|
Symbol Name ID |
Ovol2
ovo like zinc finger 2 MGI:1338039 |
| ! | Indicates phenotype varies with strain background. |
| Darker colors indicate more annotations |
| Human Phenotypes | Anterior synechiae of the anterior chamber |
Abnormal corneal endothelium morphology |
Abnormal Descemet membrane morphology |
Thinning of Descemet membrane |
Polymorphous posterior corneal dystrophy |
Band keratopathy |
Corneal opacity |
Ectopia pupillae |
Iris atrophy |
Uveal ectropion |
Photophobia |
Glaucoma |
Epiphora |
| Disease(s) Associated with OVOL2 | |||||||||||||
| posterior polymorphous corneal dystrophy 1 |
| Mouse Phenotypes | abnormal optic eminence morphology |
|
| Availability | Mouse Genotype | |
| Ovol2tm1Xdai/Ovol2tm1Xdai | ! | |
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 |
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