39 phenotypes from 3 alleles in 4 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Guloem1(IMPC)Ccpcz/Guloem1(IMPC)Ccpcz C57BL/6NCrl-Guloem1(IMPC)Ccpcz/Ccpcz	abnormal eye morphology	J:211773
	abnormal heart morphology	J:211773
	abnormal optic disk morphology	J:211773
	abnormal spleen morphology	J:211773
	anophthalmia	J:211773
	decreased lean body mass	J:211773
	enlarged heart	J:211773
	enlarged spleen	J:211773
	hyperactivity	J:211773
	increased circulating cholesterol level	J:211773
	increased circulating HDL cholesterol level	J:211773
Gulosfx-2J/Gulosfx-2J RB156Bnr/Ei Dsprul Gulosfx-2J/GrsrJ	abnormal bone mineralization	J:96441
	abnormal gait	J:96441
	abnormal retina morphology	J:96441
	abnormal trabecular bone morphology	J:96441
	cataract	J:96441
	decreased body size	J:96441
	decreased bone mineral density	J:96441
	decreased compact bone thickness	J:96441
	femur fracture	J:96441
	hindlimb paralysis	J:96441
	premature death	J:96441
	rickets	J:96441
Gulotm1Mae/Gulotm1Mae involves: 129 * C57BL/6	abnormal aorta elastic tissue morphology	J:59931
	abnormal aorta endothelium morphology	J:59931
	abnormal aorta smooth muscle morphology	J:59931
	abnormal vitamin C level	J:59931
	anemia	J:59931
	decreased circulating HDL cholesterol level	J:59931
	decreased erythrocyte cell number	J:59931
	decreased hematocrit	J:59931
	decreased mean corpuscular hemoglobin	J:59931
	gastrointestinal hemorrhage	J:59931
	hemarthrosis	J:59931
	hemorrhage	J:59931
	increased circulating cholesterol level	J:59931
	increased vascular permeability	J:59931
	postnatal growth retardation	J:59931
	premature death	J:59931
	weight loss	J:59931
Gulotm1Mae/Gulotm1Mae involves: C57BL/6	abnormal vitamin C level	J:164548
	premature death	J:164548
	rachitic rosary	J:164548