These genes were mainly enriched in the GO terms with DNA metabolic process, nuclear chromosome, and DNA repair, and in the KEGG pathways with JAK-STAT signaling pathway, novobiocin biosynthesis, Fanconi anemia pathway, cytokine–cytokine receptor interaction, homologous recombination, nonhomologous end-joining, and complement and coagulation cascades (Supplementary Figure S3). The gene discussed is SOAT1; the disease is Fanconi anemia.