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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Pik3cgtm1Pngr
targeted mutation 1, Josef M Penninger
MGI:1858013
Summary 8 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Pik3cgtm1Pngr/Pik3cgtm1Pngr B6.129P2-Pik3cgtm1Pngr MGI:3796517
hm2
Pik3cgtm1Pngr/Pik3cgtm1Pngr involves: 129P2/OlaHsd MGI:3619931
hm3
Pik3cgtm1Pngr/Pik3cgtm1Pngr involves: 129P2/OlaHsd * C57BL/6 MGI:3619226
cn4
Pik3cgtm1Pngr/Pik3cgtm1Pngr
Ptentm2Mak/Ptentm2Mak
Tg(Ckmm-cre)5Khn/0
involves: 129P2/OlaHsd * FVB MGI:3619937
cx5
Pik3cdtm1Tnr/Pik3cdtm1Tnr
Pik3cgtm1Pngr/Pik3cgtm1Pngr
B6.129-Pik3cdtm1Tnr Pik3cgtm1Pngr MGI:3796518
cx6
Pik3cdtm1Tnr/Pik3cdtm1Tnr
Pik3cgtm1Pngr/Pik3cgtm1Pngr
involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6 MGI:3796506
cx7
Pik3cdtm1Jni/Pik3cdtm1Jni
Pik3cgtm1Pngr/Pik3cgtm1Pngr
involves: 129P2/OlaHsd * C57BL/6 MGI:3796421
cx8
Ace2tm1Pngr/Y
Pik3cgtm1Pngr/Pik3cgtm1Pngr
involves: 129P2/OlaHsd * C57BL/6 MGI:5912245


Genotype
MGI:3796517
hm1
Allelic
Composition
Pik3cgtm1Pngr/Pik3cgtm1Pngr
Genetic
Background
B6.129P2-Pik3cgtm1Pngr
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Pik3cgtm1Pngr mutation (0 available); any Pik3cg mutation (59 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
immune system
• neutrophil migration in a chemotaxis assay with fMLP stimulation is reduced compared to for wild-type cells
• mice exhibit a 45% to 53% decrease in paw edema, reduced synovial inflammation, and reduced bone and cartilage erosion following administration of arthritogenic serum compared to wild-type mice
• mice exhibit a 45% to 53% decrease in paw edema, reduced synovial inflammation, and reduced bone and cartilage erosion following administration of arthritogenic serum compared to wild-type mice

skeleton
• mice exhibit a 45% to 53% decrease in paw edema, reduced synovial inflammation, and reduced bone and cartilage erosion following administration of arthritogenic serum compared to wild-type mice

cellular
• neutrophil migration in a chemotaxis assay with fMLP stimulation is reduced compared to for wild-type cells

hematopoietic system
• neutrophil migration in a chemotaxis assay with fMLP stimulation is reduced compared to for wild-type cells




Genotype
MGI:3619931
hm2
Allelic
Composition
Pik3cgtm1Pngr/Pik3cgtm1Pngr
Genetic
Background
involves: 129P2/OlaHsd
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Pik3cgtm1Pngr mutation (0 available); any Pik3cg mutation (59 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
cardiovascular system
• exhibit increased fractional shortening, velocity of circumferential fiber shortening, and peak aortic outflow velocity, indicating enhanced contractility
• individual cardiomyocytes display an increase in contractility
• treatment of cardiomyocytes with a cAMP blocker leads to a greater reduction in contractility compared to wild-type
• exhibit a significant increase in the rate of relaxation in cardiomyocytes despite the increase in peak contraction

muscle
• exhibit increased fractional shortening, velocity of circumferential fiber shortening, and peak aortic outflow velocity, indicating enhanced contractility
• individual cardiomyocytes display an increase in contractility
• treatment of cardiomyocytes with a cAMP blocker leads to a greater reduction in contractility compared to wild-type
• exhibit a significant increase in the rate of relaxation in cardiomyocytes despite the increase in peak contraction




Genotype
MGI:3619226
hm3
Allelic
Composition
Pik3cgtm1Pngr/Pik3cgtm1Pngr
Genetic
Background
involves: 129P2/OlaHsd * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Pik3cgtm1Pngr mutation (0 available); any Pik3cg mutation (59 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
immune system
• reduction in thymic cellularity
• mice have a higher percentage of CD117+ CD27+ NK cells and lower percentages of 2B4+ NK cells than in splenic NK cells from wild-type mice
• T cell development is altered however B cell development is normal
• decrease in CD4+CD8- T cells in the spleen
• thymocytes exhibit an increase in apoptosis compared to wild-type after stimulation with adenosine receptor agonists
• GRCR-induced respiratory burst is decreased in freshly isolated bone marrow neutrophils
• 70% decrease in fMLP- and C5a-induced chemotaxis of neutrophils
• accumulation of neutrophils in the peritoneal cavities is reduced in response to casein-induced peritonitis of Listeria infection
• lymphocytic choriomeningitis virus (LCMV) induced footpad-swelling is reduced, indicating impaired CD+ T cell-dependent antiviral responses
• production of antibodies to NIP after NIP-OVA immunization is reduced indicating impairment of functional T helper cell-dependent responses to hapten antigens
• NK cells are slightly less lytic than wild-type cells
• T cells exhibit impaired proliferation in response to anti-CD3 epsilon on Con A stimulation, however exhibit normal proliferation in response to PMA/Ca+ inonaphore
• T cells produce lower amounts of interferon-gamma in response to treatment with anti-CD3 epsilon and anti-CD28, Con A, or PMA/Ca+ ionaphore (J:60347)
• mice exhibit decreased IFN-gamma secretion following NK1.1 or IL-12/IL-18 stimulation compared to in wild-type mice (J:124330)
• T cells produce lower amounts of IL-2 in response to treatment with anti-CD3 epsilon and anti-CD28, Con A, or PMA/Ca+ ionaphore

hematopoietic system
• reduction in thymic cellularity
• increase in total and relative numbers of Gr1+Mac1+ myeloid cells in the spleen but not in bone marrow
• mice have a higher percentage of CD117+ CD27+ NK cells and lower percentages of 2B4+ NK cells than in splenic NK cells from wild-type mice
• T cell development is altered however B cell development is normal
• decrease in CD4+CD8- T cells in the spleen
• GRCR-induced respiratory burst is decreased in freshly isolated bone marrow neutrophils
• 70% decrease in fMLP- and C5a-induced chemotaxis of neutrophils
• accumulation of neutrophils in the peritoneal cavities is reduced in response to casein-induced peritonitis of Listeria infection
• lymphocytic choriomeningitis virus (LCMV) induced footpad-swelling is reduced, indicating impaired CD+ T cell-dependent antiviral responses
• production of antibodies to NIP after NIP-OVA immunization is reduced indicating impairment of functional T helper cell-dependent responses to hapten antigens
• NK cells are slightly less lytic than wild-type cells
• T cells exhibit impaired proliferation in response to anti-CD3 epsilon on Con A stimulation, however exhibit normal proliferation in response to PMA/Ca+ inonaphore

cellular
• 70% decrease in fMLP- and C5a-induced chemotaxis of neutrophils
• T cells exhibit impaired proliferation in response to anti-CD3 epsilon on Con A stimulation, however exhibit normal proliferation in response to PMA/Ca+ inonaphore

endocrine/exocrine glands
• reduction in thymic cellularity




Genotype
MGI:3619937
cn4
Allelic
Composition
Pik3cgtm1Pngr/Pik3cgtm1Pngr
Ptentm2Mak/Ptentm2Mak
Tg(Ckmm-cre)5Khn/0
Genetic
Background
involves: 129P2/OlaHsd * FVB
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Pik3cgtm1Pngr mutation (0 available); any Pik3cg mutation (59 available)
Ptentm2Mak mutation (4 available); any Pten mutation (88 available)
Tg(Ckmm-cre)5Khn mutation (4 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
cardiovascular system
• significantly enlarged compared to wild-type and single homozygous Pik3cgtm1Pngr mice
• extent of cardiac hypertrophy is similar to that seen in mice with cardiomyocyte-specific inactivation of Pten
• hearts are hypercontractile as assessed by increased fractional shortening, velocity or circumferential fiber shortening, and peak aortic outflow velocity
• individual cardiomyocytes display increased contractility despite the hypertrophy

muscle
• hearts are hypercontractile as assessed by increased fractional shortening, velocity or circumferential fiber shortening, and peak aortic outflow velocity
• individual cardiomyocytes display increased contractility despite the hypertrophy

growth/size/body
• significantly enlarged compared to wild-type and single homozygous Pik3cgtm1Pngr mice
• extent of cardiac hypertrophy is similar to that seen in mice with cardiomyocyte-specific inactivation of Pten




Genotype
MGI:3796518
cx5
Allelic
Composition
Pik3cdtm1Tnr/Pik3cdtm1Tnr
Pik3cgtm1Pngr/Pik3cgtm1Pngr
Genetic
Background
B6.129-Pik3cdtm1Tnr Pik3cgtm1Pngr
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Pik3cdtm1Tnr mutation (0 available); any Pik3cd mutation (45 available)
Pik3cgtm1Pngr mutation (0 available); any Pik3cg mutation (59 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
immune system
• neutrophil migration in a chemotaxis assay with LB4 or fMLP stimulation is reduced compared to for wild-type cells
• neutrophils travel shorter distances and at slower velocities than wild-type cells
• neutrophils accumulation following LTB4-stimulation is reduced greater than 70% compared to in wild-type mice
• following administration of arthritogenic serum, mice develop minimal swelling unlike in wild-type mice
• 14 days following administration of autoreactive antibodies, mice exhibit relatively normal articular surfaces, intact joint spaces and the absence of periaticular inflammation unlike wild-type mice
• following administration of arthritogenic serum, mice develop minimal swelling unlike in wild-type mice
• 14 days following administration of autoreactive antibodies, mice exhibit relatively normal articular surfaces, intact joint spaces and the absence of periaticular inflammation unlike wild-type mice

skeleton
• following administration of arthritogenic serum, mice develop minimal swelling unlike in wild-type mice
• 14 days following administration of autoreactive antibodies, mice exhibit relatively normal articular surfaces, intact joint spaces and the absence of periaticular inflammation unlike wild-type mice

cellular
• neutrophil migration in a chemotaxis assay with LB4 or fMLP stimulation is reduced compared to for wild-type cells
• neutrophils travel shorter distances and at slower velocities than wild-type cells

hematopoietic system
• neutrophil migration in a chemotaxis assay with LB4 or fMLP stimulation is reduced compared to for wild-type cells
• neutrophils travel shorter distances and at slower velocities than wild-type cells
• neutrophils accumulation following LTB4-stimulation is reduced greater than 70% compared to in wild-type mice




Genotype
MGI:3796506
cx6
Allelic
Composition
Pik3cdtm1Tnr/Pik3cdtm1Tnr
Pik3cgtm1Pngr/Pik3cgtm1Pngr
Genetic
Background
involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Pik3cdtm1Tnr mutation (0 available); any Pik3cd mutation (45 available)
Pik3cgtm1Pngr mutation (0 available); any Pik3cg mutation (59 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
immune system
• corticomedullary differentiation is lost
• total thymus cell count is reduced 27-fold compared to in wild-type mice and 10-fold compared to in Pik3cg null mice
• the population of DN3 T cells is phenotypically different from in wild-type mice due to altered marker expression
• peripheral lymph nodes and spleen exhibit decreased T cell populations compared to in wild-type mice
• mice have fewer double positive T cells due to increased apoptosis compared to in wild-type mice
• calcium fluxes in response to TCR cross-linking are absent from T cells unlike in wild-type cells

hematopoietic system
• corticomedullary differentiation is lost
• total thymus cell count is reduced 27-fold compared to in wild-type mice and 10-fold compared to in Pik3cg null mice
• the population of DN3 T cells is phenotypically different from in wild-type mice due to altered marker expression
• peripheral lymph nodes and spleen exhibit decreased T cell populations compared to in wild-type mice
• mice have fewer double positive T cells due to increased apoptosis compared to in wild-type mice
• calcium fluxes in response to TCR cross-linking are absent from T cells unlike in wild-type cells

endocrine/exocrine glands
• corticomedullary differentiation is lost
• total thymus cell count is reduced 27-fold compared to in wild-type mice and 10-fold compared to in Pik3cg null mice




Genotype
MGI:3796421
cx7
Allelic
Composition
Pik3cdtm1Jni/Pik3cdtm1Jni
Pik3cgtm1Pngr/Pik3cgtm1Pngr
Genetic
Background
involves: 129P2/OlaHsd * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Pik3cdtm1Jni mutation (0 available); any Pik3cd mutation (45 available)
Pik3cgtm1Pngr mutation (0 available); any Pik3cg mutation (59 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
immune system
• mice exhibit a high percentage of CD117+ and CD27+ NK cells and about 40% to 50% immature CD27 CD11b- cells compared to in wild-type mice
• NK cell development is blocked before the stage at which they acquire Ly49 receptors
• mice exhibit a 60% to 70% reduction in NK cells in the spleen compared to in wild-type mice
• CD3+ T cell numbers and percentages are reduced compared to in wild-type mice
• total splenocyte numbers are reduced 50% compared to in wild-type mice
• NK cells are less lytic than wild-type cells
• mice exhibit decreased IFN-gamma secretion following NK1.1 or IL-12/IL-18 stimulation compared to in wild-type mice

hematopoietic system
• mice exhibit a high percentage of CD117+ and CD27+ NK cells and about 40% to 50% immature CD27 CD11b- cells compared to in wild-type mice
• NK cell development is blocked before the stage at which they acquire Ly49 receptors
• mice exhibit a 60% to 70% reduction in NK cells in the spleen compared to in wild-type mice
• CD3+ T cell numbers and percentages are reduced compared to in wild-type mice
• total splenocyte numbers are reduced 50% compared to in wild-type mice
• NK cells are less lytic than wild-type cells




Genotype
MGI:5912245
cx8
Allelic
Composition
Ace2tm1Pngr/Y
Pik3cgtm1Pngr/Pik3cgtm1Pngr
Genetic
Background
involves: 129P2/OlaHsd * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Ace2tm1Pngr mutation (1 available); any Ace2 mutation (66 available)
Pik3cgtm1Pngr mutation (0 available); any Pik3cg mutation (59 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
cardiovascular system
• increase in basal myocardial contractility
• mice exhibit a partial reversal of myocardial hypertrophy, prevention of neutrophil infiltration into myocardial tissue, and prevention of systolic function deterioration

muscle
• increase in basal myocardial contractility
• mice exhibit a partial reversal of myocardial hypertrophy, prevention of neutrophil infiltration into myocardial tissue, and prevention of systolic function deterioration





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last database update
11/12/2024
MGI 6.24
The Jackson Laboratory