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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
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Allelic Composition
Genetic Background		 Annotated Term Reference
Mir96Dmdo/Mir96+
C3HeB/FeJ-Mir96Dmdo 		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
Mir96Dmdo/Mir96Dmdo
C3HeB/FeJ-Mir96Dmdo 		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
Mir96tm2.1Wtsi/Mir96tm2.1Wtsi
C57BL/6N-Mir96tm2.1Wtsi/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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Send questions and comments to User Support. 		last database update
12/10/2024
MGI 6.24 		The Jackson Laboratory