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Symbol Name ID |
Myh9
myosin, heavy polypeptide 9, non-muscle MGI:107717 |
| * | Aspects of the system are reported to show a normal phenotype. |
| Darker colors indicate more annotations |
| Human Phenotypes | Sensorineural hearing impairment |
Hearing impairment |
High-frequency hearing impairment |
| Disease(s) Associated with MYH9 | |||
| autosomal dominant Alport syndrome | |||
| autosomal dominant nonsyndromic deafness 17 | |||
| MYH-9 related disease |
| Mouse Phenotypes | hearing/vestibular/ear phenotype |
increased or absent threshold for auditory brainstem response |
increased susceptibility to age-related hearing loss |
impaired hearing |
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| Availability | Mouse Genotype | ||||
| Myh9Gt(Betageo-btk)1Dash/Myh9+ | |||||
| Myh9tm1.1(MYH9*)Mjk/Myh9+ | |||||
| Myh9tm1.1Dash/Myh9+ | * | ||||
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 04/23/2024 MGI 6.23 |
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