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Table 10 Overview of genes associated with monogenic, non-syndromic cardiomyopathies, and their relative contributions to different cardiomyopathic phenotypes

Gene Cardiomyopathy phenotype Associated phenotype

HCM DCM NDLVC ARVC RCM

ABCC9 a a Cantu syndrome

ACTA1

ACTC1

ACTN2b

ALPK3

ANKRD1

BAG3 a a Myofibrillar myopathy CACNA1C c c Timothy syndrome CACNB2

CALR3

CASQ2

CAV3 a a Caveolinopathy CDH2

COX15 a a Leigh syndrome

CRYAB a a Alpha-B crystallinopathy

CSRP3

CTF1

CTNNA3

DES c c Desminopathy DMD c c X-linked progressive MD DMPK

DSC2

DSG2

DSP

DTNA

EYA4

FHL1 c c Emery–Dreifuss MD

FLNC c c Myofibrillar myopathy FHOD3

FXN a a Friedreich ataxia GAA a a Pompe disease

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