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:6517A locus associated with autoimmune hemolytic anemia was mapped to mouse Chromosome 4 using 100 (NZB/Omr x NZC/Omr)F1 x NZB/Omr and 180 (NZB/Omr x NZC/Omr)F1 x NZC/Omr backcross animals. Parental strain NZB/Omr is highly susceptible (nearly 100% incidence) to spontaneous autoimmune hemolytic anemia compared to parental strain NZC/Omr (0% incidence). Aia1 (autoimmune hemolytic anemia 1) is approximately 36 cM away from Tryp1 (previously known as the coat color gene b), and thought to be located near the minor histocompatibility locus H18 (74.5 cM), a potential candidate gene. Susceptibility to hemolytic autoimmune anemia is derived from the NZB/Omr allele at Aia1. A second unmapped locus, Aia2, is thought to exist. Aia1 and Aia2 are thought to exhibit a dominant or co-dominant effect. |
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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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