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DisGeNET
DisGeNET is a knowledge management platform that integrates and standardizes the data of genes and mutations related to diseases from multiple sources. It covers entire range of human disease.
| Source | Last Updated |
|---|---|
| DisGeNET | July 29, 2024 |
| Disease ID ▲ | Disease Name | Gene Symbol | Gene ID | Gene Name | UniProt ID |
|---|---|---|---|---|---|
| C0524851 | Neurodegenerative Disorders | PLB1 | 151056 | phospholipase B1 | Q6P1J6 |
| C0524851 | Neurodegenerative Disorders | ACE | 1636 | angiotensin I converting enzyme | P12821 |
| C0524851 | Neurodegenerative Disorders | ALDH2 | 217 | aldehyde dehydrogenase 2 family member | P05091 |
| C0524851 | Neurodegenerative Disorders | FDPS | 2224 | farnesyl diphosphate synthase | P14324 |
| C0524851 | Neurodegenerative Disorders | FOLR2 | 2350 | folate receptor beta | P14207 |
| C0524851 | Neurodegenerative Disorders | ACSBG1 | 23205 | acyl-CoA synthetase bubblegum family member 1 | Q96GR2 |
| C0524851 | Neurodegenerative Disorders | ALOX12 | 239 | arachidonate 12-lipoxygenase, 12S type | P18054 |
| C0524851 | Neurodegenerative Disorders | GAD1 | 2571 | glutamate decarboxylase 1 | Q99259 |
| C0524851 | Neurodegenerative Disorders | ALPP | 250 | alkaline phosphatase, placental | P05187 |
| C0524851 | Neurodegenerative Disorders | HIBCH | 26275 | 3-hydroxyisobutyryl-CoA hydrolase | Q6NVY1 |
| C0524851 | Neurodegenerative Disorders | SLC17A5 | 26503 | solute carrier family 17 member 5 | Q9NRA2 |
| C0524851 | Neurodegenerative Disorders | ATRNL1 | 26033 | attractin like 1 | Q5VV63 |
| C0524851 | Neurodegenerative Disorders | SIGLEC7 | 27036 | sialic acid binding Ig like lectin 7 | Q9Y286 |
| C0524851 | Neurodegenerative Disorders | HPGDS | 27306 | hematopoietic prostaglandin D synthase | O60760 |
| C0524851 | Neurodegenerative Disorders | GLUL | 2752 | glutamate-ammonia ligase | P15104 |
| C0524851 | Neurodegenerative Disorders | ICAM1 | 3383 | intercellular adhesion molecule 1 | P05362 |
| C0524851 | Neurodegenerative Disorders | LIPC | 3990 | lipase C, hepatic type | P11150 |
| C0524851 | Neurodegenerative Disorders | LGALS3 | 3958 | galectin 3 | P17931 |
| C0524851 | Neurodegenerative Disorders | LPL | 4023 | lipoprotein lipase | P06858 |
| C0524851 | Neurodegenerative Disorders | ACHE | 43 | acetylcholinesterase (Cartwright blood group) | P22303 |
| C0524851 | Neurodegenerative Disorders | MRC1 | 4360 | mannose receptor C-type 1 | P22897 |
| C0524851 | Neurodegenerative Disorders | NDUFAB1 | 4706 | NADH:ubiquinone oxidoreductase subunit AB1 | O14561 |
| C0524851 | Neurodegenerative Disorders | PIK3CD | 5293 | phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta | O00329 |
| C0524851 | Neurodegenerative Disorders | PLA2G2A | 5320 | phospholipase A2 group IIA | P14555 |
| C0524851 | Neurodegenerative Disorders | TMED9 | 54732 | transmembrane p24 trafficking protein 9 | Q9BVK6 |
