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
AP1B1	gene	AP1B1	Expert Review Amber;Literature	Corneal dystrophy		Ophthalmology	BIALLELIC, autosomal or pseudoautosomal	Keratitis-ichthyosis-deafness syndrome, autosomal recessive, OMIM:242150;KID syndrome, MONDO:0018781				31630788;33452671;32969855;35144013		False	2	0;100;0	4.7	False		ENSG00000100280	ENSG00000100280	HGNC:554													
PRDX3	gene	PRDX3	Expert Review Amber;Literature	Corneal dystrophy		Ophthalmology	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Corneal dystrophy, punctiform and polychromatic pre-Descemet, OMIM:619871;corneal dystrophy, punctiform and polychromatic pre-descemet, MONDO:0859248				31782998;34369396		False	2	0;100;0	4.7	False		ENSG00000165672	ENSG00000165672	HGNC:9354