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:85562Genome scan was performed an a population of (C57BL/6J x BALB/cJ)F2 animals to detect loci associated with MPTP-induced dopamine depletion. MPTP is a neurotoxin that causes dopamine loss and Parkinson's disease symptoms in experimental animals. Parental strain C57BL/6J exhibits increased susceptibility to MPTP-induced dopamine depletion compared to BALB/cJ. Interestingly, female F2 animals exhibit a 31.6% mortality rate after MPTP administration whereas male F2 animals exhibit 0% mortality. Dpml (dopamine loss), a female specific locus mapped to approximately 32.5 cM on mouse Chromosome 15 with LOD=4.8 between 21 cM (D15Mit100) and 44.1 cM (D15Mit68). BALB/cJ-derived alleles confer increased MPTP-induced dopamine depletion at Dpml. A candidate gene mapping to this region is Hsf1. A suggestive locus mapped to 30 cM (D13Mit91) - 45 cM (D13Mit233) on mouse Chromosome 13. BALB/cJ-derived alleles confer increased MPTP-induced dopamine depletion at this locus.An interacting locus pair reaching statisticalsignificance was also identified at 29 cM on mouse Chromosome 9 and 79.4 cM on mouse Chromosome 3. Interaction occurs between D9Mit14 and D3Mit147. |
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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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