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
ADIPOR1	gene	ADIPOR1	Expert Review Amber;Royal Melbourne Hospital	Retinitis pigmentosa_Autosomal Dominant		Ophthalmological disorders	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	syndromic retinitis pigmentosa;non-syndromic autosomal dominant retinitis pigmentosa			Abnormal retinal morphology;HP:0000479	26662040;25736573;30254279;27655171		False	2	0;100;0	0.57	False		ENSG00000159346	ENSG00000159346	HGNC:24040													
ARL3	gene	ARL3	Expert Review Amber;Royal Melbourne Hospital	Retinitis pigmentosa_Autosomal Dominant		Ophthalmological disorders	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Retinitis pigmentosa 83;Joubert syndrome 35			Abnormal retinal morphology;HP:0000479	26936825;16565502;26964041;26814127;30932721;30269812		False	2	0;100;0	0.57	False		ENSG00000138175	ENSG00000138175	HGNC:694													
GUCA1B	gene	GUCA1B	Expert Review Amber;Royal Melbourne Hospital	Retinitis pigmentosa_Autosomal Dominant		Ophthalmological disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Retinitis pigmentosa 48, MIM#613827			Abnormal retinal morphology;HP:0000479	15452722;26161267		False	2	0;100;0	0.57	True		ENSG00000112599	ENSG00000112599	HGNC:4679													
PRPF6	gene	PRPF6	Expert Review Amber;Royal Melbourne Hospital	Retinitis pigmentosa_Autosomal Dominant		Ophthalmological disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Retinitis pigmentosa 60, MIM# 613983			Abnormal retinal morphology;HP:0000479	21549338;32335390		False	2	0;100;0	0.57	True		ENSG00000101161	ENSG00000101161	HGNC:15860													
VWA8	gene	VWA8	Expert Review Amber;Literature	Retinitis pigmentosa_Autosomal Dominant		Ophthalmological disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Retinitis pigmentosa 97, MIM#620422			Abnormal retinal morphology;HP:0000479	PMID: 37012052		False	2	0;100;0	0.57	True		ENSG00000102763	ENSG00000102763	HGNC:29071