36 phenotypes from 3 alleles in 3 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Trfem1(IMPC)J/Trf+ C57BL/6NJ-Trfem1(IMPC)J/Mmjax	abnormal coat/hair pigmentation	J:211773
	abnormal locomotor behavior	J:211773
	abnormal optic disk morphology	J:211773
	abnormal retina blood vessel morphology	J:211773
	abnormal retina vasculature morphology	J:211773
	abnormal vitreous body morphology	J:211773
	cataract	J:211773
	fused cornea and lens	J:211773
	impaired righting response	J:211773
	increased mean corpuscular hemoglobin	J:211773
	increased total body fat amount	J:211773
	iris synechia	J:211773
	limb grasping	J:211773
	persistence of hyaloid vascular system	J:211773
Trfem1(IMPC)J/Trfem1(IMPC)J C57BL/6NJ-Trfem1(IMPC)J/Mmjax	abnormal embryo size	J:211773
	pallor	J:211773
	preweaning lethality, complete penetrance	J:211773
Trfem1(IMPC)Rbrc/Trf+ C57BL/6NJcl-Trfem1(IMPC)Rbrc/Rbrc	abnormal circulating phosphate level	J:211773
	abnormal mean corpuscular hemoglobin	J:211773
	decreased circulating iron level	J:211773
Trfem1(IMPC)Rbrc/Trfem1(IMPC)Rbrc C57BL/6NJcl-Trfem1(IMPC)Rbrc/Rbrc	preweaning lethality, complete penetrance	J:211773
Trfhpx/Trf+ BALB/cJ-Trfhpx	abnormal iron homeostasis	J:8936, J:64456
	normal hematopoietic system phenotype	J:64456
	hemochromatosis	J:8936
	increased circulating iron level	J:8936
Trfhpx/Trfhpx BALB/cJ-Trfhpx	abnormal iron homeostasis	J:8936, J:64456
	abnormal reticulocyte morphology	J:8936
	anisocytosis	J:8936
	decreased erythrocyte cell number	J:8936
	decreased hematocrit	J:8936
	decreased hemoglobin content	J:8936
	decreased mean corpuscular hemoglobin concentration	J:8936, J:64456
	decreased mean corpuscular volume	J:8936
	hemochromatosis	J:8936, J:64456
	hypochromic anemia	J:8936, J:64456
	increased circulating iron level	J:8936
	poikilocytosis	J:8936
	postnatal growth retardation	J:8936
	postnatal lethality, complete penetrance	J:8936
	spherocytosis	J:8936