30 phenotypes from 2 alleles in 3 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Usp53em1(IMPC)Tcp/Usp53em1(IMPC)Tcp C57BL/6N-Usp53em1(IMPC)Tcp/Tcp	abnormal auditory brainstem response	J:211773
	abnormal coat/ hair morphology	J:211773
	abnormal startle reflex	J:211773
	cataract	J:211773
	decreased bone mineral content	J:211773
	decreased bone mineral density	J:211773
	decreased prepulse inhibition	J:211773
	decreased startle reflex	J:211773
	increased circulating alkaline phosphatase level	J:211773
	increased circulating bilirubin level	J:211773
	increased circulating cholesterol level	J:211773
	increased circulating total protein level	J:211773
	prolonged PR interval	J:211773
Usp53mbo/Usp53+ involves: BALB/cByJ * C57BL/6J	normal hearing/vestibular/ear phenotype	J:227841
	increased susceptibility to noise-induced hearing loss	J:227841
Usp53mbo/Usp53mbo involves: BALB/cByJ * C57BL/6J	abnormal cochlear outer hair cell morphology	J:227841
	abnormal orientation of outer hair cell stereociliary bundles	J:227841
	absent distortion product otoacoustic emissions	J:227841
	normal behavior/neurological phenotype	J:227841
	cochlear ganglion degeneration	J:227841
	cochlear hair cell degeneration	J:227841
	cochlear inner hair cell degeneration	J:227841
	cochlear outer hair cell degeneration	J:227841
	deafness	J:227841
	decreased endocochlear potential	J:227841
	Deiters cell degeneration	J:227841
	fused outer hair cell stereocilia	J:227841
	increased or absent threshold for auditory brainstem response	J:227841
	nonsyndromic hearing loss	J:227841
	organ of Corti degeneration	J:227841
Usp53mbo/Usp53mbo involves: C57BL/6J	decreased startle reflex	J:119820
	increased or absent threshold for auditory brainstem response	J:119820