In addition, both ST3GAL6-AS1 and ST3GAL6 were expressed in MM patients irrespectively of the presence of the major chromosomal aberrations, namely t(11;14), t(4;14), MAF gene translocations or hyperdiploid (HD) status, or the presence of KRAS, NRAS, TP53, BRAF, FAM46C or DIS3 gene mutations. The gene discussed is NRAS; the disease is Miyoshi myopathy.