The Venn graphic shows the DEGs common to hypothyroidism and OSA (Figure 3E), including AGT, RANBP3L, ACTA2, TCEANC2, FGR, RAMP3, IMPA2, RGS4, PLK3, UCN3, PFKFB3, MARCO, CXCL2, NLRP3, TREM2, TMSB15B, SKA3, OR51E1, ZNF252P, MSTO1, IL1RL1, FAIM, RAB20, EPPIN, CAPNS1, PIGF, CD300LB, NR4A1, NRIP1, PCDHB10, ATF3, NUDT7, MOGS, ZFP36L1, PSMD14, ERRFI1, ENC1, SLC5A3, SLC35G1, HIGD1A, TM4SF18, PTGES3, OR56A4, KIF5C, MMRN1, PLBD2, MCL1, and RPL29. This evidence concerns the gene TMSB15B and hypothyroidism.