43 phenotypes from 1 allele in 1 genetic background

Allelic Composition Genetic Background	Annotated Term	Reference
Ssr2tm1b(EUCOMM)Wtsi/Ssr2tm1b(EUCOMM)Wtsi C57BL/6N-Ssr2tm1b(EUCOMM)Wtsi/Wtsi	abnormal atrioventricular septum morphology	J:239583
	abnormal diaphragm morphology	J:239583
	abnormal digastric muscle morphology	J:239583
	abnormal ductus venosus valve morphology	J:239583
	abnormal eye muscle morphology	J:239583
	abnormal forebrain morphology	J:239583, J:261316
	abnormal hepatic vein connection	J:239583
	abnormal hyoid bone greater horn morphology	J:239583
	abnormal hypoglossal nerve topology	J:239583
	abnormal inferior vena cava valve morphology	J:239583
	abnormal infrahyoid muscle connection	J:239583
	abnormal interatrial septum morphology	J:239583
	abnormal optic chiasm morphology	J:239583
	abnormal optic cup morphology	J:239583
	abnormal optic nerve morphology	J:239583
	abnormal optic stalk morphology	J:239583
	abnormal placental labyrinth vasculature morphology	J:261316
	abnormal pulmonary valve cusp morphology	J:239583
	abnormal thymus morphology	J:239583
	abnormal Wolffian duct morphology	J:239583
	absent ductus venosus valve	J:239583
	basisphenoid bone foramen	J:239583
	common truncal valve	J:239583
	dilated lateral ventricle	J:239583
	dilated liver sinusoidal space	J:239583
	double outlet right ventricle	J:239583
	enlarged third ventricle	J:239583
	fetal growth retardation	J:239583
	fusion of vertebral arches	J:239583
	hemopericardium	J:239583
	heterochrony	J:239583
	increased trigeminal neuroma incidence	J:239583
	interrupted aortic arch, type b	J:239583
	intracerebral hemorrhage	J:239583
	muscular ventricular septal defect	J:239583
	perimembraneous ventricular septal defect	J:239583, J:261316
	persistent truncus arteriosus	J:239583
	preweaning lethality, complete penetrance	J:261316
	reduced sympathetic cervical ganglion size	J:239583
	scoliosis	J:239583
	small superior cervical ganglion	J:239583
	subcutaneous edema	J:239583
	thin myocardium compact layer	J:239583