Genetic variation in the IGSF6 gene and lack of association with inflammatory bowel disease

King, K, Moody, A, Fisher, S A, Mirza, M M, Cuthbert, A P, Hampe, J, Sutherland-Craggs, A, Sanderson, J, MacPherson, A J, Forbes, A ORCID: https://orcid.org/0000-0001-7416-9843, Mansfield, J, Schreiber, S, Lewis, C M and Mathew, C G (2003) Genetic variation in the IGSF6 gene and lack of association with inflammatory bowel disease. European Journal of Immunogenetics, 30 (3). pp. 187-190. ISSN 0960-7420

Full text not available from this repository. (Request a copy)

Abstract

The immunoglobulin superfamily 6 gene (IGSF6) on chromosome 16p11-p12 has been investigated as a positional and functional candidate for inflammatory bowel disease (IBD) susceptibility. Screening of the six exons of IGSF6 for single nucleotide polymorphisms (SNPs) detected four novel SNPs, and validated three of six SNPs listed in the international SNP database (dbSNP). The seven SNPs in IGSF6 formed five distinct linkage disequilibrium groups. There was no evidence for association of the common SNPs with disease in a large cohort of patients with IBD. The novel SNPs and the linkage disequilibrium map will be a useful resource for the analysis of IGSF6 in other immune disorders.

Item Type:	Article
Uncontrolled Keywords:	antigens, cd8,carrier proteins,case-control studies,colitis, ulcerative,crohn disease,genetic predisposition to disease,genetic variation,humans,immunoglobulins,inflammatory bowel diseases,intracellular signaling peptides and proteins,linkage disequilibrium,nod2 signaling adaptor protein,pedigree,polymorphism, single nucleotide
Faculty \ School:	Faculty of Medicine and Health Sciences > Norwich Medical School
UEA Research Groups:	Faculty of Medicine and Health Sciences > Research Groups > Gastroenterology and Gut Biology Faculty of Medicine and Health Sciences > Research Groups > Nutrition and Preventive Medicine
Depositing User:	Pure Connector
Date Deposited:	06 Aug 2014 10:48
Last Modified:	20 Oct 2022 23:59
URI:	https://ueaeprints.uea.ac.uk/id/eprint/49587
DOI:	10.1046/j.1365-2370.2003.00387.x

Actions (login required)

View Item