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
DGKE	gene	DGKE	Expert Review Red;Victorian Clinical Genetics Services	Atypical Haemolytic Uraemic Syndrome_MPGN		Renal and urinary tract disorders	BIALLELIC, autosomal or pseudoautosomal	Nephrotic syndrome, type 7, MIM# 615008			Haemolytic anaemia;HP:0001878	23274426;23542698		False	1	0;0;100	1.0	True		ENSG00000153933	ENSG00000153933	HGNC:2852													
THBD	gene	THBD	Expert Review Red;Victorian Clinical Genetics Services	Atypical Haemolytic Uraemic Syndrome_MPGN		Renal and urinary tract disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	{Hemolytic uremic syndrome, atypical, susceptibility to, 6};OMIM #612926			Haemolytic anaemia;HP:0001878	19625716		False	1	0;100;0	1.0	True		ENSG00000178726	ENSG00000178726	HGNC:11784													
VTN	gene	VTN	Expert Review Red;Victorian Clinical Genetics Services	Atypical Haemolytic Uraemic Syndrome_MPGN		Renal and urinary tract disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Atypical haemolytic uraemic syndrome			Haemolytic anaemia;HP:0001878	30377230		False	1	0;100;0	1.0	True		ENSG00000109072	ENSG00000109072	HGNC:12724