Phenotypes associated with this allele
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Find Mice |
Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Gpr132tm1Witt mutation
(1 available);
any
Gpr132 mutation
(23 available)
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immune system
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• no macrop[hage migration in response to lysophosphatidyl choline
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cellular
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• no macrop[hage migration in response to lysophosphatidyl choline
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hematopoietic system
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• no macrop[hage migration in response to lysophosphatidyl choline
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|
Find Mice |
Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Gpr132tm1Witt mutation
(1 available);
any
Gpr132 mutation
(23 available)
|
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immune system
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• hyperresponsive to surface IgM crosslinking agents
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• enhanced proliferative response to T cell receptor stimulation, even in younger mice
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• kappa and lambda light chain levels elevated
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• elevated IgG1 levels in older mice
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• although normal in young mice, after 1 year of age, secondary lymph nodes become grossly enlarged
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• expanded numbers of T and B lymphocytes
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• disrupted architecture
• 3-6X increase of single positive T lymphocytes
• 2-3X increase of B220+ B lymphocytes
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• rarely is enlarged in young mice
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• increased autoantibodies to nuclear antigens
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• heavy infiltration of lymphocytes into various organs in older mice
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• clusters of lymphocytes in liver parenchyma
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• immunoglobulin complex deposited in glomeruli
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• perivascular and interalveolar infiltration of mononuclear cells
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growth/size/body
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• start to show signs of wasting at 15-16 months of age
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• expanded numbers of T and B lymphocytes
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hematopoietic system
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• expanded numbers of T and B lymphocytes
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• hyperresponsive to surface IgM crosslinking agents
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• enhanced proliferative response to T cell receptor stimulation, even in younger mice
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• kappa and lambda light chain levels elevated
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• elevated IgG1 levels in older mice
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liver/biliary system
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• clusters of lymphocytes in liver parenchyma
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respiratory system
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• perivascular and interalveolar infiltration of mononuclear cells
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renal/urinary system
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• immunoglobulin complex deposited in glomeruli
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cellular
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• hyperresponsive to surface IgM crosslinking agents
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• enhanced proliferative response to T cell receptor stimulation, even in younger mice
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cardiovascular system
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• area in lesions occupied by macrophage is significantly increased
• reduced collagen content
• decreased apoptosis of macrophage in lesions
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immune system
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• decreased apoptosis of macrophage in atherosclerotic lesions
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cellular
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• decreased apoptosis of macrophage in atherosclerotic lesions
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hematopoietic system
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• decreased apoptosis of macrophage in atherosclerotic lesions
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