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
ITM2B	gene	ITM2B	Expert list;Expert Review Red	Congenital Stationary Night Blindness		Ophthalmological disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	?Retinal dystrophy with inner retinal dysfunction and ganglion cell abnormalities MIM#616079			Congenital stationary night blindness;HP:0007642; Retinal dystrophy;HP:0000556	24026677		False	1	0;0;100	0.23	True		ENSG00000136156	ENSG00000136156	HGNC:6174