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
FOXE3	gene	FOXE3	Expert Review Red;Victorian Clinical Genetics Services	Corneal Dystrophy		Ophthalmological disorders	BIALLELIC, autosomal or pseudoautosomal	Anterior segment dysgenesis 2, multiple subtypes, MIM# 610256			Abnormal corneal morphology;HP:0000481			False	1	0;0;100	1.11	True		ENSG00000186790	ENSG00000186790	HGNC:3808													
MAF	gene	MAF	Expert Review Red;Victorian Clinical Genetics Services	Corneal Dystrophy		Ophthalmological disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Cataract 21, multiple types, MIM# 610202			Abnormal corneal morphology;HP:0000481			False	1	0;0;100	1.11	True		ENSG00000178573	ENSG00000178573	HGNC:6776													
PITX2	gene	PITX2	Expert Review Red;Victorian Clinical Genetics Services	Corneal Dystrophy		Ophthalmological disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Anterior segment dysgenesis 4, MIM# 137600			Abnormal corneal morphology;HP:0000481			False	1	0;0;100	1.11	True		ENSG00000164093	ENSG00000164093	HGNC:9005													
PLCB3	gene	PLCB3	Expert list;Expert Review Red	Corneal Dystrophy		Ophthalmological disorders	BIALLELIC, autosomal or pseudoautosomal	"Spondylometaphyseal dysplasia with corneal dystrophy, MIM#	618961"			Abnormal corneal morphology;HP:0000481	29122926		False	1	0;0;100	1.11	True		ENSG00000149782	ENSG00000149782	HGNC:9056													
SPARCL1	gene	SPARCL1	Expert Review Red;Literature	Corneal Dystrophy		Ophthalmological disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Corneal dystrophy, MONDO:0018102			Abnormal corneal morphology;HP:0000481	PMID: 39169229		False	1	0;0;100	1.11	True		ENSG00000152583	ENSG00000152583	HGNC:11220