Otoa Phenotype Annotations

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Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Otoa
otoancorin
MGI:2149209

10 phenotypes from 2 alleles in 2 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Otoa^{tm1.1(KOMP)Vlcg}/Otoa^{tm1.1(KOMP)Vlcg} C57BL/6N-Otoa^{tm1.1(KOMP)Vlcg}/Ucd	abnormal auditory brainstem response	J:211773
	decreased mean corpuscular hemoglobin	J:211773
	decreased prepulse inhibition	J:211773
	increased startle reflex	J:211773
Otoa^tm1Gpr/Otoa^tm1Gpr involves: 129S/SvEv	abnormal cochlear nerve compound action potential	J:192263
	abnormal tectorial membrane morphology	J:192263
	absent Hensen stripe	J:192263
	detached tectorial membrane	J:192263
	normal hearing/vestibular/ear phenotype	J:192263
	impaired hearing	J:192263

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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