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
ARHGAP24	gene	ARHGAP24	Expert Review Red;Victorian Clinical Genetics Services	Proteinuria		Renal and urinary tract disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	FSGS, MONDO:0005363, ARHGAP24-related				21911940		False	1	0;0;100	0.229	True		ENSG00000138639	ENSG00000138639	HGNC:25361													
COQ8A	gene	COQ8A	Expert Review Green;Expert Review Red;Victorian Clinical Genetics Services	Proteinuria		Renal and urinary tract disorders	Unknown	Coenzyme Q10 deficiency, primary, 4, MIM#612016						False	1	50;0;50	0.229	True		ENSG00000163050	ENSG00000163050	HGNC:16812													
IL1RAP	gene	IL1RAP	Expert Review Red;Literature	Proteinuria		Renal and urinary tract disorders	BIALLELIC, autosomal or pseudoautosomal	Steroid-sensitive nephrotic syndrome				31954058		False	1	0;0;100	0.229	True		ENSG00000196083	ENSG00000196083	HGNC:5995													
ITGB4	gene	ITGB4	Expert Review Red;Victorian Clinical Genetics Services	Proteinuria		Renal and urinary tract disorders	BIALLELIC, autosomal or pseudoautosomal	Epidermolysis bullosa, junctional, with pyloric atresia, MIM#226730				10873890		False	1	0;0;100	0.229	True		ENSG00000132470	ENSG00000132470	HGNC:6158													
KANK1	gene	KANK1	Expert list;Expert Review Red	Proteinuria		Renal and urinary tract disorders	BIALLELIC, autosomal or pseudoautosomal	Nephrotic syndrome				25961457		False	1	0;0;100	0.229	True		ENSG00000107104	ENSG00000107104	HGNC:19309													
KANK4	gene	KANK4	Expert list;Expert Review Red	Proteinuria		Renal and urinary tract disorders	BIALLELIC, autosomal or pseudoautosomal					25961457		False	1	0;50;50	0.229	True		ENSG00000132854	ENSG00000132854	HGNC:27263													
KAT2B	gene	KAT2B	Expert Review Red;Literature	Proteinuria		Renal and urinary tract disorders	BIALLELIC, autosomal or pseudoautosomal	steroid-resistant nephrotic syndrome MONDO:0044765, KAT2B-related				39366742		False	1	0;0;100	0.229	True		ENSG00000114166	ENSG00000114166	HGNC:8638													
LMNA	gene	LMNA	Expert Review Red;Victorian Clinical Genetics Services	Proteinuria		Renal and urinary tract disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Familial partial lipodystrophy;FSGS				24080738		False	1	0;0;100	0.229	True		ENSG00000160789	ENSG00000160789	HGNC:6636													
NUP205	gene	NUP205	Expert list;Expert Review Red	Proteinuria		Renal and urinary tract disorders	BIALLELIC, autosomal or pseudoautosomal	Nephrotic syndrome, type 13, MIM#616893				26878725		False	1	0;0;100	0.229	True		ENSG00000155561	ENSG00000155561	HGNC:18658													
NUP37	gene	NUP37	Expert list;Expert Review Red	Proteinuria		Renal and urinary tract disorders	BIALLELIC, autosomal or pseudoautosomal	Nephrotic syndrome				30179222		False	1	0;0;100	0.229	True		ENSG00000075188	ENSG00000075188	HGNC:29929													
SPRY2	gene	SPRY2	Expert Review Red;Literature	Proteinuria		Renal and urinary tract disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	"{?IgA nephropathy, susceptibility to, 3}	MIM#616818"				25782674		False	1	0;0;100	0.229	True		ENSG00000136158	ENSG00000136158	HGNC:11270													
XPO5	gene	XPO5	Expert list;Expert Review Red	Proteinuria		Renal and urinary tract disorders	BIALLELIC, autosomal or pseudoautosomal	Nephrotic syndrome				26878725		False	1	0;100;0	0.229	True		ENSG00000124571	ENSG00000124571	HGNC:17675