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
BMP7	gene	BMP7	Expert list;Expert Review Red	Congenital anomalies of the kidney and urinary tract (CAKUT) Nonsyndromic		Renal and urinary tract disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Congenital abnormalities of the kidneys and urinary tract				24429398		False	1	0;50;50	0.153	True		ENSG00000101144	ENSG00000101144	HGNC:1074													
CBWD1	gene	CBWD1	Expert Review Red;Literature	Congenital anomalies of the kidney and urinary tract (CAKUT) Nonsyndromic		Renal and urinary tract disorders	BIALLELIC, autosomal or pseudoautosomal	CAKUT				31862704		False	1	0;0;100	0.153	True		ENSG00000172785	ENSG00000172785	HGNC:17134													
CDC5L	gene	CDC5L	Expert list;Expert Review Red	Congenital anomalies of the kidney and urinary tract (CAKUT) Nonsyndromic		Renal and urinary tract disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Congenital abnormalities of the kidneys and urinary tract				24429398		False	1	0;100;0	0.153	True		ENSG00000096401	ENSG00000096401	HGNC:1743													
CHD1L	gene	CHD1L	Expert Review Red;Victorian Clinical Genetics Services	Congenital anomalies of the kidney and urinary tract (CAKUT) Nonsyndromic		Renal and urinary tract disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	CAKUT				22146311;24429398		False	1	50;50;0	0.153	True		ENSG00000131778	ENSG00000131778	HGNC:1916													
FGF8	gene	FGF8	Expert Review Green;Expert Review Red;Victorian Clinical Genetics Services	Congenital anomalies of the kidney and urinary tract (CAKUT) Nonsyndromic		Renal and urinary tract disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Hypogonadotropic hypogonadism 6 with or without anosmia;OMIM #612702						False	1	33;33;33	0.153	True		ENSG00000107831	ENSG00000107831	HGNC:3686													
FGFR1	gene	FGFR1	Expert Review Red;Victorian Clinical Genetics Services	Congenital anomalies of the kidney and urinary tract (CAKUT) Nonsyndromic		Renal and urinary tract disorders	Unknown							False	1	100;0;0	0.153	True		ENSG00000077782	ENSG00000077782	HGNC:3688													
HOXA4	gene	HOXA4	Expert Review Red;Victorian Clinical Genetics Services	Congenital anomalies of the kidney and urinary tract (CAKUT) Nonsyndromic		Renal and urinary tract disorders	Unknown							False	1	0;0;100	0.153	True		ENSG00000197576	ENSG00000197576	HGNC:5105													
HOXB6	gene	HOXB6	Expert Review Red;Victorian Clinical Genetics Services	Congenital anomalies of the kidney and urinary tract (CAKUT) Nonsyndromic		Renal and urinary tract disorders	Unknown							False	1	0;0;100	0.153	True		ENSG00000108511	ENSG00000108511	HGNC:5117													
SIX2	gene	SIX2	Expert Review Red;Victorian Clinical Genetics Services	Congenital anomalies of the kidney and urinary tract (CAKUT) Nonsyndromic		Renal and urinary tract disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	CAKUT, MONDO:0019719, SIX2-related				24429398		False	1	0;0;100	0.153	True		ENSG00000170577	ENSG00000170577	HGNC:10888													
SOX17	gene	SOX17	Expert Review Green;Expert Review Red;Victorian Clinical Genetics Services	Congenital anomalies of the kidney and urinary tract (CAKUT) Nonsyndromic		Renal and urinary tract disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Vesicoureteral reflux 3;OMIM #613674				20960469		False	1	50;0;50	0.153	True		ENSG00000164736	ENSG00000164736	HGNC:18122													
TBC1D31	gene	TBC1D31	Expert Review Red;Literature	Congenital anomalies of the kidney and urinary tract (CAKUT) Nonsyndromic		Renal and urinary tract disorders	BIALLELIC, autosomal or pseudoautosomal	congenital anomaly of kidney and urinary tract MONDO:0019719, TBC1D31-related				37468454		False	1	0;0;100	0.153	True		ENSG00000156787	ENSG00000156787	HGNC:30888													
TNXB	gene	TNXB	Expert Review Red;Victorian Clinical Genetics Services	Congenital anomalies of the kidney and urinary tract (CAKUT) Nonsyndromic		Renal and urinary tract disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Vesicoureteral reflux 8, MIM# 615963				23620400		False	1	0;0;100	0.153	True		ENSG00000168477	ENSG00000168477	HGNC:11976													
UMOD	gene	UMOD	Expert Review Green;Expert Review Red;Victorian Clinical Genetics Services	Congenital anomalies of the kidney and urinary tract (CAKUT) Nonsyndromic		Renal and urinary tract disorders	Unknown							False	1	67;0;33	0.153	True		ENSG00000169344	ENSG00000169344	HGNC:12559													
UPK3A	gene	UPK3A	Expert Review Red;Victorian Clinical Genetics Services	Congenital anomalies of the kidney and urinary tract (CAKUT) Nonsyndromic		Renal and urinary tract disorders	Unknown	Congenital anomaly of kidney and urinary tract, MONDO:0019719						False	1	0;0;100	0.153	True		ENSG00000100373	ENSG00000100373	HGNC:12580													
WNT4	gene	WNT4	Expert Review Amber;Expert Review Red;Victorian Clinical Genetics Services	Congenital anomalies of the kidney and urinary tract (CAKUT) Nonsyndromic		Renal and urinary tract disorders	BIALLELIC, autosomal or pseudoautosomal	SERKAL syndrome;OMIM #611812				18179883		False	1	0;50;50	0.153	True		ENSG00000162552	ENSG00000162552	HGNC:12783