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
BNC2	gene	BNC2	Expert list;Expert Review Green;Literature	Congenital anomalies of the kidney and urinary tract (CAKUT) Nonsyndromic		Renal and urinary tract disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Lower urinary tract obstruction, congenital;OMIM #618612				PMID: 31656805, 31051115		False	3	100;0;0	0.119	True		ENSG00000173068	ENSG00000173068	HGNC:30988													
CDX2	gene	CDX2	Expert Review Green;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	Genetic multiple congenital anomalies/dysmorphic syndrome, MONDO:0043005;Congenital abnormalities of anus, renal and urogenital system, vertebrae and/or the limbs				29177441;34671974		False	3	50;50;0	0.119	True		ENSG00000165556	ENSG00000165556	HGNC:1806													
CHRNA3	gene	CHRNA3	Expert Review Green;Literature	Congenital anomalies of the kidney and urinary tract (CAKUT) Nonsyndromic		Renal and urinary tract disorders	BIALLELIC, autosomal or pseudoautosomal	Bladder dysfunction, autonomic, with impaired pupillary reflex and secondary CAKUT, MIM# 191800				31708116		False	3	100;0;0	0.119	True		ENSG00000080644	ENSG00000080644	HGNC:1957													
GATA3	gene	GATA3	Expert Review Green;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	Hypoparathyroidism, sensorineural deafness, and renal dysplasia, MIM# 146255				10935639;11389161;21120445;26316437;25771973;27387476;30396722		False	3	100;0;0	0.119	True		ENSG00000107485	ENSG00000107485	HGNC:4172													
GFRA1	gene	GFRA1	Expert Review Green;Literature	Congenital anomalies of the kidney and urinary tract (CAKUT) Nonsyndromic		Renal and urinary tract disorders	BIALLELIC, autosomal or pseudoautosomal	Renal hypodysplasia/aplasia 4, MIM# 619887				33020172;34737117		False	3	100;0;0	0.119	True		ENSG00000151892	ENSG00000151892	HGNC:4243													
GREB1L	gene	GREB1L	Expert Review Green;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	Renal hypodysplasia/aplasia 3, OMIM# 617805				29100091		False	3	100;0;0	0.119	True		ENSG00000141449	ENSG00000141449	HGNC:31042													
HNF1B	gene	HNF1B	Expert Review Green;Victorian Clinical Genetics Services	Congenital anomalies of the kidney and urinary tract (CAKUT) Nonsyndromic		Renal and urinary tract disorders	Unknown							False	3	100;0;0	0.119	False		ENSG00000108753	ENSG00000275410	HGNC:11630													
HPSE2	gene	HPSE2	Expert Review Green;Victorian Clinical Genetics Services	Congenital anomalies of the kidney and urinary tract (CAKUT) Nonsyndromic		Renal and urinary tract disorders	BIALLELIC, autosomal or pseudoautosomal	Urofacial syndrome 1 MIM#236730				25145936;23313374;33558177		False	3	100;0;0	0.119	True		ENSG00000172987	ENSG00000172987	HGNC:18374													
ITGA8	gene	ITGA8	Expert Review Green;Victorian Clinical Genetics Services	Congenital anomalies of the kidney and urinary tract (CAKUT) Nonsyndromic		Renal and urinary tract disorders	BIALLELIC, autosomal or pseudoautosomal	Renal hypodysplasia/aplasia 1, MIM# 191830				24439109		False	3	100;0;0	0.119	True		ENSG00000077943	ENSG00000077943	HGNC:6144													
LIFR	gene	LIFR	Expert Review Green;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, LIFR-related				28334964;38025229		False	3	50;50;0	0.119	True		ENSG00000113594	ENSG00000113594	HGNC:6597													
LRIG2	gene	LRIG2	Expert Review Green;Victorian Clinical Genetics Services	Congenital anomalies of the kidney and urinary tract (CAKUT) Nonsyndromic		Renal and urinary tract disorders	Unknown							False	3	100;0;0	0.119	False		ENSG00000198799	ENSG00000198799	HGNC:20889													
NPHP3	gene	NPHP3	Expert Review Green;Victorian Clinical Genetics Services	Congenital anomalies of the kidney and urinary tract (CAKUT) Nonsyndromic		Renal and urinary tract disorders	BIALLELIC, autosomal or pseudoautosomal	Renal-hepatic-pancreatic dysplasia 1, MIM# 208540						False	3	50;0;50	0.119	True		ENSG00000113971	ENSG00000113971	HGNC:7907													
NPNT	gene	NPNT	Expert Review Green;Literature	Congenital anomalies of the kidney and urinary tract (CAKUT) Nonsyndromic		Renal and urinary tract disorders	BIALLELIC, autosomal or pseudoautosomal	Renal agenesis, MONDO:0018470, NPNT-related				PMID: 35246978;34049960;17537792		False	3	100;0;0	0.119	True		ENSG00000168743	ENSG00000168743	HGNC:27405													
PAX2	gene	PAX2	Expert Review Green;Victorian Clinical Genetics Services	Congenital anomalies of the kidney and urinary tract (CAKUT) Nonsyndromic		Renal and urinary tract disorders	Unknown							False	3	100;0;0	0.119	False		ENSG00000075891	ENSG00000075891	HGNC:8616													
RET	gene	RET	Expert Review Green;Victorian Clinical Genetics Services	Congenital anomalies of the kidney and urinary tract (CAKUT) Nonsyndromic		Renal and urinary tract disorders	Unknown							False	3	0;0;0	0.119	False		ENSG00000165731	ENSG00000165731	HGNC:9967													
ROBO2	gene	ROBO2	Expert Review Green;Victorian Clinical Genetics Services	Congenital anomalies of the kidney and urinary tract (CAKUT) Nonsyndromic		Renal and urinary tract disorders	Unknown							False	3	100;0;0	0.119	False		ENSG00000185008	ENSG00000185008	HGNC:10250													
SLC20A1	gene	SLC20A1	Expert Review Green;Literature	Congenital anomalies of the kidney and urinary tract (CAKUT) Nonsyndromic		Renal and urinary tract disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Bladder-Exstrophy-Epispadias Complex (BEEC), MONDO:0017919, SLC20A1-related				32850778;27013921		False	3	100;0;0	0.119	True		ENSG00000144136	ENSG00000144136	HGNC:10946													
TBC1D1	gene	TBC1D1	Expert Review Green;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				26572137		False	3	100;0;0	0.119	True		ENSG00000065882	ENSG00000065882	HGNC:11578													
TBX18	gene	TBX18	Expert Review Green;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	Congenital anomalies of kidney and urinary tract 2, MIM# 143400				26235987		False	3	100;0;0	0.119	True		ENSG00000112837	ENSG00000112837	HGNC:11595													
TRAP1	gene	TRAP1	Expert Review Green;Victorian Clinical Genetics Services	Congenital anomalies of the kidney and urinary tract (CAKUT) Nonsyndromic		Renal and urinary tract disorders	BIALLELIC, autosomal or pseudoautosomal	CAKUT;VACTERL				24152966		False	3	100;0;0	0.119	True		ENSG00000126602	ENSG00000126602	HGNC:16264