WT1

Gene symbol WT1
Aliases -
Protein Name Wilms tumor protein
Function It has a tumor suppressor as well as an oncogenic role in tumor formation. Function may be isoform-specific: isoforms lacking the KTS motif may act as transcription factors.
Species Human
Editing Sites 1
Disease Acute Myeloid Leukemia;
Description WT1 is a regulatory protein with dual tumor suppressor/oncogene activity depending on the isoforms expressed, including the Lys-Thr-Ser (KTS) variant. WT1 splicing variants with excluded tripeptide (-KTS) mainly act as transcriptional regulators, while the isoforms retaining the tripeptide (+KTS) show post-transcriptional activity. Wilms Tumor 1 (WT1) mutations and variants are implicated in several diseases, including Wilms tumor and acute myeloid leukemia (AML).
RADR RADAR
REDIportal REDI portal
External links P19544(Uniport); NM_000378 (NM id); 7490 (NCBI gene id); GeneCard; GTEx
Sequence

Editing sites

Enzyme Editing type Region NT Seq Position Molecular Consequence Editing Level Tissue Editing Effect Phenotype Disease name PMID
  • APOBEC3A
G-to-A NA 1303 Nonsynonymous substitution Present Blood WT1 mutations affect the zinc finger (ZnF) domains in Wilms tumor and acute myeloid leukemia (AML). Induce mutation of wilms tumor and acute myeloid leukemia