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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Il13tm2Anjm
targeted mutation 2, Andrew NJ McKenzie
MGI:1931804
Summary 6 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Il13tm2Anjm/Il13tm2Anjm B6.129P2-Il13tm2Anjm MGI:5432708
hm2
Il13tm2Anjm/Il13tm2Anjm C.129P2(B6)-Il13tm2Anjm MGI:3038308
hm3
Il13tm2Anjm/Il13tm2Anjm involves: 129 MGI:3850549
hm4
Il13tm2Anjm/Il13tm2Anjm involves: 129P2/OlaHsd * BALB/c * C57BL/6 MGI:5432601
hm5
Il13tm2Anjm/Il13tm2Anjm involves: 129P2/OlaHsd * C57BL/6 MGI:3038307
cx6
Il13tm2Anjm/Il13tm2Anjm
Tg(SFTPC-Il18)AThos/0
involves: 129P2/OlaHsd * C57BL/6 * C57BL/6N * DBA/2 MGI:5688502


Genotype
MGI:5432708
hm1
Allelic
Composition
Il13tm2Anjm/Il13tm2Anjm
Genetic
Background
B6.129P2-Il13tm2Anjm
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Il13tm2Anjm mutation (6 available); any Il13 mutation (30 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
immune system
• decrease in the number of CD11b+ cells in the brain and spinal cord in female mice
• production of IL12 and IFNG by mononuclear cells from female mice stimulated with MOG-35?55 is significantly reduced compared to cells from male mice
• production of EAE associated chemokines by mononuclear cells from female mice is reduced compared to cells from male mice
• antigen presenting cells taken from female mice at the peak of EAE stimulated with MOG-35?55 present antigen with reduced efficiency compared to cells from male mice
• females develop EAE with reduced severity or are resistant to EAE compared to wild-type females
• however, EAE severity in males is similar to wild-type males

hematopoietic system
• decrease in the number of CD11b+ cells in the brain and spinal cord in female mice
• production of IL12 and IFNG by mononuclear cells from female mice stimulated with MOG-35?55 is significantly reduced compared to cells from male mice
• production of EAE associated chemokines by mononuclear cells from female mice is reduced compared to cells from male mice




Genotype
MGI:3038308
hm2
Allelic
Composition
Il13tm2Anjm/Il13tm2Anjm
Genetic
Background
C.129P2(B6)-Il13tm2Anjm
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Il13tm2Anjm mutation (6 available); any Il13 mutation (30 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
immune system
• neutralizing IL14 reduces response in sensitized mice down to that in unsensitized mice, unlike in wild-type mice
• neutralizing IL15 also reduces response in sensitized mutant mice but not in wild-type mice
• show a heightened response relative to wild-type mice in a model of airways hyperreactivity (sensitized and aeroallergen challenged with OVA followed by challenge with Beta-metacholine)
• however, mucus hypersecretion in this model of airways hyperreactivity is reduced
• decrease in luminal occlusion in tracheal allografts from C57BL/6 mice compared to transplants into wild-type mice
• allografts do not show a significant upregulation of TGFB1 compared to isografts
• tracheal allografts from C57BL/6 mice display prolonged maintenance of epithelial integrity and absence of luminal fibroproliferation

homeostasis/metabolism
• decreased pulmonary fibrosis is seen after FITC treatment most likely a result of an overall decrease in collagen production




Genotype
MGI:3850549
hm3
Allelic
Composition
Il13tm2Anjm/Il13tm2Anjm
Genetic
Background
involves: 129
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Il13tm2Anjm mutation (6 available); any Il13 mutation (30 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
hematopoietic system
• much fewer Th2 cells are developed in vitro when nave CD4 T cells are cultured under Th2-polarizing conditions
• Th2 cells are produced under chronic N. brasiliensis infection
• much fewer Th2 cells are found in vitro
• total IgE levels are decreased 5- to 20- fold
• however, IgE levels are comparable to wild-type when mice are immunized
• there are increased amounts of antigen-specific IgG2b levels when mice are immunized compared to controls
• there are increased amounts of antigen-specific IgM levels when mice are immunized compared to control

homeostasis/metabolism
• IL-13 are absent in these mice

immune system
• much fewer Th2 cells are developed in vitro when nave CD4 T cells are cultured under Th2-polarizing conditions
• Th2 cells are produced under chronic N. brasiliensis infection
• much fewer Th2 cells are found in vitro
• total IgE levels are decreased 5- to 20- fold
• however, IgE levels are comparable to wild-type when mice are immunized
• there are increased amounts of antigen-specific IgG2b levels when mice are immunized compared to controls
• there are increased amounts of antigen-specific IgM levels when mice are immunized compared to control
• IL-13 are absent in these mice
• IFN-gamma secretion is 2-fold compared to controls when CD4 T cells are restimulated compared to controls
• IL-10 secretion is reduced 2-fold compared to controls when nave CD4 T cells are cultured under Th2-polarizing conditions
• IL-4 secretion is dramatically decreased compared to controls when nave CD4 T cells are cultured under Th2-polarizing conditions
• schistosome eggs, an antigen that induces Th2 cell responses, induces a 2-fold decreased IL-4 response than controls
• IL-5 secretion is dramatically decreased compared to controls when nave CD4 T cells are cultured under Th2-polarizing conditions
• schistosome eggs, an antigen that induces Th2 cell responses, induces a 2-fold decreased IL-5 response than controls




Genotype
MGI:5432601
hm4
Allelic
Composition
Il13tm2Anjm/Il13tm2Anjm
Genetic
Background
involves: 129P2/OlaHsd * BALB/c * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Il13tm2Anjm mutation (6 available); any Il13 mutation (30 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• decreased mortality following acute infection with Schistosoma mansoni compared to wild-type mic

immune system
• in mice sensitized by injection of alum-precipitated chicken egg ovalbumin the exposed to low levels of aerosolized antigen little evidence of recruitment of eosinophils into the tracheal epithelium is seen
• to the liver following ischemia/reperfusion resulting from an apparent defect in transendothelial migration
• phagocytosis of Chlamydia muridarum is enhanced in vitro and in vivo
• in mice immunized with recombinant vvG levels of CCL11 and CCL22 are reduced in the lungs
• mice immunized with recombinant vvG (vaccinia virus expressing the G protein of respiratory syncytial virus (RSV)) then challenged with RSV display lower percentages and total numbers of eosinophils in the bronchoalveolar lavage (BAL) compared to wild-type mice
• in mice immunized with recombinant vvG and then challenged with RSV eosinophilia in both perivascular and interstitial regions of the lung is significantly decreased
• however, levels of eosinophils in the blood and bone marrow are similar to controls
• after respiratory infection with Chlamydia muridarum (Cmu) mice do not lose weight, show reduced bacterial loads in the lungs and reduced airway inflammation
• mice are also resistant to genital tract Cmu infection
• negligible hepatic fibrosis following infection with Schistosoma mansoni unlike in wild-type mice
• decreased mortality following acute infection with Schistosoma mansoni compared to wild-type mic

homeostasis/metabolism
• in mice immunized with recombinant vvG levels of CCL11 and CCL22 are reduced in the lungs
• increased liver damage following liver ischemia/reperfusion indicated by increased serum ALT levels and marked destruction of hepatocellular structure throughout the liver
• increased susceptibility to hepatic vascular endothelial cell injury during early periods of reperfusion

hematopoietic system
• in mice sensitized by injection of alum-precipitated chicken egg ovalbumin the exposed to low levels of aerosolized antigen little evidence of recruitment of eosinophils into the tracheal epithelium is seen
• to the liver following ischemia/reperfusion resulting from an apparent defect in transendothelial migration
• phagocytosis of Chlamydia muridarum is enhanced in vitro and in vivo




Genotype
MGI:3038307
hm5
Allelic
Composition
Il13tm2Anjm/Il13tm2Anjm
Genetic
Background
involves: 129P2/OlaHsd * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Il13tm2Anjm mutation (6 available); any Il13 mutation (30 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• decreased mortality following chronic infection with Schistosoma mansoni compared to wild-type mice

immune system
N
• development of skin lesion sin response to Leishmania mexicana infection is similar to that in wild-type mice
• homozygotes display impaired pulmonary granuloma formation in response to schistosome egg immunization
• eosinophil infiltration is impaired in response to schistosome egg immunization
• Leishmania mexicana antigen stimulated cells from L. mexicana infected mice produce increased amounts of IL12
• decreased mortality following chronic infection with Schistosoma mansoni compared to wild-type mice
• the expulsion of parasitic worms from the gut is delayed

hematopoietic system
• homozygotes display impaired pulmonary granuloma formation in response to schistosome egg immunization
• eosinophil infiltration is impaired in response to schistosome egg immunization
• Leishmania mexicana antigen stimulated cells from L. mexicana infected mice produce increased amounts of IL12




Genotype
MGI:5688502
cx6
Allelic
Composition
Il13tm2Anjm/Il13tm2Anjm
Tg(SFTPC-Il18)AThos/0
Genetic
Background
involves: 129P2/OlaHsd * C57BL/6 * C57BL/6N * DBA/2
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Il13tm2Anjm mutation (6 available); any Il13 mutation (30 available)
Tg(SFTPC-Il18)AThos mutation (0 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
growth/size/body
• mice show a decrease in body weight from 16 to 24 weeks of age, however weight loss is less than seen in single transgenic Tg(SFTPC-Il18)AThos mice

respiratory system
• mean alveolar chord lengths of 14 week old mice is shorter than in single transgenic mice
• however, pulmonary inflammation and emphysematous changes are not seen in the lungs enlarged alveolar macrophages and exudates are not present in the lungs

muscle
• decrease in quadriceps femoris muscle weight at 7 and 16 weeks of age, although muscle is heavier than in single transgenic Tg(SFTPC-Il18)AThos mice and by 25 weeks of age, weight is similar to wild-type mice
• mice show a decrease in gastrocnemius muscle weight at 7 weeks of age but not 16 and 25 weeks of age

skeleton
N
• bone mineral density is normal





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last database update
11/19/2024
MGI 6.24
The Jackson Laboratory