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Symbol
Name
ID
Otoa
otoancorin
MGI:2149209
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
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
Availability Mouse Genotype
Otoatm1.1(KOMP)Vlcg/Otoatm1.1(KOMP)Vlcg
Otoatm1Gpr/Otoatm1Gpr *

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
03/19/2024
MGI 6.23
The Jackson Laboratory