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nervous system disease
Summary
- Definition
- A disease of anatomical entity that is located_in the central nervous system or located_in the peripheral nervous system.
- Super Class
- disease of anatomical entity
Related Genes
| Gene ID | Gene Symbol | Description | Source |
|---|---|---|---|
| 4099 | MAG | myelin associated glycoprotein | |
| 4126 | MANBA | mannosidase beta | |
| 4153 | MBL2 | mannose binding lectin 2 | |
| 4245 | MGAT1 | alpha-1,3-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyltransferase | |
| 4668 | NAGA | alpha-N-acetylgalactosaminidase | |
| 4684 | NCAM1 | neural cell adhesion molecule 1 | |
| 4860 | PNP | purine nucleoside phosphorylase | |
| 4967 | OGDH | oxoglutarate dehydrogenase | |
| 5048 | PAFAH1B1 | platelet activating factor acetylhydrolase 1b regulatory subunit 1 | |
| 5168 | ENPP2 | ectonucleotide pyrophosphatase/phosphodiesterase 2 |
Related Glycoprotein
| UniProt ID | Protein Name | Source |
|---|---|---|
| Q9BZR6 | Reticulon-4 receptor | |
| Q9C0K1 | Metal cation symporter ZIP8 | |
| Q9GZR5 | Very long chain fatty acid elongase 4 | |
| Q9GZU5 | Nyctalopin | |
| Q9NY47 | Voltage-dependent calcium channel subunit alpha-2/delta-2 | |
| Q9P2R7 | Succinate--CoA ligase [ADP-forming] subunit beta, mitochondrial | |
| Q9UEF7 | Klotho | |
| Q9Y286 | Sialic acid-binding Ig-like lectin 7 |
