26 phenotypes from 6 alleles in 7 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Ern1tm1Dron/Ern1+ 129S.129S6-Ern1tm1Dron	abnormal glucose homeostasis	J:132805
	abnormal response/metabolism to endogenous compounds	J:132805
Ern1tm1Dron/Ern1tm1Dron involves: 129S6/SvEvTac	embryonic lethality during organogenesis, complete penetrance	J:132966
Ern1tm1Rjk/Ern1tm1Rjk involves: 129S1/Sv * 129X1/SvJ	abnormal cell physiology	J:124971
Ern1tm1Rjk/Ern1tm1Rjk involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	abnormal definitive hematopoiesis	J:106975
	abnormal pro-B cell morphology	J:106975
	decreased embryo size	J:106975
	embryonic growth retardation	J:106975
	embryonic lethality during organogenesis, complete penetrance	J:106975
	liver hypoplasia	J:106975
	pallor	J:106975
Ern1tm1Rjk/Ern1tm2.1Rjk Speer6-ps1Tg(Alb-cre)21Mgn/Speer6-ps1+ involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * DBA	abnormal apolipoprotein level	J:171230
	abnormal hepatocyte morphology	J:171230
	abnormal lipid level	J:171230
	decreased circulating cholesterol level	J:171230
	hepatic steatosis	J:171230
	increased hepatocyte apoptosis	J:171230
	increased liver triglyceride level	J:171230
Ern1tm1Tiw/Ern1tm1Tiw involves: 129S4/SvJae * C57BL/6	abnormal extraembryonic tissue physiology	J:153222
	abnormal placenta labyrinth morphology	J:153222
	abnormal placental labyrinth vasculature morphology	J:153222
	abnormal placental transport	J:153222
	abnormal trophoblast layer morphology	J:153222
	decreased embryo size	J:153222
	embryonic lethality during organogenesis, complete penetrance	J:153222
	small placenta	J:153222
Ern1tm2.1Rjk/Ern1tm2.1Rjk Not Specified	no abnormal phenotype detected	J:171230
Ern1tm2.1Tiw/Ern1tm2.2Tiw Meox2tm1(cre)Sor/Meox2+ involves: 129S4/SvJae * C57BL/6	normal embryo phenotype	J:153222
	normal liver/biliary system phenotype	J:153222