65 phenotypes from 2 alleles in 3 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Scarb2em2(IMPC)Tcp/Scarb2em2(IMPC)Tcp C57BL/6NCrl-Scarb2em2(IMPC)Tcp/Tcp	abnormal QT variability	J:211773
	abnormal sinus arrhythmia	J:211773
	cardiovascular system phenotype	J:211773
	decreased mean corpuscular volume	J:211773
	decreased monocyte cell number	J:211773
	decreased total body fat amount	J:211773
	enlarged kidney	J:211773
	enlarged lymph nodes	J:211773
	increased blood urea nitrogen level	J:211773
	increased bone mineral content	J:211773
	increased circulating calcium level	J:211773
	increased heart rate variability	J:211773
	increased lean body mass	J:211773
	increased leukocyte cell number	J:211773
	increased lymphocyte cell number	J:211773
	increased neutrophil cell number	J:211773
	preweaning lethality, incomplete penetrance	J:211773
	prolonged RR interval	J:211773
	thrombocytosis	J:211773
Scarb2tm1Psa/Scarb2tm1Psa involves: 129P2/OlaHsd * C57BL/6J	abnormal auditory brainstem response	J:82474, J:121998
	abnormal distortion product otoacoustic emission	J:121998
	abnormal nervous system morphology	J:82474
	abnormal otolithic membrane morphology	J:82474
	abnormal phrenic nerve morphology	J:82474
	abnormal Schwann cell morphology	J:82474
	abnormal stria vascularis morphology	J:82474, J:121998
	abnormal stria vascularis vasculature morphology	J:121998
	abnormal strial marginal cell morphology	J:82474, J:121998
	abnormal ureter morphology	J:82474
	abnormal ureter smooth muscle morphology	J:82474
	abnormal ureteropelvic junction morphology	J:82474
	abnormal urothelium morphology	J:82474
	abnormal vestibular hair cell physiology	J:121998
	absent endocochlear potential	J:82474
	absent otoliths	J:82474
	absent startle reflex	J:82474
	albuminuria	J:82474
	cochlear ganglion degeneration	J:82474, J:121998
	cochlear inner hair cell degeneration	J:82474
	cochlear outer hair cell degeneration	J:82474
	deafness	J:82474
	decreased endocochlear potential	J:82474
	decreased urine glucose level	J:82474
	decreased urine osmolality	J:82474
	demyelination	J:82474
	dilated kidney calyx	J:82474
	distended abdomen	J:82474
	hydronephrosis	J:82474
	leukocyturia	J:82474
	polydipsia	J:82474
	polyuria	J:82474
	premature death	J:82474
	sensorineural hearing loss	J:121998
	stria vascularis degeneration	J:82474, J:121998
	ureteropelvic junction obstruction	J:82474
Scarb2tm1Psa/Scarb2tm1Psa involves: 129P2/OlaHsd * C57BL/6N	abnormal behavior	J:216676
	abnormal enzyme/coenzyme activity	J:216676
	abnormal nervous system morphology	J:216676
	abnormal neuron morphology	J:216676
	astrocytosis	J:216676
	decreased body weight	J:216676
	limb grasping	J:216676
	microgliosis	J:216676
	neurodegeneration	J:216676
	paralysis	J:216676
	premature death	J:216676
	tremors	J:216676