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PTPN22 information


PTPN22
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesPTPN22, protein tyrosine phosphatase, non-receptor type 22 (lymphoid), LYP, LYP1, LYP2, PEP, PTPN8, protein tyrosine phosphatase, non-receptor type 22, PTPN22.6, PTPN22.5, protein tyrosine phosphatase non-receptor type 22
External IDsOMIM: 600716; MGI: 107170; HomoloGene: 7498; GeneCards: PTPN22; OMA:PTPN22 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001193431
NM_001308297
NM_012411
NM_015967

NM_008979

RefSeq (protein)

NP_001180360
NP_001295226
NP_036543
NP_057051

NP_033005

Location (UCSC)Chr 1: 113.81 – 113.87 MbChr 3: 103.77 – 103.82 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Protein tyrosine phosphatase non-receptor type 22 (PTPN22) is a cytoplasmatic protein encoded by gene PTPN22 and a member of PEST family of protein tyrosine phosphatases. This protein is also called "PEST-domain Enriched Phosphatase" ("PEP") or "Lymphoid phosphatase" ("LYP"). The name LYP is used strictly for the human protein encoded by PTPN22, but the name PEP is used only for its mouse homolog. However, both proteins have similar biological functions and show 70% identity in amino acid sequence. PTPN22 functions as a negative regulator of T cell receptor (TCR) signaling, which maintains homeostasis of T cell compartment.[5][6]

  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000134242 – Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000027843 – Ensembl, May 2017
  3. ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. ^ Bottini N, Peterson EJ (2014-03-21). "Tyrosine phosphatase PTPN22: multifunctional regulator of immune signaling, development, and disease". Annual Review of Immunology. 32 (1): 83–119. doi:10.1146/annurev-immunol-032713-120249. PMC 6402334. PMID 24364806.
  6. ^ Tizaoui K, Terrazzino S, Cargnin S, Lee KH, Gauckler P, Li H, et al. (June 2021). "The role of PTPN22 in the pathogenesis of autoimmune diseases: A comprehensive review". Seminars in Arthritis and Rheumatism. 51 (3): 513–522. doi:10.1016/j.semarthrit.2021.03.004. PMID 33866147. S2CID 233300534.

and 12 Related for: PTPN22 information

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PTPN22

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Protein tyrosine phosphatase non-receptor type 22 (PTPN22) is a cytoplasmatic protein encoded by gene PTPN22 and a member of PEST family of protein tyrosine...

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Allergic rhinitis

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that certain SNPs in the protein tyrosine phosphatase non-receptor 22 (PTPN22) gene and cytotoxic T-lymphocyte-associated antigen 4 (CTLA-4) gene can...

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Uveitis

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genetic factors that predispose disease onset including HLA-B27 and the PTPN22 genotype. Recent evidence has pointed to reactivation of herpes simplex...

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Autoimmunity

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of susceptibility to lupus erythematosus). In recent studies, the gene PTPN22 has emerged as a significant factor linked to various autoimmune diseases...

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Granulomatosis with polyangiitis

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people with GPA. Several genes involved in the immune system including PTPN22, CTLA4, and human leukocyte antigen genes may influence the risk of developing...

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Rheumatoid arthritis

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CD40, cytokine signaling, lymphocyte receptor activation threshold (e.g., PTPN22), and innate immune activation—appear to have less influence than HLA mutations...

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Lupus

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increased risk of SLE. Other genes that contain risk variants for SLE are IRF5, PTPN22, STAT4, CDKN1A, ITGAM, BLK, OX40L and BANK1. Some of the susceptibility...

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PADI4

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samples from North America and Sweden: association of susceptibility with PTPN22, CTLA4, and PADI4". American Journal of Human Genetics. 77 (6): 1044–1060...

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Genetic studies on Gujarati people

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Prajapati, Hiral; Marfatia, Y.S.; Begum, Rasheedunnisa (2008). "Association of PTPN22 1858C/T polymorphism with vitiligo susceptibility in Gujarat population"...

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CXorf66

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4 + 107146630 107147268 USP48 84196 241 631 89.0% 1 + 22014725 22015355 PTPN22 26191 227 281 90.0% 1 - 114365307 114365587 PSPH 5723 220 605 90.6% 7 -...

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FCRL3

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arthritis association with the FCRL3 -169C polymorphism is restricted to PTPN22 1858T-homozygous individuals in a Canadian population". Arthritis and Rheumatism...

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Lars Klareskog

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et al.: Gene-gene and gene-environment interactions involving HLA-DRB1, PTPN22, and smoking in two subsets of rheumatoid arthritis, American J. Hum. Genetics...

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