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Article

PTPN22 gene polymorphism in Behçet's disease.

Tissue antigens - 1 Nov 2007

Sahin N, Bicakcigil M, Atagunduz P, Direskeneli H, Saruhan-Direskeneli G

Abstract excerpt

A functional single nucleotide polymorphism (SNP) of PTPN22 gene encoding the protein tyrosine phosphatase has been reported to be associated with autoimmune disorders such as rheumatoid arthritis, systemic lupus erythematosus and type I diabetes. PTPN22 R620W polymorphism has a wide variation of allelic frequencies among different populations. This polymorphism is investigated in Turkish patients with Behçet's...

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Source

Identifiers

PMID: 17868256
DOI: 10.1111/j.1399-0039.2007.00928.x

Genes

PTPN22

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

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PTPN22 gene polymorphism in Behçet's disease.PMID 17868256Read ↗

Protein tyrosine phosphatase non-receptor type 2 (PTPN2) gene polymorphisms (rs2542151, rs7234029) in Egyptian Behçet's disease patients: a preliminary report.Semantic proximity Read ↗

PTPN2 rs1893217 single-nucleotide polymorphism is associated with risk of Behçet's disease in a Chinese Han population.Semantic proximity Read ↗

PTPN22 is not associated with Behçet's disease. Study spanning the complete gene region in the Spanish population and meta-analysis of the functional variant R620W.Semantic proximity Read ↗

No association of PTPN22 polymorphisms with susceptibility to ocular Behcet's disease in two Chinese Han populations.Semantic proximity Read ↗

Association of genetic variations in PTPN2 and CD122 with ocular Behcet's disease.Semantic proximity Read ↗

The association of the PTPN22 620W polymorphism with Behcet's disease.Semantic proximity Read ↗

Genetic Polymorphism of PTPN22 in Autoimmune Diseases: A Comprehensive Review.Semantic proximity Read ↗

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Association study of rs924080 and rs11209032 polymorphisms of IL23R-IL12RB2 in a Northern Chinese Han population with Behcet's disease.Semantic proximity Read ↗

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