Unexplained paediatric onset end-stage renal diseaseGene: WT1
Gene imported from the 'Renal and urinary tract disorders' panel v1.8 with a rating of Green
Created: 9 Apr 2019, 11:17 a.m.
Comment when marking as ready: Associated with phenotype in OMIM and G2P. At least five variants reported
Created: 5 Aug 2016, 1:17 p.m.
Comment on phenotypes: Also associated with Denys-Drash syndrome 194080, Frasier syndrome 136680, Meacham syndrome 608978, Mesothelioma, somatic 156240; Wilms tumor, type 1 194070
Created: 5 Aug 2016, 1:16 p.m.
Comment on list classification: Promoted from Red to Green because this gene is Green in Version 1 of the Proteinuric renal disease gene panel
Created: 17 Jun 2016, 9:29 a.m.
gene: WT1 was added gene: WT1 was added to Unexplained paediatric onset end-stage renal disease. Sources: Expert Review Green Mode of inheritance for gene: WT1 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Phenotypes for gene: WT1 were set to Nephrotic syndrome, type 4 256370