Interestingly, expression of ANKRD20A5P, SMILO, ENSG00000254343, and RHOT1P1 were significantly associated with the presence of amp(1q), while expression of PDLIM1P4 and ENSG00000249988 did not show any significant association with different MM genetic groups (Supplemental Fig. 3). The gene discussed is ANKRD20A5P; the disease is Miyoshi myopathy.