38 phenotypes from 2 alleles in 3 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Pierce1Gt(OST3440)Lex/Pierce1Gt(OST3440)Lex either: (involves: 129S5/SvEvBrd * C57BL/6J) or (involves: 129S5/SvEvBrd * C57BL/6J * FVB/N)	abnormal heart left ventricle morphology	J:252050
	abnormal heart morphology	J:252050
	abnormal kidney morphology	J:252050
	abnormal lateral plate mesoderm morphology	J:252050
	abnormal left-right axis patterning	J:252050
	abnormal liver lobule morphology	J:252050
	abnormal lung lobe morphology	J:252050
	abnormal lung position or orientation	J:252050
	abnormal mitral valve morphology	J:252050
	abnormal primitive node morphology	J:252050
	abnormal spleen morphology	J:252050
	dextrocardia	J:252050
	dilated heart atrium	J:252050
	heart hypoplasia	J:252050
	heterotaxia	J:252050
	left pulmonary isomerism	J:252050
	left sided inferior vena cava	J:252050
	lethality throughout fetal growth and development, incomplete penetrance	J:252050
	mesocardia	J:252050
	persistent truncus arteriosus	J:252050
	right pulmonary isomerism	J:252050
	right-sided stomach	J:252050
	situs inversus totalis	J:252050
	ventricular septal defect	J:252050
Pierce1tm2b(EUCOMM)Wtsi/Pierce1tm2b(EUCOMM)Wtsi C57BL/6N-Pierce1tm2b(EUCOMM)Wtsi/Wtsi	abnormal aortic valve cusp morphology	J:239583
	abnormal vertebral artery topology	J:239583
	absent segment of posterior cerebral artery	J:239583
	blood in lymph vessels	J:239583
	heterochrony	J:239583
	increased grip strength	J:211773
	muscular ventricular septal defect	J:239583
	no abnormal phenotype detected	J:239583
	retropleural edema	J:239583
	situs inversus totalis	J:239583
Pierce1tm2b(EUCOMM)Wtsi/Pierce1tm2b(EUCOMM)Wtsi involves: C57BL/6N	abnormal motile primary cilium physiology	J:316131
	abnormal respiratory motile cilium physiology	J:316131
	prenatal lethality, incomplete penetrance	J:316131
	situs ambiguus	J:316131
	situs inversus	J:316131