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. Author manuscript; available in PMC: 2016 Jul 19.
Published in final edited form as: Int J Legal Med. 2015 Nov 19;130(2):317–322. doi: 10.1007/s00414-015-1275-2

Table 1.

List of the 80 sudden cardiac arrhythmia related genes included in our panel.

Sudden cardiac arrhythmia Genes
Long QT Syndrome (LQTS) KCNQ1, KCNH2, SCN5A, ANK2, KCNE1, KCNE2, KCNJ2, CACNA1C, CAV3, SCN4B, AKAP9, SNTA1, KCNJ5
Brugada Syndrome (BrS) SCN5A, GPD1L, CACNA1C, CACNB2, SCN1B, KCNE3, SCN3B, KCND3, KCNJ8
Catecholaminergic Polymorphic Ventricular Tachycardia (CPVT) RYR2, CASQ2, ANK2, KCNJ2, TRDN
WPW Syndrome PRKAG2
Short QT Syndrome (SQTS) KCNH2, KCNJ2, CACNA1C, CACNB2, KCNQ1
Arrhythmogenic Right Ventricular Cardiomyopathy (ARVC) DSC2, DSG2, TMEM43, PKP2, DSP, RYR2, JUP, RPSA, TGFB3
Sick sinus syndrome (SSS) SCN5A, HCN4
Cardiac conduction disease (CCD) SCN5A
Hypertrophic Cardiomyopathy (HCM) MYH7, MYBPC3, TNNT2, TNNI3, TPM1, ACTC1, MYL2, MYL3, MYH6, LAMP2, PRKAG2, CSRP3, GLA, VCL, TNNC1, TTR, TTN, TCAP, MYLK2, MYOZ2, MYO6
Dilated cardiomyopathy (DCM) DES, TNNT2, MYH7, CSRP3, PLN, TCAP, ABCC9, LMNA, DMD, TAZ, TTN, VCL, EYA4, EMD, ACTN2, SGCD, ACTC1, TNNI3, TPM1, MYBPC3, LDB3, MYH6, CTF1, ANKRD1
Dilated cardiomyopathy with Cardiac conduction defect (DCM+CCD) SCN5A, LMNA
Left ventricular noncompaction (LVNC) LDB3, TAZ, MYH7, MYBPC3, ACTC1, TNNT2, SCN5A, LMNA, DMPK, DTNA, AMPD1, PMP22, LMX1B, YWHAE
Restrictive cardiomyopathy (RCM) MYH7, TNNI3, TNNT2
Atrial Fbrillation (AF) KCNQ1, KCNE2, KCNJ2, KCNH2, SCN5A, KCNA5, NPPA, NUP155, GJA5, ABCC9, GATA4, GATA5, GATA6, KCNE1L

Different types of sudden cardiac arrhythmia share the same pathogenic gene.