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
BLM	gene	BLM	Expert list;Expert Review;Expert Review Green	Wilms Tumour		Cancer Predisposition	BIALLELIC, autosomal or pseudoautosomal	Wilms tumor, MONDO:0006058;Bloom syndrome, MONDO:0008876;Bloom syndrome, MIM#210900			Nephroblastoma;HP:0002667			False	3	100;0;0	1.0	True		ENSG00000197299	ENSG00000197299	HGNC:1058													
BRCA2	gene	BRCA2	Expert list;Expert Review;Expert Review Green	Wilms Tumour		Cancer Predisposition	BIALLELIC, autosomal or pseudoautosomal	Wilms tumor, MONDO:0006058;Fanconi anemia complementation group D1,MONDO:0011584;Fanconi anemia, complementation group D1, MIM#605724			Nephroblastoma;HP:0002667			False	3	100;0;0	1.0	True		ENSG00000139618	ENSG00000139618	HGNC:1101													
BUB1B	gene	BUB1B	Expert list;Expert Review;Expert Review Green	Wilms Tumour		Cancer Predisposition	BIALLELIC, autosomal or pseudoautosomal	Wilms tumor, MONDO:0006058;Mosaic variegated aneuploidy syndrome 1, MONDO:0009759;Mosaic variegated aneuploidy syndrome 1, MIM#257300			Nephroblastoma;HP:0002667			False	3	100;0;0	1.0	True		ENSG00000156970	ENSG00000156970	HGNC:1149													
CDKN1C	gene	CDKN1C	Expert list;Expert Review;Expert Review Green	Wilms Tumour		Cancer Predisposition	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Wilms tumor, MONDO:0006058;Beckwith-Wiedemann syndrome due to CDKN1C mutation, MONDO:0016476;Beckwith-Wiedemann syndrome, MIM#130650			Nephroblastoma;HP:0002667			False	3	100;0;0	1.0	True		ENSG00000129757	ENSG00000129757	HGNC:1786													
CTR9	gene	CTR9	Expert list;Expert Review;Expert Review Green;Literature	Wilms Tumour		Cancer Predisposition	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Wilms tumor, MONDO:0006058;Wilms tumor predisposition, no MIM#			Nephroblastoma;HP:0002667	25099282;39293508;29292210		False	3	100;0;0	1.0	True		ENSG00000198730	ENSG00000198730	HGNC:16850													
DIS3L2	gene	DIS3L2	Expert list;Expert Review;Expert Review Green	Wilms Tumour		Cancer Predisposition	BIALLELIC, autosomal or pseudoautosomal	Wilms tumor, MONDO:0006058;Perlman syndrome, MONDO:0009965;Perlman syndrome, MIM#267000			Nephroblastoma;HP:0002667			False	3	100;0;0	1.0	True		ENSG00000144535	ENSG00000144535	HGNC:28648													
GPC3	gene	GPC3	Expert list;Expert Review;Expert Review Green	Wilms Tumour		Cancer Predisposition	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Wilms tumor, MONDO:0006058;Simpson-Golabi-Behmel syndrome type 1, MONDO:0020602;Simpson-Golabi-Behmel syndrome, type 1, MIM#312870			Nephroblastoma;HP:0002667			False	3	100;0;0	1.0	True		ENSG00000147257	ENSG00000147257	HGNC:4451													
PALB2	gene	PALB2	Expert list;Expert Review;Expert Review Green	Wilms Tumour		Cancer Predisposition	BIALLELIC, autosomal or pseudoautosomal	Wilms tumor, MONDO:0006058;Fanconi anemia complementation group N, MONDO:0012565;Fanconi anemia, complementation group N, MIM#610832			Nephroblastoma;HP:0002667			False	3	100;0;0	1.0	True		ENSG00000083093	ENSG00000083093	HGNC:26144													
REST	gene	REST	Expert list;Expert Review;Expert Review Green;Literature	Wilms Tumour		Cancer Predisposition	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Wilms tumor, MONDO:0006058;Wilms tumor 6, MONDO:0014779;Wilms tumor 6, susceptibility to, MIM#616806			Nephroblastoma;HP:0002667	PMID: 26551668		False	3	100;0;0	1.0	True		ENSG00000084093	ENSG00000084093	HGNC:9966													
TRIM28	gene	TRIM28	Expert list;Expert Review;Expert Review Green;Literature	Wilms Tumour		Cancer Predisposition	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Wilms tumor, MONDO:0006058;Wilms tumor predisposition, no MIM#			Nephroblastoma;HP:0002667	PMID: 29912901, 30694527, 30885698, 33565090		False	3	100;0;0	1.0	True		ENSG00000130726	ENSG00000130726	HGNC:16384													
TRIM37	gene	TRIM37	Expert list;Expert Review;Expert Review Green	Wilms Tumour		Cancer Predisposition	BIALLELIC, autosomal or pseudoautosomal	Wilms tumor, MONDO:0006058;Mulibrey nanism, MONDO:0009664;Mulibrey nanism, MIM#253250			Nephroblastoma;HP:0002667			False	3	100;0;0	1.0	True		ENSG00000108395	ENSG00000108395	HGNC:7523													
TRIP13	gene	TRIP13	Expert list;Expert Review;Expert Review Green;Literature	Wilms Tumour		Cancer Predisposition	BIALLELIC, autosomal or pseudoautosomal	Wilms tumor, MONDO:0006058;Mosaic variegated aneuploidy syndrome 3, MONDO:0054736;Mosaic variegated aneuploidy syndrome 3, MIM#617598			Nephroblastoma;HP:0002667	PMID: 28553959		False	3	100;0;0	1.0	True		ENSG00000071539	ENSG00000071539	HGNC:12307													
WT1	gene	WT1	Expert list;Expert Review;Expert Review Green	Wilms Tumour		Cancer Predisposition	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Wilms tumor, MONDO:0006058;Wilms tumor 1, MONDO:0008679;Wilms tumor, type 1, MIM#194070;Denys-Drash syndrome, MIM#194080;Frasier syndrome, MIM#136680			Nephroblastoma;HP:0002667			False	3	100;0;0	1.0	True		ENSG00000184937	ENSG00000184937	HGNC:12796