32 phenotypes from 1 allele in 1 genetic background

Allelic Composition Genetic Background	Annotated Term	Reference
Cir1tm3a(KOMP)Wtsi/Cir1tm3a(KOMP)Wtsi C57BL/6N-Cir1tm3a(KOMP)Wtsi/Wtsi	abnormal atrioventricular cushion morphology	J:239583
	abnormal eye muscle morphology	J:239583
	abnormal forebrain morphology	J:239583
	abnormal hypoglossal nerve topology	J:239583
	abnormal large intestine morphology	J:239583
	abnormal Mullerian duct morphology	J:239583
	abnormal optic cup morphology	J:239583
	abnormal placenta morphology	J:261316
	abnormal placental labyrinth vasculature morphology	J:261316
	abnormal pulmonary valve cusp morphology	J:239583
	abnormal thyroid gland morphology	J:239583
	abnormal ureter morphology	J:239583
	abnormal Wolffian duct morphology	J:239583
	absent costovertebral joint	J:239583
	absent intracranial segment of vertebral artery	J:239583
	absent vertebral pedicles	J:239583
	additional anastomosis between intracranial vertebral arteries	J:239583
	decreased cervical vertebrae number	J:239583
	decreased rib number	J:239583
	fusion of vertebral arches	J:239583
	heterochrony	J:239583
	multiple persisting craniopharyngeal ducts	J:239583
	occipital bone foramen	J:239583
	overriding aortic valve	J:239583
	perimembraneous ventricular septal defect	J:239583
	persistent trigeminal artery	J:239583
	preweaning lethality, complete penetrance	J:261316
	rib bifurcation	J:239583
	rib fusion	J:239583
	scoliosis	J:239583
	small kidney	J:239583
	subcutaneous edema	J:239583