|
Symbol Name ID |
Foxc2
forkhead box C2 MGI:1347481 |
| Darker colors indicate more annotations |
| Human Phenotypes | Conjunctivitis |
Corneal erosion |
Recurrent corneal erosions |
Corneal ulceration |
Cataract |
Microphthalmia |
Photophobia |
Ptosis |
| Disease(s) Associated with FOXC2 | ||||||||
| lymphedema-distichiasis syndrome |
| Mouse Phenotypes | abnormal orbit morphology |
abnormal iris pigment epithelium |
abnormal eye morphology |
abnormal iridocorneal angle |
abnormal canal of Schlemm morphology |
abnormal trabecular meshwork morphology |
abnormal iris morphology |
iris stroma hypoplasia |
corneal abrasion |
cataract |
ocular distichiasis |
blepharoptosis |
eye opacity |
|
| Availability | Mouse Genotype | |||||||||||||
| Foxc2tm1Blh/Foxc2+ | ||||||||||||||
| Foxc2tm1Miu/Foxc2+ | ||||||||||||||
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 04/16/2024 MGI 6.23 |
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