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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Myo15a
myosin XVA
MGI:1261811
35 phenotypes from multigenic genotypes
Export: Excel File
Allelic Composition
Genetic Background
Annotated Term Reference
Cdh23tm1.1Ugds/Cdh23tm1.1Ugds
Myo15atm1.1(cre)Ugds/Myo15a+
involves: 129S1/SvImJ * C57BL/6J
abnormal cochlear hair bundle tip links morphology J:171218
abnormal hearing electrophysiology J:171218
abnormal inner hair cell stereociliary bundle morphology J:171218
abnormal outer hair cell stereociliary bundle morphology J:171218
absent cochlear microphonics J:171218
absent distortion product otoacoustic emissions J:171218
decreased inner hair cell stereocilia number J:171218
decreased outer hair cell stereocilia number J:171218
impaired hearing J:171218
increased or absent threshold for auditory brainstem response J:171218
short inner hair cell stereocilia J:171218
short outer hair cell stereocilia J:171218
Clrn1tm1.1Ugpa/Clrn1tm1.1Ugpa
Myo15atm1.1(cre)Ugds/Myo15a+
involves: 129S1/SvImJ * C57BL/6N
abnormal cochlear IHC afferent innervation pattern J:265318
abnormal cochlear inner hair cell physiology J:265318
abnormal cochlear nerve compound action potential J:265318
abnormal cochlear nerve fiber response J:265318
abnormal cochlear nerve morphology J:265318
abnormal inner hair cell stereociliary bundle morphology J:265318
abnormal outer hair cell stereociliary bundle morphology J:265318
abnormal ribbon synapse morphology J:265318
abnormal synapse morphology J:265318
abnormal synaptic vesicle exocytosis J:265318
cochlear inner hair cell degeneration J:265318
cochlear outer hair cell degeneration J:265318
deafness J:265318
increased or absent distortion product otoacoustic emission threshold J:265318
increased or absent threshold for auditory brainstem response J:265318
sensorineural hearing loss J:265318
Myo15ash2/Myo15a+
Myo6sv/Myo6+
involves: B10.HA/(33NX)Sn
increased susceptibility to age-related hearing loss J:86379
Myo15ash2/Myo15ash2
Myo6sv/Myo6sv
involves: B10.HA/(33NX)Sn
abnormal cochlear hair cell stereociliary bundle morphology J:86379
abnormal organ of Corti morphology J:86379
decreased body size J:86379
short cochlear hair cell stereocilia J:86379
Myo15atm1.1(cre)Ugds/Myo15a+
Ush1gtm1.1Ugds/Ush1gtm1.1Ugds
involves: 129S1/SvImJ * C57BL/6J
abnormal cochlear hair bundle tip links morphology J:171218
abnormal hair cell mechanoelectric transduction J:171218
abnormal hair cell physiology J:171218
abnormal hearing electrophysiology J:171218
abnormal inner hair cell stereociliary bundle morphology J:171218
abnormal outer hair cell stereociliary bundle morphology J:171218
abnormal vestibular system physiology J:171218
absent cochlear microphonics J:171218
absent distortion product otoacoustic emissions J:171218
circling J:171218
deafness J:171218
decreased inner hair cell stereocilia number J:171218
decreased outer hair cell stereocilia number J:171218
increased or absent threshold for auditory brainstem response J:171218
short inner hair cell stereocilia J:171218
short outer hair cell stereocilia J:171218
Pcdh15tm1.1Ugds/Pcdh15tm1.1Ugds
Myo15atm1.1(cre)Ugds/Myo15a+
involves: 129S1/SvImJ * C57BL/6J
abnormal auditory brainstem response J:209275
abnormal cochlear hair bundle tip links morphology J:209275
abnormal cochlear nerve compound action potential J:209275
abnormal hair cell mechanoelectric transduction J:209275
abnormal outer hair cell stereociliary bundle morphology J:209275
deafness J:209275
decreased inner hair cell stereocilia number J:209275
decreased outer hair cell stereocilia number J:209275
increased or absent threshold for auditory brainstem response J:209275
short inner hair cell stereocilia J:209275
short outer hair cell stereocilia J:209275

Contributing Projects:
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
12/10/2024
MGI 6.24
The Jackson Laboratory