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Phenotypes Associated with This Genotype
Genotype
MGI:3629084
Allelic
Composition
Ctsetm1Kjy/Ctsetm1Kjy
Genetic
Background
involves: C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Ctsetm1Kjy mutation (0 available); any Ctse mutation (29 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
immune system
• homozygotes housed under conventional conditions have an increased ratio of CD4+CD8+ T cells among splenic lymphocytes compared to wild-type
• peripheral blood has an increased number of eosinophils compared to that of mice raised under SPF conditions
• in 14-week old homozygotes raised under conventional conditions from birth, serum IgE is ~10-fold higher than in wild-type animals;
• accumulation and reduced turnover of Il18 and Il1b is observed in homozygotes raised under conventional conditions
• accumulation and reduced turnover of Il18 and Il1b is observed in homozygotes raised under conventional conditions
• amounts of Il4 and Il5 in supernatants of stimulated cultures spleen cells are 6-fold and 3-fold greater respectively for mutants compared to wild-type
• amounts of Il4 and Il5 in supernatants of stimulated cultures spleen cells are 6-fold and 3-fold greater respectively for mutants compared to wild-type
• homozygous nulls develop dermatitis similar to atopic dermatitis seen in humans
• mutants raised under conventional conditions show increased sensitivity to hapten-induced experimental contact dermatitis compared to wild-type littermates and NC mice; rate of development and severity are greater
• 5 weeks after administration of TCNB, abscesses with infiltration and thickening of the epidermis is apparent in mutant mice

hematopoietic system
• homozygotes housed under conventional conditions have an increased ratio of CD4+CD8+ T cells among splenic lymphocytes compared to wild-type
• peripheral blood has an increased number of eosinophils compared to that of mice raised under SPF conditions
• in 14-week old homozygotes raised under conventional conditions from birth, serum IgE is ~10-fold higher than in wild-type animals;

homeostasis/metabolism
• accumulation and reduced turnover of Il18 and Il1b is observed in homozygotes raised under conventional conditions
• accumulation and reduced turnover of Il18 and Il1b is observed in homozygotes raised under conventional conditions

integument
• homozygous nulls develop dermatitis similar to atopic dermatitis seen in humans
• mutants raised under conventional conditions show increased sensitivity to hapten-induced experimental contact dermatitis compared to wild-type littermates and NC mice; rate of development and severity are greater
• 5 weeks after administration of TCNB, abscesses with infiltration and thickening of the epidermis is apparent in mutant mice
• dermis of homozygous mice has a large accumuation of eosinophils, mast cells, macrophages and lymphocytes
• epidermis is thickened by hyperplasia
• under conventional housing conditions, homozygous mice develop spontaneous skin atopic dermatitis-like lesions; cultured samples from lesions identified S. aureus as a preferential bacterium
• lesions of various grades are apparent on the face, neck, ears, nose and dorsal skin of mice depending on the age and duration of exposure to conventional conditions; onl a small percentage of heterozygotes developed lesions under the same conditions
• 50-week old animals showed more severe lesions than 14-week old mice; if mice are raised in conventional conditions from time of birth, lesions become apparent at 10 weeks of age and the time for induction of dermatitis decreases with age at time of transfer to conventional housing
• homozygotes at 50 weeks of age display other clinical signs of dermatitis such as itching, crust formation, and erosion

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
atopic dermatitis DOID:3310 OMIM:603165
OMIM:PS603165
J:108745


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
09/03/2024
MGI 6.24
The Jackson Laboratory