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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 |
|---|---|---|---|---|---|
| C0264408 | Childhood asthma | CLEC16A | 23274 | C-type lectin domain containing 16A | Q2KHT3 |
| C0264408 | Childhood asthma | ALOX5 | 240 | arachidonate 5-lipoxygenase | P09917 |
| C0264408 | Childhood asthma | ACAA1 | 30 | acetyl-CoA acyltransferase 1 | P09110 |
| C0264490 | Acute respiratory failure | ABO | 28 | ABO, alpha 1-3-N-acetylgalactosaminyltransferase and alpha 1-3-galactosyltransferase | P16442 |
| C0264490 | Acute respiratory failure | PARP1 | 142 | poly(ADP-ribose) polymerase 1 | P09874 |
| C0264490 | Acute respiratory failure | IDH1 | 3417 | isocitrate dehydrogenase (NADP(+)) 1 | O75874 |
| C0264490 | Acute respiratory failure | CYP1A1 | 1543 | cytochrome P450 family 1 subfamily A member 1 | P04798 |
| C0264490 | Acute respiratory failure | MBL2 | 4153 | mannose binding lectin 2 | P11226 |
| C0264490 | Acute respiratory failure | PIK3C3 | 5289 | phosphatidylinositol 3-kinase catalytic subunit type 3 | Q8NEB9 |
| C0264490 | Acute respiratory failure | SFTPD | 6441 | surfactant protein D | P35247 |
| C0264490 | Acute respiratory failure | SFTPA2 | 729238 | surfactant protein A2 | Q8IWL1 |
| C0264490 | Acute respiratory failure | SLC2A10 | 81031 | solute carrier family 2 member 10 | O95528 |
| C0264490 | Acute respiratory failure | PTEN | 5728 | phosphatase and tensin homolog | P60484 |
| C0264611 | Apraxia of Phonation | COG4 | 25839 | component of oligomeric golgi complex 4 | Q9H9E3 |
| C0264611 | Apraxia of Phonation | GALT | 2592 | galactose-1-phosphate uridylyltransferase | P07902 |
| C0264611 | Apraxia of Phonation | PTEN | 5728 | phosphatase and tensin homolog | P60484 |
| C0264694 | Chronic myocardial ischemia | TM7SF2 | 7108 | transmembrane 7 superfamily member 2 | O76062 |
| C0264766 | Rheumatic mitral stenosis | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
| C0264893 | Nodal rhythm disorder | GPD1L | 23171 | glycerol-3-phosphate dehydrogenase 1 like | Q8N335 |
| C0264893 | Nodal rhythm disorder | CACNA2D1 | 781 | calcium voltage-gated channel auxiliary subunit alpha2delta 1 | P54289 |
| C0264956 | Atheroma | PARP1 | 142 | poly(ADP-ribose) polymerase 1 | P09874 |
| C0264995 | Occlusion of artery (disorder) | NT5E | 4907 | 5'-nucleotidase ecto | P21589 |
| C0264995 | Occlusion of artery (disorder) | AGXT | 189 | alanine--glyoxylate and serine--pyruvate aminotransferase | P21549 |
| C0265004 | Dilatation of aorta | SMUG1 | 23583 | single-strand-selective monofunctional uracil-DNA glycosylase 1 | Q53HV7 |
| C0265004 | Dilatation of aorta | VCAN | 1462 | versican | P13611 |
