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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Ltbtm1Krn
targeted mutation 1, Heinrich Korner
MGI:2384499
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Ltbtm1Krn/Ltbtm1Krn C57BL/6-Ltbtm1Krn MGI:3768355


Genotype
MGI:3768355
hm1
Allelic
Composition
Ltbtm1Krn/Ltbtm1Krn
Genetic
Background
C57BL/6-Ltbtm1Krn
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Ltbtm1Krn mutation (0 available); any Ltb mutation (19 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• unlike wild-type mice, infection with Leishmania major results in skin lesions that progress to ulcers and mortality within 8 to 14 weeks

immune system
• while white pulp structure and B cell follicular structures are conserved there is limited B cell penetration into T cell areas
• the spleen is hypercellular and double the wild-type size
• 38% of mice exhibit 1 to 3 large mesenteric lymph nodes, 38% exhibit small or normal lymph nodes and 24% exhibit no lymphoid aggregates
• unlike wild-type mice, 7 days after infection with Leishmania major no specific antigen response has been mounted and only a weak T cell response is visible by 28 days
• however, immune response to Con A is normal
• IgG1 production during the first 3 weeks following infection with Leishmania major is lower than in wild-type mice
• IgG2a production during the first 3 weeks following infection with Leishmania major is virtually absent unlike in wild-type mice
• IgM production during the first 3 weeks following infection with Leishmania major is higher than in wild-type mice
• unlike wild-type mice, infection with Leishmania major results in skin lesions that progress to ulcers and mortality within 8 to 14 weeks
• parasite content in the spleen is 500x higher than in wild-type mice after 14 days (5 viable parasites per 1000 splenocytes compared to 0.01 viable parasites per 1000 splenocytes in wild-type mice)

hematopoietic system
• while white pulp structure and B cell follicular structures are conserved there is limited B cell penetration into T cell areas
• the spleen is hypercellular and double the wild-type size
• IgG1 production during the first 3 weeks following infection with Leishmania major is lower than in wild-type mice
• IgG2a production during the first 3 weeks following infection with Leishmania major is virtually absent unlike in wild-type mice
• IgM production during the first 3 weeks following infection with Leishmania major is higher than in wild-type mice

growth/size/body
• the spleen is hypercellular and double the wild-type size





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