31 phenotypes from 4 alleles in 5 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Ccbe1em1(IMPC)Mbp/Ccbe1+ C57BL/6NCrl-Ccbe1em1(IMPC)Mbp/MbpMmucd	abnormal eye morphology	J:211773
	abnormal liver morphology	J:211773
	abnormal retina blood vessel morphology	J:211773
	abnormal retina morphology	J:211773
	abnormal retina vasculature morphology	J:211773
	abnormal uterus morphology	J:211773
	enlarged uterus	J:211773
	microphthalmia	J:211773
	persistence of hyaloid vascular system	J:211773
	small liver	J:211773
Ccbe1em1(IMPC)Mbp/Ccbe1em1(IMPC)Mbp C57BL/6NCrl-Ccbe1em1(IMPC)Mbp/MbpMmucd	abnormal craniofacial morphology	J:211773
	abnormal placenta morphology	J:211773
	abnormal placenta vasculature	J:211773
	edema	J:211773
	microphthalmia	J:211773
	pale liver	J:211773
	preweaning lethality, complete penetrance	J:211773
Ccbe1tm1Lex/Ccbe1tm1Lex involves: 129S5/SvEvBrd	abnormal lymphangiogenesis	J:186594
	absent lymphatic vessels	J:186594
	edema	J:186594
	prenatal lethality, complete penetrance	J:186594
Ccbe1tm1Mlkn/Ccbe1tm1Mlkn either: B6.129-Ccbe1tm1Mlkn or (involves: 129 * C57BL/6)	abnormal erythropoiesis	J:196696
	abnormal liver morphology	J:196696
	abnormal macrophage physiology	J:196696
	absent lymphatic vessels	J:196696
	anemia	J:196696
	decreased fetal derived definitive erythrocyte cell number	J:196696
	decreased hematocrit	J:196696
	decreased macrophage cell number	J:196696
	edema	J:196696
	increased apoptosis	J:196696
	increased nucleated erythrocyte cell number	J:196696
	pallor	J:196696
	prenatal lethality	J:196696
	small liver	J:196696
Ccbe1tm2.1Mlkn/Ccbe1tm2.1Mlkn Ndor1Tg(UBC-cre/ERT2)1Ejb/0 involves: 129 * C57BL/6	normal hematopoietic system phenotype	J:196696
Ccbe1tm2.1Mlkn/Ccbe1tm2.1Mlkn Tg(VAV1-cre)1Graf/0 involves: 129	no abnormal phenotype detected	J:196696