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:108420Linkage analysis was performed on 420 female animals from a (C57BL/6Slc x SCG/Knj)F2 intercross to identify QTL for renal phenotypes. Parental strain SCG/Knj is derived from BXSB/Mp and MRL/Mp-Faslpr, and spontaneously develops crescentic glomerulonephritis and vascularitis. The Fas-lpr mutation is largely responsible for the disease phenotype but this experiment seeks to identify non-Fas disease-associated loci. 102 polymorphic markers covering 85% of the genome at a 20 cM resolution was used for the genome scan. F2 animals were analyzed by cohorts grouped according to genotype at the Fas locus. Significant linkage to total serum IgM at 12 weeks of age (LOD=4.8; 17% of variance) and total serum IgM and IgG at 24 weeks of age (LOD=6.7 and 4.4, respectively; 27% and 6% of variance, respectfully) mapped to mouse Chromosome 13 between D13Mit60 (16 cM) and D13Mit144 (48 cM). This locus is named Scgq5 (spontaneous crescentic glomerulonephritis QTL 5). SCG/Knj-derived alleles at Scgq5 confer increased IgG and IgM with a recessive mode of inheritance. Previously identified immune QTL mapping near Sgcq5 include Sgp3 (43 cM) and a locus reported by Haywood et al in 2001. |
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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 12/17/2024 MGI 6.24 |
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