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
CA4	gene	CA4	Expert Review Red;Royal Melbourne Hospital	Retinitis pigmentosa_Autosomal Dominant		Ophthalmological disorders	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Retinitis pigmentosa 17, 600852			Abnormal retinal morphology;HP:0000479	15563508;15090652;17652713;16260723		False	1	0;0;100	0.57	True		ENSG00000167434	ENSG00000167434	HGNC:1375													
FSCN2	gene	FSCN2	Expert Review Red;Royal Melbourne Hospital	Retinitis pigmentosa_Autosomal Dominant		Ophthalmological disorders	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Retinitis pigmentosa 30 MIM#607921;Macular degeneration			Abnormal retinal morphology;HP:0000479	16043865;18450588		False	1	0;0;100	0.57	True		ENSG00000186765	ENSG00000186765	HGNC:3960													
PITPNM3	gene	PITPNM3	Expert Review Red;Royal Melbourne Hospital	Retinitis pigmentosa_Autosomal Dominant		Ophthalmological disorders	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Cone-rod dystrophy 5, 600977			Abnormal retinal morphology;HP:0000479	22405330;17377520		False	1	0;0;100	0.57	False		ENSG00000091622	ENSG00000091622	HGNC:21043													
PRKCG	gene	PRKCG	Expert list	Retinitis pigmentosa_Autosomal Dominant		Ophthalmological disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Retinitis pigmentosa 11 MIM#600138			Abnormal retinal morphology;HP:0000479	9545390;16828200		False	1	0;0;100	0.57	False		ENSG00000126583	ENSG00000126583	HGNC:9402													
RP9	gene	RP9	Expert Review Red;Royal Melbourne Hospital	Retinitis pigmentosa_Autosomal Dominant		Ophthalmological disorders	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Retinitis pigmentosa 9, 180104			Abnormal retinal morphology;HP:0000479	16799052;16671097		False	1	0;0;100	0.57	True		ENSG00000164610	ENSG00000164610	HGNC:10288													
SAG	gene	SAG	Expert Review Red;Royal Melbourne Hospital	Retinitis pigmentosa_Autosomal Dominant		Ophthalmological disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Retinitis pigmentosa 47, MIM# 613758			Abnormal retinal morphology;HP:0000479	28549094;33047631		False	1	0;50;50	0.57	True		ENSG00000130561	ENSG00000130561	HGNC:10521													
SEMA4A	gene	SEMA4A	Expert Review Red;Royal Melbourne Hospital	Retinitis pigmentosa_Autosomal Dominant		Ophthalmological disorders	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Cone-rod dystrophy 10, 610283;Retinitis pigmentosa 35, 610282			Abnormal retinal morphology;HP:0000479	16199541;28805479;23360997;15277503		False	1	0;0;100	0.57	True		ENSG00000196189	ENSG00000196189	HGNC:10729													
SPP2	gene	SPP2	Expert Review Red;Royal Melbourne Hospital	Retinitis pigmentosa_Autosomal Dominant		Ophthalmological disorders	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Autosomal dominant retinitis pigmentosa			Abnormal retinal morphology;HP:0000479	26459573		False	1	0;0;100	0.57	False		ENSG00000072080	ENSG00000072080	HGNC:11256