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A Missense Single-Nucleotide Polymorphism in a Gene Encoding a Protein Tyrosine Phosphatase (PTPN22) Is Associated with Rheumatoid Arthritis

The American Journal of Human Genetics · 2004 · Vol. 75(2) · pp. 330–337

Ann B. Begovich✉Victoria CarltonLee HonigbergSteven J. SchrodiAnand P. ChokkalingamHeather C. AlexanderKristin ArdlieQiqing Huang(The University of Texas MD Anderson Cancer Center)Ashley M. SmithJill M. SpoerkeMarion ConnMonica ChangSheng-Yung ChangRandall K. SaikiJoseph J. CataneseDiane U. LeongVeronica GarciaLinda McAllisterDouglas A. JefferyAnnette T. LeeFranak BatliwallaElaine F. Remmers(National Institute of Arthritis and Musculoskeletal and Skin Diseases)Lindsey A. Criswell(University of California, San Francisco)Michael F. Seldin(University of California, Davis)Daniel L. Kastner(National Institute of Arthritis and Musculoskeletal and Skin Diseases)Christopher I. Amos(The University of Texas MD Anderson Cancer Center)John J. SninskyPeter K. Gregersen

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Protein Tyrosine Phosphatases Galectins and Cancer Biology Diabetes and associated disordersMissense mutationProtein tyrosine phosphataseSingle-nucleotide polymorphismPTPN22Rheumatoid arthritisGeneGeneticsBiologyMedicineGenotype

MeSH terms

Arthritis, RheumatoidGene FrequencyHumansMolecular Sequence DataOrgan SpecificityRNA, MessengerProtein Tyrosine PhosphatasesMutation, MissensePolymorphism, Single NucleotideProtein Tyrosine Phosphatase, Non-Receptor Type 1

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