FREAC3 Antibody Blocking Peptide

This gene belongs to the forkhead family of transcription factors which is characterized by a distinct DNA-binding forkhead domain. The specific function of this gene has not yet been determined; however， it has been shown to play a role in the regulation of embryonic and ocular development. Mutations in this gene cause various glaucoma phenotypes including primary congenital glaucoma， autosomal dominant iridogoniodysgenesis anomaly， and Axenfeld-Rieger anomaly.