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Mapping Data
Experiment
  • Experiment
    TEXT-QTL
  • Chromosome
    5
  • Reference
    J:81446 Battersby BJ, et al., Nuclear genetic control of mitochondrial DNA segregation. Nat Genet. 2003 Feb;33(2):183-6
  • ID
    MGI:2656786
Genes
GeneAlleleAssay TypeDescription
Smdq1 visible phenotype
D5Mit25 PCR amplified length variant
Notes
  • Experiment
    Genome scan was performed on a (BALB/c x CAST/Ei)F2 intercross population to identify QTLs affecting mitochondrial DNA (mtDNA) segregation. Three loci were mapped to mouse Chromosomes 2, 5, and 6. Smdq1 maps to 61 cM on mouse Chromosome 5 at D5Mit25 (LOD=31.5) in linkage to mtDNA segregation in the liver at 3 months of age and accounts for 35% of the phenotypic variance. CAST/Ei-derived alleles at Smdq1 appear to influence mtDNA segregation in a dominantly-inherited manner. Smdq2 maps to 51.4 cM on mouse Chromosome 2 at D2Mit480 (LOD=4.0) in linkage to mtDNA segregation in the kidney at 3 months of age and accounts for 16% of the phenotypic variance. CAST/Ei-derived alleles appear to be associated with mtDNA segregation at Smdq2 in a recessive manner. Smdq3 maps to 3.6 cM on mouse Chromosome 6 at D6Mit266 (LOD=4.4) in linkage to mtDNA segregation in the spleen at 12 months of age and accounts for 20% of the phenotypic variance.

Contributing Projects:
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
04/30/2024
MGI 6.23
The Jackson Laboratory