HMOX1 and Miyoshi myopathy: Among the 96 genes, we found 16 common genes in both datasets (BCL2, BCL2L1, C3, CCR4, CD28, CD68, CD8A, CSF1, HMOX1, IL18, IL1A, IL1B, PTGS2, PTPRC, SELP, STAT3) that were significantly altered between AL amyloidosis and MM patients (p < 0.05; Figure 2C,D).