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
ADGRA3	gene	ADGRA3	Expert Review Red;Royal Melbourne Hospital	Retinitis Pigmentosa Superpanel		Ophthalmological disorders	BIALLELIC, autosomal or pseudoautosomal	Retinitis pigmentosa, MONDO:0019200, ADGRA3-related			Abnormal retinal morphology;HP:0000479	23105016		False	1	0;0;100	0.214	True		ENSG00000152990	ENSG00000152990	HGNC:13839													
CA4	gene	CA4	Expert Review Red;Royal Melbourne Hospital	Retinitis Pigmentosa Superpanel		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	0.214	True		ENSG00000167434	ENSG00000167434	HGNC:1375													
CCT2	gene	CCT2	Expert Review Red;NHS GMS	Retinitis Pigmentosa Superpanel		Ophthalmological disorders	BIALLELIC, autosomal or pseudoautosomal	Leber's congenital amaurosis			Abnormal retinal morphology;HP:0000479	27645772;29450543		False	1	0;0;100	0.214	True		ENSG00000166226	ENSG00000166226	HGNC:1615													
FSCN2	gene	FSCN2	Expert Review Red;Royal Melbourne Hospital;Royal Melbourne Hospital	Retinitis Pigmentosa Superpanel		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	0.214	True		ENSG00000186765	ENSG00000186765	HGNC:3960													
HKDC1	gene	HKDC1	Expert Review Red;Expert list	Retinitis Pigmentosa Superpanel		Ophthalmological disorders	BIALLELIC, autosomal or pseudoautosomal	"Retinitis pigmentosa 92, MIM#	619614"			Abnormal retinal morphology;HP:0000479	30085091		False	1	0;0;100	0.214	True		ENSG00000156510	ENSG00000156510	HGNC:23302													
PITPNM3	gene	PITPNM3	Expert Review Red;Royal Melbourne Hospital	Retinitis Pigmentosa Superpanel		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	0.214	False		ENSG00000091622	ENSG00000091622	HGNC:21043													
PMPCA	gene	PMPCA	Expert Review Red;Royal Melbourne Hospital	Retinitis Pigmentosa Superpanel		Ophthalmological disorders	BIALLELIC, autosomal or pseudoautosomal	Spinocerebellar ataxia, autosomal recessive 2			Abnormal retinal morphology;HP:0000479			False	1	0;0;100	0.214	False		ENSG00000165688	ENSG00000165688	HGNC:18667													
PRKCG	gene	PRKCG	Expert list	Retinitis Pigmentosa Superpanel		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	0.214	False		ENSG00000126583	ENSG00000126583	HGNC:9402													
RGR	gene	RGR	Expert Review Red;Royal Melbourne Hospital	Retinitis Pigmentosa Superpanel		Ophthalmological disorders	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Retinitis pigmentosa 44, 613769			Abnormal retinal morphology;HP:0000479	10581022;30347075;27748892;27623334		False	1	0;0;100	0.214	True		ENSG00000148604	ENSG00000148604	HGNC:9990													
RP9	gene	RP9	Expert Review Red;Royal Melbourne Hospital	Retinitis Pigmentosa Superpanel		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	0.214	True		ENSG00000164610	ENSG00000164610	HGNC:10288													
SAG	gene	SAG	Expert Review Red;Royal Melbourne Hospital	Retinitis Pigmentosa Superpanel		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	0.214	True		ENSG00000130561	ENSG00000130561	HGNC:10521													
SAMD11	gene	SAMD11	Expert Review Red;Royal Melbourne Hospital	Retinitis Pigmentosa Superpanel		Ophthalmological disorders	BIALLELIC, autosomal or pseudoautosomal	Autosomal recessive retinitis pigmentosa			Abnormal retinal morphology;HP:0000479	27734943		False	1	0;0;100	0.214	False		ENSG00000187634	ENSG00000187634	HGNC:28706													
SCAPER	gene	SCAPER	Expert Review Red;Expert list;Literature	Retinitis Pigmentosa Superpanel		Ophthalmological disorders	BIALLELIC, autosomal or pseudoautosomal	Intellectual developmental disorder and retinitis pigmentosa MIM#618195			Abnormal retinal morphology;HP:0000479	28794130;31069901;31192531;30723319;30561111		False	1	0;0;100	0.214	True		ENSG00000140386	ENSG00000140386	HGNC:13081													
SCLT1	gene	SCLT1	Literature	Retinitis Pigmentosa Superpanel		Ophthalmological disorders	BIALLELIC, autosomal or pseudoautosomal	Nonsyndromic retinitis pigmentosa			Abnormal retinal morphology;HP:0000479	30425282		False	1	0;0;100	0.214	False		ENSG00000151466	ENSG00000151466	HGNC:26406													
SEMA4A	gene	SEMA4A	Expert Review Red;Royal Melbourne Hospital	Retinitis Pigmentosa Superpanel		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	0.214	True		ENSG00000196189	ENSG00000196189	HGNC:10729													
SLC39A12	gene	SLC39A12	Expert Review Red;Literature	Retinitis Pigmentosa Superpanel		Ophthalmological disorders	BIALLELIC, autosomal or pseudoautosomal	Retinitis pigmentosa, MONDO:0019200, SLC39A12-related			Abnormal retinal morphology;HP:0000479	PMID: 35486108		False	1	0;0;100	0.214	True		ENSG00000148482	ENSG00000148482	HGNC:20860													
SLC7A14	gene	SLC7A14	Expert Review Red;Royal Melbourne Hospital	Retinitis Pigmentosa Superpanel		Ophthalmological disorders	BIALLELIC, autosomal or pseudoautosomal	Retinitis pigmentosa 68, 615725 (3)			Abnormal retinal morphology;HP:0000479	27028480;24670872		False	1	0;0;100	0.214	True		ENSG00000013293	ENSG00000013293	HGNC:29326													
SPP2	gene	SPP2	Expert Review Red;Royal Melbourne Hospital	Retinitis Pigmentosa Superpanel		Ophthalmological disorders	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Autosomal dominant retinitis pigmentosa			Abnormal retinal morphology;HP:0000479	26459573		False	1	0;0;100	0.214	False		ENSG00000072080	ENSG00000072080	HGNC:11256													
WDR34	gene	WDR34	Expert Review Red;Literature	Retinitis Pigmentosa Superpanel		Ophthalmological disorders	BIALLELIC, autosomal or pseudoautosomal	Retinitis pigmentosa			Abnormal retinal morphology;HP:0000479	33124039		False	1	0;0;100	0.214	True		ENSG00000119333	ENSG00000119333	HGNC:28296