41 phenotypes from 2 alleles in 2 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Pfdn1em1(IMPC)J/Pfdn1+ C57BL/6NJ-Pfdn1em1(IMPC)J/Mmjax	abnormal locomotor behavior	J:211773
	decreased exploration in new environment	J:211773
	limb grasping	J:211773
Pfdn1em1(IMPC)J/Pfdn1em1(IMPC)J C57BL/6NJ-Pfdn1em1(IMPC)J/Mmjax	abnormal embryo size	J:211773
	abnormal tail morphology	J:211773
	cleft palate	J:211773
	hemorrhage	J:211773
	preweaning lethality, complete penetrance	J:211773
Pfdn1Gt(GTR1.3)1Rul/Pfdn1Gt(GTR1.3)1Rul involves: 129	abnormal B cell activation	J:137415
	abnormal B cell differentiation	J:137415
	abnormal B cell morphology	J:137415
	abnormal brain commissure morphology	J:137415
	abnormal brain white matter morphology	J:137415
	abnormal cerebellum morphology	J:137415
	abnormal corpus callosum morphology	J:137415
	abnormal erythrocyte morphology	J:137415
	abnormal neutrophil morphology	J:137415
	abnormal spleen morphology	J:137415
	abnormal spleen red pulp morphology	J:137415
	abnormal spleen white pulp morphology	J:137415
	abnormal splenic cell ratio	J:137415
	abnormal T cell activation	J:137415
	abnormal thymus cell ratio	J:137415
	abnormal thymus morphology	J:137415
	decreased B-1 B cell number	J:137415
	decreased B-2 B cell number	J:137415
	decreased birth body size	J:137415
	decreased bone marrow cell number	J:137415
	decreased corpus callosum size	J:137415
	decreased erythrocyte cell number	J:137415
	decreased pre-B cell number	J:137415
	decreased thymus weight	J:137415
	hydrocephaly	J:137415
	impaired coordination	J:137415
	premature death	J:137415
	sinus inflammation	J:137415
	slow postnatal weight gain	J:137415
	small spleen	J:137415
	spleen hypoplasia	J:137415
	thymus hypoplasia	J:137415
	weight loss	J:137415