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Symbol
Name
ID

Usp53
ubiquitin specific peptidase 53
MGI:2139607

Phenotype annotations related to nervous system

Darker colors indicate more annotations

Human Phenotypes	Cognitive impairment
Disease(s) Associated with USP53	Cognitive impairment
progressive familial intrahepatic cholestasis

Mouse Phenotypes		abnormal orientation of outer hair cell stereociliary bundles	fused outer hair cell stereocilia	cochlear inner hair cell degeneration	abnormal cochlear outer hair cell morphology	cochlear outer hair cell degeneration	cochlear hair cell degeneration	cochlear ganglion degeneration	decreased prepulse inhibition
Availability	Mouse Genotype		fused outer hair cell stereocilia	cochlear inner hair cell degeneration	abnormal cochlear outer hair cell morphology	cochlear outer hair cell degeneration	cochlear hair cell degeneration	cochlear ganglion degeneration	decreased prepulse inhibition
	Usp53^em1(IMPC)Tcp/Usp53^em1(IMPC)Tcp
	Usp53^mbo/Usp53^mbo

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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