40 phenotypes from multigenic genotypes

Allelic Composition Genetic Background	Annotated Term	Reference
Cisd2tm1Tfts/Cisd2+ B6.129S7-Cisd2tm1Tfts	decreased bone mineral density of femur	J:148467
	premature death	J:148467
Cisd2tm1Tfts/Cisd2tm1Tfts B6.129S7-Cisd2tm1Tfts	abnormal coat/hair pigmentation	J:148467
	abnormal defecation	J:148467
	abnormal glucose homeostasis	J:148467
	abnormal mitochondrial morphology	J:148467
	abnormal muscle fiber morphology	J:148467
	abnormal myocardium layer morphology	J:148467
	abnormal optic nerve morphology	J:148467
	abnormal respiratory electron transport chain	J:148467
	abnormal respiratory function	J:148467
	axon degeneration	J:148467
	blindness	J:148467
	corneal opacity	J:148467
	decreased body mass index	J:148467
	decreased body size	J:148467
	decreased body weight	J:148467
	decreased bone mineral density of femur	J:148467
	decreased fluid intake	J:148467
	decreased food intake	J:148467
	decreased hair follicle number	J:148467
	decreased insulin secretion	J:148467
	decreased oxygen consumption	J:148467
	decreased subcutaneous adipose tissue amount	J:148467
	decreased tidal volume	J:148467
	decreased total body fat amount	J:148467
	decreased trabecular bone thickness	J:148467
	demyelination	J:148467
	exophthalmos	J:148467
	impaired glucose tolerance	J:148467
	increased insulin sensitivity	J:148467
	lordokyphosis	J:148467
	muscle degeneration	J:148467
	neurodegeneration	J:148467
	oliguria	J:148467
	postnatal growth retardation	J:148467
	premature aging	J:148467
	premature death	J:148467
	prominent ears	J:148467
	retina neovascularization	J:148467
	small thoracic cavity	J:148467
	thick epidermis	J:148467
Cisd2tm1Tfts/Cisd2tm1Tfts involves: 129S7/SvEvBrd * C57BL/6	premature aging	J:148467