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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Ikbkbtm2Mka
targeted mutation 2, Michael Karin
MGI:2445462
Summary 5 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
cn1
Ikbkbtm2Mka/Ikbkbtm2.1Mka
Tg(Vil-cre)1Mka/0
involves: 129 MGI:3038976
cn2
Ikbkbtm2Mka/Ikbkbtm2Mka
Tg(Ckmm-cre)1Lrsn/0
involves: 129 MGI:3799267
cn3
Ikbkbtm2Mka/Ikbkbtm2Mka
Lyz2tm1(cre)Ifo/Lyz2+
involves: 129/Sv * 129P2/OlaHsd MGI:4843279
cn4
Cd19tm1(cre)Cgn/Cd19+
Ikbkbtm2Mka/Ikbkbtm2Mka
involves: 129/Sv * 129P2/OlaHsd * C57BL/6 MGI:2657004
cn5
Ikbkbtm2Mka/Ikbkbtm2.1Mka
Tg(Vil-cre)1Mka/0
involves: 129/Sv * C57BL/6 MGI:2662291


Genotype
MGI:3038976
cn1
Allelic
Composition
Ikbkbtm2Mka/Ikbkbtm2.1Mka
Tg(Vil-cre)1Mka/0
Genetic
Background
involves: 129
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Ikbkbtm2.1Mka mutation (0 available); any Ikbkb mutation (54 available)
Ikbkbtm2Mka mutation (0 available); any Ikbkb mutation (54 available)
Tg(Vil-cre)1Mka mutation (0 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
cellular
• small intestinal crypt epithelial cells are more sensitive to gamma-radiation, showing an increase in apoptosis after irradiation
• LPS injection alone induces apoptosis in intestinal epithelial cells of mutants but not controls
• small intestinal crypt epithelial cells exhibit an increase in apoptosis after gamma-irradiation
• LPS injection before ionizing radiation significantly increases the number of apoptotic intestinal epithelial cells in mutants by about 70%

digestive/alimentary system
• LPS injection alone induces apoptosis in intestinal epithelial cells of mutants but not controls
• small intestinal crypt epithelial cells exhibit an increase in apoptosis after gamma-irradiation
• LPS injection before ionizing radiation significantly increases the number of apoptotic intestinal epithelial cells in mutants by about 70%




Genotype
MGI:3799267
cn2
Allelic
Composition
Ikbkbtm2Mka/Ikbkbtm2Mka
Tg(Ckmm-cre)1Lrsn/0
Genetic
Background
involves: 129
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Ikbkbtm2Mka mutation (0 available); any Ikbkb mutation (54 available)
Tg(Ckmm-cre)1Lrsn mutation (0 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
muscle
• under long-term differentiation conditions without medium replenishment, myotubes are 48% less atrophic compared to similarly treated wild-type mouse embryonic fibroblasts
• the number of intermediate fibers is increased compared to in wild-type mice




Genotype
MGI:4843279
cn3
Allelic
Composition
Ikbkbtm2Mka/Ikbkbtm2Mka
Lyz2tm1(cre)Ifo/Lyz2+
Genetic
Background
involves: 129/Sv * 129P2/OlaHsd
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Ikbkbtm2Mka mutation (0 available); any Ikbkb mutation (54 available)
Lyz2tm1(cre)Ifo mutation (14 available); any Lyz2 mutation (41 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
immune system
• bone marrow-derived macrophages exhibit LPS-induced apoptosis unlike control cells

cellular
• bone marrow-derived macrophages exhibit LPS-induced apoptosis unlike control cells

hematopoietic system
• bone marrow-derived macrophages exhibit LPS-induced apoptosis unlike control cells




Genotype
MGI:2657004
cn4
Allelic
Composition
Cd19tm1(cre)Cgn/Cd19+
Ikbkbtm2Mka/Ikbkbtm2Mka
Genetic
Background
involves: 129/Sv * 129P2/OlaHsd * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Cd19tm1(cre)Cgn mutation (11 available); any Cd19 mutation (56 available)
Ikbkbtm2Mka mutation (0 available); any Ikbkb mutation (54 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
hematopoietic system
• decrease in survival of B cells
• reduction in populations of some peripheral B cell subsets, particularly the lymph node compartment
• B cell generation is not impaired
• reduced number of peritoneal B-1 cells
• mutants fail to mount effective antibody responses to T cell-dependent and independent antigens
• hypoproliferation in response to anti-IgM, LPS, and anti-Tnfrsf5 (anti9-CD40)
• decrease in basal IgG levels
• decrease in basal IgM levels

immune system
• decrease in survival of B cells
• reduction in populations of some peripheral B cell subsets, particularly the lymph node compartment
• B cell generation is not impaired
• reduced number of peritoneal B-1 cells
• mutants fail to mount effective antibody responses to T cell-dependent and independent antigens
• hypoproliferation in response to anti-IgM, LPS, and anti-Tnfrsf5 (anti9-CD40)
• decrease in basal IgG levels
• decrease in basal IgM levels

cellular
• decrease in survival of B cells
• hypoproliferation in response to anti-IgM, LPS, and anti-Tnfrsf5 (anti9-CD40)




Genotype
MGI:2662291
cn5
Allelic
Composition
Ikbkbtm2Mka/Ikbkbtm2.1Mka
Tg(Vil-cre)1Mka/0
Genetic
Background
involves: 129/Sv * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Ikbkbtm2.1Mka mutation (0 available); any Ikbkb mutation (54 available)
Ikbkbtm2Mka mutation (0 available); any Ikbkb mutation (54 available)
Tg(Vil-cre)1Mka mutation (0 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
digestive/alimentary system
• loss of mucosal integrity and increased number of apoptotic cells after gut ischemia-reperfusion
• mutants develop severe intestinal edematous change in response to gut ischemia-reperfusion compared to only mild edema in controls

immune system
• neutrophil migration/recruitment into the lung after gut ischemia-reperfusion is reduced and lung edema is prevented
• the increase in serum TNF-alpha that is observed in controls at 4 hours after gut ischemia-reperfusion is abolished
• reduction in systemic inflammatory response following gut ischemia-reperfusion

homeostasis/metabolism
• mutants develop severe intestinal edematous change in response to gut ischemia-reperfusion compared to only mild edema in controls
• the increase in serum TNF-alpha that is observed in controls at 4 hours after gut ischemia-reperfusion is abolished
• mutants show increased local injury but prevention of systemic inflammation following intestinal ischemia-reperfusion

hematopoietic system
• neutrophil migration/recruitment into the lung after gut ischemia-reperfusion is reduced and lung edema is prevented





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
04/30/2024
MGI 6.23
The Jackson Laboratory