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
FSCN2	gene	FSCN2	Expert Review Red;Royal Melbourne Hospital	Macular Dystrophy/Stargardt Disease		Ophthalmological disorders	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Retinitis pigmentosa 30 MIM#607921;Macular degeneration			Macular dystrophy;HP:0007754	11527955;16043865;16280978;17251446;18450588		False	1	0;0;100	0.45	True		ENSG00000186765	ENSG00000186765	HGNC:3960													
HMCN1	gene	HMCN1	Expert Review Red;Royal Melbourne Hospital	Macular Dystrophy/Stargardt Disease		Ophthalmological disorders	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Macular Degeneration			Macular dystrophy;HP:0007754			False	1	0;0;100	0.45	True		ENSG00000143341	ENSG00000143341	HGNC:19194													
PITPNM3	gene	PITPNM3	Expert Review Red;Royal Melbourne Hospital	Macular Dystrophy/Stargardt Disease		Ophthalmological disorders	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Cone-rod dystrophy 5, 600977			Macular dystrophy;HP:0007754	17377520;22405330		False	1	0;0;100	0.45	True		ENSG00000091622	ENSG00000091622	HGNC:21043