29 phenotypes from 3 alleles in 5 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Myl2tm1(cre)Krc/Myl2+ Srsf2tm1Xdfu/Srsf2tm1Xdfu involves: 129S4/SvJae	cardiac interstitial fibrosis	J:88432
	normal cardiovascular system phenotype	J:88432
	decreased ventricle muscle contractility	J:88432
	dilated cardiomyopathy	J:88432
	pregnancy-related premature death	J:88432
Srsf2tm1.1Oaw/Srsf2+ Tg(Mx1-cre)1Cgn/? B6.Cg-Tg(Mx1-cre)1Cgn Srsf2tm1.1Oaw	abnormal cell cycle	J:221404
	abnormal erythroid progenitor cell morphology	J:221404
	abnormal erythropoiesis	J:221404
	abnormal hematopoietic stem cell physiology	J:221404
	abnormal hematopoietic system physiology	J:221404
	abnormal myelopoiesis	J:221404
	abnormal neutrophil morphology	J:221404
	decreased B cell number	J:221404
	failure of myelopoiesis	J:221404
	impaired hematopoiesis	J:221404
	increased apoptosis	J:221404
	increased hematopoietic stem cell number	J:221404
	macrocytic anemia	J:221404
Srsf2tm1.1Xdfu/Srsf2tm1.1Xdfu involves: 129S4/SvJae * FVB/N	embryonic lethality between implantation and somite formation, complete penetrance	J:88432
Srsf2tm1Xdfu/Srsf2+ Tg(Lck-cre)I57Jxm/? involves: 129S4/SvJae * 129X1/SvJ * ICR	decreased thymocyte number	J:88668
	decreased thymus weight	J:88668
Srsf2tm1Xdfu/Srsf2tm1Xdfu Tg(Lck-cre)I57Jxm/? involves: 129S4/SvJae * 129X1/SvJ * ICR	abnormal spleen white pulp morphology	J:88668
	abnormal T cell differentiation	J:88668
	absent thymus corticomedullary boundary	J:88668
	decreased double-positive T cell number	J:88668
	decreased T cell number	J:88668
	decreased thymocyte number	J:88668
	increased double-negative T cell number	J:88668
	small thymus	J:88668
Srsf2tm1Xdfu/Srsf2tm1Xdfu Tg(Mx1-cre)1Cgn/? involves: 129S4/SvJae * C57BL/6J * CBA/J	abnormal hematopoietic system physiology	J:221404
	bone marrow failure	J:221404
	impaired hematopoiesis	J:221404