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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 |
|---|---|---|---|---|---|
| C0004096 | Asthma | SLC17A5 | 26503 | solute carrier family 17 member 5 | Q9NRA2 |
| C0362046 | Prediabetes syndrome | SLC17A5 | 26503 | solute carrier family 17 member 5 | Q9NRA2 |
| C0017661 | IGA Glomerulonephritis | SLC17A5 | 26503 | solute carrier family 17 member 5 | Q9NRA2 |
| C0038454 | Cerebrovascular accident | SLC17A5 | 26503 | solute carrier family 17 member 5 | Q9NRA2 |
| C3888065 | ECTODERMAL DYSPLASIA 10A, HYPOHIDROTIC/HAIR/NAIL TYPE, AUTOSOMAL DOMINANT | SLC17A5 | 26503 | solute carrier family 17 member 5 | Q9NRA2 |
| C0042769 | Virus Diseases | SLC17A5 | 26503 | solute carrier family 17 member 5 | Q9NRA2 |
| C0019100 | Severe Dengue | SLC17A5 | 26503 | solute carrier family 17 member 5 | Q9NRA2 |
| C0015310 | Exotropia | SLC17A5 | 26503 | solute carrier family 17 member 5 | Q9NRA2 |
| C0004153 | Atherosclerosis | SLC17A5 | 26503 | solute carrier family 17 member 5 | Q9NRA2 |
| C0028738 | Nystagmus | SLC17A5 | 26503 | solute carrier family 17 member 5 | Q9NRA2 |
| C0030312 | Pancytopenia | SLC17A5 | 26503 | solute carrier family 17 member 5 | Q9NRA2 |
| C1852438 | CATARACT, COPPOCK-LIKE | SLC17A5 | 26503 | solute carrier family 17 member 5 | Q9NRA2 |
| C3463824 | MYELODYSPLASTIC SYNDROME | SLC17A5 | 26503 | solute carrier family 17 member 5 | Q9NRA2 |
| C0025517 | Metabolic Diseases | SLC17A5 | 26503 | solute carrier family 17 member 5 | Q9NRA2 |
| C0566602 | Primary sclerosing cholangitis | SLC17A5 | 26503 | solute carrier family 17 member 5 | Q9NRA2 |
| C3714636 | Pneumonitis | SLC17A5 | 26503 | solute carrier family 17 member 5 | Q9NRA2 |
| C0005745 | Blepharoptosis | SLC17A5 | 26503 | solute carrier family 17 member 5 | Q9NRA2 |
| C1956346 | Coronary Artery Disease | SLC17A5 | 26503 | solute carrier family 17 member 5 | Q9NRA2 |
| C0027726 | Nephrotic Syndrome | SLC17A5 | 26503 | solute carrier family 17 member 5 | Q9NRA2 |
| C0019187 | Hepatitis, Alcoholic | SLC17A5 | 26503 | solute carrier family 17 member 5 | Q9NRA2 |
| C0948008 | Ischemic stroke | SLC17A5 | 26503 | solute carrier family 17 member 5 | Q9NRA2 |
| C0015652 | Fascioliasis | SLC17A5 | 26503 | solute carrier family 17 member 5 | Q9NRA2 |
| C3887494 | ECTODERMAL DYSPLASIA 10B, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMAL RECESSIVE | SLC17A5 | 26503 | solute carrier family 17 member 5 | Q9NRA2 |
| C1168401 | Squamous cell carcinoma of the head and neck | SLC17A5 | 26503 | solute carrier family 17 member 5 | Q9NRA2 |
| C1565489 | Renal Insufficiency | SLC17A5 | 26503 | solute carrier family 17 member 5 | Q9NRA2 |
