Symbol Name ID |
Casp3
caspase 3 MGI:107739 |
* | Aspects of the system are reported to show a normal phenotype. |
Darker colors indicate more annotations |
Human Phenotypes | Diplopia |
Color vision defect |
Disease(s) Associated with CASP3 | ||
Parkinson's disease |
Mouse Phenotypes | vision/eye phenotype |
abnormal retina pigment epithelium morphology |
abnormal eye morphology |
abnormal lens development |
abnormal lens epithelium morphology |
cataract |
abnormal eye development |
abnormal optic stalk morphology |
microphthalmia |
abnormal retina morphology |
abnormal retina inner nuclear layer morphology |
retina fold |
|
Availability | Mouse Genotype | ||||||||||||
Casp3tm1Flv/Casp3tm1Flv | * |
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 03/12/2024 MGI 6.23 |
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