Symbol Name ID |
Otof
otoferlin MGI:1891247 |
* | Aspects of the system are reported to show a normal phenotype. |
Darker colors indicate more annotations |
Human Phenotypes | Absence of acoustic reflex |
Sensorineural hearing impairment |
Disease(s) Associated with OTOF | ||
autosomal recessive nonsyndromic deafness 9 |
Mouse Phenotypes | hearing/vestibular/ear phenotype |
abnormal cochlear hair cell stereociliary bundle morphology |
abnormal cochlear inner hair cell morphology |
abnormal inner hair cell synaptic ribbon morphology |
abnormal cochlear inner hair cell physiology |
abnormal hearing electrophysiology |
increased or absent threshold for auditory brainstem response |
deafness |
|
Availability | Mouse Genotype | ||||||||
Otofdeaf5Jcs/Otofdeaf5Jcs | * | ||||||||
Otofpga/Otofpga | |||||||||
Otoftm1.1Erei/Otoftm1.1Erei | |||||||||
Otoftm1Ugds/Otoftm1Ugds | * | ||||||||
Otofdeaf5Jcs/Otof+ | * |
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 04/23/2024 MGI 6.23 |
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