Species: Hu, Mu, Ze
Applications: WB, ELISA, ICC/IF, IHC, ChIP, KO, Mycoplasma
Host: Goat Polyclonal
Species: Hu, Mu, Rt
Applications: ICC/IF, IHC, IP
Host: Rabbit Polyclonal
Species: Hu
Applications: WB
Host: Mouse Monoclonal
Species: Hu
Applications: WB
Species: Hu
Applications: AC
Description
FOXC1 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
Bioinformatics
| Entrez |
Mouse
Human
|
| Uniprot |
Human
Human
Human
|
| Product By Gene ID |
2296 |
| Alternate Names |
- ARA
- FKHL7RIEG3
- forkhead box C1
- forkhead box protein C1
- forkhead, drosophila, homolog-like 7
- forkhead/winged helix-like transcription factor 7
- forkhead-related activator 3
- Forkhead-related protein FKHL7
- Forkhead-related transcription factor 3
- FREAC-3
- FREAC3IRID1
- IGDA
- IHG1
- myeloid factor-delta
|
Research Areas for FoxC1
Find related products by research area and learn more about each of the different research areas below.
Cancer
