Symbol Name ID |
Coch
cochlin MGI:1278313 |
* | 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 |
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Availability | Mouse Genotype | ||||
Cochtm1.1Stw/Cochtm1.1Stw | * | ||||
Cochtm1Mrtn/Cochtm1Mrtn | |||||
Cochtm1.1Stw/Coch+ | * | ||||
Cochtm1Mrtn/Coch+ |
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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