Myo3a Phenotype Annotations

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Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Myo3a
myosin IIIA
MGI:2183924

10 phenotypes from 3 alleles in 3 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Myo3a^tm1.1Mckg/Myo3a^tm1.1Mckg C57BL/6-Myo3a^tm1.1Mckg	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
Myo3a^{tm1b(KOMP)Wtsi}/Myo3a^{tm1b(KOMP)Wtsi} C57BL/6N-Myo3a^{tm1b(KOMP)Wtsi}/J	abnormal auditory brainstem response	J:211773
	decreased thigmotaxis	J:211773
	hyperactivity	J:211773
	impaired glucose tolerance	J:211773
Myo3a^tm1Pgg/Myo3a^tm1Pgg B6.129-Myo3a^tm1Pgg	normal hearing/vestibular/ear phenotype	J:236347

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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