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Phenotypes Associated with This Genotype
Genotype
MGI:4417904
Allelic
Composition
Junbtm3Wag/Junbtm3Wag
Tg(KRT5-cre)1Tak/0
Genetic
Background
involves: 129/Sv * 129P2/OlaHsd * C3H * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Junbtm3Wag mutation (1 available); any Junb mutation (19 available)
Tg(KRT5-cre)1Tak mutation (0 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• mice die before 20 months

immune system
• mice exhibit an increase in plasma cells in the blood, lymph node and spleen unlike wild-type mice
• from epidermal cells
• mice exhibit skin ulcerations, the lupus band in the epidermal-dermal junction, increased IL-6 secretion, mesangial hypercellularity with glomerular basement membrane thickening and luminal obstruction, small and strophic kidney, increased anti-histone antibodies, and decreased survival compared with wild-type mice
• UV-treated mice exhibit inflammatory perivascular infiltrates with abundant CD3+ T lymphocytes in the liver and lungs unlike similarly treated Junbtm3Wag homozygotes
• UV-treated mice develop swelling of the paws with functional articular impairment, synovial proliferation, and synovial membrane inflammation unlike similarly treated Junbtm3Wag homozygotes
• unlike wild-type controls, mice develop immunocomplex glomerulonephritis (IC-GN) characterized by mesangial hypercellularity, lobulation of the glomerular tuft with basement membrane thickening, endocapillary hypercellularity, and luminal obstruction by immuno complex deposits
• UV-treated mice develop IC-GN accompanied by tubulo-interstitial nephritis and perivascular CD3+ T-cell-rich infiltrates unlike similarly treated Junbtm3Wag homozygotes
• UV-treated mice develop IC-GN accompanied by tubulo-interstitial nephritis and perivascular CD3+ T-cell-rich infiltrates unlike similarly treated Junbtm3Wag homozygotes
• starting at 3 months, mice exhibit dermatitis of ears, snouts, upper thorax region, and paws unlike wild-type mice

renal/urinary system
• mice display endocapillary hypercellularity and luminal obstruction by immuno complex deposits
• mice exhibit mesangial hypercellularity
• unlike wild-type controls, mice develop immunocomplex glomerulonephritis (IC-GN) characterized by mesangial hypercellularity, lobulation of the glomerular tuft with basement membrane thickening, endocapillary hypercellularity, and luminal obstruction by immuno complex deposits
• UV-treated mice develop IC-GN accompanied by tubulo-interstitial nephritis and perivascular CD3+ T-cell-rich infiltrates unlike similarly treated Junbtm3Wag homozygotes
• UV-treated mice develop IC-GN accompanied by tubulo-interstitial nephritis and perivascular CD3+ T-cell-rich infiltrates unlike similarly treated Junbtm3Wag homozygotes
• mice exhibit podocyte foot process effacement in most glomerular capillary loops
• mice exhibit lobulation of the glomerular tuft

homeostasis/metabolism

hematopoietic system
• mice exhibit an increase in plasma cells in the blood, lymph node and spleen unlike wild-type mice

integument
• starting at 3 months, mice exhibit dermatitis of ears, snouts, upper thorax region, and paws unlike wild-type mice
• mice exhibit the lupus band in the epidermal-dermal junction unlike wild-type mice

cardiovascular system
• mice display endocapillary hypercellularity and luminal obstruction by immuno complex deposits

cellular
• mice exhibit mesangial hypercellularity


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
04/16/2024
MGI 6.23
The Jackson Laboratory