|
Symbol Name ID |
Myo15a
myosin XVA MGI:1261811 |
| * | Aspects of the system are reported to show a normal phenotype. |
| Darker colors indicate more annotations |
| Human Phenotypes | Profound sensorineural hearing impairment |
| Disease(s) Associated with MYO15A | |
| autosomal recessive nonsyndromic deafness 3 |
| Mouse Phenotypes | hearing/vestibular/ear phenotype |
abnormal cochlear hair cell morphology |
absent cochlear hair cells |
abnormal cochlear hair cell inter-stereocilial links morphology |
abnormal inner hair cell stereociliary bundle morphology |
short inner hair cell stereocilia |
short outer hair cell stereocilia |
short cochlear hair cell stereocilia |
thin cochlear hair cell stereocilia |
abnormal cochlear outer hair cell morphology |
cochlear hair cell degeneration |
abnormal organ of Corti morphology |
organ of Corti degeneration |
abnormal stria vascularis morphology |
abnormal tectorial membrane morphology |
abnormal utricular macula morphology |
abnormal cochlear inner hair cell physiology |
increased or absent threshold for auditory brainstem response |
absent distortion product otoacoustic emissions |
deafness |
|
| Availability | Mouse Genotype | ||||||||||||||||||||
| Myo15ampc190H/Myo15ampc190H | |||||||||||||||||||||
| Myo15ash2-2J/Myo15ash2-2J | |||||||||||||||||||||
| Myo15ash2-3J/Myo15ash2-3J | * | ||||||||||||||||||||
| Myo15ash2/Myo15ash2 | |||||||||||||||||||||
| Myo15atm1.1Jebd/Myo15atm1.1Jebd | |||||||||||||||||||||
| Myo15ash2-J/Myo15atm1.1Jebd | |||||||||||||||||||||
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO) |
||
|
Citing These Resources Funding Information Warranty Disclaimer, Privacy Notice, Licensing, & Copyright Send questions and comments to User Support. |
last database update 04/16/2024 MGI 6.23 |
|
|
|
||
Analysis Tools