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Variants in CCL16 are associated with blood plasma and cerebrospinal fluid CCL16 protein levels.
Ebbert, Mark T W; Staley, Lyndsay A; Parker, Joshua; Parker, Sheradyn; Bailey, Matthew; Ridge, Perry G; Goate, Alison M; Kauwe, John S K.
Afiliação
  • Ebbert MT; Department of Biology, Brigham Young University, Provo, UT, 84602, USA.
  • Staley LA; Department of Biology, Brigham Young University, Provo, UT, 84602, USA.
  • Parker J; Department of Biology, Brigham Young University, Provo, UT, 84602, USA.
  • Parker S; Department of Biology, Brigham Young University, Provo, UT, 84602, USA.
  • Bailey M; Biology and Biomedical Sciences, Washington University, St. Louis, MO, 63110, USA.
  • Ridge PG; Department of Biology, Brigham Young University, Provo, UT, 84602, USA.
  • Goate AM; Department of Neuroscience Icahn School of Medicine, New York, NY, 10029, USA.
  • Kauwe JS; Department of Biology, Brigham Young University, Provo, UT, 84602, USA. Kauwe@byu.edu.
BMC Genomics ; 17 Suppl 3: 437, 2016 06 29.
Article em En | MEDLINE | ID: mdl-27357396
ABSTRACT

BACKGROUND:

CCL16 is a chemokine predominantly expressed in the liver, but is also found in the blood and brain, and is known to play important roles in immune response and angiogenesis. Little is known about the gene's regulation.

METHODS:

Here, we test for potential causal SNPs that affect CCL16 protein levels in both blood plasma and cerebrospinal fluid in a genome-wide association study across two datasets. We then use METAL to performed meta-analyses with a significance threshold of p < 5x10(-8). We removed SNPs where the direction of the effect was different between the two datasets.

RESULTS:

We identify 10 SNPs associated with increased CCL16 protein levels in both biological fluids.

CONCLUSIONS:

Our results will help understand CCL16's regulation, allowing researchers to better understand the gene's effects on human health.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Metanálise como Assunto / Quimiocinas CC / Polimorfismo de Nucleotídeo Único / Estudo de Associação Genômica Ampla Tipo de estudo: Risk_factors_studies / Systematic_reviews Limite: Aged / Aged80 / Humans / Middle aged Idioma: En Revista: BMC Genomics Assunto da revista: GENETICA Ano de publicação: 2016 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Metanálise como Assunto / Quimiocinas CC / Polimorfismo de Nucleotídeo Único / Estudo de Associação Genômica Ampla Tipo de estudo: Risk_factors_studies / Systematic_reviews Limite: Aged / Aged80 / Humans / Middle aged Idioma: En Revista: BMC Genomics Assunto da revista: GENETICA Ano de publicação: 2016 Tipo de documento: Article País de afiliação: Estados Unidos