FOXC2
| forkhead box C2 (MFH-1, mesenchyme forkhead 1)
| |
| Identifiers | |
| Symbol | FOXC2 |
| Alt. Symbols | FKHL14 |
| Entrez | 2303 |
| HUGO | 3801 |
| OMIM | 602402 |
| RefSeq | NM_005251 |
| UniProt | Q99958 |
| Other data | |
| Locus | Chr. 16 q22-16q24 |
FOXC2 is a gene associated with lymphedema distichiasis, and that has been studied to determine if it is associated with varicose veins.
External links
- Ng M, Andrew T, Spector T, Jeffery S (2005). "Linkage to the FOXC2 region of chromosome 16 for varicose veins in otherwise healthy, unselected sibling pairs.". J Med Genet 42 (3): 235-9. PMID 15744037.
Navigation WikiDoc | WikiPatient | Popular pages | Recently Edited Pages | Recently Added
Pictures
There is no pharmaceutical or device industry support for this site and we need your viewer supported Donations | Editorial Board | Governance | Licensing | Disclaimers | Avoid Plagiarism | Policies
Table of Contents In Alphabetical Order | By Individual Diseases | Signs and Symptoms | Physical Examination | Lab Tests | Drugs
Editor Tools Become an Editor | Editors Help Menu | Create a Page | Edit a Page | Upload a Picture or File | Printable version | Permanent link | Maintain Pages | What Pages Link HereThere is no pharmaceutical or device industry support for this site and we need your viewer supported Donations | Editorial Board | Governance | Licensing | Disclaimers | Avoid Plagiarism | Policies
