Symbol Name ID |
Pdzd7
PDZ domain containing 7 MGI:3608325 |
* | 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 PDZD7 | ||||
autosomal recessive nonsyndromic deafness 57 | ||||
Usher syndrome type 2A | ||||
Usher syndrome type 2C |
Mouse Phenotypes | hearing/vestibular/ear phenotype |
abnormal outer hair cell kinocilium location or orientation |
abnormal outer hair cell stereociliary bundle morphology |
decreased outer hair cell stereocilia number |
abnormal cochlear outer hair cell morphology |
abnormal cochlear outer hair cell physiology |
decreased cochlear microphonics |
abnormal hair cell mechanoelectric transduction |
increased or absent threshold for auditory brainstem response |
abnormal distortion product otoacoustic emission |
deafness |
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Availability | Mouse Genotype | |||||||||||
Pdzd7mpc265H/Pdzd7mpc265H | ||||||||||||
Pdzd7tm1a(EUCOMM)Wtsi/Pdzd7tm1a(EUCOMM)Wtsi | * |
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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