41 phenotypes from 2 alleles in 3 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Xpnpep1Gt(S22-1B1)Sor/Xpnpep1Gt(S22-1B1)Sor B6.129S4-Xpnpep1Gt(S22-1B1)Sor	postnatal lethality, complete penetrance	J:193753
Xpnpep1Gt(S22-1B1)Sor/Xpnpep1Gt(S22-1B1)Sor involves: 129S4/SvJae * C57BL/6J	abnormal survival	J:193753
	abnormal urine color	J:193753
	decreased birth body size	J:193753
	decreased body length	J:193753
	decreased body size	J:193753
	decreased body weight	J:193753
	decreased brain size	J:193753
	forebrain hypoplasia	J:193753
	increased urine protein level	J:193753
	microcephaly	J:193753
	postnatal growth retardation	J:193753
	postnatal lethality, incomplete penetrance	J:193753
	prenatal lethality, incomplete penetrance	J:193753
Xpnpep1tm1a(KOMP)Wtsi/Xpnpep1tm1a(KOMP)Wtsi C57BL/6N-Xpnpep1tm1a(KOMP)Wtsi/Wtsi	abnormal aortic valve morphology	J:239583
	abnormal bile duct morphology	J:239583
	abnormal cranium morphology	J:211773
	abnormal eye muscle morphology	J:239583
	abnormal hypoglossal nerve topology	J:239583
	abnormal inferior vena cava morphology	J:239583
	abnormal inferior vena cava valve morphology	J:239583
	abnormal infrahyoid muscle connection	J:239583
	abnormal infrahyoid muscle morphology	J:239583
	abnormal intestine placement	J:239583
	abnormal mitral valve morphology	J:239583
	abnormal Mullerian duct morphology	J:239583
	abnormal superior vena cava morphology	J:239583
	abnormal thymus morphology	J:239583
	abnormal umbilical vein topology	J:239583
	abnormal vertebral artery topology	J:239583
	abnormal vitelline vein topology	J:239583
	blood in lymph vessels	J:239583
	dilated liver sinusoidal space	J:239583
	embryo tumor	J:239583
	increased gamma-delta T cell number	J:211773
	increased hemangioma incidence	J:239583
	increased NK cell number	J:211773
	increased trigeminal neuroma incidence	J:239583
	muscular ventricular septal defect	J:239583
	preweaning lethality, incomplete penetrance	J:211773
	subcutaneous edema	J:239583