35 phenotypes from 2 alleles in 2 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Ssr1em1(IMPC)Mbp/Ssr1+ C57BL/6N-Ssr1em1(IMPC)Mbp/MbpMmucd	abnormal kidney morphology	J:211773
	abnormal liver morphology	J:211773
	abnormal placenta morphology	J:211773
	abnormal skin morphology	J:211773
	abnormal spleen morphology	J:211773
	abnormal testis morphology	J:211773
	abnormal vitreous body morphology	J:211773
	cataract	J:211773
	embryonic growth retardation	J:211773
	enlarged spleen	J:211773
	enlarged testis	J:211773
	microphthalmia	J:211773
	persistence of hyaloid vascular system	J:211773
	small kidney	J:211773
	small liver	J:211773
Ssr1em1(IMPC)Mbp/Ssr1em1(IMPC)Mbp C57BL/6N-Ssr1em1(IMPC)Mbp/MbpMmucd	abnormal blood vessel morphology	J:211773
	abnormal placenta morphology	J:211773
	abnormal placenta size	J:211773
	abnormal placenta vasculature	J:211773
	edema	J:211773
	embryonic growth retardation	J:211773
	preweaning lethality, complete penetrance	J:211773
Ssr1Gt(ble-lacZl)16Brr/Ssr1Gt(ble-lacZl)16Brr involves: 129S2/SvPas	abnormal cardiac epithelial to mesenchymal transition	J:115006
	abnormal heart development	J:115006
	abnormal heart ventricle morphology	J:115006
	abnormal interventricular septum morphology	J:115006
	abnormal semilunar valve morphology	J:115006
	abnormal truncus arteriosus septation	J:115006
	aorticopulmonary septal defect	J:115006
	decreased fetal size	J:115006
	dilated heart left ventricle	J:115006
	dilated heart right ventricle	J:115006
	double outlet right ventricle	J:115006
	edema	J:115006
	enlarged heart	J:115006
	failure of conotruncal ridge closure	J:115006
	neonatal lethality, complete penetrance	J:115006
	persistent truncus arteriosus	J:115006