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
CIB2	gene	CIB2	Expert Review Red;Royal Melbourne Hospital	Usher Syndrome		Ophthalmological disorders	BIALLELIC, autosomal or pseudoautosomal	Usher syndrome, type IJ, 614869			Usher syndrome;MONDO:0019501	23023331;23023331;26173970;26473954;27344577;26226137;26445815		False	1	0;0;100	1.5	True		ENSG00000136425	ENSG00000136425	HGNC:24579													
ESPN	gene	ESPN	Expert Review Red;Royal Melbourne Hospital	Usher Syndrome		Ophthalmological disorders	BIALLELIC, autosomal or pseudoautosomal	Usher syndrome, type 1M, MIM#618632			Usher syndrome;MONDO:0019501	29572253		False	1	0;0;100	1.5	True		ENSG00000187017	ENSG00000187017	HGNC:13281													
HARS	gene	HARS	Expert Review Red;Royal Melbourne Hospital;Victorian Clinical Genetics Services	Usher Syndrome		Ophthalmological disorders	BIALLELIC, autosomal or pseudoautosomal	Usher syndrome type 3B			Usher syndrome;MONDO:0019501			False	1	0;0;100	1.5	True		ENSG00000170445	ENSG00000170445	HGNC:4816