FOXC1 (C Term) polyclonal, anti-human, mouse, zebrafish

Background:
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.

Other Names:
Forkhead box protein C1, Forkhead-related protein FKHL7, Forkhead-related transcription factor 3, FREAC-3, FOXC1, FKHL7, FREAC3

Antigen Types:
Synthetic Peptide

Gene Name:
FOXC1
Gene ID:
2296
Primary Accession: Q12948
Other Accession: NP_001444;2296;17300 (mouse);