SPRYD7 and Miyoshi myopathy: Notably, in MM characterized by t(11;14) translocation the analysis unraveled the upregulation of lnc-LRRC47-1 and lnc-SEL1L3-6, and the downregulation of lnc-MC2R-2 and lnc-SPRYD7-2, the latter of which may have 25 putative transcripts, eight of which corresponding to DLEU2. Patients carrying t(4;14) translocation upregulated lnc-WHSC2-2, a pseudogene located in the intron 19 of MMSET gene, which encodes the histone methyltransferase deregulated as the result of t(4;14) translocation.