Sequence variants in the autophagy gene IRGM and multiple other replicating loci contribute to Crohn's disease susceptibility.

Journal article

A genome-wide association scan in individuals with Crohn's disease by the Wellcome Trust Case Control Consortium detected strong association at four novel loci. We tested 37 SNPs from these and other loci for association in an independent case-control sample. We obtained replication for the autophagy-inducing IRGM gene on chromosome 5q33.1 (replication P = 6.6 x 10(-4), combined P = 2.1 x 10(-10)) and for nine other loci, including NKX2-3, PTPN2 and gene deserts on chromosomes 1q and 5p13.

Authors: Parkes, M; Barrett, J; Prescott, N; Tremelling, M; Anderson, C

• Publication status: Published
• Journal: Nature genetics
• Volume: 39
• Issue: 7
• Pages: 830-832
• Publication date: 2007-07-01
• DOI: 10.1038/ng2061
• EISSN: 1546-1718
• ISSN: 1061-4036
• Language: English
• Keywords: Sequence Analysis, DNA; Crohn Disease; Wellcome Trust Case Control Consortium; Animals; Polymorphism, Single Nucleotide; Genetic Variation; Autophagy; Humans; Case-Control Studies; Genetic Predisposition to Disease; GTP-Binding Proteins; Mice