|
Symbol Name ID |
Cldn14
claudin 14 MGI:1860425 |
| Darker colors indicate more annotations |
| Human Phenotypes | Sensorineural hearing impairment |
Hearing impairment |
| Disease(s) Associated with CLDN14 | ||
| autosomal recessive nonsyndromic deafness 29 |
| Mouse Phenotypes | abnormal inner hair cell stereociliary bundle morphology |
absent outer hair cell stereocilia |
cochlear inner hair cell degeneration |
cochlear outer hair cell degeneration |
cochlear hair cell degeneration |
increased or absent threshold for auditory brainstem response |
deafness |
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| Availability | Mouse Genotype | |||||||
| Cldn14tm1Tbf/Cldn14tm1Tbf | ||||||||
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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