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 09/03/2024 MGI 6.24 |
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