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Symbol Name ID |
Foxl2
forkhead box L2 MGI:1349428 |
| Darker colors indicate more annotations |
| Human Phenotypes | Microcornea |
Microphthalmia |
Strabismus |
Nystagmus |
Hypermetropia |
Ptosis |
| Disease(s) Associated with FOXL2 | ||||||
| blepharophimosis, ptosis, and epicanthus inversus syndrome |
| Mouse Phenotypes | abnormal eye morphology |
eyelid hypoplasia |
eyelids open at birth |
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| Availability | Mouse Genotype | |||
| Foxl2tm1Gpil/Foxl2tm1Gpil | ||||
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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