69 phenotypes from 3 alleles in 3 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Epg5em1(IMPC)H/Epg5em1(IMPC)H C57BL/6NTac-Epg5em1(IMPC)H/H	abnormal gait	J:211773
	decreased circulating glucose level	J:211773
	decreased circulating serum albumin level	J:211773
	decreased lymphocyte cell number	J:211773
	decreased prepulse inhibition	J:211773
	decreased startle reflex	J:211773
	hyperactivity	J:211773
	increased basophil cell number	J:211773
	increased bone mineral density	J:211773
	increased circulating alanine transaminase level	J:211773
	increased circulating alkaline phosphatase level	J:211773
	increased circulating amylase level	J:211773
	increased circulating aspartate transaminase level	J:211773
	increased circulating iron level	J:211773
	increased heart rate	J:211773
	increased large unstained cell number	J:211773
	increased leukocyte cell number	J:211773
	increased lymphocyte cell number	J:211773
	increased monocyte cell number	J:211773
	increased neutrophil cell number	J:211773
	increased red blood cell distribution width	J:211773
	increased spleen weight	J:211773
	short tibia	J:211773
	tremors	J:211773
Epg5M1Btlr/Epg5M1Btlr C57BL/6J-Epg5M1Btlr	circling	J:272115
	tremors	J:272115
Epg5tm1Ygz/Epg5tm1Ygz involves: 129S1/Sv * 129X1/SvJ * C57BL/6N	abnormal autophagy	J:196603
	abnormal electroretinogram waveform feature	J:279837
	abnormal hippocampus morphology	J:196603
	abnormal hippocampus pyramidal cell layer	J:196603
	abnormal innervation	J:196603
	abnormal motor capabilities/coordination/movement	J:196603
	abnormal motor neuron morphology	J:196603
	abnormal muscle fiber morphology	J:196603
	abnormal photoreceptor inner segment morphology	J:279837
	abnormal photoreceptor outer segment size	J:279837
	abnormal Z line morphology	J:196603
	astrocytosis	J:279837
	axonal spheroids	J:196603
	centrally nucleated skeletal muscle fibers	J:196603
	decreased b-wave amplitude	J:279837
	decreased body weight	J:196603
	decreased cerebral cortex pyramidal cell number	J:196603
	decreased hippocampus pyramidal cell number	J:196603
	decreased motor neuron number	J:196603
	decreased retina cone cell number	J:279837
	decreased skeletal muscle fiber size	J:196603
	decreased white adipose tissue amount	J:196603
	decreased white fat cell lipid droplet size	J:196603
	decreased white fat cell size	J:196603
	hindlimb paralysis	J:196603
	impaired autophagy	J:279837
	impaired coordination	J:196603
	increased mitochondrial size	J:196603
	increased retina apoptosis	J:279837
	kyphosis	J:196603
	limb grasping	J:196603
	normal liver/biliary system phenotype	J:196603
	microgliosis	J:196603
	muscular atrophy	J:196603
	neuronal cytoplasmic inclusions	J:196603
	poor grooming	J:196603
	postnatal growth retardation	J:196603
	premature death	J:196603, J:279837
	retina outer nuclear layer degeneration	J:279837
	retina photoreceptor degeneration	J:279837
	retina rod cell degeneration	J:279837
	rough coat	J:196603
	skeletal muscle fiber degeneration	J:196603
	thin retina outer nuclear layer	J:279837