VDAC1 and Miyoshi myopathy: We observed that SLC25A4, PHB2, CERS1, VPS13C, HUWE1, VDAC1, and SLC25A5 were significantly upregulated, while OGT, ATG13, PINK1, and OPTN were significantly downregulated in MM patients (supplementary Fig. 2A and 2B).