50 phenotypes from 2 alleles in 2 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Atp11atm1a(KOMP)Wtsi/Atp11atm1a(KOMP)Wtsi C57BL/6N-Atp11atm1a(KOMP)Wtsi/Wtsi	abnormal adenohypophysis morphology	J:239583
	abnormal artery morphology	J:239583
	abnormal carotid artery morphology	J:239583
	abnormal coronary sinus connection	J:239583
	abnormal elbow joint morphology	J:239583
	abnormal eye morphology	J:239583
	abnormal eye muscle morphology	J:239583
	abnormal larynx morphology	J:239583
	abnormal Meckel's cartilage morphology	J:239583
	abnormal Mullerian duct morphology	J:239583
	abnormal nasal cavity morphology	J:239583
	abnormal olfactory bulb morphology	J:239583
	abnormal olfactory nerve morphology	J:239583
	abnormal optic cup morphology	J:239583
	abnormal optic stalk morphology	J:239583
	abnormal placental labyrinth vasculature morphology	J:261316
	abnormal thymus morphology	J:239583
	abnormal umbilical vein topology	J:239583
	abnormal vertebral artery morphology	J:239583
	abnormal vitelline vein topology	J:239583
	absent ductus venosus valve	J:239583
	absent olfactory nerve	J:239583
	absent pectinate muscle	J:239583
	additional anastomosis between intracranial vertebral arteries	J:239583
	aorta coarctation	J:239583
	aphakia	J:239583
	dilated liver sinusoidal space	J:239583
	exencephaly	J:239583
	herniated liver	J:239583
	heterochrony	J:239583
	increased rib number	J:239583
	increased trigeminal neuroma incidence	J:239583
	liver hypoplasia	J:239583
	multiple persisting craniopharyngeal ducts	J:239583
	muscular ventricular septal defect	J:239583, J:261316
	narrow eye opening	J:239583
	overriding aortic valve	J:239583
	perimembraneous ventricular septal defect	J:239583
	persistent trigeminal artery	J:239583
	placenta hemorrhage	J:261316
	preweaning lethality, complete penetrance	J:261316
	reduced sympathetic cervical ganglion size	J:239583
	small placenta	J:261316
	small superior cervical ganglion	J:239583
	subcutaneous edema	J:239583
	thin myocardium compact layer	J:239583
	umbilical vein stenosis	J:239583
Atp11atm1c(KOMP)Wtsi/Atp11atm1c(KOMP)Wtsi Myf5tm3(cre)Sor/Myf5+ involves: 129S4/SvJaeSor * C57BL/6JJcl * C57BL/6N	abnormal myoblast differentiation	J:262981
	abnormal skeletal muscle regeneration	J:262981
	normal muscle phenotype	J:262981