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
CD151	gene	CD151	Expert Review Red;Radboud University Medical Center, Nijmegen	Epidermolysis bullosa	Skin fragility disorders	Dermatological disorders	BIALLELIC, autosomal or pseudoautosomal	Nephropathy with pretibial epidermolysis bullosa and deafness, 609057;[Blood group, Raph], 179620;Kindler syndrome-like epidermolysis bullosa				29138120		False	1	0;0;100	1.12	False		ENSG00000177697	ENSG00000177697	HGNC:1630													
MMP1	gene	MMP1	Radboud University Medical Center, Nijmegen	Epidermolysis bullosa	Skin fragility disorders	Dermatological disorders		COPD, rate of decline of lung function in, 606963; {Epidermolysis bullosa dystrophica, autosomal recessive, modifier of}, 226600						False	1	0;0;100	1.12	False		ENSG00000196611	ENSG00000196611	HGNC:7155