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
GNE	gene	GNE	Expert Review Red;Mackenzie's Mission	Prepair 500+		Screening	BIALLELIC, autosomal or pseudoautosomal	Nonaka myopathy MIM#605820;Thrombocytopenia 12 with or without myopathy MIM#620757				25257349;17549255;25061177;30171045;29941673		False	1	0;100;0	2.1	True		ENSG00000159921	ENSG00000159921	HGNC:23657													
GPR143	gene	GPR143	Expert Review Red;Mackenzie's Mission	Prepair 500+		Screening	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Nystagmus 6, congenital, X-linked, MIM#300814;Ocular albinism, type I, Nettleship-Falls type, MIM#300500				30555098;29761529		False	1	0;100;0	2.1	True		ENSG00000101850	ENSG00000101850	HGNC:20145