Summary |
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Variant origin |
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Variant description |
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Phenotypes |
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View phenotypes and curated references for all genotypes (concatenated display).
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Expression |
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Notes |
Mapping and Phenotype information for this QTL, its variants and associated markersJ:26266The authors show the following order of loci in mouse Chromosome 4: The number between the loci represents the genetic distance based on percent recombination in crosses involving NZW and NZB mice: Imm1- 38.6 - Mup1 - 15.6 - b - 28.7 - Imh1. J:49899Linkage analysis was performed on 127 male animals from a NZW/Slc x (NZW/Slc x BXSB/Slc)F1 backcross to identify QTL associated with systemic lupus erythematosus (SLE) traits, such as anticardiolipin antibody production, platelet-binding autoantibody production, thrombocytopenia, and myocardial infarction. 108 polymorphic markers were used for the genome scan. Male F1 animals carrying the BXSB-derived Yaa locus exhibit significantly elevated anticardiolipin antibodies and an increased frequency of myocardial infarction, and serve as a mouse model of human SLE-associated antiphospholipid syndrome. Linkage to platelet-binding IgG antibodies and thrombocytopenia mapped to 17.4 cM on mouse Chromosome 17 near D17Mit16 (close to the H2 locus) and 11 cM on mouse Chromosome 8 near D8Mit96. These loci are designated Pbat1 (platelet-binding antibody-associated thrombocytopenia 1) and Pbat2, respectively. BXSB-derived alleles at Pbat1 and Pbat2 confer increased platelet binding IgG production and increased thrombocytopenia with a dominant mode of inheritance. Potential candidate genes mapping near Pbat2 include Scat (5 cM) and Plat (9 cM). Linkage to anti-cardiolipin antibody production mapped to 17.4 cM on mouse Chromosome 17 near D17Mit16 and 44.5 cM on mouse Chromosome 4 near D4Mit9. These loci are designated Acla1 (anticardiolipin antibody 1) and Acla2, respectively. BSXB/Slc-derived alleles at Acla1 and Acla2 confer increased anti-cardiolipin antibody production witha dominant mode of inheritance. Ifna (42.6 cM) and Ifnb1 (42.6 cM) are potential candidate genes for Acla2. Previously identified QTLs Imh1 (66 cM) and Mott1 (66 cM) map near Acla2. Linkage to myocardial infarction mapped to 69 cM on mouse Chromosome 7 near D7Mit14 and 39 cM on mouse Chromosome 14 near D14Mit68. These loci are designated Myci1 (myocardial infarction 1) and Myci2, respectively. BXSB-derived alleles at Myci1 and Myci2 confer increased incidence of myocardial infarction with a dominant mode of inheritance. A potential candidate genes for Myci1 is Il4r (62 cM) and a potential candidate gene for Myci2 is amd (30.5 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 08/02/2024 MGI 6.24 |
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