|
Symbol Name ID |
Ctnna1
catenin alpha 1 MGI:88274 |
| Darker colors indicate more annotations |
| Human Phenotypes | Foveal hyperpigmentation |
Pattern dystrophy of the retina |
Drusen |
Reduced visual acuity |
| Disease(s) Associated with CTNNA1 | ||||
| patterned macular dystrophy 2 |
| Mouse Phenotypes | retina cone cell degeneration |
retina rod cell degeneration |
retina photoreceptor degeneration |
abnormal retina pigment epithelium morphology |
abnormal retina pigmentation |
abnormal ocular fundus morphology |
thin retina outer nuclear layer |
abnormal retina outer limiting membrane morphology |
retina spots |
decreased a-wave amplitude |
decreased b-wave amplitude |
abnormal c-wave shape |
abnormal eye electrophysiology |
abnormal rod electrophysiology |
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| Availability | Mouse Genotype | ||||||||||||||
| Ctnna1Tvrm5/Ctnna1Tvrm5 | |||||||||||||||
| Ctnna1Tvrm5/Ctnna1+ | |||||||||||||||
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 05/21/2024 MGI 6.23 |
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