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Phenotypes Associated with This Genotype
Genotype
MGI:5440219
Allelic
Composition
Tcrbtm1Mom/Tcrbtm1Mom
Tcrdtm1Mom/Tcrdtm1Mom
Traf3ip2tm1.1Lix/Traf3ip2tm1.1Lix
Genetic
Background
B6.129-Tcrbtm1Mom Traf3ip2tm1.1Lix Tcrdtm1Mom
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Tcrbtm1Mom mutation (12 available); any Tcrb mutation (98 available)
Tcrdtm1Mom mutation (13 available); any Tcrd mutation (16 available)
Traf3ip2tm1.1Lix mutation (0 available); any Traf3ip2 mutation (41 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
immune system
N
• triple mutants exhibit reduced lupus-like phenotypes compared to Traf3ip2 single homozygotes, with normal spleen weight and cellularity, normal B cell numbers (B cell numbers however are decreased compared to Tcrb and Tcrd double homozygous mutants), normal cervical lymph node weight and cellularity, significantly less total IgG antibodies and anti-nuclear antigen specific IgG autoantibodies, and no IgG deposition in the kidney glomeruli
• 16-18 week old mutants exhibit a trend toward an increase in numbers of immature B cells
• ratios of T2:T1 and T3:T1 B cells are increased compared to wild-type mice
• mutants exhibit increased levels of marginal zone B cells compared to wild-type mice, however levels are similar to that seen in Traf3ip2 single homozygotes or to Tcrb and Tcrd double homozygous mutants, indicating no further increase in levels
• decrease in the number of T cells in the spleen compared to wild-type mice and Traf3ip2 single homozygotes
• mutants develop significantly less total IgG antibodies (IgG, IgG1, IgG2c) and anti-nuclear antigen specific IgG autoantibodies than Traf3ip2 single homozygotes
• the IgG deposition within the kidney glomeruli that is seen in Traf3ip2 single homozygotes is not seen in triple mutants
• mutants exhibit elevated levels of IgM deposition within kidney glomeruli
• serum levels of anti-chromatin IgM, anti-histone IgM, and anti-dsDNA Igm are elevated in triple mutants compared to Traf3ip2 single homozygotes
• serum levels of anti-chromatin IgM are elevated in triple mutants compared to Traf3ip2 single homozygotes
• serum levels anti-dsDNA IgM are elevated in triple mutants compared to Traf3ip2 single homozygotes
• serum levels of anti-histone IgM are elevated in triple mutants compared to Traf3ip2 single homozygotes

hematopoietic system
• 16-18 week old mutants exhibit a trend toward an increase in numbers of immature B cells
• ratios of T2:T1 and T3:T1 B cells are increased compared to wild-type mice
• mutants exhibit increased levels of marginal zone B cells compared to wild-type mice, however levels are similar to that seen in Traf3ip2 single homozygotes or to Tcrb and Tcrd double homozygous mutants, indicating no further increase in levels
• decrease in the number of T cells in the spleen compared to wild-type mice and Traf3ip2 single homozygotes
• mutants develop significantly less total IgG antibodies (IgG, IgG1, IgG2c) and anti-nuclear antigen specific IgG autoantibodies than Traf3ip2 single homozygotes
• the IgG deposition within the kidney glomeruli that is seen in Traf3ip2 single homozygotes is not seen in triple mutants
• mutants exhibit elevated levels of IgM deposition within kidney glomeruli
• serum levels of anti-chromatin IgM, anti-histone IgM, and anti-dsDNA Igm are elevated in triple mutants compared to Traf3ip2 single homozygotes

cardiovascular system
• kidneys show occasional obstruction of the capillary lumina

renal/urinary system
• kidneys show occasional obstruction of the capillary lumina
• kidneys show moderate hypercellularity of the glomerular mesangium and occasional obstruction of the capillary lumina, however no signs of mononuclear cell infiltrates or signs of tubulointerstitial disease
• mutants exhibit elevated levels of IgM deposition within kidney glomeruli

cellular
• kidneys show moderate hypercellularity of the glomerular mesangium and occasional obstruction of the capillary lumina, however no signs of mononuclear cell infiltrates or signs of tubulointerstitial disease


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
03/18/2025
MGI 6.24
The Jackson Laboratory