68 phenotypes from 10 alleles in 12 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Relatm1.1Gho/Relatm1.1Gho involves: 129S6/SvEvTac * C57BL/6	abnormal eye development	J:134684
	abnormal limb morphology	J:134684
	anophthalmia	J:134684
	embryonic lethality, incomplete penetrance	J:134684
	microphthalmia	J:134684
Relatm1.2Gho/Relatm1.2Gho involves: 129S6/SvEvTac * C57BL/6	increased hepatocyte apoptosis	J:134684
	lethality throughout fetal growth and development, complete penetrance	J:134684
Relatm1Asba/Relatm1Asba Tg(Vil1-cre)997Gum/0 involves: 129 * C57BL/6J * SJL	abnormal intestinal epithelium morphology	J:131977
	abnormal small intestinal villus morphology	J:131977
	abnormal small intestine crypts of Lieberkuhn morphology	J:131977
	abnormal small intestine morphology	J:131977
	decreased survivor rate	J:131977
	diarrhea	J:131977
	impaired intestine regeneration	J:131977
	increased susceptibility to induced colitis	J:131977
	increased susceptibility to xenobiotic induced morbidity/mortality	J:131977
	megacolon	J:131977
	premature death	J:131977
	slow postnatal weight gain	J:131977
Relatm1Bal/Relatm1Bal B6.129S4-Relatm1Bal	increased hepatocyte apoptosis	J:111325
	internal hemorrhage	J:111325
	lethality throughout fetal growth and development, complete penetrance	J:111325
Relatm1Bal/Relatm1Bal B6;129S4-Relatm1Bal/J	normal homeostasis/metabolism phenotype	J:91366
Relatm1Bal/Relatm1Bal involves: 129S4/SvJae	abnormal cell death	J:28390
	abnormal neuron physiology	J:119844
	abnormal trigeminal nerve morphology	J:119844
	decreased marginal zone B cell number	J:65246
	normal immune system phenotype	J:113514
	increased neuron apoptosis	J:119844
Relatm1Bal/Relatm1Bal involves: 129S4/SvJae * C57BL/6J	increased hepatocyte apoptosis	J:28390
	internal hemorrhage	J:28390
	lethality throughout fetal growth and development, complete penetrance	J:28390
	liver degeneration	J:28390
Relatm1Mpa/Relatm1Mpa Tg(Alb1-cre)7Gsc/0 involves: FVB/N	increased susceptibility to endotoxin shock	J:137861
Relatm1Rsch/Relatm1Rsch Ptf1atm1(cre)Hnak/? involves: C57BL/6	abnormal interleukin level	J:122194
	abnormal response/metabolism to endogenous compounds	J:122194
	abnormal tumor necrosis factor level	J:122194
	increased susceptibility to xenobiotic induced morbidity/mortality	J:122194
	lung inflammation	J:122194
	pancreas inflammation	J:122194
Relatm1Rsch/Relatm1Rsch Tg(Cd4-cre)1Cwi/0 involves: C57BL/6 * DBA/2	abnormal gamma-delta T cell morphology	J:169863
Relatm1Rsch/Relatm1Rsch Tg(Lck-cre)I57Jxm/0 involves: ICR	abnormal gamma-delta T cell morphology	J:169863
	decreased interleukin-17 secretion	J:169863
	normal immune system phenotype	J:169863
	increased susceptibility to bacterial infection	J:169863
Relatm1Ukl/Relatm1Ukl B6.129S1-Relatm1Ukl/J	no abnormal phenotype detected	J:101977
Relatm1Yuo/Relatm1Yuo involves: 129S/SvEv	abnormal hepatocyte morphology	J:63099
	abnormal liver morphology	J:63099
	abnormal lymphocyte physiology	J:63099
	abnormal myogenesis	J:135692
	decreased B cell proliferation	J:63099
	decreased double-positive T cell number	J:63099
	decreased IgA level	J:63099
	decreased IgG1 level	J:63099
	decreased T cell proliferation	J:63099
	lethality throughout fetal growth and development, complete penetrance	J:63099
Relatm2.1Gho/Relatm2.1Gho involves: 129S6/SvEvTac * C57BL/6	abnormal bone structure	J:163663
	abnormal brain morphology	J:163663
	abnormal colon morphology	J:163663
	abnormal heart morphology	J:163663
	abnormal spleen morphology	J:163663
	decreased body size	J:163663
	distorted hair follicle pattern	J:163663
	epidermal hyperplasia	J:163663
	epidermal necrosis	J:163663
	extramedullary hematopoiesis	J:163663
	hepatic necrosis	J:163663
	increased inflammatory response	J:163663
	increased neutrophil cell number	J:163663
	interstitial pneumonia	J:163663
	liver fibrosis	J:163663
	liver hypoplasia	J:163663
	liver inflammation	J:163663
	lung inflammation	J:163663
	myositis	J:163663
	postnatal growth retardation	J:163663
	premature death	J:163663
	skin fibrosis	J:163663
	small hair follicles	J:163663
Relatm2.1Mpa/Relatm2.1Mpa involves: C57BL/6	no abnormal phenotype detected	J:148519