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 |
---|---|---|---|---|---|
C0007131 | Non-Small Cell Lung Carcinoma | SLC17A5 | 26503 | solute carrier family 17 member 5 | Q9NRA2 |
C0011581 | Depressive disorder | SLC17A5 | 26503 | solute carrier family 17 member 5 | Q9NRA2 |
C0036572 | Seizures | SLC17A5 | 26503 | solute carrier family 17 member 5 | Q9NRA2 |
C3714756 | Intellectual Disability | SLC17A5 | 26503 | solute carrier family 17 member 5 | Q9NRA2 |
C0014518 | Toxic Epidermal Necrolysis | SLC17A5 | 26503 | solute carrier family 17 member 5 | Q9NRA2 |
C0032285 | Pneumonia | SLC17A5 | 26503 | solute carrier family 17 member 5 | Q9NRA2 |
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 |
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Last updated: August 19, 2024