|
Symbol Name ID |
Ush2a
usherin MGI:1341292 |
| Darker colors indicate more annotations |
| Human Phenotypes | Photophobia |
Cerebral cortical atrophy |
Subcortical cerebral atrophy |
Aplasia/Hypoplasia of the cerebellum |
Ataxia |
Depression |
Anxiety |
Psychosis |
Schizophrenia |
Hallucinations |
Hyperacusis |
Cognitive impairment |
Intellectual disability |
Hyperreflexia |
| Disease(s) Associated with USH2A | ||||||||||||||
| retinitis pigmentosa | ||||||||||||||
| Usher syndrome | ||||||||||||||
| Usher syndrome type 2 |
| Mouse Phenotypes | decreased cochlear outer hair cell number |
abnormal retina photoreceptor morphology |
short photoreceptor inner segment |
short photoreceptor outer segment |
retina cone cell degeneration |
retina photoreceptor degeneration |
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| Availability | Mouse Genotype | ||||||
| Ush2atm1Tili/Ush2atm1Tili | |||||||
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 04/30/2024 MGI 6.23 |
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