Summary |
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Variant origin |
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Variant description |
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Phenotypes |
View phenotypes and curated references for all genotypes (concatenated display).
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Notes |
Mapping and Phenotype information for this QTL, its variants and associated markersJ:96562Linkage analysis was performed on a population of (B10.S-H2s/J x A.SW-H2s/J)F2 animals to identify QTLs associated with experimental autoimmune myocarditis. Parental strain A.SW-H2s/J is susceptible to experimental autoimmune myocarditis after immunization with mouse cardiac myosin, which is characterized by the production of cardiac-specfic autoantibodies and diffuse mononuclear infiltratation. Parental strain B10.S-H2s/J is resistant to experimentally induced myocarditis and exhibits minimal inflammation. 81 polymorphic markers at an average spacing of 20 cM were used in the genome scan. 144 phenotypically extreme F2 animals were used for the initial genome scan. Linkage was detected on mouse Chromosome 1, 4, and 6. After genotyping remainingF2 progeny (total n=296) significant linkage was confirmed for mouse Chromosome 6. This locus is named Eamcd2 (experimental autoimmune myocarditis 2). Eamcd2 is a male specific locus and maps to 74.3 cM (LOD=5.7 at D6Mit373). The 1.5 LOD support intervalspans 9 cM around the peak. A/J-derived alleles from A.SW-H2s confer increased susceptibility to autoimmune myocarditis in male animals at Eamcd2.Previously identified diabetes QTL Idd6 (73 cM) overlaps with Eamcd2. Idd6 was identified in diabetes susceptible strain NOD. Idd6 also exhibits a greater effect in male animals similar to Eamcd2. Highly suggestive linkage mapped to mouse Chromosome 1 (LOD=3.26) but this locus warrants further analysis and mapping. This region of chromosome 1 overlaps with a previously identified diabetes QTL named Idd5 (40 cM). |
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References |
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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 11/12/2024 MGI 6.24 |
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