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Symbol Name ID |
Cldn9
claudin 9 MGI:1913100 |
| Darker colors indicate more annotations |
| Human Phenotypes | Sensorineural hearing impairment |
| Disease(s) Associated with CLDN9 | |
| autosomal recessive nonsyndromic deafness 116 |
| Mouse Phenotypes | decreased cochlear outer hair cell number |
decreased outer hair cell stereocilia number |
cochlear outer hair cell degeneration |
abnormal organ of Corti morphology |
increased or absent threshold for auditory brainstem response |
deafness |
abnormal perilymph physiology |
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| Availability | Mouse Genotype | |||||||
| Cldn9nmf329/Cldn9nmf329 | ||||||||
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 04/09/2024 MGI 6.23 |
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