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Browse result for Lymphoproliferative syndrome

※ introduction

    Autoimmune lymphoproliferative syndrome (ALPS) is a form of lymphoproliferative disorder (LPDs). It affects lymphocyte apoptosis. It is a rare genetic disorder of abnormal lymphocyte survival caused by defective Fas mediated apoptosis. Normally, after infectious insult, the immune system down-regulates by increasing Fas expression on activated B and T lymphocytes and Fas-ligand on activated T lymphocytes. Fas and Fas-ligand interact to trigger the caspase cascade, leading to cell apoptosis. Patients with ALPS have a defect in this apoptotic pathway, leading to chronic non-malignant lymphoproliferation, autoimmune disease, and secondary cancers.

Reference
Wiki: Lymphoproliferative syndrome



PTMD IDUniProt AccessionEntrez IDGene NameProtein NameOrganism
PTMD00639P98170331
XIAP
E3 ubiquitin-protein ligase XIAP
Homo sapiens
PTMD06305Q088813702
ITK
Tyrosine-protein kinase ITK/TSK
Homo sapiens