※ PTMD 2.0 database Online Browse Options
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
Reference
Wiki: Lymphoproliferative syndrome
| PTMD ID | UniProt Accession | Entrez ID | Gene Name | Protein Name | Organism |
|---|---|---|---|---|---|
| PTMD00639 | P98170 | 331 | XIAP | E3 ubiquitin-protein ligase XIAP | Homo sapiens |
| PTMD06305 | Q08881 | 3702 | ITK | Tyrosine-protein kinase ITK/TSK | Homo sapiens |
