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Browse result for Autoimmune 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: Autoimmune lymphoproliferative syndrome



PTMD IDUniProt AccessionEntrez IDGene NameProtein NameOrganism
PTMD00193P25445355
FAS
Tumor necrosis factor receptor superfamily member 6
Homo sapiens
PTMD00689Q14790841
CASP8
Caspase-8 [Cleaved into: Caspase-8 subunit p18; Caspase-8 subunit p10]
Homo sapiens
PTMD01300Q056555580
PRKCD
Protein kinase C delta type [Cleaved into: Protein kinase C delta type regulatory subunit; Protein kinase C delta type catalytic subunit ]
Homo sapiens
PTMD05217P48023356
FASLG
Tumor necrosis factor ligand superfamily member 6 [Cleaved into: Tumor necrosis factor ligand superfamily member 6, membrane form; Tumor necrosis factor ligand superfamily member 6, soluble form ; ADAM10-processed FasL form ; FasL intracellular domain ]
Homo sapiens
PTMD10832Q92851843
CASP10
Caspase-10 [Cleaved into: Caspase-10 subunit p23/17; Caspase-10 subunit p12]
Homo sapiens