Myo6 Phenotype Annotations - Multigenic Genotypes

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Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Myo6
myosin VI
MGI:104785

9 phenotypes from multigenic genotypes

Allelic Composition Genetic Background	Annotated Term	Reference
Bmp5^se Myo6^sv/Bmp5^se Myo6^sv involves: B10.HA/(33NX)Sn * C57BL/6J	prenatal lethality, incomplete penetrance	J:5044
In(9Bmp5-Myo6)5Rl/Bmp5^se Myo6^sv involves: 101/Rl * C3H/Rl	circling	J:100221
	impaired hearing	J:100221
	short ears	J:100221
Myo15a^sh2/Myo15a⁺ Myo6^sv/Myo6⁺ involves: B10.HA/(33NX)Sn	increased susceptibility to age-related hearing loss	J:86379
Myo15a^sh2/Myo15a^sh2 Myo6^sv/Myo6^sv 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

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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