Mir96 Phenotype Annotations

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Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Mir96
microRNA 96
MGI:3619440

15 phenotypes from 2 alleles in 2 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Mir96^Dmdo/Mir96⁺ C3HeB/FeJ-Mir96^Dmdo	abnormal cochlear hair cell stereociliary bundle morphology	J:151354
	abnormal pinna reflex	J:151354
	cochlear hair cell degeneration	J:151354
	cochlear outer hair cell degeneration	J:151354
	decreased cochlear nerve compound action potential	J:151354
	fused vestibular hair cell stereocilia	J:151354
	impaired hearing	J:151354
Mir96^Dmdo/Mir96^Dmdo C3HeB/FeJ-Mir96^Dmdo	abnormal cochlear hair cell stereociliary bundle morphology	J:151354
	abnormal gait	J:151354
	absent cochlear nerve compound action potential	J:151354
	absent pinna reflex	J:151354
	circling	J:151354
	cochlear hair cell degeneration	J:151354
	deafness	J:151354
	decreased cochlear hair cell number	J:151354
	head bobbing	J:151354
Mir96^tm2.2Wtsi/Mir96^tm2.2Wtsi C57BL/6N-Mir96^tm2.2Wtsi/Wtsi	no abnormal phenotype detected	J:239583

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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