Symbol Name ID |
Otoa
otoancorin MGI:2149209 |
* | Aspects of the system are reported to show a normal phenotype. |
Darker colors indicate more annotations |
Human Phenotypes | Sensorineural hearing impairment |
Disease(s) Associated with OTOA | |
autosomal recessive nonsyndromic deafness 22 |
Mouse Phenotypes | hearing/vestibular/ear phenotype |
absent Hensen stripe |
abnormal tectorial membrane morphology |
detached tectorial membrane |
abnormal auditory brainstem response |
abnormal cochlear nerve compound action potential |
impaired hearing |
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Availability | Mouse Genotype | |||||||
Otoatm1.1(KOMP)Vlcg/Otoatm1.1(KOMP)Vlcg | ||||||||
Otoatm1Gpr/Otoatm1Gpr | * |
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 03/19/2024 MGI 6.23 |
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