Symbol
| FOXF1
| contributors: mct/npt - updated : 07-04-2014
|
HGNC name
| forkhead box F1
|
HGNC id
| 3809
|
corresponding disease(s)
|
ACDMPV
|
Other morbid association(s)
|
Type | Gene Modification | Chromosome rearrangement | Protein expression | Protein Function
|
---|
tumoral
|  
|  
|  
|  
|
predominantly silenced in breast and colorectal cancer cell lines with inactive T53¨ | |
Variant & Polymorphism
|
| |
Candidate gene
Marker
Therapy target
| | | |
| Foxf1 heterozygous mice display abnormalities in lung and gallbladder development | |
Foxf1 deletion from smooth muscle cells causes esophageal defects in newborn mice |