Mine Disruption Phenotype

Gene Info

  • Species: Mouse (Mus musculus)
  • GeneID: 19255
  • Symbol: Ptpn2
  • Description: protein tyrosine phosphatase, non-receptor type 2
Export (tab separated) Export to Excel
Gene ID Entry Entry Name Protein Name Type Information
19255 Q06180 PTN2_MOUSE Tyrosine-protein phosphatase non-receptor type 2 (Protein-tyrosine phosphatase PTP-2) (EC 3.1.3.48) (MPTP) DISRUPTION PHENOTYPE Newborn mice are viable and do not display physical abnormalities. However, by 3 to 5 weeks of age they develop hunched posture, diarrhea and anemia. They do not survive beyond 5 weeks of age due to severe anemia, hematopoietic defects and the development of progressive systemic inflammatory disease. They display splenomegaly, lymphadenopathy and thymic atrophy, associated with altered B-cell differentiation, altered erythropoiesis, and impaired T- and B-cell functions. The inflammatory disease is characterized by high levels of circulating pro-inflammatory cytokines and lymphocytic infiltrates in non-lymphoid tissues. Heterozygous Ptpn2+/- mice exhibit decreased gluconeogenesis and hepatic glucose production while muscle-specific disruption of Ptpn2 has no effect on insulin signaling and glucose homeostasis in this tissue. {ECO:0000269|PubMed:14726372, ECO:0000269|PubMed:20484139, ECO:0000269|PubMed:22080863, ECO:0000269|PubMed:22124607, ECO:0000269|PubMed:9271584}.