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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 |
|---|---|---|---|---|---|
| C3495559 | Juvenile arthritis | ALOX12 | 239 | arachidonate 12-lipoxygenase, 12S type | P18054 |
| C3495559 | Juvenile arthritis | ICAM1 | 3383 | intercellular adhesion molecule 1 | P05362 |
| C3495559 | Juvenile arthritis | MBL2 | 4153 | mannose binding lectin 2 | P11226 |
| C3495559 | Juvenile arthritis | NCAM1 | 4684 | neural cell adhesion molecule 1 | P13591 |
| C3495559 | Juvenile arthritis | PRNP | 5621 | prion protein | P04156 |
| C3495559 | Juvenile arthritis | SLC2A3 | 6515 | solute carrier family 2 member 3 | P11169 |
| C3495559 | Juvenile arthritis | VTCN1 | 79679 | V-set domain containing T cell activation inhibitor 1 | Q7Z7D3 |
| C3495559 | Juvenile arthritis | CAT | 847 | catalase | P04040 |
| C3495559 | Juvenile arthritis | TNFRSF10C | 8794 | TNF receptor superfamily member 10c | O14798 |
| C3495559 | Juvenile arthritis | CD14 | 929 | CD14 molecule | P08571 |
| C3495559 | Juvenile arthritis | NAMPT | 10135 | nicotinamide phosphoribosyltransferase | P43490 |
| C3495559 | Juvenile arthritis | DAG1 | 1605 | dystroglycan 1 | Q14118 |
| C3495559 | Juvenile arthritis | FCN2 | 2220 | ficolin 2 | Q15485 |
| C3495559 | Juvenile arthritis | CLEC16A | 23274 | C-type lectin domain containing 16A | Q2KHT3 |
| C3495559 | Juvenile arthritis | ACACA | 31 | acetyl-CoA carboxylase alpha | Q13085 |
| C3495559 | Juvenile arthritis | OLR1 | 4973 | oxidized low density lipoprotein receptor 1 | P78380 |
| C3495559 | Juvenile arthritis | PLAUR | 5329 | plasminogen activator, urokinase receptor | Q03405 |
| C3495559 | Juvenile arthritis | PRNP | 5621 | prion protein | F7VJQ1 |
| C3495559 | Juvenile arthritis | PCYT1B | 9468 | phosphate cytidylyltransferase 1, choline, beta | Q9Y5K3 |
| C3495498 | Cardiomyopathy, Familial Hypertrophic, 1 (disorder) | CALR3 | 125972 | calreticulin 3 | Q96L12 |
| C3495489 | Rieger eye malformation sequence | CYP1B1 | 1545 | cytochrome P450 family 1 subfamily B member 1 | Q16678 |
| C3495439 | Inflammatory disorder of breast | CRLS1 | 54675 | cardiolipin synthase 1 | Q9UJA2 |
| C3495436 | American cutaneous leishmaniasis | B3GAT1 | 27087 | beta-1,3-glucuronyltransferase 1 | Q9P2W7 |
| C3495427 | Fanconi-Bickel Syndrome | AGPAT2 | 10555 | 1-acylglycerol-3-phosphate O-acyltransferase 2 | O15120 |
| C3495427 | Fanconi-Bickel Syndrome | SLC2A2 | 6514 | solute carrier family 2 member 2 | P11168 |
