Symbol Name ID |
Foxc1
forkhead box C1 MGI:1347466 |
Darker colors indicate more annotations |
Human Phenotypes | Redundant skin |
Disease(s) Associated with FOXC1 | |
Axenfeld-Rieger syndrome |
Mouse Phenotypes | abnormal vibrissa number |
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Availability | Mouse Genotype | |
Foxc1ch/Foxc1ch |
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 08/02/2024 MGI 6.24 |
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