30 phenotypes from 2 alleles in 2 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Apelaem1Shx/Apelaem1Shx involves: C57BL/6J * CBA/Ca2J	no abnormal phenotype detected	J:330639
Apelatm1.2Brre/Apela+ B6(Cg)-Apelatm1.2Brre	abnormal litter size	J:244834
	maternal effect	J:244834
Apelatm1.2Brre/Apelatm1.2Brre B6(Cg)-Apelatm1.2Brre	abnormal angiogenesis	J:244834
	abnormal cardiovascular system morphology	J:244834
	abnormal dorsal aorta morphology	J:244834
	abnormal glomerular capillary endothelium morphology	J:244834
	abnormal heart tube morphology	J:244834
	abnormal intersomitic artery morphology	J:244834
	abnormal litter size	J:244834
	abnormal placenta morphology	J:244834
	abnormal placental labyrinth vasculature morphology	J:244834
	abnormal syncytiotrophoblast morphology	J:244834
	abnormal vascular development	J:244834
	abnormal visceral yolk sac morphology	J:244834
	absent cardiac outflow tract	J:244834
	absent glomerular endothelium fenestra	J:244834
	absent vitelline blood vessels	J:244834
	decreased embryo weight	J:244834
	normal embryo phenotype	J:244834
	embryonic growth retardation	J:244834
	glomerular capillary congestion	J:244834
	increased placenta apoptosis	J:244834
	increased systemic arterial blood pressure	J:244834
	increased urine protein level	J:244834
	lethality, incomplete penetrance	J:244834
	maternal effect	J:244834
	pale yolk sac	J:244834
	pericardial edema	J:244834
	renal glomerular protein deposits	J:244834
	normal renal/urinary system phenotype	J:244834
	thin placenta labyrinth	J:244834