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
ADCY10	gene	ADCY10	Expert list;Expert Review Amber;Victorian Clinical Genetics Services	Kidneyome_SuperPanel_KidGen_VCGS		Renal and urinary tract disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Hypercalciuria, absorptive, susceptibility to, MIM#143870				11932268		False	2	0;0;0	0.7	False		ENSG00000143199	ENSG00000143199	HGNC:21285													
APOL1	gene	APOL1	Expert Review Amber;Victorian Clinical Genetics Services	Kidneyome_SuperPanel_KidGen_VCGS		Renal and urinary tract disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	{Glomerulosclerosis, focal segmental, 4, susceptibility to}, MIM#612551				20635188;20647424;24206458		False	2	0;0;0	0.7	False		ENSG00000100342	ENSG00000100342	HGNC:618													
BMP7	gene	BMP7	Expert list;Expert Review Amber	Kidneyome_SuperPanel_KidGen_VCGS		Renal and urinary tract disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Congenital abnormalities of the kidneys and urinary tract				24429398		False	2	0;0;0	0.7	False		ENSG00000101144	ENSG00000101144	HGNC:1074													
CDC5L	gene	CDC5L	Expert list;Expert Review Amber	Kidneyome_SuperPanel_KidGen_VCGS		Renal and urinary tract disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Congenital abnormalities of the kidneys and urinary tract				24429398		False	2	0;0;0	0.7	False		ENSG00000096401	ENSG00000096401	HGNC:1743													
DACT1	gene	DACT1	Expert list;Expert Review Amber	Kidneyome_SuperPanel_KidGen_VCGS		Renal and urinary tract disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Townes-Brocks syndrome 2, MIM#617466				28054444		False	2	0;0;0	0.7	False		ENSG00000165617	ENSG00000165617	HGNC:17748													
FGF20	gene	FGF20	Expert list;Expert Review Amber	Kidneyome_SuperPanel_KidGen_VCGS		Renal and urinary tract disorders	BIALLELIC, autosomal or pseudoautosomal	Renal hypodysplasia/aplasia 2, MIM#615721				22698282		False	2	0;0;0	0.7	False		ENSG00000078579	ENSG00000078579	HGNC:3677													
KANK1	gene	KANK1	Expert list;Expert Review Amber	Kidneyome_SuperPanel_KidGen_VCGS		Renal and urinary tract disorders	BIALLELIC, autosomal or pseudoautosomal	Nephrotic syndrome				25961457		False	2	0;0;0	0.7	False		ENSG00000107104	ENSG00000107104	HGNC:19309													
KANK4	gene	KANK4	Expert list;Expert Review Amber	Kidneyome_SuperPanel_KidGen_VCGS		Renal and urinary tract disorders	BIALLELIC, autosomal or pseudoautosomal					25961457		False	2	0;0;0	0.7	False		ENSG00000132854	ENSG00000132854	HGNC:27263													
SOX11	gene	SOX11	Expert list;Expert Review Amber	Kidneyome_SuperPanel_KidGen_VCGS		Renal and urinary tract disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Congenital abnormalities of the kidneys and urinary tract				29459093;24886874		False	2	0;0;0	0.7	False		ENSG00000176887	ENSG00000176887	HGNC:11191													
VTN	gene	VTN	Expert Review Amber;Victorian Clinical Genetics Services	Kidneyome_SuperPanel_KidGen_VCGS		Renal and urinary tract disorders	Unknown							False	2	0;0;0	0.7	False		ENSG00000109072	ENSG00000109072	HGNC:12724													
XPO5	gene	XPO5	Expert list;Expert Review Amber	Kidneyome_SuperPanel_KidGen_VCGS		Renal and urinary tract disorders	BIALLELIC, autosomal or pseudoautosomal	Nephrotic syndrome				26878725		False	2	0;0;0	0.7	False		ENSG00000124571	ENSG00000124571	HGNC:17675