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Symbol Name ID |
Msrb3
methionine sulfoxide reductase B3 MGI:2443538 |
| * | Aspects of the system are reported to show a normal phenotype. |
| Darker colors indicate more annotations |
| Human Phenotypes | Hearing impairment |
| Disease(s) Associated with MSRB3 | |
| autosomal recessive nonsyndromic deafness 74 |
| Mouse Phenotypes | hearing/vestibular/ear phenotype |
abnormal outer hair cell stereociliary bundle morphology |
absent outer hair cell stereocilia |
cochlear inner hair cell degeneration |
cochlear outer hair cell degeneration |
increased or absent threshold for auditory brainstem response |
deafness |
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| Availability | Mouse Genotype | |||||||
| Msrb3tm1Hyk/Msrb3tm1Hyk | * | |||||||
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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