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Genome wide association study in Swedish Labrador retrievers identifies genetic loci associated with hip dysplasia and body weight

Kieler, Ida Nordang (author)
Univ Copenhagen, Dept Vet Clin Sci, Copenhagen, Denmark.
Persson, Sofia Malm (author)
Swedish Kennel Club, Dept Breeding & Hlth, Stockholm, Sweden.
Hagman, Ragnvi (author)
Swedish Univ Agr Sci, Dept Clin Sci, Uppsala, Sweden.
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Marinescu, Voichita (author)
Uppsala universitet,Institutionen för medicinsk biokemi och mikrobiologi
Hedhammar, Åke (author)
Swedish Univ Agr Sci, Dept Clin Sci, Uppsala, Sweden.
Strandberg, Erling (author)
Swedish Univ Agr Sci, Dept Anim Breeding & Genet, Uppsala, Sweden.
Lindblad-Toh, Kerstin (author)
Uppsala universitet,Institutionen för medicinsk biokemi och mikrobiologi,Science for Life Laboratory, SciLifeLab,Broad Inst MIT & Harvard, Cambridge, MA USA.
Arendt, Maja Louise (author)
Uppsala universitet,Institutionen för medicinsk biokemi och mikrobiologi,Science for Life Laboratory, SciLifeLab,Univ Copenhagen, Dept Vet Clin Sci, Copenhagen, Denmark.
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Univ Copenhagen, Dept Vet Clin Sci, Copenhagen, Denmark Swedish Kennel Club, Dept Breeding & Hlth, Stockholm, Sweden. (creator_code:org_t)
Springer Nature, 2024
2024
English.
In: Scientific Reports. - : Springer Nature. - 2045-2322. ; 14:1
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Genome wide association studies (GWAS) have been utilized to identify genetic risk loci associated with both simple and complex inherited disorders. Here, we performed a GWAS in Labrador retrievers to identify genetic loci associated with hip dysplasia and body weight. Hip dysplasia scores were available for 209 genotyped dogs. We identified a significantly associated locus for hip dysplasia on chromosome 24, with three equally associated SNPs (p = 4.3 x 10-7) in complete linkage disequilibrium located within NDRG3, a gene which in humans has been shown to be differentially expressed in osteoarthritic joint cartilage. Body weight, available for 85 female dogs, was used as phenotype for a second analysis. We identified two significantly associated loci on chromosome 10 (p = 4.5 x 10-7) and chromosome 31 (p = 2.5 x 10-6). The most associated SNPs within these loci were located within the introns of the PRKCE and CADM2 genes, respectively. PRKCE has been shown to play a role in regulation of adipogenesis whilst CADM2 has been associated with body weight in multiple human GWAS. In summary, we identified credible candidate loci explaining part of the genetic inheritance for hip dysplasia and body weight in Labrador retrievers with strong candidate genes in each locus previously implicated in the phenotypes investigated.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Medicinsk genetik (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Medical Genetics (hsv//eng)

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