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Phenotypes Associated with This Genotype
Genotype
MGI:3842820
Allelic
Composition
H2b/H2g7
Tg(TcraR28,TcrbR28)KRNDim/0
Genetic
Background
involves: C57BL/6 * NOD * SJL
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
H2b mutation (30 available); any H2 mutation (282 available)
H2g7 mutation (24 available); any H2 mutation (282 available)
Tg(TcraR28,TcrbR28)KRNDim mutation (0 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
immune system
• mitral valve inflammation begins at 3 weeks of age and by 8 weeks, accumulation of inflammatory cells and interstitial thickening is obvious indicating fibroinflammatory mitral valve disease
• mononuclear phagocytes (macrophages and monocytes) constitute the vast majority of accumulated leukocytes
• frequency of TNF- and IL-6-producing phagocytes in inflamed mitral valve tissue is elevated, indicating an enrichment of cytokine-producing phagocytes within the inflamed mitral valves
• antibody blockade of either TNF or IL-6 beginning at the onset of mitral valve inflammation reduces mitral valve fibrosis and thickening
• rheumatoid arthritis occurs with disease onset transpiring between 25 and 35 days of age (J:36815)
• arthritis occurrence is established by joint inspection and measure of ankle thickness, and histological confirmation in several mice (J:36815)

cardiovascular system
• mitral valve hydroxyproline content is elevated
• by 8 weeks of age, mitral valves are fibrotic and thickened
• TNFR2 neutralization with a monoclonal antibody exacerbates mitral valve fibrosis and thickening
• blockade of either VLA-4 or VCAM-1 with monoclonal antibodies attenuates valve fibrosis and thickening
• mitral valve inflammation begins at 3 weeks of age and by 8 weeks, accumulation of inflammatory cells and interstitial thickening is obvious indicating fibroinflammatory mitral valve disease
• mononuclear phagocytes (macrophages and monocytes) constitute the vast majority of accumulated leukocytes
• frequency of TNF- and IL-6-producing phagocytes in inflamed mitral valve tissue is elevated, indicating an enrichment of cytokine-producing phagocytes within the inflamed mitral valves
• antibody blockade of either TNF or IL-6 beginning at the onset of mitral valve inflammation reduces mitral valve fibrosis and thickening

homeostasis/metabolism
• mitral valve hydroxyproline content is elevated

skeleton
• rheumatoid arthritis occurs with disease onset transpiring between 25 and 35 days of age (J:36815)
• arthritis occurrence is established by joint inspection and measure of ankle thickness, and histological confirmation in several mice (J:36815)

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
mitral valve disease DOID:61 J:275827
rheumatoid arthritis DOID:7148 OMIM:180300
J:36815


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
11/19/2024
MGI 6.24
The Jackson Laboratory