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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Ifngr2tm1Pbro
targeted mutation 1, Paul B Rothman
MGI:1930965
Summary 2 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Ifngr2tm1Pbro/Ifngr2tm1Pbro involves: 129S1/Sv MGI:3603844
hm2
Ifngr2tm1Pbro/Ifngr2tm1Pbro NOD.129S1-Ifngr2tm1Pbro MGI:3603845


Genotype
MGI:3603844
hm1
Allelic
Composition
Ifngr2tm1Pbro/Ifngr2tm1Pbro
Genetic
Background
involves: 129S1/Sv
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Ifngr2tm1Pbro mutation (2 available); any Ifngr2 mutation (23 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
immune system
• class switching to IgG2a inhibited when stimulated with IFN-gamma
• class switching to IgE and IgG1 caused by Il-4 fails
• differentiation of Th1 cells inhibited
• increased susceptibility to Listeria monocytogenes infection

hematopoietic system
• class switching to IgG2a inhibited when stimulated with IFN-gamma
• class switching to IgE and IgG1 caused by Il-4 fails
• differentiation of Th1 cells inhibited




Genotype
MGI:3603845
hm2
Allelic
Composition
Ifngr2tm1Pbro/Ifngr2tm1Pbro
Genetic
Background
NOD.129S1-Ifngr2tm1Pbro
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Ifngr2tm1Pbro mutation (2 available); any Ifngr2 mutation (23 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
cellular
• CD8+ T cells injected into Ifngr2-deficient NOD mice are less able to cause diabetes, due to impaired homing ability and impaired diapedesis

immune system
• CD8+ T cells injected into Ifngr2-deficient NOD mice are less able to cause diabetes, due to impaired homing ability and impaired diapedesis
• enhanced Th2 responses
• CD8+ T cells injected into Ifngr2-deficient NOD mice are less able to cause diabetes, due to impaired homing ability and impaired diapedesis
• when diabetogenic splenocytes are injected into Ifngr2-deficient NOD mice, diabetes development is delayed compared to wild-type NOD mice

homeostasis/metabolism
N
• unexpectedly, incidence of type 1 diabetes in females was unchanged

hematopoietic system
• CD8+ T cells injected into Ifngr2-deficient NOD mice are less able to cause diabetes, due to impaired homing ability and impaired diapedesis
• enhanced Th2 responses
• CD8+ T cells injected into Ifngr2-deficient NOD mice are less able to cause diabetes, due to impaired homing ability and impaired diapedesis

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
type 1 diabetes mellitus DOID:9744 OMIM:222100
J:72818





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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
04/23/2024
MGI 6.23
The Jackson Laboratory