50 phenotypes from 3 alleles in 4 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Ppt1tm1.1Dprc/Ppt1tm1.1Dprc involves: 129S6/SvEvTac * BALB/cJ * C57BL/6	abnormal microglial cell activation	J:213552
	abnormal motor coordination/balance	J:213552
	astrocytosis	J:213552
	decreased exploration in new environment	J:213552
	impaired coordination	J:213552
	increased body weight	J:213552
	lipofuscinosis	J:213552
Ppt1tm1Aj/Ppt1tm1Aj involves: 129S4/SvJae * C57BL/6	abnormal brain morphology	J:95522
	abnormal cerebral cortex morphology	J:95522
	abnormal hippocampus morphology	J:95522
	abnormal kidney morphology	J:95522
	abnormal liver morphology	J:95522
	abnormal podocyte morphology	J:95522
	abnormal retina neuronal layer morphology	J:95522
	abnormal spleen morphology	J:95522
	blindness	J:95522
	brain atrophy	J:95522
	brain inflammation	J:95522
	decreased brain weight	J:95522
	hindlimb paralysis	J:95522
	limb grasping	J:95522
	loss of cortex neurons	J:95522
	loss of GABAergic neurons	J:95522
	myoclonus	J:95522
	neurodegeneration	J:95522
	premature death	J:95522
	seizures	J:95522
Ppt1tm1Hof/Ppt1tm1Hof involves: 129P2/OlaHsd * 129S2/SvPas * 129S6/SvEvTac * C57BL/6	abnormal brain morphology	J:177265
	abnormal cytokine level	J:177265
	abnormal visual cortex morphology	J:177265
	astrocytosis	J:177265
	brain atrophy	J:177265
	brain inflammation	J:177265
	decreased brain weight	J:177265
	hippocampal neuron degeneration	J:177265
	neurodegeneration	J:177265
	premature death	J:177265
	thin cerebral cortex	J:177265
Ppt1tm1Hof/Ppt1tm1Hof involves: 129S6/SvEvTac * C57BL/6J	abnormal aggression-related behavior	J:72931
	abnormal brain morphology	J:72931
	abnormal gait	J:72931
	abnormal retina cone bipolar cell morphology	J:280337
	abnormal retina rod bipolar cell morphology	J:280337
	astrocytosis	J:280337
	decreased brain size	J:72931
	decreased grooming behavior	J:72931
	decreased retina cone cell number	J:280337
	decreased retina photoreceptor cell number	J:280337
	decreased total retina thickness	J:280337
	hindlimb paralysis	J:72931
	hippocampal neuron degeneration	J:72931
	jerky movement	J:72931
	microgliosis	J:280337
	myoclonus	J:72931
	neurodegeneration	J:72931
	premature death	J:72931
	Purkinje cell degeneration	J:72931
	retina deposits	J:280337
	retina ganglion cell degeneration	J:280337
	retina gliosis	J:280337
	retina photoreceptor degeneration	J:280337
	thick neurocranium	J:72931
	thin retina inner nuclear layer	J:280337
	thin retina outer nuclear layer	J:280337