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autoimmune lymphoproliferative syndrome
Summary
- Synonym
-
- ALPS
- Canale-Smith syndrome
- Definition
- A hypersensitivity reaction type IV disease that is an inherited disorder in which the body cannot properly regulate the number of immune system cells (lymphocytes). It is characterized by the production of an abnormally large number of lymphocytes. Accumulation of excess lymphocytes results in enlargement of the lymph nodes, the liver, and the spleen.
- Super Class
- hypersensitivity reaction type IV disease
Related Genes
| Gene ID | Gene Symbol | Description | Source |
|---|---|---|---|
| 7167 | TPI1 | triosephosphate isomerase 1 | |
| 7412 | VCAM1 | vascular cell adhesion molecule 1 | |
| 8505 | PARG | poly(ADP-ribose) glycohydrolase | |
| 8807 | IL18RAP | interleukin 18 receptor accessory protein | |
| 8809 | IL18R1 | interleukin 18 receptor 1 | |
| 8877 | SPHK1 | sphingosine kinase 1 | |
| 9173 | IL1RL1 | interleukin 1 receptor like 1 | |
| 9993 | DGCR2 | DiGeorge syndrome critical region gene 2 | |
| 10135 | NAMPT | nicotinamide phosphoribosyltransferase | |
| 10159 | ATP6AP2 | ATPase H+ transporting accessory protein 2 |
Related Glycoprotein
| UniProt ID | Protein Name | Source |
|---|---|---|
| Q15125 | 3-beta-hydroxysteroid-Delta(8),Delta(7)-isomerase | |
| Q15485 | Ficolin-2 | |
| Q16394 | Exostosin-1 | |
| Q16706 | Alpha-mannosidase 2 | |
| Q29983 | MHC class I polypeptide-related sequence A | |
| Q2KHT3 | Protein CLEC16A | |
| Q5SRI9 | Glycoprotein endo-alpha-1,2-mannosidase | |
| Q6P1J6 | Phospholipase B1, membrane-associated | |
| Q7Z7D3 | V-set domain-containing T-cell activation inhibitor 1 | |
| Q86W56 | Poly(ADP-ribose) glycohydrolase |
