These genes represent coordinated axes of T‐cell dysfunction in sepsis, including dysregulated inflammatory/innate signaling (IL1R2, LTB, PRKCA, MARCO, SLC11A1, RNF10, and COMMD6), mitochondrial and bioenergetic stress programs (COX7B, PPM1K, IER5, WHAMM, and NUCKS1), and impaired trafficking and activation signaling (S1PR1, TESPA1, and CD96). The gene discussed is CD96; the disease is Sepsis.