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Qbis1C57BLKS/J
QTL Variant Detail
Summary
QTL variant: Qbis1C57BLKS/J
Name: QTL for body weight independent of sex 1; C57BLKS/J
MGI ID: MGI:3612520
QTL: Qbis1  Location: unknown  Genetic Position: Chr4, cM position of peak correlated region/allele: 70.02 cM
QTL Note: genome coordinates based on the marker associated with the peak LOD score
Variant
origin
Strain of Specimen:  C57BLKS/J
Variant
description
Allele Type:    QTL
Mutation:    Undefined
    This allele confers increased body weight and fat pad weight compared to DBA/2Jcl. (J:104466)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Structures Affected by this Mutation: 2 anatomical structure(s)
Notes

Mapping and Phenotype information for this QTL, its variants and associated markers

J:104466

Linkage analysis was performed on 634 animals from a (BKS.Cg-m+/+ Leprdb/Jcl x DBA/2Jcl)F2 intercross to identify QTL associated with diabetes-related traits. Parental strain BKS.Cg-m+/+ Leprdb/Jcl is diabetic, obese, and exhibits higher fasting blood glucose levels compared to parental strain DBA/2Jcl. F2 animals homozygous for the Leprdb mutation exhibit higher body weight, fat pad weight, and fasting glucose levels compared to wild type or heterozygous F2 animals. Genotype and sex were considered inthe phenotypic analysis. Animals were maintained on standard chow diet. 227 microsatellite markers covering the autosomes were used for the genome scan. The X chromosome was not analyzed due to lack of polymorphisms between the parental strains.

Four major sex-independent QTL named Qbis1, Qbis2, Qbis3, and Qbis4 mapped to mouse Chromosome 4, 5, 11, and 15, respectively. Twenty-seven significant interacting locus pairs were also identified, some of which involve Qbis1, Qbis2, Qbis3, or Qbis4.

Qbis1(QTL for body weight independent of sex 1) mapped to 66 cM (133.1 Mb) on mouse Chromosome 4 near D4Mit54 in the homozygous Leprdb F2 population. This locus is linked to body weight at 4 weeks of age in males (LOD=3.98; 11% of variance) and body weight at8 and 9 weeks of age in females (LOD=4.20; 13% of variance). Qbis1 is also linked to fat pad weight in females (LOD=5.18; 15% of variance). Homozygosity for C57BLKS/Jcl-derived alleles at Qbis1 confer increased body weight and fat pad weight.

Qbis2 mapped to approximately 41 cM - 45 cM (67.5 Mb - 84.1 Mb) on mouse Chromosome 5 near D5Mit356 - D5Mit40 in the homozygous Leprdb F2 population. In males, this locus is linked to body weight at 6, 7, 8, and 9 weeks of age (LOD=4.69; 13% of variance) and fatpad weight at 9 weeks of age (LOD=3.86; 11% of variance). In females, this locus is linked to body weight (LOD=3.87; 13% of variance) and fat pad weight (LOD=4.01; 13% of variance) at 9 weeks of age. Homozygosity for DBA/2Jcl-derived alleles at Qbis2 confer increased body weight and fat pad weight. A previously identified obesity QTL named Nobq1 (28 cM) maps near Qbis2.

Qbis3 mapped to 47.6 cM (90.4 Mb) in males and to 52 cM (96.5 Mb) in females on mouse Chromosome 11 near D11Mit36 and D11Mit179, respectively,in the heterozygous Leprdb F2 population. This locus is linked to body weight at 5, 6, and 7 weeks of age in males (LOD=4.75; 12% of variance) and body weight at 8, 9, and 10 weeks in females (LOD=4.99; 11% of variance). Homozygosity for DBA/2Jcl-derived alleles at Qbis3 confer increased body weight.

Qbis4 mapped to 48.2 cM (78.2 Mb) on mouse Chromosome 15 near D15Mit239 in the heterozygous Leprdb F2 population. This locus is linked to body weight at 8 weeks in males (LOD=4.49; 10% of variance)and body weight at 10 weeks in females (LOD=3.65; 9% of variance). Homozygosity for DBA/2Jcl-derived alleles at Qbis4 confer increased body weight.

References
Original:  J:104466 Togawa K, et al., Multidimensional genome scans identify the combinations of genetic loci linked to diabetes-related phenotypes in mice. Hum Mol Genet. 2006 Jan 1;15(1):113-28
All:  1 reference(s)

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
04/09/2024
MGI 6.23
The Jackson Laboratory