Acromicric dysplasia: genes and variants
Acromicric dysplasia is linked to 1 analyzed protein (FBN1). 6 DNA variants are known to cause it; 39 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 Acromicric dysplasia
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.
6 disease-causing and 39 uncertain variants in FBN1 are linked to Acromicric dysplasia.
Where Acromicric dysplasia variants cluster
- FBN1 C-terminal domain (positions 1528–2731): 5 of 6 disease-causing changes, 2.0× more than its size predicts.
Known disease-causing variants in Acromicric dysplasia
| Variant | Position | Protein part | Clinical label |
|---|---|---|---|
| FBN1 C1562R | 1562 | TB 6 | Disease-causing (★★) |
| FBN1 C2210Y | 2210 | EGF-like 38 | Disease-causing (★★) |
| FBN1 C734R | 734 | EGF-like 11 | Disease-causing (★) |
| FBN1 G1762C | 1762 | C-terminal domain | Disease-causing (★) |
| FBN1 C2541W | 2541 | EGF-like 44 | Disease-causing (★) |
| FBN1 A1728T | 1728 | TB 7 | Disease-causing |
Same protein, different disease
- Marfan syndrome is also caused by FBN1 variants; they fall mostly in different places as the Acromicric dysplasia 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 Acromicric dysplasia variants (406 disease-causing).
- Isolated thoracic aortic aneurysm is also caused by FBN1 variants; they fall mostly in different places as the Acromicric dysplasia 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 Acromicric dysplasia variants (10 disease-causing).
- Ectopia lentis 1, isolated, autosomal dominant is also caused by FBN1 variants; they fall mostly in different places as the Acromicric dysplasia variants (6 disease-causing).
Diseases related to Acromicric dysplasia
- 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
- Geleophysic dysplasia, also linked to FBN1
- MASS syndrome, also linked to FBN1
- Weill-Marchesani syndrome 2, dominant, also linked to FBN1
- Stiff skin syndrome, also linked to FBN1
Frequently asked questions
Which genes are linked to Acromicric dysplasia?
In CATVariant, Acromicric dysplasia is linked to 1 analyzed protein: FBN1 (Fibrillin-1).
How many genetic variants are linked to Acromicric dysplasia?
48 variants: 6 are classified as disease-causing (pathogenic or likely pathogenic) in ClinVar and 39 are of uncertain significance or have conflicting reports.
Which uncertain variants in Acromicric dysplasia 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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