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Symbol Name ID |
Otog
otogelin MGI:1202064 |
| Darker colors indicate more annotations |
| Human Phenotypes | Vestibular hypofunction |
Sensorineural hearing impairment |
| Disease(s) Associated with OTOG | ||
| autosomal recessive nonsyndromic deafness 18B |
| Mouse Phenotypes | abnormal cochlea morphology |
abnormal tectorial membrane morphology |
decreased vestibular hair cell stereocilia number |
abnormal semicircular canal morphology |
abnormal crista ampullaris morphology |
abnormal utricle morphology |
abnormal vestibular saccule morphology |
abnormal vestibular saccular macula morphology |
abnormal otolithic membrane morphology |
abnormal otolith morphology |
detached otolithic membrane |
abnormal ear physiology |
abnormal auditory brainstem response |
increased or absent threshold for auditory brainstem response |
impaired hearing |
deafness |
nonsyndromic hearing impairment |
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| Availability | Mouse Genotype | |||||||||||||||||
| Otogem1(IMPC)J/Otogem1(IMPC)J | ||||||||||||||||||
| Otogtm1Prs/Otogtm1Prs | ||||||||||||||||||
| Otogtwt-2J/Otogtwt-2J | ||||||||||||||||||
| Otogtwt-3J/Otogtwt-3J | ||||||||||||||||||
| Otogtwt-4J/Otogtwt-4J | ||||||||||||||||||
| Otogtwt-5J/Otogtwt-5J | ||||||||||||||||||
| Otogtwt/Otogtwt | ||||||||||||||||||
| Otogvbd/Otogvbd | ||||||||||||||||||
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 04/30/2024 MGI 6.23 |
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