FOXF1 belongs to the forkhead family of transcription factors which is characterized by a distinct forkhead domain. The specific function of FOXF1 has not yet been determined; however, it may play a role in the regulation of pulmonary genes as well as embryonic development. FOXF1 (Forkhead Box F1) is a Protein Coding gene. Diseases associated with FOXF1 include Alveolar Capillary Dysplasia With Misalignment Of Pulmonary Veins and Alveolar Capillary Dysplasia. Among its related pathways are Embryonic and Induced Pluripotent Stem Cell Differentiation Pathways and Lineage-specific Markers and FOXA2 and FOXA3 transcription factor networks.
