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newGenome View

candidate Crohn's disease genes
on chromosome 16
Databases

PubMed
the literature
LocusLink
collection of gene-related information
OMIM
catalog of human genes and disorders
Information

Fact sheet
from the National Institute for Diabetes and Digestive and Kidney Diseases, NIH
The Crohn's disease WebPage
information and links
The Crohn's and colitis pharmacist
disease and medication information
MEDLINEplus
links on Crohn's disease compiled by the National Library of Medicine

INFLAMMATORY BOWEL DISEASE (IBD) is a group of chronic disorders that cause inflammation or ulceration in the small and large intestines. Most often, IBD is classified either as ulcerative colitis or Crohn's disease. While ulcerative colitis affects the inner lining of the colon and rectum, Crohn's disease extends into the deeper layers of the intestinal wall. It is a chronic condition and may recur at various times over a lifetime.
  About 20% of cases of Crohn's disease appear to run in families. It is a 'complex trait', which means that several genes at different locations in the genome may contribute to the disease. A susceptibility locus for the disease was recently mapped to chromosome 16. Candidate genes found in this region include several involved in the inflamatory response, including: CD19, involved in B-lymphocyte function; sialophorin, involved in leukocyte adhesion; the CD11 integrin cluster, involved in microbacterial cell adhesion; and the interleukin-4 receptor, which is interesting, as IL-4-mediated functions are altered in IBDs.
  Because some of the genetic factors involved in Crohn's disease may also contribute to ulcerative colitis susceptibility, research into Crohn's disease may assist in further understanding both types of IBD.