|
Symbol Name ID |
Foxf1
forkhead box F1 MGI:1347470 |
| Darker colors indicate more annotations |
| Human Phenotypes | Cystic hygroma |
Thickened nuchal skin fold |
Omphalocele |
Diastasis recti |
| Disease(s) Associated with FOXF1 | ||||
| persistent fetal circulation syndrome |
| Mouse Phenotypes | weight loss |
|
| Availability | Mouse Genotype | |
| Foxf1em1Vvk/Foxf1+ | ||
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO) |
||
|
Citing These Resources Funding Information Warranty Disclaimer, Privacy Notice, Licensing, & Copyright Send questions and comments to User Support. |
last database update 04/23/2024 MGI 6.23 |
|
|
|
||
Analysis Tools