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. The gene discussed is CXCL2; the disease is obstructive sleep apnea syndrome.