Becker muscular dystrophy, Cardiomyopathy, Duchenne muscular dystrophy, Dystrophin deficiency: genes and variants
Becker muscular dystrophy, Cardiomyopathy, Duchenne muscular dystrophy, Dystrophin deficiency is linked to 1 analyzed protein (DMD). 1 DNA variants are known to cause it; 74 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 Becker muscular dystrophy, Cardiomyopathy, Duchenne muscular dystrophy, Dystrophin deficiency
DMD: Dystrophin
Its dystrophin product mechanically links the actin cytoskeleton of muscle fibers to the extracellular matrix and stabilizes the sarcolemma during contraction. Severe loss causes Duchenne muscular dystrophy, while variants preserving partial function more often cause Becker muscular dystrophy.
1 disease-causing and 74 uncertain variants in DMD are linked to Becker muscular dystrophy, Cardiomyopathy, Duchenne muscular dystrophy, Dystrophin deficiency.
Known disease-causing variants in Becker muscular dystrophy, Cardiomyopathy, Duchenne muscular dystrophy, Dystrophin deficiency
| Variant | Position | Protein part | Clinical label |
|---|---|---|---|
| DMD G2097V | 2097 | Spectrin 16 | Disease-causing (★★) |
Diseases related to Becker muscular dystrophy, Cardiomyopathy, Duchenne muscular dystrophy, Dystrophin deficiency
- Dilated cardiomyopathy, also linked to DMD
- Muscular dystrophy, also linked to DMD
- Familial isolated dilated cardiomyopathy, also linked to DMD
- Duchenne muscular dystrophy, also linked to DMD
- Neuromuscular disease caused by qualitative or quantitative defects of dystrophin, also linked to DMD
Frequently asked questions
Which genes are linked to Becker muscular dystrophy, Cardiomyopathy, Duchenne muscular dystrophy, Dystrophin deficiency?
In CATVariant, Becker muscular dystrophy, Cardiomyopathy, Duchenne muscular dystrophy, Dystrophin deficiency is linked to 1 analyzed protein: DMD (Dystrophin).
How many genetic variants are linked to Becker muscular dystrophy, Cardiomyopathy, Duchenne muscular dystrophy, Dystrophin deficiency?
75 variants: 1 are classified as disease-causing (pathogenic or likely pathogenic) in ClinVar and 74 are of uncertain significance or have conflicting reports.
Which uncertain variants in Becker muscular dystrophy, Cardiomyopathy, Duchenne muscular dystrophy, Dystrophin deficiency 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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