42 phenotypes from 2 alleles in 2 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Man2a1em1(IMPC)Hmgu/Man2a1em1(IMPC)Hmgu C57BL/6N-Man2a1em1(IMPC)Hmgu/Ieg	abnormal cecum morphology	J:211773
	abnormal vitreous body morphology	J:211773
	decreased blood urea nitrogen level	J:211773
	decreased circulating alkaline phosphatase level	J:211773
	decreased circulating iron level	J:211773
	decreased hemoglobin content	J:211773
	decreased mean corpuscular volume	J:211773
	increased cardiac output	J:211773
	increased circulating amylase level	J:211773
	increased circulating aspartate transaminase level	J:211773
	increased circulating bilirubin level	J:211773
	increased heart weight	J:211773
	increased mean platelet volume	J:211773
	increased red blood cell distribution width	J:211773
	thrombocytopenia	J:211773
Man2a1tm1Jxm/Man2a1tm1Jxm involves: 129S1/Sv * 129X1/SvJ * C57BL/6	abnormal erythrocyte morphology	J:41621
	abnormal hematopoietic system morphology/development	J:41621
	abnormal immune serum protein physiology	J:74579
	abnormal immune system physiology	J:74579
	abnormal renal glomerulus morphology	J:74579
	abnormal renal/urinary system physiology	J:74579
	abnormal self tolerance	J:74579
	abnormal spleen morphology	J:74579
	anemia	J:41621
	anisocytosis	J:41621
	decreased erythrocyte osmotic fragility	J:41621
	enlarged spleen	J:41621
	glomerulonephritis	J:74579
	hematuria	J:74579
	normal immune system phenotype	J:74579
	increased hematopoietic stem cell number	J:41621
	increased IgA level	J:74579
	increased IgG level	J:74579
	increased IgM level	J:74579
	increased memory T cell number	J:74579
	increased urine protein level	J:74579
	liver inflammation	J:74579
	lung inflammation	J:74579
	premature death	J:74579
	renal fibrosis	J:74579
	renal glomerular immunoglobulin deposits	J:74579
	reticulocytosis	J:41621