The WT1 gene homepage

General information
Gene symbol WT1
Gene name Wilms tumor 1
Chromosome 11
Chromosomal band p13
Imprinted Unknown
Genomic reference NG_009272.1
Transcript reference NM_024426.4
Exon/intron information NM_024426.4 exon/intron table
Associated with diseases DDS, Frasier, Meacham, MESOM, NPHS, NPHS4, WAGR, WAGRO, WT1
Citation reference(s) -
Refseq URL Genomic reference sequence
Curators (1) Olga Beltcheva
Total number of public variants reported 134
Unique public DNA variants reported 87
Individuals with public variants 42
Hidden variants 21
Date created April 29, 2010
Date last updated November 27, 2023
Version WT1:231127

Graphical displays and utilities
Graphs Graphs displaying summary information of all variants in the database »
Reading frame checker The Reading-frame checker generates a prediction of the effect of whole-exon changes. Active for: NM_024426.4.
UCSC Genome Browser Show variants in the UCSC Genome Browser (full view, compact view)
Ensembl Genome Browser Show variants in the Ensembl Genome Browser (full view, compact view)
NCBI Sequence Viewer Show distribution histogram of variants in the NCBI Sequence Viewer

Links to other resources
Homepage URL
HGNC 12796
Entrez Gene 7490
PubMed articles WT1
OMIM - Gene 607102
OMIM - Diseases DDS (Denys-Drash syndrome (DDS))
Frasier (Frasier syndrome)
Meacham (Meacham syndrome)
MESOM (mesothelioma, malignant (MESOM))
NPHS4 (nephrotic syndrome, type 4 (NPHS-4))
WAGR (Wilms tumor, aniridia, genitourinary anomalies, mental retardation syndrome (WAGR, 11p partial monosomy syndrome))
WT1 (Wilms tumor, type 1, somatic (WT-1, nephroblastoma))
GeneCards WT1
GeneTests WT1
Orphanet WT1

Active transcripts




NCBI ID     

NCBI Protein ID     

00023961 11 transcript variant D NM_024426.4 NP_077744.3 134

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