MnM (CG14964) seems to be a hub gene within the interaction network of sarcomere genes, as shown in Fig. 3A. Four interaction partners of MYOM2 are known to carry mutations causing cardiomyopathies (MYH7, ANKRD1, ACTN2 and TTN), whereas two are known to cause muscular dystrophy (DYSF and CAPN3). The gene discussed is MYOM2; the disease is muscular dystrophy.