Table 7.
Arrhythmia-related Genes Studied
| Inherited Primary Arrhythmia Syndromes | |
|---|---|
| Diseases | Associated Genes |
| Brugada Syndrome | ABCC9*, CACNA1C*, CACNA2D1, CACNB2, GPD1L, HCN4, KCND3, KCNE3, KCNE5, KCNJ8, PKP2*, RANGRF, SCN1B, SCN2B, SCN3B, SCN5A*†, SCN10A |
| Catecholaminergic Polymorphic Ventricular Tachycardia | CASQ2, RYR2*†, TRDN*† |
| Familial Atrial Fibrillation | ABCC9*, KCNA5, KCNH2*, KCNJ2*, KCNQ1*, LMNA*, RYR2*, SCN5A* |
| Long QT Syndrome | AKAP9, ANK2, CACNA1C*†, CALM1, CALM2, CALM3, CAV3, KCNE1, KCNE2, KCNH2*†, KCNJ2*†, KCNJ5, KCNQ1*†, SCN4B, SCN5A*, SNTA1, TRDN* |
| Short QT Syndrome | CACNA1C*, KCNH2*, KCNJ2*, KCNQ1* |
| Arrhythmogenic Cardiomyopathies | |
| Diseases | Associated Genes |
| Arrhythmogenic Right Ventricular Cardiomyopathy | DSC2, DSG2, DSP*†, JUP, PKP2*†, RYR2*, SCN5A* |
| Hypertrophic Cardiomyopathy | ACTC1, MYBPC3, MYH7, MYL2, MYL3, TNNI3, TNNT2, TPM1 |
| Other Arrhythmogenic Cardiomyopathies | ABCC9*†, CTNNA3, DES, DSP*, FLNC, KCNH2*, KCNQ1*, LDB3, LMNA*†, PLN, SCN5A*, TMEM43, TRPM4 |
Genes associated with >1 disease
Most common disease association for genes associated with >1 disease