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Symbol
Name
ID

Foxc1
forkhead box C1
MGI:1347466

Phenotype annotations related to integument

Darker colors indicate more annotations

Human Phenotypes	Redundant skin
Disease(s) Associated with FOXC1	Redundant skin
Axenfeld-Rieger syndrome

Mouse Phenotypes		abnormal vibrissa number
Availability	Mouse Genotype	abnormal vibrissa number
	Foxc1^ch/Foxc1^ch

Contributing Projects: 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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