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
CDH2	gene	CDH2	Expert list;Expert Review Amber	Arrhythmogenic Cardiomyopathy		Cardiovascular disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Arrhythmogenic right ventricular dysplasia, familial, 14, OMIM#618920			Arrhythmia;HP:0011675;Cardiomyopathy;HP:0001638			False	2	0;100;0	0.68	True		ENSG00000170558	ENSG00000170558	HGNC:1759													
CTNNA3	gene	CTNNA3	Expert Review Amber;Other	Arrhythmogenic Cardiomyopathy		Cardiovascular disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	"Arrhythmogenic right ventricular cardiomyopathy;Arrhythmogenic right ventricular dysplasia, familial, 13	MIM#615616"			Arrhythmia;HP:0011675;Cardiomyopathy;HP:0001638	23136403;21254927;22421363;30415094;31539150		False	2	0;100;0	0.68	False		ENSG00000183230	ENSG00000183230	HGNC:2511													
KBTBD13	gene	KBTBD13	Expert Review Amber;Literature	Arrhythmogenic Cardiomyopathy		Cardiovascular disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Intrinsic cardiomyopathy MONDO:0000591			Arrhythmia;HP:0011675;Cardiomyopathy;HP:0001638	36335629		False	2	0;100;0	0.68	True		ENSG00000234438	ENSG00000234438	HGNC:37227													
LEMD2	gene	LEMD2	Expert Review Amber;Literature	Arrhythmogenic Cardiomyopathy		Cardiovascular disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	arrhythmogenic right ventricular cardiomyopathy, MONDO:0016587			Arrhythmia;HP:0011675;Cardiomyopathy;HP:0001638	31061923;26788539;30905398;36377660		False	2	0;100;0	0.68	True		ENSG00000161904	ENSG00000161904	HGNC:21244													
LMNA	gene	LMNA	Expert list;Expert Review Amber	Arrhythmogenic Cardiomyopathy		Cardiovascular disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	"Cardiomyopathy, dilated, 1A, MIM#	115200;Arrhythmogenic right ventricular cardiomyopathy"			Arrhythmia;HP:0011675;Cardiomyopathy;HP:0001638	22199124;25837155;26620845		False	2	0;100;0	0.68	True		ENSG00000160789	ENSG00000160789	HGNC:6636													
PLN	gene	PLN	Expert list;Expert Review Amber	Arrhythmogenic Cardiomyopathy		Cardiovascular disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Arrhythmogenic right ventricular cardiomyopathy			Arrhythmia;HP:0011675;Cardiomyopathy;HP:0001638	22820313;33831308		False	2	0;100;0	0.68	True		ENSG00000198523	ENSG00000198523	HGNC:9080