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Symbol
Name
ID
Coch
cochlin
MGI:1278313
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
Cochlear degeneration
Abnormal vestibular function
Vertigo
Sensorineural hearing impairment
Postlingual sensorineural hearing impairment
Tinnitus
Disease(s) Associated with COCH
autosomal dominant nonsyndromic deafness 9
autosomal recessive nonsyndromic deafness 110

Mouse Phenotypes
hearing/vestibular/ear phenotype
increased or absent threshold for auditory brainstem response
abnormal distortion product otoacoustic emission
reduced linear vestibular evoked potential
Availability Mouse Genotype
Cochtm1.1Stw/Cochtm1.1Stw *
Cochtm1Mrtn/Cochtm1Mrtn
Cochtm1.1Stw/Coch+ *
Cochtm1Mrtn/Coch+

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