCNN3 		0.310 Biomarker disease GENOMICS_ENGLAND A de novo mutation in KCNN3 associated with autosomal dominant idiopathic non-cirrhotic portal hypertension. 26658685 2016