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Symbol
Name
ID

Tprn
taperin
MGI:2139535

Phenotype annotations related to hearing/vestibular/ear

*	Aspects of the system are reported to show a normal phenotype.
	Darker colors indicate more annotations

Human Phenotypes	Sensorineural hearing impairment	Progressive sensorineural hearing impairment
Disease(s) Associated with TPRN	Sensorineural hearing impairment	Progressive sensorineural hearing impairment
autosomal recessive nonsyndromic deafness 79

Mouse Phenotypes		hearing/vestibular/ear phenotype	decreased inner hair cell stereocilia number	decreased outer hair cell stereocilia number	cochlear inner hair cell degeneration	cochlear outer hair cell degeneration	abnormal auditory brainstem response	increased or absent threshold for auditory brainstem response	nonsyndromic hearing loss
Availability	Mouse Genotype	hearing/vestibular/ear phenotype	decreased inner hair cell stereocilia number	decreased outer hair cell stereocilia number	cochlear inner hair cell degeneration	cochlear outer hair cell degeneration	abnormal auditory brainstem response		nonsyndromic hearing loss
	Tprn^em1Pghu/Tprn^em1Pghu	*
	Tprn^{tm1.1(KOMP)Vlcg}/Tprn^{tm1.1(KOMP)Vlcg}

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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