35 phenotypes from 2 alleles in 2 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Ehbp1l1em1Aha/Ehbp1l1em1Aha Not Specified	abnormal small intestinal microvillus morphology	J:236573
	anemia	J:236573
	decreased small intestinal microvillus size	J:236573
	neonatal lethality, complete penetrance	J:236573
Ehbp1l1tm1a(EUCOMM)Wtsi/Ehbp1l1tm1a(EUCOMM)Wtsi C57BL/6N-Ehbp1l1tm1a(EUCOMM)Wtsi/Wtsi	abnormal aortic valve cusp morphology	J:239583
	abnormal bile duct morphology	J:239583
	abnormal cystic duct morphology	J:239583
	abnormal ductus venosus valve morphology	J:239583
	abnormal eye muscle morphology	J:239583
	abnormal lens morphology	J:239583
	abnormal Mullerian duct morphology	J:239583
	abnormal Mullerian duct topology	J:239583
	abnormal nasal cavity morphology	J:239583
	abnormal nasal septum morphology	J:239583
	abnormal optic chiasm morphology	J:239583
	abnormal optic cup morphology	J:239583
	abnormal optic stalk morphology	J:239583
	absent celiac artery	J:239583
	absent ductus venosus valve	J:239583
	absent olfactory nerve	J:239583
	additional anastomosis between intracranial vertebral arteries	J:239583
	aphakia	J:239583
	blood in lymph vessels	J:239583
	coloboma	J:239583
	decreased tongue size	J:239583
	dilated liver sinusoidal space	J:239583
	dual inferior vena cava	J:239583
	embryo tumor	J:239583
	fused incisors	J:239583
	increased trigeminal neuroma incidence	J:239583
	perimembraneous ventricular septal defect	J:239583
	preweaning lethality, complete penetrance	J:211773
	retrolental blood	J:239583
	subcutaneous edema	J:239583
	thin myocardium	J:239583