11p partial monosomy syndrome: genes and variants
11p partial monosomy syndrome is linked to 1 analyzed protein (WT1). 5 DNA variants are known to cause it; 3 more are uncertain, and 0 of those already look disease-causing on computable evidence.
Last updated 2026-09-30. Research information, not medical advice.
Genes linked to 11p partial monosomy syndrome
WT1: Wilms tumor protein
It controls transcriptional programs required for kidney and gonadal development and also restrains or promotes cell growth in a context-dependent manner. Germline pathogenic variants cause Wilms-tumor predisposition and Denys-Drash or Frasier syndromes, while somatic alterations occur in some leukemias.
5 disease-causing and 2 uncertain variants in WT1 are linked to 11p partial monosomy syndrome.
Weakly linked (only a few uncertain records): PAX6.
Where 11p partial monosomy syndrome variants cluster
- WT1 C2H2-type 3 (positions 383–405): 3 of 5 disease-causing changes, 11.7× more than its size predicts.
Known disease-causing variants in 11p partial monosomy syndrome
| Variant | Position | Protein part | Clinical label |
|---|---|---|---|
| WT1 R366C | 366 | C2H2-type 2 | Disease-causing (★★) |
| WT1 R366H | 366 | C2H2-type 2 | Disease-causing (★★) |
| WT1 D396N | 396 | C2H2-type 3 | Disease-causing (★★) |
| WT1 D396G | 396 | C2H2-type 3 | Disease-causing (★) |
| WT1 C385R | 385 | C2H2-type 3 | Disease-causing (★) |
Diseases related to 11p partial monosomy syndrome
- Nephrotic syndrome, also linked to WT1
- Acute myeloid leukemia, also linked to WT1
- Wilms tumor, also linked to WT1
- Frasier syndrome, also linked to WT1
- Kidney disorder, also linked to WT1
- Meacham syndrome, also linked to WT1
Frequently asked questions
Which genes are linked to 11p partial monosomy syndrome?
In CATVariant, 11p partial monosomy syndrome is linked to 1 analyzed protein: WT1 (Wilms tumor protein).
How many genetic variants are linked to 11p partial monosomy syndrome?
8 variants: 5 are classified as disease-causing (pathogenic or likely pathogenic) in ClinVar and 3 are of uncertain significance or have conflicting reports.
Which uncertain variants in 11p partial monosomy syndrome look disease-causing?
None of the uncertain variants currently reaches the likely-pathogenic range on computable evidence alone.
About this data
Variant–disease links come from ClinVar, Open Targets and UniProt, pooled from the latest public CATVariant analysis of each human protein. Evidence scores use the ACMG/AMP Bayesian points scale with computable criteria only (position among known disease variants, rarity in gnomAD, calibrated predictors, deep mutational scanning); there is no family or patient data, so they prioritise variants for expert review and never classify them.
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