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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Trim65em1Cya
endonuclease-mediated mutation 1, Cyagen Biosciences
MGI:6356825
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Trim65em1Cya/Trim65em1Cya involves: C57BL/6 MGI:6822325


Genotype
MGI:6822325
hm1
Allelic
Composition
Trim65em1Cya/Trim65em1Cya
Genetic
Background
involves: C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Trim65em1Cya mutation (0 available); any Trim65 mutation (30 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• after i.p. infection with encephalomyocarditis virus (EMCV), all mice die within 3 days post-infection i.e. significantly sooner than similarly infected wild-type controls

immune system
• 12 h after i.v. inoculation with EMCV, serum interferon-alpha levels are markedly lower than those in similarly infected wild-type controls
• 12 h after i.v. inoculation with EMCV, serum interferon-beta levels are markedly lower than those in similarly infected wild-type controls
• in contrast, 12 h after i.v. inoculation with vesicular stomatitis virus (VSV, Indiana strain), serum interferon-beta levels are comparable to those in wild-type controls
• following infection with EMCV, IFN-alpha secretion by bone marrow derived macrophages (BMDMs) is completely inhibited
• in contrast, following infection with VSV, IFN-alpha secretion by BMDMs is normal
• following EMCV infection, induction of IFN-beta mRNA expression and IFN-beta secretion by BMDMs is completely inhibited
• following stimulation with HMW poly I:C or EMCV-RNA, induction of IFN-beta mRNA expression in BMDMs is abrogated
• in contrast, VSV infection-induced IFN-beta secretion by BMDMs is normal
• IFN-beta mRNA expression in BMDMs is also normal following adenovirus infection, or after stimulation with 5'-triphosphate RNA (3pRNA, an agonist for RIG-I), extracellular LPS (agonist for TLR4), poly I:C (agonist for TLR3) or VSV-RNA
• 48 h after i.p. infection with encephalomyocarditis virus (EMCV, strain D), mice exhibit more severe tissue damage and higher virus titer in the pancreas than EMCV-infected wild-type controls
• in contrast, no differences in virus titer are observed in the pancreas 24 h after VSV infection
• after i.p. infection with encephalomyocarditis virus (EMCV), all mice die within 3 days post-infection i.e. significantly sooner than similarly infected wild-type controls

homeostasis/metabolism
• 12 h after i.v. inoculation with EMCV, serum interferon-alpha levels are markedly lower than those in similarly infected wild-type controls
• 12 h after i.v. inoculation with EMCV, serum interferon-beta levels are markedly lower than those in similarly infected wild-type controls
• in contrast, 12 h after i.v. inoculation with vesicular stomatitis virus (VSV, Indiana strain), serum interferon-beta levels are comparable to those in wild-type controls





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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
05/07/2024
MGI 6.23
The Jackson Laboratory