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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
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Allelic Composition
Genetic Background		 Annotated Term Reference
Otoatm1.1(KOMP)Vlcg/Otoatm1.1(KOMP)Vlcg
C57BL/6N-Otoatm1.1(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
Otoatm1Gpr/Otoatm1Gpr
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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Send questions and comments to User Support. 		last database update
04/16/2024
MGI 6.23 		The Jackson Laboratory