Gene: KCNH1 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 3756
Gene Symbol: KCNH1
KCNH1 		0.300 Biomarker phenotype CTD_human De novo variants in neurodevelopmental disorders with epilepsy. 29942082 2018
Entrez Id: 3756
Gene Symbol: KCNH1
KCNH1 		0.300 Biomarker phenotype CTD_human Mutations in the voltage-gated potassium channel gene KCNH1 cause Temple-Baraitser syndrome and epilepsy. 25420144 2015