WT1 Transcription Factor

Alternative Names

  • WT1
  • WT1/EWS Fusion Gene

Associated Diseases

Nephrotic Syndrome, Type 4
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OMIM Number

607102

NCBI Gene ID

7490

Uniprot ID

P19544

Length

48,111 bases

No. of Exons

12

No. of isoforms

9

Protein Name

Wilms tumor protein

Molecular Mass

49188 Da

Amino Acid Count

499

Genomic Location

chr11:32,387,775-32,435,885

Gene Map Locus
11p13

Description

This gene encodes a transcription factor that contains four zinc-finger motifs at the C-terminus and a proline/glutamine-rich DNA-binding domain at the N-terminus. It has an essential role in the normal development of the urogenital system, and it is mutated in a small subset of patients with Wilms tumor. This gene exhibits complex tissue-specific and polymorphic imprinting pattern, with biallelic, and monoallelic expression from the maternal and paternal alleles in different tissues. Multiple transcript variants have been described. In several variants, there is evidence for the use of a non-AUG (CUG) translation initiation codon upstream of, and in-frame with the first AUG. [From RefSeq]

Epidemiology in the Arab World

View Map
Variant NameCountryGenomic LocationClinvar Clinical SignificanceCTGA Clinical Significance Condition(s)HGVS ExpressionsdbSNPClinvar
NM_024426.6:c.1250G>TLebanonchr11:32396271PathogenicNephrotic Syndrome, Type 4NG_009272.1:g.44271G>T; NM_024426.6:c.1250G>T; NP_077744.4:p.Ser417Ile1440971275
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