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Article

The PTPN22 620W allele is a risk factor for Wegener's granulomatosis.

Arthritis and rheumatism - 1 Dec 2005

Jagiello Peter, Aries Peer, Arning Larissa, Wagenleiter Sonja E N, Csernok Elena, Hellmich Bernhard, Gross Wolfgang L, Epplen Joerg T

Abstract excerpt

OBJECTIVE: Analyses of families with multiple autoimmune disorders have revealed a functional polymorphism, 620W, in the intracellular tyrosine phosphatase gene PTPN22 as a predisposing factor for type 1 diabetes, seropositive rheumatoid arthritis, systemic lupus erythematosus, and Hashimoto thyr...

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Share to Granulomatosis with Polyangiitis
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Share to Antibodies, Antineutrophil Cytoplasmic

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Polymorphism, Genetic

Share to Protein Tyrosine Phosphatase, Non-Receptor Type 1

Share to Protein Tyrosine Phosphatase, Non-Receptor Type 22

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Source

Identifiers

PMID: 16320352
DOI: 10.1002/art.21487

Genes

PTPN22

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-16320352-2026-09-04.1. Manifest publication-graph-cohort-2026-09-04.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

Related research

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Research trail→

Click a neighbor to travelStep 1 · 12 closest

The PTPN22 620W allele is a risk factor for Wegener's granulomatosis.PMID 16320352Read ↗

PTPN22 R620W polymorphism in the ANCA-associated vasculitides.Semantic proximity Read ↗

PTPN22 R620W polymorphism and ANCA disease risk in white populations: a metaanalysis.Semantic proximity Read ↗

Pathways to gene identification in rheumatoid arthritis: PTPN22 and beyond.Semantic proximity Read ↗

PTPN22 genetic variation: evidence for multiple variants associated with rheumatoid arthritis.Semantic proximity Read ↗

The protein tyrosine phosphatase nonreceptor 22 C1858T polymorphism and vasculitis: a meta-analysis.Semantic proximity Read ↗

[Relevance of the gene variant PTPN22 620W for rheumatology].Semantic proximity Read ↗

PTPN22 gene polymorphisms in autoimmune diseases with special reference to systemic lupus erythematosus disease susceptibility.Semantic proximity Read ↗

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

Genetic association of the R620W polymorphism of protein tyrosine phosphatase PTPN22 with human SLE.Semantic proximity Read ↗

Why is PTPN22 a good candidate susceptibility gene for autoimmune disease?Semantic proximity Read ↗

Multiplex family-based study in systemic lupus erythematosus: association between the R620W polymorphism of PTPN22 and the FcgammaRIIa (CD32A) R131 allele.Semantic proximity Read ↗

Lack of association between the protein tyrosine phosphatase non-receptor 22 (PTPN22)*620W allele and systemic sclerosis in the French Caucasian population.Semantic proximity Read ↗

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