Tprn Phenotype Annotations

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Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Tprn
taperin
MGI:2139535

10 phenotypes from 2 alleles in 2 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Tprn^em1Pghu/Tprn^em1Pghu B6.Cg-Tprn^em1Pghu	cochlear inner hair cell degeneration	J:240563
	cochlear outer hair cell degeneration	J:240563
	decreased inner hair cell stereocilia number	J:240563
	decreased outer hair cell stereocilia number	J:240563
	normal hearing/vestibular/ear phenotype	J:240563
	increased or absent threshold for auditory brainstem response	J:240563
	nonsyndromic hearing loss	J:240563
Tprn^{tm1.1(KOMP)Vlcg}/Tprn^{tm1.1(KOMP)Vlcg} C57BL/6N-Tprn^{tm1.1(KOMP)Vlcg}/J	abnormal auditory brainstem response	J:211773
	decreased prepulse inhibition	J:211773
	decreased startle reflex	J:211773

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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