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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 |
|---|---|---|---|---|---|
| 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 |
| C0019693 | HIV Infections | TMED1 | 11018 | transmembrane p24 trafficking protein 1 | Q13445 |
| C0006142 | Malignant neoplasm of breast | TMED1 | 11018 | transmembrane p24 trafficking protein 1 | Q13445 |
| C0751882 | Myasthenic Syndromes, Congenital | CHAT | 1103 | choline O-acetyltransferase | P28329 |
| C1568363 | Tendinosis | CHAT | 1103 | choline O-acetyltransferase | P28329 |
| C3714756 | Intellectual Disability | CHAT | 1103 | choline O-acetyltransferase | P28329 |
| C0028043 | Nicotine Dependence | CHAT | 1103 | choline O-acetyltransferase | P28329 |
| C0004096 | Asthma | CHAT | 1103 | choline O-acetyltransferase | P28329 |
| C0270824 | Visual seizure | CHAT | 1103 | choline O-acetyltransferase | P28329 |
| C0699790 | Colon Carcinoma | CHAT | 1103 | choline O-acetyltransferase | P28329 |
| C0038454 | Cerebrovascular accident | CHAT | 1103 | choline O-acetyltransferase | P28329 |
| C0022972 | Lambert-Eaton Myasthenic Syndrome | CHAT | 1103 | choline O-acetyltransferase | P28329 |
