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Genome-wide association analysis of eosinophilic esophagitis provides insight into the tissue specificity of this allergic disease.

Authors: Kottyan, LC  Davis, BP  Sherrill, JD  Liu, K  Rochman, M  Kaufman, K  Weirauch, MT  Vaughn, S  Lazaro, S  Rupert, AM  Kohram, M  Stucke, EM  Kemme, KA  Magnusen, A  He, H  Dexheimer, P  Chehade, M  Wood, RA  Pesek, RD  Vickery, BP  Fleischer, DM  Lindbad, R  Sampson, HA  Mukkada, VA  Putnam, PE  Abonia, JP  Martin, LJ  Harley, JB  Rothenberg, ME 
Citation: Kottyan LC, etal., Nat Genet. 2014 Aug;46(8):895-900. doi: 10.1038/ng.3033. Epub 2014 Jul 13.
Pubmed: (View Article at PubMed) PMID:25017104
DOI: Full-text: DOI:10.1038/ng.3033

Eosinophilic esophagitis (EoE) is a chronic inflammatory disorder associated with allergic hypersensitivity to food. We interrogated >1.5 million genetic variants in EoE cases of European ancestry and subsequently in a multi-site cohort with local and out-of-study control subjects. In addition to replicating association of the 5q22 locus (meta-analysis P=1.9x10(-16)), we identified an association at 2p23 spanning CAPN14 (P=2.5x10(-10)). CAPN14 was specifically expressed in the esophagus, was dynamically upregulated as a function of disease activity and genetic haplotype and after exposure of epithelial cells to interleukin (IL)-13, and was located in an epigenetic hotspot modified by IL-13. Genes neighboring the top 208 EoE-associated sequence variants were enriched for esophageal expression, and multiple loci for allergic sensitization were associated with EoE susceptibility (4.8x10(-2)

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CRRD Object Information
CRRD ID: 11100049
Created: 2016-06-14
Species: All species
Last Modified: 2016-06-14
Status: ACTIVE



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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.