Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 775
Gene Symbol: CACNA1C
CACNA1C
0.410 Biomarker phenotype GENOMICS_ENGLAND Emerging therapeutic targets in the short QT syndrome. 29697308 2018
Entrez Id: 1832
Gene Symbol: DSP
DSP
0.400 Biomarker phenotype CTD_human We discovered rare variants in three genes that are clinically associated with sudden cardiac death-TMEM43, DSP, and MYBPC3. 20435227 2010
Entrez Id: 79188
Gene Symbol: TMEM43
TMEM43
0.400 Biomarker phenotype CTD_human We discovered rare variants in three genes that are clinically associated with sudden cardiac death-TMEM43, DSP, and MYBPC3. 20435227 2010
Entrez Id: 4000
Gene Symbol: LMNA
LMNA
0.400 Biomarker phenotype CTD_human Familial progressive sinoatrial and atrioventricular conduction disease of adult onset with sudden death, dilated cardiomyopathy, and brachydactyly. A new type of heart-hand syndrome? 15996213 2005
Entrez Id: 10848
Gene Symbol: PPP1R13L
PPP1R13L
0.300 Biomarker phenotype GENOMICS_ENGLAND Here, we show that iASPP is expressed at intercalated discs in human and mouse postmitotic cardiomyocytes. iASPP interacts with desmoplakin and desmin in cardiomyocytes to maintain the integrity of desmosomes and intermediate filament networks in vitro and in vivo. iASPP deficiency specifically induces right ventricular dilatation in mouse embryos at embryonic day 16.5. iASPP-deficient mice with exon 8 deletion (Ppp1r13l(Δ8/Δ8)) die of sudden cardiac death, displaying features of ARVC. 25691752 2015
Entrez Id: 4607
Gene Symbol: MYBPC3
MYBPC3
0.300 Biomarker phenotype CTD_human We discovered rare variants in three genes that are clinically associated with sudden cardiac death-TMEM43, DSP, and MYBPC3. 20435227 2010
Entrez Id: 10848
Gene Symbol: PPP1R13L
PPP1R13L
0.300 Biomarker phenotype GENOMICS_ENGLAND A mutation in NFkappaB interacting protein 1 causes cardiomyopathy and woolly haircoat syndrome of Poll Hereford cattle. 19016676 2009
Entrez Id: 7139
Gene Symbol: TNNT2
TNNT2
0.300 Biomarker phenotype CTD_human Knock-in mouse model of dilated cardiomyopathy caused by troponin mutation. 17556660 2007
Entrez Id: 10848
Gene Symbol: PPP1R13L
PPP1R13L
0.300 Biomarker phenotype GENOMICS_ENGLAND A mutation in NFkB interacting protein 1 results in cardiomyopathy and abnormal skin development in wa3 mice. 15661756 2005
Entrez Id: 1482
Gene Symbol: NKX2-5
NKX2-5
0.300 Biomarker phenotype GENOMICS_ENGLAND