These pathways included the hematopoietic cell lineage, primary immunodeficiency, the T-cell receptor signaling pathway, the PI3K-Akt signaling pathway, focal adhesion, leukocyte transendothelial migration, cytokine‒cytokine receptor interaction, graft-versus–host disease, natural killer cell-mediated cytotoxicity, the cell cycle, malaria, and the Toll-like receptor signaling pathway. Here, AKT1 is linked to inborn error of immunity.