44 phenotypes from 3 alleles in 5 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Hbb-b1MommeD7/Hbb-b1+ involves: FVB/N	abnormal definitive hematopoiesis	J:190446
	anisocytosis	J:190446
	anisopoikilocytosis	J:190446
	decreased mean corpuscular hemoglobin	J:190446
	decreased mean corpuscular volume	J:190446
	enlarged spleen	J:142335, J:190446
	extramedullary hematopoiesis	J:190446
	hypochromic microcytic anemia	J:190446
	increased erythrocyte clearance	J:190446
	increased nucleated erythrocyte cell number	J:190446
	increased red blood cell distribution width	J:190446
	increased spleen red pulp amount	J:190446
	leptocytosis	J:190446
	microcytic anemia	J:190446
	poikilocytosis	J:190446
	polychromatophilia	J:190446
	reticulocytosis	J:142335
	schistocytosis	J:190446
	spherocytosis	J:190446
Hbb-b1MommeD7/Hbb-b1MommeD7 involves: FVB/N	abnormal liver morphology	J:190446
	decreased erythrocyte cell number	J:142335
	lethality throughout fetal growth and development, complete penetrance	J:190446
	liver hypoplasia	J:190446
	pallor	J:142335, J:190446
	postnatal lethality	J:142335
Hbb-b1Rbc13/Hbb-b1+ involves: BALB/c * C57BL/6	abnormal definitive hematopoiesis	J:190446
	anisocytosis	J:190446
	anisopoikilocytosis	J:190446
	decreased mean corpuscular hemoglobin	J:190446
	decreased mean corpuscular volume	J:190446
	enlarged spleen	J:190446
	extramedullary hematopoiesis	J:190446
	hypochromic microcytic anemia	J:190446
	increased erythrocyte clearance	J:190446
	increased nucleated erythrocyte cell number	J:190446
	increased red blood cell distribution width	J:190446
	increased spleen red pulp amount	J:190446
	leptocytosis	J:190446
	microcytic anemia	J:190446
	poikilocytosis	J:190446
	polychromatophilia	J:190446
	schistocytosis	J:190446
	spherocytosis	J:190446
Hbb-b1Rbc13/Hbb-b1MommeD7 involves: BALB/c * C57BL/6 * FVB/N	pallor	J:190446
Hbb-b1Rbc13/Hbb-b1Rbc13 involves: BALB/c * C57BL/6	abnormal liver morphology	J:190446
	lethality throughout fetal growth and development, complete penetrance	J:190446
	liver hypoplasia	J:190446
	pallor	J:190446
Hbb-b1tm1Shs/Hbb-b1+ involves: C57BL/6CrSlc	abnormal aerobic respiration	J:81902
	abnormal hemoglobin	J:81902
	abnormal skeletal muscle fiber type ratio	J:81902
	acidosis	J:81902
	anemia	J:81902
	decreased hemoglobin content	J:81902
	decreased pulmonary ventilation	J:81902
	hyperoxia	J:81902
	increased aerobic running capacity	J:81902
	increased carbon dioxide production	J:81902
	increased oxygen consumption	J:81902
Hbb-b1tm1Shs/Hbb-b1tm1Shs involves: C57BL/6	abnormal erythrocyte physiology	J:78271
	abnormal erythropoiesis	J:78271
	anisopoikilocytosis	J:78271
	decreased erythrocyte cell number	J:78271
	decreased hematocrit	J:78271
	decreased mean corpuscular hemoglobin	J:78271
	decreased mean corpuscular volume	J:78271
	enlarged spleen	J:78271
	extramedullary hematopoiesis	J:78271
	hemolytic anemia	J:78271
	hypochromic anemia	J:78271
	increased erythroid progenitor cell number	J:78271
	increased number of Heinz bodies	J:78271
	increased spleen iron level	J:78271
	reticulocytosis	J:78271