This is a public repository collecting the gene annotations Eric Fauman has contributed to various published GWAS
Specifically, these annotations come from the following three publications:
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Stacey D, Fauman EB, Ziemek D, et al. ProGeM: a framework for the prioritization of candidate causal genes at molecular quantitative trait loci. Nucleic Acids Res. 2019;47(1):e3. doi:10.1093/nar/gky837
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Yin X, Chan LS, Bose D, et al. Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Nat Commun. 2022;13(1):1644. Published 2022 Mar 28. doi:10.1038/s41467-022-29143-5
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Surendran P, Stewart ID, Au Yeung VPW, et al. Rare and common genetic determinants of metabolic individuality and their effects on human health. Nat Med. 2022;28(11):2321-2332. doi:10.1038/s41591-022-02046-0
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https://pubmed.ncbi.nlm.nih.gov/30239796/
- Stacey D, Fauman EB, Ziemek D, et al.
- ProGeM: a framework for the prioritization of candidate causal genes at molecular quantitative trait loci.
- Nucleic Acids Res. 2019;47(1):e3.
- doi:10.1093/nar/gky837
- https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6326795/bin/gky837_supplemental_files.zip
- Table S1
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https://pubmed.ncbi.nlm.nih.gov/35347128/
- Yin X, Chan LS, Bose D, et al.
- Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci.
- Nat Commun. 2022;13(1):1644. Published 2022 Mar 28.
- doi:10.1038/s41467-022-29143-5
- https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8960770/bin/41467_2022_29143_MOESM4_ESM.xlsx
- Supplementary Data 3
- Supplementary Data 7
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https://pubmed.ncbi.nlm.nih.gov/36357675/
- Surendran P, Stewart ID, Au Yeung VPW, et al.
- Rare and common genetic determinants of metabolic individuality and their effects on human health.
- Nat Med. 2022;28(11):2321-2332.
- doi:10.1038/s41591-022-02046-0
- https://static-content.springer.com/esm/art%3A10.1038%2Fs41591-022-02046-0/MediaObjects/41591_2022_2046_MOESM2_ESM.xlsx
- Supplementary Table 7
In each of the 3 papers above I specifically annotated a SNP-metabolite pair with one or more causal genes. In cases like the FADS1|FADS2 locus I explicitly annotated the association with the pair because biochemistry along can't uniquely identify the causal gene (for most metabolites). I collected the smallest p-value for any metabolite assigned to each particular causal gene across the 3 papers. The attached file, egea_met.txt, lists one entry for each causal gene, or set of nearby causal genes (e.g., FADS1|FADS2), representing the strongest metabolite (or metabolite ratio) association at that locus. The column headers are:
- gene - Eric Fauman's annotation as to the causal gene at the locus. If more than one gene is listed it means I can't ascertain a unique causal gene because the paralogs at the locus have similar functions. But I am fairly certain that the true causal gene is one (or more) of the listed genes
- nlp - the -log10(p) of the strongest association assigned to the gene/locus across the 3 publications
- trait - the name of the metabolite (or metabolite ratio) with the smallest p-value at the locus
- rsid - the rsid of the sentinel or lead SNP
- explanation - the biochemical rational for my selection of the causal gene, as reported in one of the 3 papers
- explanation_source - the pubmedid of the original functional/experimental work linking the gene to the metabolite
- gwas_source - the pubmedid of the GWAS generating the p-value for this SNP and this metabolite
- annotation_source - the pubmedid containing the original causal gene annotation (one of the 3 papers listed above)
Eric Fauman, November 28, 2020