32 phenotypes from 4 alleles in 5 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Bnip3lGt(XT0573)Wtsi/Bnip3lGt(XT0573)Wtsi B6.Cg-Bnip3lGt(XT0573)Wtsi	abnormal erythrocyte morphology	J:137609
	abnormal erythrocyte physiology	J:137609
	abnormal reticulocyte morphology	J:137609
	decreased erythrocyte cell number	J:137609
	decreased mean corpuscular volume	J:137609
	increased erythrocyte osmotic fragility	J:137609
	polychromatophilia	J:137609
	reticulocytosis	J:137609
Bnip3ltm1.1Gwd/Bnip3ltm1.1Gwd involves: 129	normal cardiovascular system phenotype	J:145086
Bnip3ltm1.1Gwd/Bnip3ltm1.1Gwd involves: 129 * C57BL/6	abnormal bone marrow cell number	J:141583
	abnormal definitive hematopoiesis	J:141583
	abnormal erythroblast number	J:141583
	abnormal erythrocyte morphology	J:141583
	abnormal spleen morphology	J:141583
	abnormal thrombopoiesis	J:141583
	anisocytosis	J:141583
	decreased body length	J:141583
	decreased body weight	J:141583
	enlarged spleen	J:141583
	increased mean corpuscular volume	J:141583
	increased spleen red pulp amount	J:141583
	poikilocytosis	J:141583
	polychromatophilia	J:141583
	postnatal growth retardation	J:141583
	reticulocytosis	J:141583
Bnip3ltm1Gwd/Bnip3ltm1Gwd Nkx2-5tm1(cre)Rjs/Nkx2-5+ involves: 129 * 129S7/SvEvBrd	abnormal heart left ventricle morphology	J:145086
	abnormal response of heart to induced stress	J:145086
	cardiac fibrosis	J:145086
	decreased cardiomyocyte apoptosis	J:145086
	increased cardiac muscle contractility	J:145086
Bnip3ltm1Ney/Bnip3ltm1Ney Not Specified	abnormal definitive hematopoiesis	J:141545
	abnormal erythrocyte morphology	J:141545
	abnormal mitophagy	J:141545
	anemia	J:141545
	decreased erythrocyte cell number	J:141545
	decreased hematocrit	J:141545
	enlarged spleen	J:141545
	poikilocytosis	J:141545
	polychromatophilia	J:141545
	reticulocytosis	J:141545
	spherocytosis	J:141545
	spleen hyperplasia	J:141545