About   Help   FAQ
Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Tg(Igk-V21-Bax)1967Bvn
transgene insertion 1967, Brian Van Ness
MGI:3046400
Summary 3 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
cx1
Ighatm1(Myc)Janz/Igha+
Tg(Igk-V21-Bax)1967Bvn/0
involves: 129S1/Sv * C57BL/6 * FVB/N MGI:3046405
cx2
Tg(IghMyc)22Bri/0
Tg(Igk-V21-Bax)1967Bvn/0
involves: C57BL/6 * FVB/N MGI:3046406
tg3
Tg(Igk-V21-Bax)1967Bvn/0 involves: FVB/N MGI:3046404


Genotype
MGI:3046405
cx1
Allelic
Composition
Ighatm1(Myc)Janz/Igha+
Tg(Igk-V21-Bax)1967Bvn/0
Genetic
Background
involves: 129S1/Sv * C57BL/6 * FVB/N
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Ighatm1(Myc)Janz mutation (1 available); any Igha mutation (18 available)
Tg(Igk-V21-Bax)1967Bvn mutation (0 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
growth/size/body
• 8 week old double transgenic exhibit splenomegaly with massive accumulation of plasma cells in extrafollicular areas

mortality/aging
• survival of double transgenics is markedly decreased as a result of malignant plasma cell tumors

neoplasm
• in some cases plasma cell leukemia is seen
• malignant plasma cell tumors develop rapidly with a mean onset of 135 days, are fully penetrant, proliferate vigorously, occur in multiple tissues including the spleen, bone marrow, and lymph nodes, and may have monocentric or multicentric origins
• bone sections from double transgenic mice with less advanced tumors show multifocal lesions of aberrant pleomorphic plasma cells next to diminished of dissolved osseous trabeculae
• pathalogical fractures of the long bones are seen in some double transgenic mice

hematopoietic system
• B cell apoptosis is increased compared to normal B cells but decreased compared to B cells from Igh-2tm1Janz single transgenics
• 8 week old double transgenic exhibit splenomegaly with massive accumulation of plasma cells in extrafollicular areas
• plasma cells participate in cell cycling unlike in normal mice
• the bone marrow and spleen contain on average 42% and 34% plasma cells, respectively, compared to less than 2% in normal mice
• elevation of IgG accompanied the increase in plasma cell numbers
• elevation of IgM accompanied the increase in plasma cell numbers

immune system
• B cell apoptosis is increased compared to normal B cells but decreased compared to B cells from Igh-2tm1Janz single transgenics
• 8 week old double transgenic exhibit splenomegaly with massive accumulation of plasma cells in extrafollicular areas
• plasma cells participate in cell cycling unlike in normal mice
• the bone marrow and spleen contain on average 42% and 34% plasma cells, respectively, compared to less than 2% in normal mice
• elevation of IgG accompanied the increase in plasma cell numbers
• elevation of IgM accompanied the increase in plasma cell numbers

cellular
• B cell apoptosis is increased compared to normal B cells but decreased compared to B cells from Igh-2tm1Janz single transgenics




Genotype
MGI:3046406
cx2
Allelic
Composition
Tg(IghMyc)22Bri/0
Tg(Igk-V21-Bax)1967Bvn/0
Genetic
Background
involves: C57BL/6 * FVB/N
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Tg(IghMyc)22Bri mutation (1 available)
Tg(Igk-V21-Bax)1967Bvn mutation (0 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• 50% of double transgenics die of a lymphoproliferative disorder by 5.5 weeks

neoplasm
• multifocal to coalescent infiltrations of mononuclear cells with large round to polygonal hypochromatic nuclei are seen in the kidneys, spleen, lymph node, liver, ung, heart, thymus, pancreas, and sternal bone marrow
• osteolytic lesions with cheets of pleomorphic plasmacytic cells adjacent to lysed osseous trabeculae are seen

hematopoietic system
• 4 - 6 week old double transgenic exhibit severe splenomegaly
• the number of immature/transitional B cells is increased

immune system
• 4 - 6 week old double transgenic exhibit severe splenomegaly
• the number of immature/transitional B cells is increased

liver/biliary system
• multiple beige nodules up to 2 mm in diameter are seen

growth/size/body
• 4 - 6 week old double transgenic exhibit severe splenomegaly




Genotype
MGI:3046404
tg3
Allelic
Composition
Tg(Igk-V21-Bax)1967Bvn/0
Genetic
Background
involves: FVB/N
Find Mice Using the International Mouse Strain Resource (IMSR)
No mouse lines available in IMSR.
See publication links below for author information.
phenotype observed in females
phenotype observed in males
N normal phenotype
hematopoietic system
• the number of immature/transitional B cells is increased
• plasma cell foci are seen in the kidney, bone marrow and other lymphoid tissues
• in response to a T cell independent antigen transgenic mice produce 65% more specific Igs compared to littermate controls
• IgA serum levels are increased
• IgE serum levels are increased
• a moderate elevation of 3 isotypes of IgG is seen (J:90901)
• serum levels are increased
• serum levels are increased
• IgM serum levels are increased

homeostasis/metabolism
• some transgenic mice have detectable levels of Ig proteins in their urine

immune system
• the number of immature/transitional B cells is increased
• plasma cell foci are seen in the kidney, bone marrow and other lymphoid tissues
• in response to a T cell independent antigen transgenic mice produce 65% more specific Igs compared to littermate controls
• IgA serum levels are increased
• IgE serum levels are increased
• a moderate elevation of 3 isotypes of IgG is seen (J:90901)
• serum levels are increased
• serum levels are increased
• IgM serum levels are increased

renal/urinary system
• some transgenic mice have detectable levels of Ig proteins in their urine
• multiple perivascular foci of lymphocytes are seen in the kidney
• hyaline renal tubular casts presumably made of Ig proteins are found





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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
11/12/2024
MGI 6.24
The Jackson Laboratory