56 phenotypes from multigenic genotypes

Allelic Composition Genetic Background	Annotated Term	Reference
Bidtm1Sjk/Bidtm1Sjk Relatm1Bal/Relatm1Bal involves: 129S4/SvJae * 129X1/SvJ * C57BL/6	abnormal liver morphology	J:132334
	decreased fibroblast apoptosis	J:117693
	lethality throughout fetal growth and development, complete penetrance	J:117693
	liver hemorrhage	J:132334
Nfkb1tm1Bal/Nfkb1tm1Bal Relatm1Bal/Rela+ involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6	abnormal colon morphology	J:67107
	cecum inflammation	J:67107
	diarrhea	J:67107
	increased susceptibility to bacterial infection	J:67107
	large intestinal inflammation	J:67107
	peritoneal inflammation	J:67107
Nfkb1tm1Bal/Nfkb1tm1Bal Relatm1Bal/Relatm1Bal involves: 129P2/OlaHsd * 129S4/SvJae	abnormal dendritic cell differentiation	J:113514
	decreased dendritic cell number	J:113514
Nfkb1tm1Bal/Nfkb1tm1Bal Relatm1Bal/Relatm1Bal Tnftm1Ljo/Tnftm1Ljo involves: 129P2/OlaHsd * 129S1/Sv * 129S4/SvJae	neonatal lethality, complete penetrance	J:91366
	prenatal lethality, incomplete penetrance	J:91366
	thin epidermis	J:91366
Reltm1Grd/Reltm1Grd Relatm1Bal/Relatm1Bal B6.129S-Reltm1Grd Relatm1Bal	abnormal erythropoiesis	J:111325
	abnormal monocyte differentiation	J:111325
	decreased common myeloid progenitor cell number	J:111325
	embryonic lethality during organogenesis, complete penetrance	J:111325
	normal hematopoietic system phenotype	J:111325
	hyperchromasia	J:111325
	increased granulocyte number	J:111325
	increased hepatocyte apoptosis	J:111325
	internal hemorrhage	J:111325
Reltm1Grd/Reltm1Grd Relatm1Bal/Relatm1Bal Tnftm1Ljo/Tnftm1Ljo involves: 129P2/OlaHsd * 129S1/Sv * 129S4/SvJae	abnormal cell cycle	J:91366
	abnormal epidermal layer morphology	J:91366
	abnormal epidermis stratum basale morphology	J:91366
	abnormal hair follicle placode formation	J:91366
	abnormal keratinocyte morphology	J:91366
	decreased cell proliferation	J:91366
	decreased embryo size	J:91366
	decreased hair follicle number	J:91366
	neonatal lethality, complete penetrance	J:91366
	thin epidermis	J:91366
	underdeveloped hair follicles	J:91366
Relatm1.1Gho/Relatm1.1Gho Tnfrsf1atm1Mak/Tnfrsf1atm1Mak involves: 129S2/SvPas * 129S6/SvEvTac * C57BL/6	abnormal eye development	J:134684
	blindness	J:134684
	premature death	J:134684
	prenatal lethality, incomplete penetrance	J:134684
Relatm1.2Gho/Relatm1.2Gho Tnfrsf1atm1Mak/Tnfrsf1atm1Mak involves: 129S2/SvPas * 129S6/SvEvTac * C57BL/6	premature death	J:134684
Relatm1Bal/Relatm1Bal Tg(SERPINA1-BCL2)1Pva/0 involves: 129S4/SvJae * C57BL/6 * DBA/2	increased hepatocyte apoptosis	J:126292
Relatm1Bal/Relatm1Bal Tnftm1Ljo/Tnftm1Ljo involves: 129S1/Sv * 129S4/SvJae * C57BL/6	abnormal nervous system physiology	J:124444
Relatm1Bal/Relatm1Bal Tnfrsf1atm1Imx/Tnfrsf1atm1Imx involves: 129S4/SvJae * C57BL/6	abnormal spleen germinal center morphology	J:60742
	abnormal thymus morphology	J:60742
	decreased body size	J:60742
	decreased spleen white pulp amount	J:60742
	extramedullary hematopoiesis	J:60742
	focal hepatic necrosis	J:60742
	heart inflammation	J:60742
	liver inflammation	J:60742
	lung inflammation	J:60742
	postnatal lethality, complete penetrance	J:60742
Relatm1Yuo/Relatm1Yuo Tnftm1Ljo/Tnftm1Ljo involves: 129S/SvEv * 129S1/Sv	abnormal myogenesis	J:135692
	decreased skeletal muscle fiber diameter	J:135692
	increased skeletal muscle fiber number	J:135692
Relatm2.1Gho/Relatm2.1Gho Tnfrsf1atm1Mak/Tnfrsf1atm1Mak involves: 129S2/SvPas * 129S6/SvEvTac	abnormal corneal epithelium morphology	J:163663
	corneal vascularization	J:163663
	decreased cornea thickness	J:163663
	increased corneal epithelium thickness	J:163663
	increased incidence of corneal inflammation	J:163663
	liver fibrosis	J:163663
	liver inflammation	J:163663
	premature death	J:163663