Symbol Name ID |
Foxc2
forkhead box C2 MGI:1347481 |
Darker colors indicate more annotations |
Human Phenotypes | Nonimmune hydrops fetalis |
Disease(s) Associated with FOXC2 | |
lymphedema-distichiasis syndrome |
Mouse Phenotypes | abnormal fourth pharyngeal arch artery morphology |
abnormal third pharyngeal arch artery morphology |
spina bifida occulta |
kinked neural tube |
abnormal multipotent stem cell morphology |
abnormal somite shape |
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Availability | Mouse Genotype | ||||||
Foxc2tm1Blh/Foxc2tm1Blh | |||||||
Foxc2tm1Miu/Foxc2tm1Miu |
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 09/03/2024 MGI 6.24 |
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