35 phenotypes from 2 alleles in 2 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Coro1ctm1a(KOMP)Wtsi/Coro1c+ C57BL/6N-Coro1ctm1a(KOMP)Wtsi/Wtsi	decreased mean corpuscular hemoglobin	J:211773
	increased erythrocyte cell number	J:211773
Coro1ctm1a(KOMP)Wtsi/Coro1ctm1a(KOMP)Wtsi C57BL/6N-Coro1ctm1a(KOMP)Wtsi/Wtsi	abnormal cervical rib	J:239583
	abnormal coronary sinus connection	J:239583
	abnormal cystic duct morphology	J:239583
	abnormal eye muscle morphology	J:239583
	abnormal forebrain morphology	J:239583
	abnormal inferior vena cava valve morphology	J:239583
	abnormal interatrial septum morphology	J:239583
	abnormal ovary morphology	J:239583
	abnormal third ventricle morphology	J:239583
	abnormal vertebral artery topology	J:239583
	abnormal viscerocranium morphology	J:239583
	abnormal vitelline vein connection	J:239583
	absent ductus venosus valve	J:239583
	basisphenoid bone foramen	J:239583
	blood in lymph vessels	J:239583
	decreased parotid gland size	J:239583
	dilated bile duct	J:239583
	dilated liver sinusoidal space	J:239583
	embryo tumor	J:239583
	epididymal cyst	J:239583
	exencephaly	J:239583
	heterochrony	J:239583
	multiple persisting craniopharyngeal ducts	J:239583
	no abnormal phenotype detected	J:239583
	small superior cervical ganglion	J:239583
	subcutaneous edema	J:239583
Coro1ctm1d(KOMP)Wtsi/Coro1ctm1d(KOMP)Wtsi involves: C57BL/6N	abnormal platelet morphology	J:290447
	decreased locomotor activity	J:290447
	decreased startle reflex	J:290447
	decreased urination frequency	J:290447
	increased circulating alkaline phosphatase level	J:290447
	increased or absent threshold for auditory brainstem response	J:290447
	thrombocytosis	J:290447