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 |
Desp2 exhibits epistatic interactions with loci at DXMit172 and D6Mit183 to increase immobility time in the tail suspension test when C57BL/6-derived alleles are present at each locus pair.
Mapping and Phenotype information for this QTL, its variants and associated markersJ:75441QTLs associated with behavioral despair were mapped in 560 (C57BL/6 x C3H/He)F2 intercross animals using 120 markers at an average density of 11 cM. Animals were subjected to forced swim tests (FST) and tail suspension tests (TST). The amount of time theanimal spent immobile during the tests was used as a measure of despair using the assumption the animal had given up all hope of escape. Parental strain C57BL/6 exhibits the longest periods of immobility indicating greater propensity for despair whereas parental strain C3H/He exhibits the shortest immobility times. Desp1 mapped to 47 cM on mouse Chromosome 8 in linkage to immobility during FST at D8Mit242 with LOD=4.2. C57BL/6-derived alleles confer increased despair in an additive fashion at Desp1. Desp2 mapped to 21 cM on mouse Chromosome 11 in linkage to immobility during both FST and TST at D11Mit271 with LOD=3.7 and LOD=3.6, respectively. C3H/He-derived alleles confer decreased despair in a dominant fashion at Desp2. Potential candidate genes for Desp2 include Gabrb2, Gabra1, Gabrg2, and Gabra6. Quantitative RT-PCR analysis revealed decreased expression of Gabra1 in the frontal cortex of C57BL/6 animals compared to C3H/He3 animals. Two-locus interaction analysis detected additive interactions between Desp2 and loci at DXMit172 and D6Mit183. Homozygosity for C57BL/6 alleles at each locus pair appears to amplify immobility during TST. |
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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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