FOXF1 (Forkhead Box F1) is a Protein Coding gene. Diseases associated with FOXF1 include Alveolar Capillary Dysplasia With Misalignment Of Pulmonary Veins and Persistent Fetal Circulation Syndrome. Among its related pathways are Embryonic and Induced Pluripotent Stem Cell Differentiation Pathways and Lineage-specific Markers and FOXA2 and FOXA3 transcription factor networks. Gene Ontology (GO) annotations related to this gene include DNA binding transcription factor activity and transcription regulatory region DNA binding. An important paralog of this gene is FOXF2.
Related Pathway/CSCs feature
 FOXF1 mediates mesenchymal stem cell fusion-induced reprogramming of lung cancer cells.
Oncotarget.2014 Oct 15;5(19):9514-29. [ 25237908 ]