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
ANLN	gene	ANLN	Expert Review Amber;Victorian Clinical Genetics Services	Proteinuria		Renal and urinary tract disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Focal segmental glomerulosclerosis 8, OMIM #616032				24676636;30002222		False	2	0;100;0	0.229	True		ENSG00000011426	ENSG00000011426	HGNC:14082													
APOL1	gene	APOL1	Expert Review Amber;Victorian Clinical Genetics Services	Proteinuria		Renal and urinary tract disorders	BIALLELIC, autosomal or pseudoautosomal	{Glomerulosclerosis, focal segmental, 4, susceptibility to}, MIM#612551				20647424;24206458;20635188;25993319;34350953		False	2	25;50;25	0.229	True	Other	ENSG00000100342	ENSG00000100342	HGNC:618													
EHD1	gene	EHD1	Expert Review Amber;Literature	Proteinuria		Renal and urinary tract disorders	BIALLELIC, autosomal or pseudoautosomal	Inherited renal tubular disease, MONDO:0015962, EHD1-related				35149593		False	2	0;100;0	0.229	True		ENSG00000110047	ENSG00000110047	HGNC:3242													
EMP2	gene	EMP2	Expert Review Amber;Victorian Clinical Genetics Services	Proteinuria		Renal and urinary tract disorders	BIALLELIC, autosomal or pseudoautosomal	nephrotic syndrome, type 10 MONDO:0014373				24814193;31508419		False	2	0;100;0	0.229	True		ENSG00000213853	ENSG00000213853	HGNC:3334													
KIRREL1	gene	KIRREL1	Expert Review Amber;Literature	Proteinuria		Renal and urinary tract disorders	BIALLELIC, autosomal or pseudoautosomal	Nephrotic syndrome, type 23, MIM# 619201				31472902		False	2	0;100;0	0.229	True		ENSG00000183853	ENSG00000183853	HGNC:15734													
MEFV	gene	MEFV	Expert Review Amber;Expert Review Green;Literature;Victorian Clinical Genetics Services	Proteinuria		Renal and urinary tract disorders	BIALLELIC, autosomal or pseudoautosomal	Familial Mediterranean fever MIM#134610;Familial Mediterranean fever MIM#249100;Neutrophilic dermatosis, acute febrile MIM#608068				PMID: 27956278		False	2	50;50;0	0.229	True	Other	ENSG00000103313	ENSG00000103313	HGNC:6998													
PRDM15	gene	PRDM15	Expert Review Amber;Literature	Proteinuria		Renal and urinary tract disorders	BIALLELIC, autosomal or pseudoautosomal	Steroid resistant nephrotic syndrome				31950080		False	2	0;100;0	0.229	True		ENSG00000141956	ENSG00000141956	HGNC:13999													
RCAN1	gene	RCAN1	Expert Review Amber;Literature	Proteinuria		Renal and urinary tract disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	FSGS;proteinuria				33863784		False	2	0;100;0	0.229	True		ENSG00000159200	ENSG00000159200	HGNC:3040