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IBD2 inflammatory bowel disease 2 [ Homo sapiens (human) ]

Gene ID: 3378, updated on 31-Aug-2024

Summary

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Official Symbol
IBD2provided by HGNC
Official Full Name
inflammatory bowel disease 2provided by HGNC
Primary source
MIM:601458
Gene type
unknown
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo

Genomic context

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Location:
12p13.2-q24.1

Bibliography

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Related articles in PubMed

  1. Association of ulcerative colitis with the inflammatory bowel disease susceptibility locus IBD2 in non-Jewish Caucasians and evidence of genetic heterogeneity among racial and ethnic populations with Crohn disease. Uthoff SM, et al. Am J Med Genet, 2002 Dec 1. PMID 12439891
  2. Linkage and association between inflammatory bowel disease and a locus on chromosome 12. Duerr RH, et al. Am J Hum Genet, 1998 Jul. PMID 9634527, Free PMC Article
  3. Genetic analysis of inflammatory bowel disease in a large European cohort supports linkage to chromosomes 12 and 16. Curran ME, et al. Gastroenterology, 1998 Nov. PMID 9797359
  4. An autosomal screen for genes that predispose to celiac disease in the western counties of Ireland. Zhong F, et al. Nat Genet, 1996 Nov. PMID 8896565
  5. Two stage genome-wide search in inflammatory bowel disease provides evidence for susceptibility loci on chromosomes 3, 7 and 12. Satsangi J, et al. Nat Genet, 1996 Oct. PMID 8841195

See all (7) citations in PubMed

GeneRIFs: Gene References Into Functions

What's a GeneRIF?
  1. Observational study of gene-disease association. (HuGE Navigator)
    Title: Association of ulcerative colitis with the inflammatory bowel disease susceptibility locus IBD2 in non-Jewish Caucasians and evidence of genetic heterogeneity among racial and ethnic populations with Crohn disease.
Submit: New GeneRIF Correction

Phenotypes

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Associated conditions

Description Tests
inflammatory bowel disease 2
OMIM: 601458GeneReviews: Not available

General gene information

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Markers

Property

  • phenotype only

Gene LinkOut

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