Tprn Phenotype Annotations

About Help FAQ

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
	abnormal startle reflex	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)
Citing These Resources Funding Information Warranty Disclaimer, Privacy Notice, Licensing, & Copyright Send questions and comments to User Support.	last database update 12/10/2024 MGI 6.24