|
Symbol Name ID |
Rd3
retinal degeneration 3 MGI:1921273 |
| Darker colors indicate more annotations |
| Human Phenotypes | Encephalocele |
Aplasia/Hypoplasia of the cerebellar vermis |
Abnormality of neuronal migration |
Hemiplegia/hemiparesis |
Intellectual disability |
Global developmental delay |
Seizure |
| Disease(s) Associated with RD3 | |||||||
| Leber congenital amaurosis |
| Mouse Phenotypes | absent retina rod cells |
retina photoreceptor degeneration |
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| Availability | Mouse Genotype | ||
| Rd3rd3/Rd3rd3 | |||
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 04/23/2024 MGI 6.23 |
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