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Symbol
Name
ID
Foxc2
forkhead box C2
MGI:1347481
Phenotype annotations related to embryo
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
Availability Mouse Genotype
Foxc2tm1Blh/Foxc2tm1Blh
Foxc2tm1Miu/Foxc2tm1Miu

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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last database update
03/19/2024
MGI 6.23
The Jackson Laboratory