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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Myo3a
myosin IIIA
MGI:2183924
7 phenotypes from 2 alleles in 2 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Myo3atm1.1Mckg/Myo3atm1.1Mckg
C57BL/6-Myo3atm1.1Mckg
cochlear inner hair cell degeneration J:166812
cochlear outer hair cell degeneration J:166812
decreased cochlear hair cell number J:166812
decreased cochlear outer hair cell number J:166812
normal hearing/vestibular/ear phenotype J:166812
impaired hearing J:166812
Myo3atm1b(KOMP)Wtsi/Myo3atm1b(KOMP)Wtsi
C57BL/6N-Myo3atm1b(KOMP)Wtsi/J
abnormal behavioral response to light J:211773

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Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
09/18/2018
MGI 6.12
The Jackson Laboratory