Patient-specific induced pluripotent stem cells as “disease-in-a-dish” models for inherited cardiomyopathies and channelopathies – 15 years of research

Table 2 Main genes associated with inherited channelopathies

Condition	Genotype	Ref.
LQTS1	KCNQ1	[16]
LQTS2	KCNH2	[16]
LQTS3	SCN5A	[16]
LQTS4	ANK2	[17]
LQTS5	KCNE1	[17]
LQTS6	KCNE2	[17]
LQTS7	KCNJ2	[17]
LQTS8	CACNA1C	[17]
LQTS9	CAV3	[17]
LQTS10	SCN4B	[17]
LQTS11	AKAP9	[17]
LQTS12	SNTA1	[17]
LQTS13	KCNJ5	[17]
LQTS14	CALM1	[17]
LQTS15	CALM2	[17]
JLN1	KCNQ1	[17]
JLN2	KCNE1	[17]
CPVT1	RYR2	[16]
CPVT2	CASQ2	[16]
SQTS	KCNH2, KCNQ1, KCNJ2	[16]
BrS	SCN5A	[18]

BrS: Brugada syndrome; CPVT: Catecholaminergic polymorphic ventricular tachycardia; LQTS: Long QT syndrome; SQTS: Short QT syndrome.