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
CDX2	gene	CDX2	Expert Review Red;Victorian Clinical Genetics Services	Kidneyome_SuperPanel_KidGen_VCGS		Renal and urinary tract disorders	Unknown							False	1	0;0;0	0.7	False		ENSG00000165556	ENSG00000165556	HGNC:1806													
COL4A2	gene	COL4A2	Expert Review Red;Victorian Clinical Genetics Services	Kidneyome_SuperPanel_KidGen_VCGS		Renal and urinary tract disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Brain small vessel disease 2, MIM#614483						False	1	0;0;0	0.7	False		ENSG00000134871	ENSG00000134871	HGNC:2203													
COQ8A	gene	COQ8A	Expert Review Red;Victorian Clinical Genetics Services	Kidneyome_SuperPanel_KidGen_VCGS		Renal and urinary tract disorders	Unknown	Coenzyme Q10 deficiency, primary, 4, MIM#612016						False	1	0;0;0	0.7	False		ENSG00000163050	ENSG00000163050	HGNC:16812													
EZH2	gene	EZH2	Expert Review Red;Victorian Clinical Genetics Services	Kidneyome_SuperPanel_KidGen_VCGS		Renal and urinary tract disorders	Unknown							False	1	0;0;0	0.7	False		ENSG00000106462	ENSG00000106462	HGNC:3527													
FGFR1	gene	FGFR1	Expert Review Red;Victorian Clinical Genetics Services	Kidneyome_SuperPanel_KidGen_VCGS		Renal and urinary tract disorders	Unknown							False	1	0;0;0	0.7	False		ENSG00000077782	ENSG00000077782	HGNC:3688													
HOXA4	gene	HOXA4	Expert Review Red;Victorian Clinical Genetics Services	Kidneyome_SuperPanel_KidGen_VCGS		Renal and urinary tract disorders	Unknown							False	1	0;0;0	0.7	False		ENSG00000197576	ENSG00000197576	HGNC:5105													
HOXB6	gene	HOXB6	Expert Review Red;Victorian Clinical Genetics Services	Kidneyome_SuperPanel_KidGen_VCGS		Renal and urinary tract disorders	Unknown							False	1	0;0;0	0.7	False		ENSG00000108511	ENSG00000108511	HGNC:5117													
ITGB4	gene	ITGB4	Expert Review Red;Victorian Clinical Genetics Services	Kidneyome_SuperPanel_KidGen_VCGS		Renal and urinary tract disorders	BIALLELIC, autosomal or pseudoautosomal	Epidermolysis bullosa, junctional, with pyloric atresia, MIM#226730				10873890		False	1	0;0;0	0.7	False		ENSG00000132470	ENSG00000132470	HGNC:6158													
LMNA	gene	LMNA	Expert Review Red;Victorian Clinical Genetics Services	Kidneyome_SuperPanel_KidGen_VCGS		Renal and urinary tract disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	FSGS;Familial partial lipodystrophy				24080738		False	1	0;0;0	0.7	False		ENSG00000160789	ENSG00000160789	HGNC:6636													
NUP160	gene	NUP160	Expert Review Red;Literature	Kidneyome_SuperPanel_KidGen_VCGS		Renal and urinary tract disorders	BIALLELIC, autosomal or pseudoautosomal	Nephrotic syndrome, type 19, MIM#618178				30179222		False	1	0;0;0	0.7	False		ENSG00000030066	ENSG00000030066	HGNC:18017													
NUP205	gene	NUP205	Expert list;Expert Review Red	Kidneyome_SuperPanel_KidGen_VCGS		Renal and urinary tract disorders	BIALLELIC, autosomal or pseudoautosomal	Nephrotic syndrome, type 13, MIM#616893				26878725		False	1	0;0;0	0.7	False		ENSG00000155561	ENSG00000155561	HGNC:18658													
NUP37	gene	NUP37	Expert list;Expert Review Red	Kidneyome_SuperPanel_KidGen_VCGS		Renal and urinary tract disorders	BIALLELIC, autosomal or pseudoautosomal	Nephrotic syndrome				30179222		False	1	0;0;0	0.7	False		ENSG00000075188	ENSG00000075188	HGNC:29929													
SEC63	gene	SEC63	Expert list;Expert Review Red	Kidneyome_SuperPanel_KidGen_VCGS		Renal and urinary tract disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Polycystic liver disease 2, MIM#617004				15133510		False	1	0;0;0	0.7	False		ENSG00000025796	ENSG00000025796	HGNC:21082													
SEMA3A	gene	SEMA3A	Expert Review Red;Victorian Clinical Genetics Services	Kidneyome_SuperPanel_KidGen_VCGS		Renal and urinary tract disorders	Unknown							False	1	0;0;0	0.7	False		ENSG00000075213	ENSG00000075213	HGNC:10723													
UPK3A	gene	UPK3A	Expert Review Red;Victorian Clinical Genetics Services	Kidneyome_SuperPanel_KidGen_VCGS		Renal and urinary tract disorders	Unknown							False	1	0;0;0	0.7	False		ENSG00000100373	ENSG00000100373	HGNC:12580