Symbol Name ID |
Pcdh15
protocadherin 15 MGI:1891428 |
* | Aspects of the system are reported to show a normal phenotype. |
Darker colors indicate more annotations |
Human Phenotypes | Abnormal vestibular function |
Sensorineural hearing impairment |
Congenital sensorineural hearing impairment |
Hearing impairment |
Disease(s) Associated with PCDH15 | ||||
autosomal recessive nonsyndromic deafness 23 | ||||
Usher syndrome type 1D | ||||
Usher syndrome type 1F |
Mouse Phenotypes | hearing/vestibular/ear phenotype |
abnormal vestibuloocular dark reflex |
abnormal vestibuloocular light reflex |
abnormal inner hair cell kinocilium morphology |
abnormal inner hair cell kinocilium location or orientation |
abnormal outer hair cell kinocilium morphology |
abnormal outer hair cell kinocilium location or orientation |
abnormal vestibular hair cell kinocilium morphology |
abnormal cochlear sensory epithelium morphology |
abnormal cochlear hair cell morphology |
abnormal cochlear hair cell stereociliary bundle morphology |
abnormal cochlear hair cell inter-stereocilial links morphology |
abnormal cochlear hair bundle tip links morphology |
abnormal inner hair cell stereociliary bundle morphology |
abnormal orientation of inner hair cell stereociliary bundles |
decreased inner hair cell stereocilia number |
fused inner hair cell stereocilia |
short inner hair cell stereocilia |
abnormal orientation of cochlear hair cell stereociliary bundles |
abnormal orientation of outer hair cell stereociliary bundles |
abnormal outer hair cell stereociliary bundle morphology |
short outer hair cell stereocilia |
decreased outer hair cell stereocilia number |
short cochlear hair cell stereocilia |
cochlear inner hair cell degeneration |
abnormal cochlear outer hair cell morphology |
cochlear outer hair cell degeneration |
cochlear hair cell degeneration |
abnormal organ of Corti morphology |
abnormal organ of Corti supporting cell morphology |
abnormal Hensen cell morphology |
abnormal pillar cell morphology |
absent tunnel of Corti |
organ of Corti degeneration |
vestibular hair cell degeneration |
abnormal vestibular saccule morphology |
vestibular saccular macula degeneration |
vestibular saccular degeneration |
abnormal otolithic membrane morphology |
abnormal otolith morphology |
decreased otolith number |
enlarged otoliths |
abnormal hair cell mechanoelectric transduction |
abnormal auditory brainstem response |
increased or absent threshold for auditory brainstem response |
abnormal cochlear nerve compound action potential |
absent distortion product otoacoustic emissions |
deafness |
abnormal vestibular system physiology |
absent linear vestibular evoked potential |
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Availability | Mouse Genotype | ||||||||||||||||||||||||||||||||||||||||||||||||||
Pcdh15av-2J/Pcdh15av-2J | * | ||||||||||||||||||||||||||||||||||||||||||||||||||
Pcdh15av-3J/Pcdh15av-3J | * | ||||||||||||||||||||||||||||||||||||||||||||||||||
Pcdh15av-5J/Pcdh15av-5J | |||||||||||||||||||||||||||||||||||||||||||||||||||
Pcdh15av-6J/Pcdh15av-6J | * | ||||||||||||||||||||||||||||||||||||||||||||||||||
Pcdh15av-J/Pcdh15av-J | * | ||||||||||||||||||||||||||||||||||||||||||||||||||
Pcdh15av-Jfb/Pcdh15av-Jfb | |||||||||||||||||||||||||||||||||||||||||||||||||||
Pcdh15av-Tg2742Rpw/Pcdh15av-Tg2742Rpw | * | ||||||||||||||||||||||||||||||||||||||||||||||||||
Pcdh15av/Pcdh15av | |||||||||||||||||||||||||||||||||||||||||||||||||||
Pcdh15em1Zma/Pcdh15em1Zma | |||||||||||||||||||||||||||||||||||||||||||||||||||
Pcdh15roda/Pcdh15roda | |||||||||||||||||||||||||||||||||||||||||||||||||||
Pcdh15tm1.1Mll/Pcdh15tm1.1Mll | * | ||||||||||||||||||||||||||||||||||||||||||||||||||
Pcdh15tm2.1Mll/Pcdh15tm2.1Mll | |||||||||||||||||||||||||||||||||||||||||||||||||||
Pcdh15tm3.1Mll/Pcdh15tm3.1Mll | * | ||||||||||||||||||||||||||||||||||||||||||||||||||
Pcdh15av-3J/Pcdh15+ | |||||||||||||||||||||||||||||||||||||||||||||||||||
Pcdh15tm1.1Ugds/Pcdh15tm1.1Ugds Myo15atm1.1(cre)Ugds/Myo15a+ (conditional) |
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 08/02/2024 MGI 6.24 |
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