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Article

Software and database for the analysis of mutations in the human WT1 gene.

Nucleic acids research - 1 Jan 1998

Jeanpierre C, Béroud C, Niaudet P, Junien C

Abstract excerpt

The WT1 gene, located at 11p13, encodes a zinc finger transcription factor involved in renal and gonadal development and in Wilms' tumor. Constitutional mutations of this gene have been described in most patients with Denys Drash syndrome (mesangial sclerosis associated with male pseudohermaphrodism and/or Wilms' tumor), but also in patients with genitourinary abnormalities and Wilms' tumor (WT) or presenting...

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Identifiers

PMID: 9399851
DOI: 10.1093/nar/26.1.271
PMCID: PMC147190

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Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

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Research trail→

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Software and database for the analysis of mutations in the human WT1 gene.PMID 9399851Read ↗

Novel WT1 mutation (C388Y) in a female child with Denys-Drash syndrome.Semantic proximity Read ↗

Identification of constitutional WT1 mutations, in patients with isolated diffuse mesangial sclerosis, and analysis of genotype/phenotype correlations by use of a computerized mutation database.Semantic proximity Read ↗

WT1 Pathogenic Variants are Associated with a Broad Spectrum of Differences in Sex Development Phenotypes and Heterogeneous Progression of Renal Disease.Semantic proximity Read ↗

Twenty-four new cases of WT1 germline mutations and review of the literature: genotype/phenotype correlations for Wilms tumor development.Semantic proximity Read ↗

Clinical Characterization of a National Cohort of Patients With Germline WT1 Variants Including Late-Onset PhenotypesSemantic proximity Read ↗

Clinical and molecular characterization of patients with heterozygous mutations in wilms tumor suppressor gene 1.Semantic proximity Read ↗

A clinical overview of WT1 gene mutations.Semantic proximity Read ↗

Genotype/phenotype correlations in Wilms' tumor.Semantic proximity Read ↗

Zinc finger point mutations within the WT1 gene in Wilms tumor patients.Semantic proximity Read ↗

Clinical pictures and novel mutations of WT1-associated Denys-Drash syndrome in two Chinese children.Semantic proximity Read ↗

WT1 and glomerular diseases.Semantic proximity Read ↗

The role of WT1 in Wilms tumorigenesis.Semantic proximity Read ↗

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