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
DOLK	gene	DOLK	Expert Review Amber;Literature	Dilated Cardiomyopathy		Cardiovascular disorders	BIALLELIC, autosomal or pseudoautosomal	"Congenital disorder of glycosylation, type Im	MIM#610768"			Dilated cardiomyopathy;HP:0001644	31741824;28816422;24144945;22242004		False	2	0;100;0	1.37	True		ENSG00000175283	ENSG00000175283	HGNC:23406													
DSG2	gene	DSG2	Expert Review Amber;Victorian Clinical Genetics Services	Dilated Cardiomyopathy		Cardiovascular disorders	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Arrhythmogenic right ventricular dysplasia, 10, 610193;Cardiomyopathy, dilated, 1BB, 612877			Dilated cardiomyopathy;HP:0001644	23071725;33949662;18678517;21859740;28764973;35941102		False	2	50;50;0	1.37	True		ENSG00000046604	ENSG00000046604	HGNC:3049													
EMD	gene	EMD	Expert Review Amber;Literature	Dilated Cardiomyopathy		Cardiovascular disorders	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Emery-Dreifuss muscular dystrophy 1, X-linked MIM#310300			Dilated cardiomyopathy;HP:0001644	24997722		False	2	0;100;0	1.37	True		ENSG00000102119	ENSG00000102119	HGNC:3331													
FKTN	gene	FKTN	Expert Review Amber;Literature	Dilated Cardiomyopathy		Cardiovascular disorders	BIALLELIC, autosomal or pseudoautosomal	Cardiomyopathy, dilated, 1X MIM#611615			Dilated cardiomyopathy;HP:0001644	17036286;19015585		False	2	0;100;0	1.37	True		ENSG00000106692	ENSG00000106692	HGNC:3622													
GATA6	gene	GATA6	Expert Review Amber;Literature	Dilated Cardiomyopathy		Cardiovascular disorders	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Dilated cardiomyopathy			Dilated cardiomyopathy;HP:0001644	25119427;31301121;20705924		False	2	0;100;0	1.37	True		ENSG00000141448	ENSG00000141448	HGNC:4174													
JPH2	gene	JPH2	Expert Review Amber;Literature	Dilated Cardiomyopathy		Cardiovascular disorders	BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal	Cardiomyopathy, dilated, 2E, MIM# 619492			Dilated cardiomyopathy;HP:0001644	29540472;31227780;29165669;27471098;30384889;31227780;10949023;23715556		False	2	0;100;0	1.37	True		ENSG00000149596	ENSG00000149596	HGNC:14202													
JUP	gene	JUP	Expert Review Amber;Literature	Dilated Cardiomyopathy		Cardiovascular disorders	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	"Arrhythmogenic right ventricular dysplasia 12 (MIM#611528);Naxos disease, MIM#	601214"			Dilated cardiomyopathy;HP:0001644			False	2	0;100;0	1.37	True		ENSG00000173801	ENSG00000173801	HGNC:6207													
LDB3	gene	LDB3	Expert Review Amber;Victorian Clinical Genetics Services	Dilated Cardiomyopathy		Cardiovascular disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Cardiomyopathy, dilated, 1C, with or without LVNC MIM#601493			Dilated cardiomyopathy;HP:0001644	26419279;16427346;14660611;14662268		False	2	0;100;0	1.37	True		ENSG00000122367	ENSG00000122367	HGNC:15710													
NEBL	gene	NEBL	Expert Review Amber;Literature	Dilated Cardiomyopathy		Cardiovascular disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Hypertrophic cardiomyopathy;dilated cardiomyopathy			Dilated cardiomyopathy;HP:0001644	27186169		False	2	100;0;0	1.37	True		ENSG00000078114	ENSG00000078114	HGNC:16932													
PLEKHM2	gene	PLEKHM2	Expert Review Amber;Literature	Dilated Cardiomyopathy		Cardiovascular disorders	BIALLELIC, autosomal or pseudoautosomal	Dilated cardiomyopathy MONDO:0005021			Dilated cardiomyopathy;HP:0001644	35862026;26464484;38942823;38490981;37349842		False	2	0;100;0	1.37	True		ENSG00000116786	ENSG00000116786	HGNC:29131													
SLC6A6	gene	SLC6A6	Expert Review Amber;Literature	Dilated Cardiomyopathy		Cardiovascular disorders	BIALLELIC, autosomal or pseudoautosomal	Hypotaurinaemic retinal degeneration and cardiomyopathy (HTRDC), MIM#145350;Early retinal degeneration;cardiomyopathy			Dilated cardiomyopathy;HP:0001644	31345061;31903486;29886034		False	2	0;100;0	1.37	True		ENSG00000131389	ENSG00000131389	HGNC:11052													
TMEM43	gene	TMEM43	Expert Review Amber;Literature	Dilated Cardiomyopathy		Cardiovascular disorders	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	"Arrhythmogenic right ventricular dysplasia 5 (MIM# 	604400)"			Dilated cardiomyopathy;HP:0001644	18313022;21214875;23812740;22725725;24598986		False	2	0;100;0	1.37	True		ENSG00000170876	ENSG00000170876	HGNC:28472