Analysis of the GSE136831 dataset revealed an elevation in the DC population within IPF patients’ lungs, with significant accumulations specifically in cDC2 (marked by FCGR2B, CLEC10A, FOXN3, ABHD12) and Langerhans cells (indicated by CD1A, FCER1A, CD1E, HLA-DQB2, S100B). The gene discussed is FOXN3; the disease is idiopathic pulmonary fibrosis.