GeneSet Information

Tier I GS269553 • GWAS Catalog Data for metabolite measurement in 862 European ancestry male individuals

DESCRIPTION:

List of positional candidate genes after correcting for multiple testing and controlling the false discovery rate from genome wide association studies (GWAS) retrieved from the NHGRI-EBI Catalog of published genome-wide association studies (http://www.ebi.ac.uk/gwas/). The disease/trait examined in this study, as reported by the authors, was Urinary metabolites. The EFO term metabolite measurement was annotated to this set after curation by NHGRI-EBI. Intergenic SNPS were mapped to both the upstream and downstream gene. P-value uploaded. This gene set was generated using gwas2gs v. 0.1.8 and the GWAS Catalog v. 1.0.1.

LABEL:

GWAS: metabolite measurement

SCORE TYPE:

P-Value

DATE ADDED:

2017-05-02

DATE UPDATED:

2024-04-25

SPECIES:

AUTHORS:

K Suhre, H Wallaschofski, J Raffler, N Friedrich, R Haring, K Michael, C Wasner, A Krebs, F Kronenberg, D Chang, C Meisinger, HE Wichmann, W Hoffmann, H Völzke, U Völker, A Teumer, R Biffar, T Kocher, SB Felix, T Illig, HK Kroemer, C Gieger, W Römisch-Margl, M Nauck

TITLE:

A genome-wide association study of metabolic traits in human urine.

JOURNAL:

Nature genetics Jun 2011, Vol 43, pp. 565-9

ABSTRACT:

We present a genome-wide association study of metabolic traits in human urine, designed to investigate the detoxification capacity of the human body. Using NMR spectroscopy, we tested for associations between 59 metabolites in urine from 862 male participants in the population-based SHIP study. We replicated the results using 1,039 additional samples of the same study, including a 5-year follow-up, and 992 samples from the independent KORA study. We report five loci with joint P values of association from 3.2 × 10(-19) to 2.1 × 10(-182). Variants at three of these loci have previously been linked with important clinical outcomes: SLC7A9 is a risk locus for chronic kidney disease, NAT2 for coronary artery disease and genotype-dependent response to drug toxicity, and SLC6A20 for iminoglycinuria. Moreover, we identify rs37369 in AGXT2 as the genetic basis of hyper-β-aminoisobutyric aciduria. PUBMED: 21572414
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metabolite measurement (EFO:0004725)

Gene List • 8 Genes

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