43 phenotypes from 9 alleles in 10 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Eportm1.1(EGFP/icre)Uk/Eportm1.1(EGFP/icre)Uk involves: BALB/cJ	embryonic lethality during organogenesis, complete penetrance	J:92235
Eportm1Cos/Eportm1Cos involves: 129S/SvEv * C57BL/6J	abnormal embryonic erythrocyte morphology	J:31156
	abnormal erythrocyte morphology	J:31156
	abnormal erythropoiesis	J:31156
	anemia	J:31156
	decreased erythrocyte cell number	J:31156
	embryonic lethality, complete penetrance	J:31156
	pale liver	J:31156
	small liver	J:31156
Eportm1Hwu/Eportm1Hwu Tg(GFAP-cre)25Mes/? involves: 129 * C57BL/6 * FVB/N	abnormal postnatal subventricular zone morphology	J:104816
Eportm1Jae/Epor+ either: (involves: 129S4/SvJae * BALB/c) or (involves: 129S4/SvJae * C57BL/6)	pale liver	J:29254
Eportm1Jae/Eportm1Jae either: (involves: 129S4/SvJae * BALB/c) or (involves: 129S4/SvJae * C57BL/6)	abnormal erythropoiesis	J:29254
	abnormal placenta morphology	J:29254
	anemia	J:29254
	increased erythroid progenitor cell number	J:29254
	increased hepatocyte apoptosis	J:29254
	lethality throughout fetal growth and development, complete penetrance	J:29254
	pale liver	J:29254
	small liver	J:29254
Eportm1Jae/Eportm1Jae involves: 129S4/SvJae	abnormal blood vessel morphology	J:53885
	abnormal heart development	J:53885
	abnormal heart morphology	J:53885
	abnormal interventricular groove morphology	J:53885
	abnormal interventricular septum morphology	J:53885
	abnormal myocardial fiber physiology	J:53885
	anemia	J:53885
	decreased angiogenesis	J:128893
	detached epicardium	J:53885
	edema	J:53885
	lethality throughout fetal growth and development, complete penetrance	J:53885
	pericardial edema	J:53885
	thick ventricular wall	J:53885
	ventricular hypoplasia	J:53885
Eportm1Jni/Eportm1Jni involves: 129S1/Sv * C57BL/6	abnormal erythropoiesis	J:70036
	increased hematocrit	J:70036
Eportm1Lizon/Eportm1Lizon involves: 129S4/SvJae * C57BL/6	absent erythroid progenitor cell	J:35594
	anemia	J:35594
	decreased erythrocyte cell number	J:35594
	embryonic lethality during organogenesis, complete penetrance	J:35594
	normal hematopoietic system phenotype	J:35594
	impaired hematopoiesis	J:35594
	increased hepatocyte apoptosis	J:35594
	liver hypoplasia	J:35594
	normal nervous system phenotype	J:35594
	pale liver	J:35594
	pale yolk sac	J:35594
	small liver	J:35594
Eportm1Lizon/Eportm1Lizon Tg(Gata1-Epor)AMym/0 involves: 129S4/SvJae * C57BL/6 * DBA	abnormal heart right ventricle pressure	J:121500
	abnormal lung vasculature morphology	J:121500
	abnormal physiological neovascularization	J:82257
	abnormal response to injury	J:121500
	abnormal vascular endothelial cell migration	J:121500
	heart right ventricle hypertrophy	J:121500
	increased susceptibility to induced morbidity/mortality	J:121500
	pulmonary hypertension	J:121500
Eportm2Jni/Eportm2Jni involves: 129P2/OlaHsd * C57BL/6	abnormal erythropoiesis	J:70036
	decreased hematocrit	J:70036
Hprt1tm1(ACTB-Epor)Unc/Y involves: 129P2/OlaHsd	abnormal definitive hematopoiesis	J:81859
	normal hematopoietic system phenotype	J:81859
Hprt1tm1(ACTB-Epor)Unc/Hprt1tm1(ACTB-Epor)Unc involves: 129P2/OlaHsd	abnormal definitive hematopoiesis	J:81859
	normal hematopoietic system phenotype	J:81859