44 phenotypes from multigenic genotypes

Allelic Composition Genetic Background	Annotated Term	Reference
Cdkn1atm1Tyj/Cdkn1atm1Tyj Cdkn2dtm1Maro/Cdkn2dtm1Maro involves: 129P2/OlaHsd * 129S2/SvPas * 129X1/SvJ * C57BL/6 * CD-1	abnormal cochlear hair cell physiology	J:118337
	abnormal cochlear inner hair cell morphology	J:118337
	decreased cochlear hair cell number	J:118337
	decreased cochlear inner hair cell number	J:118337
	decreased cochlear outer hair cell number	J:118337
	increased cochlear hair cell number	J:118337
	polyploidy	J:118337
Cdkn1btm1Mlf/Cdkn1btm1Mlf Cdkn2dtm1Maro/Cdkn2dtm1Maro involves: 129X1/SvJ * C57BL/6	abnormal behavior	J:58522
	abnormal mitosis	J:58522
	abnormal neuron morphology	J:58522
	bradykinesia	J:58522
	cachexia	J:58522
	decreased body size	J:58522
	dehydration	J:58522
	impaired righting response	J:58522
	increased cell proliferation	J:58522
	increased mitotic index	J:58522
	increased neuron apoptosis	J:58522
	limb grasping	J:58522
	muscle hypertonia	J:58522
	normal nervous system phenotype	J:58522
	paresis	J:58522
	photosensitivity	J:58522
	postnatal lethality, complete penetrance	J:58522
	respiratory distress	J:58522
	seizures	J:58522
	tremors	J:58522
	weight loss	J:58522
Cdkn2ctm1Bbd/Cdkn2ctm1Bbd Cdkn2dtm1Maro/Cdkn2dtm1Maro involves: 129P2/OlaHsd * 129S1/Sv * C57BL/6	abnormal germ cell morphology	J:68829
	abnormal Leydig cell differentiation	J:68829
	abnormal male meiosis	J:68829
	abnormal spermatogenesis	J:68829
	asthenozoospermia	J:68829
	decreased circulating testosterone level	J:68829
	decreased germ cell number	J:68829
	increased body weight	J:68829
	increased circulating follicle stimulating hormone level	J:68829
	increased Leydig cell number	J:68829
	increased pheochromocytoma incidence	J:68829
	increased pituitary adenoma incidence	J:68829
	male infertility	J:68829
	oligozoospermia	J:68829
	seminiferous tubule degeneration	J:68829
	testicular atrophy	J:68829