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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
Reference
Wiki: Autoimmune lymphoproliferative syndrome
| PTMD ID | UniProt Accession | Entrez ID | Gene Name | Protein Name | Organism |
|---|---|---|---|---|---|
| PTMD00193 | P25445 | 355 | FAS | Tumor necrosis factor receptor superfamily member 6 | Homo sapiens |
| PTMD00689 | Q14790 | 841 | CASP8 | Caspase-8 [Cleaved into: Caspase-8 subunit p18; Caspase-8 subunit p10] | Homo sapiens |
| PTMD01300 | Q05655 | 5580 | PRKCD | Protein kinase C delta type [Cleaved into: Protein kinase C delta type regulatory subunit; Protein kinase C delta type catalytic subunit ] | Homo sapiens |
| PTMD05217 | P48023 | 356 | 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 |
| PTMD10832 | Q92851 | 843 | CASP10 | Caspase-10 [Cleaved into: Caspase-10 subunit p23/17; Caspase-10 subunit p12] | Homo sapiens |
