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amyloidosis
Summary
- Synonym
-
- amyloid disease
- Definition
- A disease of metabolsism that is characterized by extracellular tissue deposition of mis-folded amyloid fibrils built up by twisted protofilaments, deposited in the spaces between the cells of vital organs, causing disruption of organ tissue structure and function. These deposits may result in a wide range of clinical manifestations depending upon their type, location, and the amount of deposition.
- Super Class
- disease of metabolism
Related Genes
| Gene ID | Gene Symbol | Description | Source |
|---|---|---|---|
| 2876 | GPX1 | glutathione peroxidase 1 | |
| 3290 | HSD11B1 | hydroxysteroid 11-beta dehydrogenase 1 | |
| 3339 | HSPG2 | heparan sulfate proteoglycan 2 | |
| 4069 | LYZ | lysozyme | |
| 4099 | MAG | myelin associated glycoprotein | |
| 4153 | MBL2 | mannose binding lectin 2 | |
| 4166 | CHST6 | carbohydrate sulfotransferase 6 | |
| 4669 | NAGLU | N-acetyl-alpha-glucosaminidase | |
| 4684 | NCAM1 | neural cell adhesion molecule 1 | |
| 5290 | PIK3CA | phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha |
Related Glycoprotein
| UniProt ID | Protein Name | Source |
|---|---|---|
| Q6YHK3 | CD109 antigen | |
| Q8IV08 | 5'-3' exonuclease PLD3 | |
| Q8IWL2 | Pulmonary surfactant-associated protein A1 | |
| Q8TD20 | Solute carrier family 2, facilitated glucose transporter member 12 | |
| Q9BXN2 | C-type lectin domain family 7 member A | |
| Q9GZX3 | Carbohydrate sulfotransferase 6 | |
| Q9P2R7 | Succinate--CoA ligase [ADP-forming] subunit beta, mitochondrial | |
| Q9Y6A2 | Cholesterol 24-hydroxylase |
