Summary |
|
|||||||||||||
Variant origin |
|
|||||||||||||
Variant description |
|
|||||||||||||
Phenotypes |
View phenotypes and curated references for all genotypes (concatenated display).
|
|||||||||||||
Notes |
Mapping and Phenotype information for this QTL, its variants and associated markersJ:145043A previously mapped genetic locus on mouse Chromosome 1 exhibiting suggestive linkage to autoimmune myocarditis susceptibility was confirmed in this study using congenic line analysis. A 50 cM region (D1Mit65 to D1Mit334) containing Eamcd1 (experimental autoimmune myocarditis 1) derived from myocarditis susceptible strain A.SW-H2s/J was isolated on a resistant B10.S-H2s/J genetic background. This congenic line displays increased incidence of autoimmune myocarditis and is designated B10.A-(D1Mit65-D1Mit334). Experimental autoimmune myocarditis is characterized by the production of cardiac-specfic autoantibodies and diffuse mononuclear infiltratation after immunization with mouse cardiac myosin. Congenic animals also displayed decreased activation of caspase 3, 8 and 9 in CD4+ T cells after myosin antigen challenge. However, the severity of induced autoimmune myocarditis in B10.A-(D1Mit65-D1Mit334) congenic animals is lessened compared to that of susceptible donor strain A.SW. Icos (32 cM) and Il1r2 (19.5 cM) are two potential candidate genes located in the Eamcd1 QTL interval from 8.4 cM to 49.7 cM. Following myosin antigen challenge, Icos and Il1r2 mRNA expression is higher in the lymph nodes of B10.S-H2s/J mice compared to A.SW-H2s/J mice. |
|||||||||||||
References |
|
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 |
|
|