AKT1S1 and leishmaniasis: Results showed differential enrichment in leishmaniasis, cytokine receptor interactions, anti-inflammatory response, vascular endothelial cell surface interactions, cellular aging, chemokine signaling pathways, FC epsilon receptor I signaling pathway, immune regulation interactions in lymphoid and non-lymphoid cells, and DNA double-strand break repair in PRAS40 mRNA expression with positive correlation phenotypes (Table 2, Figure 5).