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Phenotypes Associated with This Genotype
Genotype
MGI:3693616
Allelic
Composition
Ifngr1tm1Agt/Ifngr1tm1Agt
Genetic
Background
involves: 129S7/SvEvBrd * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Ifngr1tm1Agt mutation (13 available); any Ifngr1 mutation (52 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• in vesicular somatitis virus (VSV)-infected mice

immune system
• splenocytes proliferate against the antigen and a mitogen more vigorously than those from wild-type
• in trinitrophenyl-conjugated ovalbumin-treated mice
• in trinitrophenyl-conjugated ovalbumin-treated mice
• mice exhibit a slightly reduced CTL response against lymphocytic choriomeningitis virus (LCMV) infection with enhanced viral replication compared with similarly treated wild-type mice
• stimulation of splenocytes with an antigen or a mitogen induces a higher production of IFN-gamma than in wild-type
• stimulation of splenocytes with an antigen induces a higher production of IL-4, IL-6, IL-13 and IFN-gamma than in wild-type
• stimulation of splenocytes with a mitogen induces a higher production of IL-13
• following induction of experimental myasthenia gravis, mice exhibit less severe disease compared with wild-type mice
• exhibit increased incidence and severity of induced experimental autoimmune uveoretinitis compared to wild-type (59.3% vs. 40% of wild-type)
• upon uveoretinitis induction, see a significant infiltration of eosinophils into the eyes compared to wild-type
• following infection with Listeria monocytogenes, mice exhibit 100-fold increase in bacterial titers in the liver and 10-fold in the spleen compared to in similarly treated wild-type mice
• mice infected with vesicular somatitis virus (VSV) exhibit a 100- to 1000-fold increase in viral titers and increased lethality compared with similarly treated wild-type mice
• mice exhibit a slightly reduced CTL response against lymphocytic choriomeningitis virus (LCMV) infection with enhanced viral replication compared with similarly treated wild-type mice
• in vesicular somatitis virus (VSV)-infected mice

neoplasm
• tumor growth in tumor-bearing mice treated with Th-17-polarized cells from Tg(Tcra,Tcrb)9Rest cells is minimally delayed, and develop progressive disease

liver/biliary system
N
• mice show no liver injury on treatment with HBsAg-specific Th1 cells and HBsAg

hematopoietic system
• splenocytes proliferate against the antigen and a mitogen more vigorously than those from wild-type
• in trinitrophenyl-conjugated ovalbumin-treated mice
• in trinitrophenyl-conjugated ovalbumin-treated mice
• mice exhibit a slightly reduced CTL response against lymphocytic choriomeningitis virus (LCMV) infection with enhanced viral replication compared with similarly treated wild-type mice

cellular
• splenocytes proliferate against the antigen and a mitogen more vigorously than those from wild-type


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
05/07/2024
MGI 6.23
The Jackson Laboratory