They indicated that significant diagnostic potential in MM was found for decreased expression of AFF2, circMYBL2, circ_0000190, and increased expression of PTK2, CDYL, ATP10A, PVT1, circ_0000142, circ_0001821, circ_0069767, and circ_0007841 [49]. This evidence concerns the gene ATP10A and Miyoshi myopathy.