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
APRT	gene	APRT	Expert list;Expert Review Amber	Unexplained kidney failure in young people	Disorders of function	Renal and urinary tract disorders	BIALLELIC, autosomal or pseudoautosomal	interstitial nephritis;chronic kidney disease;end stage renal disease;nephrolithiaisis;Adenine phosphoribosyltransferase deficiency 614723				30355577;30106368;25307253;22212387		False	2	100;0;0	1.125	False		ENSG00000198931	ENSG00000198931	HGNC:626													
CD151	gene	CD151	Eligibility statement prior genetic testing;Expert Review Amber	Unexplained kidney failure in young people	Disorders of function	Renal and urinary tract disorders	BIALLELIC, autosomal or pseudoautosomal	Nephropathy with pretibial epidermolysis bullosa and deafness 609057				15265795;29138120;17015618		False	2	0;0;0	1.125	False		ENSG00000177697	ENSG00000177697	HGNC:1630