Unexplained kidney failure in young people
Gene: WT1Comment when marking as ready: Associated with phenotype in OMIM and G2P. At least five variants reportedCreated: 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 194070Created: 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 panelCreated: 17 Jun 2016, 9:29 a.m.
Phenotypes for gene: WT1 were changed from Nephrotic syndrome, type 4 256370 to Nephrotic syndrome, type 4 256370
Promoted to version 1 17th August 2016
This gene has been classified as Green List (High Evidence).
Phenotypes for WT1 were set to Nephrotic syndrome, type 4 256370
WT1 was added to Unexplained kidney failure in young peoplepanel. Sources: Emory Genetics Laboratory,Illumina TruGenome Clinical Sequencing Services,Radboud University Medical Center, Nijmegen,UKGTN
Phenotypes for WT1 were set to Nephrotic syndrome, type 4 256370
Mode of inheritance for WT1 was changed to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
This gene has been classified as Green List (High Evidence).
WT1 was created by sleigh
WT1 was added to Unexplained kidney failure in young peoplepanel. Sources: Eligibility statement prior genetic testing