38 phenotypes from 2 alleles in 3 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Ppiaem1(IMPC)Mbp/Ppiaem1(IMPC)Mbp C57BL/6NCrl-Ppiaem1(IMPC)Mbp/MbpMmucd	abnormal auditory brainstem response	J:211773
	abnormal colon morphology	J:211773
	abnormal eye morphology	J:211773
	abnormal kidney morphology	J:211773
	abnormal spleen morphology	J:211773
	abnormal vitreous body morphology	J:211773
	cataract	J:211773
	decreased body length	J:211773
	decreased erythrocyte cell number	J:211773
	decreased heart weight	J:211773
	enlarged spleen	J:211773
	increased blood urea nitrogen level	J:211773
	increased circulating alkaline phosphatase level	J:211773
	increased mean corpuscular hemoglobin	J:211773
	increased mean corpuscular volume	J:211773
	increased mean platelet volume	J:211773
	increased red blood cell distribution width	J:211773
	increased spleen weight	J:211773
	megacolon	J:211773
	microphthalmia	J:211773
	small kidney	J:211773
Ppiatm1Lubn/Ppiatm1Lubn 129S6.129P2-Ppiatm1Lubn	abnormal CD4-positive, alpha-beta T cell physiology	J:93591
	blepharitis	J:93591
	heart inflammation	J:93591
	increased circulating interleukin-4 level	J:93591
	increased IgE level	J:93591
	increased IgG1 level	J:93591
	increased immunoglobulin level	J:93591
	increased inflammatory response	J:93591
	increased interleukin-2 secretion	J:93591
	increased interleukin-4 secretion	J:93591
	increased susceptibility to type I hypersensitivity reaction	J:93591
	increased T cell number	J:93591
	liver inflammation	J:93591
	pancreas inflammation	J:93591
	postnatal lethality, incomplete penetrance	J:93591
	prenatal lethality, incomplete penetrance	J:93591
	spleen hyperplasia	J:93591
Ppiatm1Lubn/Ppiatm1Lubn involves: 129P2/OlaHsd * MF1	prenatal lethality, incomplete penetrance	J:93591