28 phenotypes from 3 alleles in 4 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Flvcr1tm1.1Jlab/Flvcr1+ involves: 129S4/SvJae * C57BL/6 * DBA/2	no abnormal phenotype detected	J:132057
Flvcr1tm1.1Jlab/Flvcr1tm1.1Jlab B6.129S4-Flvcr1tm1.1Jlab	abnormal craniofacial morphology	J:132057
	abnormal limb development	J:132057
	embryonic lethality during organogenesis, incomplete penetrance	J:132057
Flvcr1tm1.1Jlab/Flvcr1tm1.1Jlab involves: 129S4/SvJae * C57BL/6 * DBA/2	abnormal autopod morphology	J:132057
	abnormal erythropoiesis	J:132057
	abnormal spleen morphology	J:132057
	anemia	J:132057
	decreased body size	J:132057
	enlarged heart	J:132057
	enlarged spleen	J:132057
	hyperchromic macrocytic anemia	J:132057
	reticulocytopenia	J:132057
Flvcr1tm1Etol/Flvcr1tm1Etol either: (involves: 129) or (involves: 129 * C57BL/6)	abnormal cartilage morphology	J:194202
	abnormal digit development	J:194202
	abnormal skeleton morphology	J:194202
	abnormal vascular development	J:194202
	absent mandible	J:194202
	normal hematopoietic system phenotype	J:194202
	hemorrhage	J:194202
	lethality throughout fetal growth and development, complete penetrance	J:194202
	skin edema	J:194202
	small Meckel's cartilage	J:194202
Flvcr1tm1Jlab/Flvcr1tm1Jlab Tg(Mx1-cre)1Cgn/0 involves: 129S4/SvJae * C57BL/6 * CBA	abnormal autopod morphology	J:132057
	abnormal craniofacial morphology	J:132057
	abnormal digit development	J:132057
	abnormal limb development	J:132057
	normal cardiovascular system phenotype	J:132057
	embryonic lethality during organogenesis, incomplete penetrance	J:132057
	lethality throughout fetal growth and development, incomplete penetrance	J:132057
	normal renal/urinary system phenotype	J:132057
	normal reproductive system phenotype	J:132057
	normal respiratory system phenotype	J:132057