Table 1 Panel of genes responsible for cardiomyopathies and channelopathies implicated in arrhythmias. Mutation of SCN9A has been associated to “Paroxysmal Extreme Pain disorder” which can present as breath-holding spells and episodes of extreme bradycardia in infancy
From: Cardiac arrest in a toddler treated with propranolol for infantile Hemangioma: a case report
Arrhythmias | Cardiomyopathies |
|---|---|
ABCC9 | ACTC1 |
AKAP9 | ACTN2 |
ANK2 | ANKRD1 |
CACNA1C | BAG3 |
CACNB2 | BRAF |
CALM1 | CALR3 |
CASQ2 | CAV3 |
CAV3 | CRYAB |
DSC2 | CSRP3 |
DSG2 | DES |
DSP | DMD |
GJA5 | DTNA |
GPD1L | EYA4 |
HCN4 | FKTN |
JUP | GATAD1 |
KCNA5 | GLA |
KCND3 | JPH2 |
KCNE1 | KRAS |
KCNE2 | LAMA4 |
KCNE3 | LAMP2 |
KCNH2 | LDB3 |
KCNJ2 | MIB1 |
KCNJ5 | MYBPC3 |
KCNQ1 | MYH6 |
KCNQ1 | MYH7 |
LMNA | MYL2 |
NPPA | MYL3 |
NUP155 | MYOZ2 |
PKP2 | MYPN |
RYR2 | NEXN |
SCN1B | NF1 |
SCN2B | NNT |
SCN3B | NRAS |
SCN4B | PLN |
SCN5A | PRDM16 |
SNT1 | PRKAG2 |
TGFB3 | PTPN11 |
TMEM43 | RAF1 |
TRDN | RBM20 |
SCN9A | RIT1 |
SGCD | |
SOS1 | |
TAZ | |
TCAP | |
TMPO | |
TNNC1 |