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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Expression |
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Notes |
Mapping and Phenotype information for this QTL, its variants and associated markersJ:89267Linkage analysis was performed on 217 (C3H/HeJ x SWR/J)F2 intercross animals to identify QTLs associated with blood pressure. Parental strain SWR/J is hypertensive compared to parental strain C3H/HeJ. Genome scan was conducted using 103 polymorphic markers. Bpq8 (blood pressure QTL 8) mapped to 78 cM on mouse Chromosome 1 with LOD=3.5 at D1Mit105. This locus explains 4.5% of the phenotypic variance. The QTL range of Bpq8 is broad spanning 64 cM - 106 cM. SWR/J-derived alleles confer increased blood pressure with dominant inheritance at this locus. Bpq8 overlaps with a previously identified blood pressure QTL named Bpq2 (81.6 cM). The QTL interval was narrowed significantly by combining data from the Bpq8 and Bpq2 crosses. Combining data narrowed the Bpq8 QTL range to 68 cM -86 cM and increased the LOD score to 6.38. Haplotype analysis comparing the allelic differences between hypertensive strains (C57BL/6J, SWR/J) and normotensive strains (A/J, C3H/HeJ) further reduced the Bpq8 interval to a 2.3 cM region centered around 81.6 cM.Bpq9 mapped to 56 cM on mouse Chromosome 16 with LOD=3.6 at D16Mit158. This locus explains 5.9% of the phenotypic variance. The QTL range of Bpq9 spans 46 cM - 58 cM. Interestingly, homozygosity for SWR/J-derived alleles or homozygosity for C3H/HeJ-derived alleles confer increased blood pressure compared to heterozygotes. Further analysis gave evidence of two separate but closely linked QTLs at 44 cM and 54 cM with opposite allele effects. |
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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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