Genomics England

WT1

Wilms tumor 1

Panel	Mode of inheritance	Details
Filter panels7 panels
Green in Adult solid tumours cancer susceptibility Signed-off version 2.2	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Phenotypes Familial Wilms tumor
Green in Childhood solid tumours R-numbers: R359 Signed-off version 4.0	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Phenotypes Wagner Syndrome, Frasier syndrome, 136680, Nephrotic syndrome, type 4, 256370, Denys-Drash syndrome, 194080, Familial Wilms tumor, Wilms Tumor 1, Wilms Tumor, Wilms tumour, Meacham syndrome, 608978, Mesothelioma, somatic, 156240, Denys-Drash Syndrome, Wilms tumor, type 1, 194070
Green in DDG2P Component of the following Super Panels: - Paediatric disorders Signed-off version 4.15	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Phenotypes DENYS-DRASH SYNDROME 194080, FRASIER SYNDROME FRASIER SYNDROME FRASIER SYNDROME 136680
Green in Differences in sex development R-numbers: R146 Signed-off version 4.5	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Phenotypes Denys-Drash syndrome 194080, Frasier syndrome 136680, Meacham syndrome 608978
Green in Fetal anomalies R-numbers: R21, R412 Signed-off version 4.195	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Phenotypes FRASIER SYNDROME FRASIER SYNDROME FRASIER SYNDROME, DENYS-DRASH SYNDROME
Green in Proteinuric renal disease Component of the following Super Panels: - Unexplained young onset end-stage renal disease R-numbers: R195 Signed-off version 4.15	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Phenotypes Denys-Drash syndrome #194080, Frasier syndrome #136680, Wilms tumor, type 1 #194070
Green in Wilms tumour with features suggestive of predisposition R-numbers: R220 Signed-off version 1.0	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Phenotypes Wilms tumor, type 1, OMIM:194070