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Symbol Name ID |
Rdx
radixin MGI:97887 |
| Darker colors indicate more annotations |
| Human Phenotypes | Profound sensorineural hearing impairment |
| Disease(s) Associated with RDX | |
| autosomal recessive nonsyndromic deafness 24 |
| Mouse Phenotypes | abnormal cochlear hair cell stereociliary bundle morphology |
abnormal inner hair cell stereociliary bundle morphology |
fused inner hair cell stereocilia |
short inner hair cell stereocilia |
abnormal outer hair cell stereociliary bundle morphology |
short outer hair cell stereocilia |
fused outer hair cell stereocilia |
cochlear hair cell degeneration |
organ of Corti degeneration |
increased or absent threshold for auditory brainstem response |
deafness |
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| Availability | Mouse Genotype | |||||||||||
| Rdxtm1Sts/Rdxtm1Sts | ||||||||||||
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 05/07/2024 MGI 6.23 |
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