Entity Name	Entity type	Gene Symbol	Sources(; separated)	Level4	Level3	Level2	Model_Of_Inheritance	Phenotypes	Omim	Orphanet	HPO	Publications	Description	Flagged	GEL_Status	UserRatings_Green_amber_red	version	ready	Mode of pathogenicity	EnsemblId(GRch37)	EnsemblId(GRch38)	HGNC	Position Chromosome	Position GRCh37 Start	Position GRCh37 End	Position GRCh38 Start	Position GRCh38 End	STR Repeated Sequence	STR Normal Repeats	STR Pathogenic Repeats	Region Haploinsufficiency Score	Region Triplosensitivity Score	Region Required Overlap Percentage	Region Variant Type	Region Verbose Name
DES	gene	DES	Expert list;Expert Review Green	Arrhythmogenic Cardiomyopathy		Cardiovascular disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	"Cardiomyopathy, dilated, 1I, MIM#	604765;Myopathy, myofibrillar, 1	, MIM#601419;Arrhythmogenic right ventricular cardiomyopathy"			Arrhythmia;HP:0011675;Cardiomyopathy;HP:0001638	19879535;20423733;24200904;22395865;29212896;23168288;20829228		False	3	100;0;0	0.68	True		ENSG00000175084	ENSG00000175084	HGNC:2770													
DSC2	gene	DSC2	Expert Review Green;Victorian Clinical Genetics Services	Arrhythmogenic Cardiomyopathy		Cardiovascular disorders	BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal	Arrhythmogenic right ventricular dysplasia 11, MIM# 610476;Arrhythmogenic right ventricular dysplasia 11 with mild palmoplantar keratoderma and woolly hair, MIM# 610476			Arrhythmia;HP:0011675;Cardiomyopathy;HP:0001638	17963498;21062920;23863954;17186466;18957847;17033975;28339476;33831308		False	3	100;0;0	0.68	True		ENSG00000134755	ENSG00000134755	HGNC:3036													
DSG2	gene	DSG2	Expert Review Green;Victorian Clinical Genetics Services	Arrhythmogenic Cardiomyopathy		Cardiovascular disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Arrhythmogenic right ventricular dysplasia 10, MIM# 610193			Arrhythmia;HP:0011675;Cardiomyopathy;HP:0001638	33831308		False	3	100;0;0	0.68	True		ENSG00000046604	ENSG00000046604	HGNC:3049													
DSP	gene	DSP	Expert Review Green;Victorian Clinical Genetics Services	Arrhythmogenic Cardiomyopathy		Cardiovascular disorders	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Arrhythmogenic right ventricular dysplasia 8, MIM# 607450;Carvajal syndrome			Arrhythmia;HP:0011675;Cardiomyopathy;HP:0001638	15941723;25765472;23954618;20864495;21397041;24938629;22240500;31073624;30345701;11063735;33831308		False	3	100;0;0	0.68	True		ENSG00000096696	ENSG00000096696	HGNC:3052													
FLNC	gene	FLNC	Expert list;Expert Review Green	Arrhythmogenic Cardiomyopathy		Cardiovascular disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Arrhythmogenic right ventricular cardiomyopathy			Arrhythmia;HP:0011675;Cardiomyopathy;HP:0001638	31924696;31627847		False	3	50;50;0	0.68	True		ENSG00000128591	ENSG00000128591	HGNC:3756													
JUP	gene	JUP	Expert Review Green;Victorian Clinical Genetics Services	Arrhythmogenic Cardiomyopathy		Cardiovascular disorders	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Arrhythmogenic right ventricular dysplasia 12 MIM# 611528;Naxos disease MIM# 601214			Arrhythmia;HP:0011675;Cardiomyopathy;HP:0001638	16722579;17924338;33831308		False	3	100;0;0	0.68	True		ENSG00000173801	ENSG00000173801	HGNC:6207													
PKP2	gene	PKP2	Expert Review Green;Victorian Clinical Genetics Services	Arrhythmogenic Cardiomyopathy		Cardiovascular disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Arrhythmogenic right ventricular dysplasia 9, MIM# 609040			Arrhythmia;HP:0011675;Cardiomyopathy;HP:0001638	33831308		False	3	100;0;0	0.68	True		ENSG00000057294	ENSG00000057294	HGNC:9024													
TMEM43	gene	TMEM43	Expert Review Green;Victorian Clinical Genetics Services	Arrhythmogenic Cardiomyopathy		Cardiovascular disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Arrhythmogenic right ventricular dysplasia 5, MIM# 604400			Arrhythmia;HP:0011675;Cardiomyopathy;HP:0001638	18313022;21214875;23812740;22725725;24598986;29980933;33831308		False	3	100;0;0	0.68	True		ENSG00000170876	ENSG00000170876	HGNC:28472