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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 |
|---|---|---|---|---|---|
| C1261473 | Sarcoma | SLC27A5 | 10998 | solute carrier family 27 member 5 | Q9Y2P5 |
| C4551720 | Primary Ciliary Dyskinesia | SLC27A5 | 10998 | solute carrier family 27 member 5 | Q9Y2P5 |
| C1527407 | Eosinophilic Pneumonia | SLC27A5 | 10998 | solute carrier family 27 member 5 | Q9Y2P5 |
| C0023530 | Leukopenia | SLC27A5 | 10998 | solute carrier family 27 member 5 | Q9Y2P5 |
| 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 |
| C0003873 | Rheumatoid Arthritis | HTD2 | 109703458 | hydroxyacyl-thioester dehydratase type 2 | P86397 |
| C0151744 | Myocardial Ischemia | ACOT2 | 10965 | acyl-CoA thioesterase 2 | P49753 |
| C0011860 | Diabetes Mellitus, Non-Insulin-Dependent | ACOT2 | 10965 | acyl-CoA thioesterase 2 | P49753 |
