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 |
---|---|---|---|---|---|
C0035222 | Respiratory Distress Syndrome, Adult | SLC27A5 | 10998 | solute carrier family 27 member 5 | Q9Y2P5 |
C0022283 | Incontinentia Pigmenti Achromians | SLC27A5 | 10998 | solute carrier family 27 member 5 | Q9Y2P5 |
C0524620 | Metabolic Syndrome X | SLC27A5 | 10998 | solute carrier family 27 member 5 | Q9Y2P5 |
C1332206 | Adult Lymphoma | SLC27A5 | 10998 | solute carrier family 27 member 5 | Q9Y2P5 |
C0006267 | Bronchiectasis | SLC27A5 | 10998 | solute carrier family 27 member 5 | Q9Y2P5 |
C0340076 | Asthmatic pulmonary eosinophilia | SLC27A5 | 10998 | solute carrier family 27 member 5 | Q9Y2P5 |
C0023890 | Liver Cirrhosis | SLC27A5 | 10998 | solute carrier family 27 member 5 | Q9Y2P5 |
C1306459 | Primary malignant neoplasm | SLC27A5 | 10998 | solute carrier family 27 member 5 | Q9Y2P5 |
C0751606 | Adult Acute Lymphocytic Leukemia | SLC27A5 | 10998 | solute carrier family 27 member 5 | Q9Y2P5 |
C0034068 | Pulmonary Eosinophilia | SLC27A5 | 10998 | solute carrier family 27 member 5 | Q9Y2P5 |
C0162309 | Adrenoleukodystrophy | SLC27A5 | 10998 | solute carrier family 27 member 5 | Q9Y2P5 |
C0023467 | Leukemia, Myelocytic, Acute | SLC27A5 | 10998 | solute carrier family 27 member 5 | Q9Y2P5 |
C1850900 | Familial primary gastric lymphoma | SLC27A5 | 10998 | solute carrier family 27 member 5 | Q9Y2P5 |
C0028754 | Obesity | SLC27A5 | 10998 | solute carrier family 27 member 5 | Q9Y2P5 |
C0162557 | Liver Failure, Acute | SLC27A5 | 10998 | solute carrier family 27 member 5 | Q9Y2P5 |
C0023452 | Childhood Acute Lymphoblastic Leukemia | SLC27A5 | 10998 | solute carrier family 27 member 5 | Q9Y2P5 |
C0279626 | Squamous cell carcinoma of esophagus | SLC27A5 | 10998 | solute carrier family 27 member 5 | Q9Y2P5 |
C0023449 | Acute lymphocytic leukemia | SLC27A5 | 10998 | solute carrier family 27 member 5 | Q9Y2P5 |
C0010691 | Cystinuria | SLC3A1 | 6519 | solute carrier family 3 member 1 | Q07837 |
C1848030 | Hypotonia-Cystinuria Syndrome | SLC3A1 | 6519 | solute carrier family 3 member 1 | Q07837 |
C0022661 | Kidney Failure, Chronic | SLC3A1 | 6519 | solute carrier family 3 member 1 | Q07837 |
C0017636 | Glioblastoma | SLC3A1 | 6519 | solute carrier family 3 member 1 | Q07837 |
C1621958 | Glioblastoma Multiforme | SLC3A1 | 6519 | solute carrier family 3 member 1 | Q07837 |
C1857388 | Cystinuria, Type A | SLC3A1 | 6519 | solute carrier family 3 member 1 | Q07837 |
C0027709 | Nephrocalcinosis | SLC3A1 | 6519 | solute carrier family 3 member 1 | Q07837 |
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Last updated: August 19, 2024