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Symbol
Name
ID
Myo3a
myosin IIIA
MGI:2183924
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
Progressive sensorineural hearing impairment
Progressive hearing impairment
Disease(s) Associated with MYO3A
autosomal recessive nonsyndromic deafness 30

Mouse Phenotypes
hearing/vestibular/ear phenotype
decreased cochlear hair cell number
decreased cochlear outer hair cell number
cochlear inner hair cell degeneration
cochlear outer hair cell degeneration
impaired hearing
Availability Mouse Genotype
Myo3atm1.1Mckg/Myo3atm1.1Mckg *

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
09/11/2018
MGI 6.12
The Jackson Laboratory