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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 |
|---|---|---|---|---|---|
| C0003873 | Rheumatoid Arthritis | SLC17A5 | 26503 | solute carrier family 17 member 5 | Q9NRA2 |
| C0007384 | Cataplexy | SLC17A5 | 26503 | solute carrier family 17 member 5 | Q9NRA2 |
| C1848200 | SUBCORTICAL BAND HETEROTOPIA, X-LINKED | SLC17A5 | 26503 | solute carrier family 17 member 5 | Q9NRA2 |
| C0345904 | Malignant neoplasm of liver | SLC17A5 | 26503 | solute carrier family 17 member 5 | Q9NRA2 |
| C0020456 | Hyperglycemia | SLC17A5 | 26503 | solute carrier family 17 member 5 | Q9NRA2 |
| C0001973 | Alcoholic Intoxication, Chronic | SLC17A5 | 26503 | solute carrier family 17 member 5 | Q9NRA2 |
| C0086438 | Hypogammaglobulinemia | SLC17A5 | 26503 | solute carrier family 17 member 5 | Q9NRA2 |
| C0002895 | Anemia, Sickle Cell | SLC17A5 | 26503 | solute carrier family 17 member 5 | Q9NRA2 |
| C0018802 | Congestive heart failure | SLC17A5 | 26503 | solute carrier family 17 member 5 | Q9NRA2 |
| C0376480 | Gingival Overgrowth | SLC17A5 | 26503 | solute carrier family 17 member 5 | Q9NRA2 |
| C0233794 | Memory impairment | SLC17A5 | 26503 | solute carrier family 17 member 5 | Q9NRA2 |
| C0162739 | HELLP Syndrome | SLC17A5 | 26503 | solute carrier family 17 member 5 | Q9NRA2 |
| C1845052 | AMELOGENESIS IMPERFECTA, HYPOPLASTIC/HYPOMATURATION, X-LINKED 1 | SLC17A5 | 26503 | solute carrier family 17 member 5 | Q9NRA2 |
| C0085078 | Lysosomal Storage Diseases | SLC17A5 | 26503 | solute carrier family 17 member 5 | Q9NRA2 |
| C0085409 | Polyendocrinopathies, Autoimmune | SLC17A5 | 26503 | solute carrier family 17 member 5 | Q9NRA2 |
| C0041296 | Tuberculosis | SLC17A5 | 26503 | solute carrier family 17 member 5 | Q9NRA2 |
| C0020538 | Hypertensive disease | SLC17A5 | 26503 | solute carrier family 17 member 5 | Q9NRA2 |
| C0011311 | Dengue Fever | SLC17A5 | 26503 | solute carrier family 17 member 5 | Q9NRA2 |
| C4721555 | Autoimmune hepatitis | SLC17A5 | 26503 | solute carrier family 17 member 5 | Q9NRA2 |
| 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 |
