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Symbol Name ID |
Fanci
Fanconi anemia, complementation group I MGI:2384790 |
| Darker colors indicate more annotations |
| Human Phenotypes | Abnormality of the eye |
Astigmatism |
Cataract |
Aplasia/Hypoplasia of the iris |
Optic nerve hypoplasia |
Hypertelorism |
Proptosis |
Microphthalmia |
Strabismus |
Nystagmus |
Myopia |
Abnormality of vision |
Visual impairment |
Ptosis |
| Disease(s) Associated with FANCI | ||||||||||||||
| Fanconi anemia | ||||||||||||||
| Fanconi anemia complementation group I |
| Mouse Phenotypes | abnormal lens development |
abnormal retina development |
microphthalmia |
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| Availability | Mouse Genotype | |||
| Fancitm1.1Itl/Fancitm1.1Itl | ||||
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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