By contrast, the downregulated DEGs were mainly responsible for butanoate metabolism, DNA replication, Fanconi anemia pathway, homologous recombination, viral protein interaction with cytokine and cytokine receptor, oocyte meiosis, IL-17 signaling pathway, pyrimidine metabolism, cell cycle, and cytokine-cytokine receptor interaction (Fig. 4D). This evidence concerns the gene IL17A and Fanconi anemia.