23 phenotypes from 6 alleles in 5 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Nle1l11Jus1/Nle1l11Jus1 Not Specified	absent egg cylinders	J:109155
	embryonic lethality between implantation and somite formation, complete penetrance	J:109155
Nle1l11Jus4/Nle1l11Jus4 Not Specified	embryonic lethality between implantation and somite formation, complete penetrance	J:109155
Nle1rs13468707-C/Nle1rs13468707-C C57BL/6J	embryonic lethality between implantation and somite formation, complete penetrance	J:193532
Nle1tm1.2Cota/Nle1tm1.2Cota involves: 129S2/SvPas	abnormal embryo development	J:204063
	failure of blastocyst to hatch from the zona pellucida	J:204063
Nle1tm1Cba/Nle1tm1.1Cota Cd19tm1(cre)Cgn/Cd19+ involves: 129P2/OlaHsd * 129S2/SvPas	normal hematopoietic system phenotype	J:204063
	normal immune system phenotype	J:204063
Nle1tm1Cba/Nle1tm1.1Cota Gt(ROSA)26Sortm2(cre/ERT2)Brn/Gt(ROSA)26Sor+ involves: 129P2/OlaHsd * 129S2/SvPas	abnormal bone marrow cell morphology/development	J:204063
	abnormal common lymphocyte progenitor cell morphology	J:204063
	abnormal hematopoietic stem cell physiology	J:204063
	abnormal immune system organ morphology	J:204063
	abnormal intestinal epithelium morphology	J:204063
	abnormal ribosome biogenesis	J:204063
	decreased bone marrow cell number	J:204063
	decreased common myeloid progenitor cell number	J:204063
	decreased granulocyte number	J:204063
	decreased macrophage cell number	J:204063
	decreased NK cell number	J:204063
	decreased T cell number	J:204063
	normal hematopoietic system phenotype	J:204063
	impaired hematopoiesis	J:204063
	premature death	J:204063
	spleen hypoplasia	J:204063
	thymus hypoplasia	J:204063
Nle1tm1Cba/Nle1tm1Cba involves: 129S2/SvPas * C57BL/6 * SJL/J	abnormal inner cell mass apoptosis	J:108385
	embryonic lethality between implantation and somite formation, complete penetrance	J:108385
	failure of blastocyst to hatch from the zona pellucida	J:108385