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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Rela
v-rel reticuloendotheliosis viral oncogene homolog A (avian)
MGI:103290
68 phenotypes from 10 alleles in 12 genetic backgrounds
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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 intestine regeneration 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
increased sensitivity to xenobiotic induced morbidity/mortality J:131977
increased susceptibility to induced colitis 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 sensitivity 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

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB), Gene Ontology (GO)
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last database update
01/07/2020
MGI 6.14
The Jackson Laboratory