|
Symbol Name ID |
Foxc2
forkhead box C2 MGI:1347481 |
| Darker colors indicate more annotations |
| Human Phenotypes | Abnormality of the musculature |
Muscle weakness |
| Disease(s) Associated with FOXC2 | ||
| lymphedema-distichiasis syndrome |
| Mouse Phenotypes | thin myocardium |
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| Availability | Mouse Genotype | |
| Foxc2tm1.2Tsku/Foxc2tm1.2Tsku | ||
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO) |
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last database update 05/14/2024 MGI 6.23 |
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