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Phenotypes Associated with This Genotype
Genotype
MGI:3693641
Allelic
Composition
Lyntm1Tya/Lyntm1Tya
Genetic
Background
involves: 129P2/OlaHsd * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Lyntm1Tya mutation (1 available); any Lyn mutation (66 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• homozygotes tend to die with age

immune system
• number of lymphocytes in the periphery is about 2/3 of wild-type, although the number of red blood cells is normal
• population of B220+mIgM+ B cells is reduced by 70 to 35% in the peripheral tissues such as the lymph node and spleen, however bone marrow shows normal levels
• population of B220hiIgM+ cells, but not B220loIgM+ cells is slightly decreased, suggesting that only recirculating B cells in the bone marrow are affected
• spleen shows accumulation of a significant number of plasma cells and unusual lymphoblast-like cells carrying Mac1 antigen and cytoplasmic IgM
• evident in mutants older than 3 months of age
• increase in the mass of the white pulp, which contains large lymphoblast-like cells
• population of splenic B cells is reduced by half
• splenic B cells survive longer time periods than those from wild-type
• the proliferative response of splenic B cells to surface IgM cross-linking, CD40 ligand, and LPS is impaired
• serum levels of all isotypes are higher than in wild-type in the absence of antigenic stimulation, indicating some abnormalities in class switching
• 5-fold elevation in the absence of antigenic challenge
• IgA production is higher when challenged with DNP-KLH or TNP-LPS
• 28-fold elevation in the absence of antigenic challenge
• IgM production is higher when challenged with DNP-KLH or TNP-LPS
• Peyer's patches are smaller or undetectable
• anti-dsDNA antibodies elevated, most of which are IgM
• develop severe renal disease with hypercellularity, lobularity, and global sclerosis as age, an indication of autoimmune disease

renal/urinary system
• develop severe renal disease with hypercellularity, lobularity, and global sclerosis as age, an indication of autoimmune disease

hematopoietic system
• significant number of mutants older than 8 months of age are severely anemic
• number of lymphocytes in the periphery is about 2/3 of wild-type, although the number of red blood cells is normal
• population of B220+mIgM+ B cells is reduced by 70 to 35% in the peripheral tissues such as the lymph node and spleen, however bone marrow shows normal levels
• population of B220hiIgM+ cells, but not B220loIgM+ cells is slightly decreased, suggesting that only recirculating B cells in the bone marrow are affected
• spleen shows accumulation of a significant number of plasma cells and unusual lymphoblast-like cells carrying Mac1 antigen and cytoplasmic IgM
• evident in mutants older than 3 months of age
• increase in the mass of the white pulp, which contains large lymphoblast-like cells
• population of splenic B cells is reduced by half
• splenic B cells survive longer time periods than those from wild-type
• the proliferative response of splenic B cells to surface IgM cross-linking, CD40 ligand, and LPS is impaired
• serum levels of all isotypes are higher than in wild-type in the absence of antigenic stimulation, indicating some abnormalities in class switching
• 5-fold elevation in the absence of antigenic challenge
• IgA production is higher when challenged with DNP-KLH or TNP-LPS
• 28-fold elevation in the absence of antigenic challenge
• IgM production is higher when challenged with DNP-KLH or TNP-LPS

cellular
• the proliferative response of splenic B cells to surface IgM cross-linking, CD40 ligand, and LPS is impaired

growth/size/body
• evident in mutants older than 3 months of age


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
03/25/2025
MGI 6.24
The Jackson Laboratory