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Symbol
Name
ID
Otof
otoferlin
MGI:1891247
Phenotype annotations related to hearing/vestibular/ear
*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+ *

Contributing Projects:
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
The Jackson Laboratory