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
GUCA1B	gene	GUCA1B	Expert Review Amber;Royal Melbourne Hospital	Macular Dystrophy/Stargardt Disease		Ophthalmological disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Retinitis pigmentosa 48, MIM#613827			Macular dystrophy;HP:0007754	15452722;26161267		False	2	0;100;0	0.45	True		ENSG00000112599	ENSG00000112599	HGNC:4679													
RBP3	gene	RBP3	Expert Review Amber;Royal Melbourne Hospital	Macular Dystrophy/Stargardt Disease		Ophthalmological disorders	BIALLELIC, autosomal or pseudoautosomal	Retinitis pigmentosa 66, 615233			Macular dystrophy;HP:0007754	25766589;19074801		False	2	0;100;0	0.45	True		ENSG00000107618	ENSG00000265203	HGNC:9921													
TEAD1	gene	TEAD1	Expert list;Expert Review Amber	Macular Dystrophy/Stargardt Disease		Ophthalmological disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sveinsson chorioretinal atrophy MIM#108985			Macular dystrophy;HP:0007754	15016762;17689488;30903741;26091538		False	2	0;100;0	0.45	True		ENSG00000187079	ENSG00000187079	HGNC:11714