Source: ALL

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 10021
Gene Symbol: HCN4
HCN4
CUI: C1142166
Disease: Brugada Syndrome (disorder)
Brugada Syndrome (disorder) 		0.320 GeneticVariation BEFREE In the present study, the potential correlation between HCN4 gene variations and the occurrence of SUNDS was investigated. 30452770

2019
Entrez Id: 10021
Gene Symbol: HCN4
HCN4
CUI: C1142166
Disease: Brugada Syndrome (disorder)
Brugada Syndrome (disorder) 		0.320 GeneticVariation BEFREE Mutation in S6 domain of HCN4 channel in patient with suspected Brugada syndrome modifies channel function. 27553229

2016
Entrez Id: 10021
Gene Symbol: HCN4
HCN4
CUI: C1142166
Disease: Brugada Syndrome (disorder)
Brugada Syndrome (disorder) 		0.320 Biomarker CLINGEN Mutation in S6 domain of HCN4 channel in patient with suspected Brugada syndrome modifies channel function. 27553229

2016
Entrez Id: 10021
Gene Symbol: HCN4
HCN4
CUI: C1142166
Disease: Brugada Syndrome (disorder)
Brugada Syndrome (disorder) 		0.320 Biomarker CLINGEN Spectrum and prevalence of mutations involving BrS1- through BrS12-susceptibility genes in a cohort of unrelated patients referred for Brugada syndrome genetic testing: implications for genetic testing. 22840528

2012
Entrez Id: 10021
Gene Symbol: HCN4
HCN4
CUI: C1142166
Disease: Brugada Syndrome (disorder)
Brugada Syndrome (disorder) 		0.320 Biomarker CLINGEN Role of HCN4 channel in preventing ventricular arrhythmia. 19165230

2009
Entrez Id: 10021
Gene Symbol: HCN4
HCN4
CUI: C1142166
Disease: Brugada Syndrome (disorder)
Brugada Syndrome (disorder) 		0.320 Biomarker CLINGEN Functional characterization of a trafficking-defective HCN4 mutation, D553N, associated with cardiac arrhythmia. 15123648

2004