Symbol Name ID |
Fanca
Fanconi anemia, complementation group A MGI:1341823 |
* | Aspects of the system are reported to show a normal phenotype. |
! | Indicates phenotype varies with strain background. |
Darker colors indicate more annotations |
Human Phenotypes | Abnormality of the eye |
Astigmatism |
Cataract |
Aplasia/Hypoplasia of the iris |
Hypertelorism |
Proptosis |
Microphthalmia |
Strabismus |
Nystagmus |
Abnormality of vision |
Visual impairment |
Ptosis |
Disease(s) Associated with FANCA | ||||||||||||
Fanconi anemia | ||||||||||||
Fanconi anemia complementation group A |
Mouse Phenotypes | vision/eye phenotype |
microphthalmia |
|
Availability | Mouse Genotype | ||
Fancatm1.1Wong/Fancatm1.1Wong | * | ! | |
Fancatm1Wong/Fancatm1Wong | ! |
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 08/02/2024 MGI 6.24 |
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