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Symbol
Name
ID

Tprn
taperin
MGI:2139535

Phenotype annotations related to nervous system

Darker colors indicate more annotations

Human Phenotypes	Delayed speech and language development
Disease(s) Associated with TPRN	Delayed speech and language development
autosomal recessive nonsyndromic deafness 79

Mouse Phenotypes		decreased inner hair cell stereocilia number	decreased outer hair cell stereocilia number	cochlear inner hair cell degeneration	cochlear outer hair cell degeneration	decreased prepulse inhibition
Availability	Mouse Genotype	decreased inner hair cell stereocilia number	decreased outer hair cell stereocilia number	cochlear inner hair cell degeneration	cochlear outer hair cell degeneration	decreased prepulse inhibition
	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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