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CELIAC2 celiac disease 2 [ Homo sapiens (human) ]

Gene ID: 317782, updated on 31-Aug-2024

Summary

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Official Symbol
CELIAC2provided by HGNC
Official Full Name
celiac disease 2provided by HGNC
Primary source
MIM:609754
Gene type
unknown
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
CD; GSE

Genomic context

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Location:
5q31-q33

Bibliography

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Related articles in PubMed

  1. An autosomal genome-wide screen for celiac disease in Bedouin families. Ding YC, et al. Genes Immun, 2008 Jan. PMID 17943142
  2. Genome-wide linkage analysis of Scandinavian affected sib-pairs supports presence of susceptibility loci for celiac disease on chromosomes 5 and 11. Naluai AT, et al. Eur J Hum Genet, 2001 Dec. PMID 11840196
  3. Existence of a genetic risk factor on chromosome 5q in Italian coeliac disease families. Greco L, et al. Ann Hum Genet, 2001 Jan. PMID 11415521

GeneRIFs: Gene References Into Functions

What's a GeneRIF?
  1. An autosomal genome-wide screen for celiac disease in Bedouin families is reported.
    Title: An autosomal genome-wide screen for celiac disease in Bedouin families.
Submit: New GeneRIF Correction

Phenotypes

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Associated conditions

Description Tests
celiac disease 2
OMIM: 609754GeneReviews: Not available

General gene information

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Property

  • phenotype only

Gene LinkOut

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