Rare Muscle Disorder Models

Rare diseases affecting muscles are predominantly genetic muscle disorders, such as Duchenne muscular dystrophy, progressive muscular dystrophy, facioscapulohumeral muscular dystrophy, myotonic dystrophy, spinal muscular atrophy, peroneal muscular atrophy, glycogen storage diseases, lipid metabolism myopathies, and mitochondrial encephalomyopathies. Cyagen has developed a series of gene knockout, knock-in, and point mutation models for muscular diseases. We also offer customization and collaboration options to meet the specific needs of researchers.


Disease Name Target Genes Targeting Methods Ordering
Myotonic dystrophy type 1, DM1 Dmpk TG Order Now
Duchenne muscular dystrophy, DMD Dmd Mu, Humanization(WT, Mu, KO) Order Now
Limb-girdle muscular dystrophy,type 2D, LGMD2D Sgca KO Order Now
Danon disease Lamp2 KO Order Now