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
COQ7	gene	COQ7	Expert list;Expert Review Amber;Expert Review Green	Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic		Renal and urinary tract disorders	BIALLELIC, autosomal or pseudoautosomal	Coenzyme Q10 deficiency, primary, 8, MIM#616733				31240163;28409910;26084283		False	2	67;0;33	0.145	True		ENSG00000167186	ENSG00000167186	HGNC:2244													
DACT1	gene	DACT1	Expert list;Expert Review Amber;NHS GMS	Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic		Renal and urinary tract disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Townes-Brocks syndrome 2, MIM#617466				28054444		False	2	0;67;33	0.145	True		ENSG00000165617	ENSG00000165617	HGNC:17748													
FOXC1	gene	FOXC1	Expert Review Amber;Victorian Clinical Genetics Services	Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic		Renal and urinary tract disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Congenital anomalies of the kidney and urinary tract (CAKUT)				32475988		False	2	0;100;0	0.145	True		ENSG00000054598	ENSG00000054598	HGNC:3800													
SIX5	gene	SIX5	Expert Review Amber;Victorian Clinical Genetics Services	Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic		Renal and urinary tract disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Branchiootorenal syndrome 2, MIM# 610896				17357085;33624842;20301554;24730701;22447252;21280147;14704431;11950062;10802667;10802668		False	2	0;100;0	0.145	True		ENSG00000177045	ENSG00000177045	HGNC:10891													
TSHZ3	gene	TSHZ3	Expert Review Amber;Literature	Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic		Renal and urinary tract disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	congenital anomaly of kidney and urinary tract MONDO:0019719				27668656;34919690;36553458;39420202		False	2	0;100;0	0.145	True		ENSG00000121297	ENSG00000121297	HGNC:30700