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 09/03/2024 MGI 6.24 |
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