Weill-Marchesani syndrome 2, dominant: genes and variants
Weill-Marchesani syndrome 2, dominant is linked to 1 analyzed protein (FBN1). 3 DNA variants are known to cause it; 40 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 Weill-Marchesani syndrome 2, dominant
FBN1: Fibrillin-1
Its fibrillin-1 microfibrils provide mechanical support to elastic tissues and regulate local availability of growth factors such as TGF-beta. Pathogenic variants cause Marfan syndrome and related fibrillinopathies affecting the aorta, skeleton, eyes, skin, and lungs.
3 disease-causing and 40 uncertain variants in FBN1 are linked to Weill-Marchesani syndrome 2, dominant.
Known disease-causing variants in Weill-Marchesani syndrome 2, dominant
| Variant | Position | Protein part | Clinical label |
|---|---|---|---|
| FBN1 C1374Y | 1374 | EGF-like 23 | Disease-causing (★★) |
| FBN1 G1754D | 1754 | C-terminal domain | Disease-causing (★★) |
| FBN1 S110C | 110 | EGF-like 1 | Disease-causing (★) |
Same protein, different disease
- Marfan syndrome is also caused by FBN1 variants; they fall mostly in different places as the Weill-Marchesani syndrome 2, dominant variants (434 disease-causing).
- Familial thoracic aortic aneurysm and aortic dissection is also caused by FBN1 variants; they fall mostly in different places as the Weill-Marchesani syndrome 2, dominant variants (406 disease-causing).
- Isolated thoracic aortic aneurysm is also caused by FBN1 variants; they fall mostly in different places as the Weill-Marchesani syndrome 2, dominant variants (12 disease-causing).
- Marfan syndrome/loeys-dietz syndrome/familial thoracic aortic aneurysms and dissections is also caused by FBN1 variants; they fall mostly in different places as the Weill-Marchesani syndrome 2, dominant variants (10 disease-causing).
- Acromicric dysplasia is also caused by FBN1 variants; they fall mostly in different places as the Weill-Marchesani syndrome 2, dominant variants (6 disease-causing).
Diseases related to Weill-Marchesani syndrome 2, dominant
- Familial thoracic aortic aneurysm and aortic dissection, also linked to FBN1
- Marfan syndrome, also linked to FBN1
- Perrault syndrome, also linked to FBN1
- Connective tissue disorder, also linked to FBN1
- Familial aortopathy, also linked to FBN1
- Isolated thoracic aortic aneurysm, also linked to FBN1
- Marfan syndrome/loeys-dietz syndrome/familial thoracic aortic aneurysms and dissections, also linked to FBN1
- Ectopia lentis 1, isolated, autosomal dominant, also linked to FBN1
- Acromicric dysplasia, also linked to FBN1
- Geleophysic dysplasia, also linked to FBN1
- MASS syndrome, also linked to FBN1
- Stiff skin syndrome, also linked to FBN1
Frequently asked questions
Which genes are linked to Weill-Marchesani syndrome 2, dominant?
In CATVariant, Weill-Marchesani syndrome 2, dominant is linked to 1 analyzed protein: FBN1 (Fibrillin-1).
How many genetic variants are linked to Weill-Marchesani syndrome 2, dominant?
43 variants: 3 are classified as disease-causing (pathogenic or likely pathogenic) in ClinVar and 40 are of uncertain significance or have conflicting reports.
Which uncertain variants in Weill-Marchesani syndrome 2, dominant 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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