Summary |
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Variant origin |
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Variant description |
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Notes |
Mapping and Phenotype information for this QTL, its variants and associated markersJ:94027Two different methods were used to assess lesion phenotypes of the colon and cecum and their power to detect colitis QTLs. 259 (C3Bir.129P2-Il10tm1Cgn/J x B6.129P2-Il10tm1Cgn/J)F1 x C3Bir.129P2-Il10tm1Cgn/J backcross animals were used for linkage analysis. A total of 359 mice were analyzed, which includes parental and F1 hybrid animals. All animals were assessed using both scoring methods. Parental strain C3H/HeJBir is susceptible to colitis while parental strain C57BL/6J is resistant. The more detailed scoring method by The Jackson Lab (TJL) was more powerful in detecting a colitis susceptibility locus, Cdcs11, on mouse Chromosome 3 compared to the less detailed Hanover Medical School (MHH) method. In this study, TJL method detected linkage to distal colon phenotypes at D3Mit257 (70.3 cM, LOD=2.61) and total colon phenotypes at D3Mit199 (60.5 cM, LOD=2.64). Linkage to total parameters (which included severity, hyperplasia, ulceration, and area involved) yielded higher LOD scores at D3Mit199 (LOD=4.08) and D3Mit257 (LOD=4.28) using TJL method. Using the more simple MHH method, only linkage to distal colon phenotypes, represented by QTL Cdcs12, could be detected at D3Mit18 (76 cM) with a lower LOD score (LOD=1.77). |
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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 12/10/2024 MGI 6.24 |
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