FOXC1 Antibody

Forkhead box C1 (FOXC1) belongs to the forkhead family of transcription factors which is characterized by a distinct DNA-binding forkhead domain. The specific function of FOXC1 has not yet been determined; however, the gene has been shown to play a role in the regulation of embryonic and ocular development. Mutations in the FOXC1 gene cause various glaucoma phenotypes including primary congenital glaucoma, autosomal dominant iridogoniodysgenesis anomaly, and Axenfeld-Rieger anomaly.[taken from NCBI Entrez Gene (Gene ID: 2296)].

Alternative names for FOXC1 Antibody include forkhead-related protein FKHL7 antibody, forkhead related transcription factor 3 antibody, FREAC-3 antibody, ARA antibody, IGDA antibody, IHG1 antibody, FKHL7 antibody, IRID1 antibody, RIEG3 antibody, FREAC3 antibody.