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Symbol
Name
ID
Foxc2
forkhead box C2
MGI:1347481
Phenotype annotations related to craniofacial
*Aspects of the system are reported to show a normal phenotype.
Darker colors indicate more annotations
Human Phenotypes
Micrognathia
Cleft upper lip
Cleft palate
Conjunctivitis
Distichiasis
Ectropion
Disease(s) Associated with FOXC2
lymphedema-distichiasis syndrome

Mouse Phenotypes
craniofacial phenotype
abnormal fourth pharyngeal arch artery morphology
abnormal third pharyngeal arch artery morphology
abnormal craniofacial bone morphology
small basioccipital bone
abnormal basisphenoid bone morphology
abnormal Meckel's cartilage morphology
small Meckel's cartilage
small interparietal bone
small exoccipital bone
abnormal supraoccipital bone morphology
absent supraoccipital bone
abnormal sphenoid bone morphology
abnormal alisphenoid bone morphology
abnormal presphenoid bone morphology
absent presphenoid bone
abnormal pterygoid process morphology
small pterygoid bone
small temporal bone squamous part
abnormal orbit morphology
small mandible
abnormal palatine bone horizontal plate morphology
absent palatine bone horizontal plate
absent palatine bone
abnormal middle ear ossicle morphology
absent incus
abnormal malleus morphology
abnormal gonial bone morphology
gonial bone hypoplasia
malleus hypoplasia
absent stapes
absent soft palate
cleft secondary palate
cleft palate
periorbital edema
Availability Mouse Genotype
Foxc2tm1Blh/Foxc2tm1Blh
Foxc2tm1Miu/Foxc2tm1Miu
Foxc2tm1Miu/Foxc2+
Foxc2tm1.1Miu/Foxc2tm1.1Miu
Nkx2-5tm1(cre)Rjs/Nkx2-5+  (conditional)
*
Foxc2tm1.1Miu/Foxc2tm1.1Miu
Tg(Tek-cre)1Ywa/0  (conditional)
*

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
04/30/2024
MGI 6.23
The Jackson Laboratory