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 |
---|---|---|---|---|---|
C0006142 | Malignant neoplasm of breast | SLC2A12 | 154091 | solute carrier family 2 member 12 | Q8TD20 |
C0400966 | Non-alcoholic Fatty Liver Disease | SLC2A12 | 154091 | solute carrier family 2 member 12 | Q8TD20 |
C1859726 | ARTERIAL TORTUOSITY SYNDROME | SLC2A10 | 81031 | solute carrier family 2 member 10 | O95528 |
C0152013 | Adenocarcinoma of lung (disorder) | SLC2A10 | 81031 | solute carrier family 2 member 10 | O95528 |
C1257931 | Mammary Neoplasms, Human | SLC2A10 | 81031 | solute carrier family 2 member 10 | O95528 |
C0684249 | Carcinoma of lung | SLC2A10 | 81031 | solute carrier family 2 member 10 | O95528 |
C0011860 | Diabetes Mellitus, Non-Insulin-Dependent | SLC2A10 | 81031 | solute carrier family 2 member 10 | O95528 |
C0032285 | Pneumonia | SLC2A10 | 81031 | solute carrier family 2 member 10 | O95528 |
C0242379 | Malignant neoplasm of lung | SLC2A10 | 81031 | solute carrier family 2 member 10 | O95528 |
C0001418 | Adenocarcinoma | SLC2A10 | 81031 | solute carrier family 2 member 10 | O95528 |
C0027651 | Neoplasms | SLC2A10 | 81031 | solute carrier family 2 member 10 | O95528 |
C0235833 | Congenital diaphragmatic hernia | SLC2A10 | 81031 | solute carrier family 2 member 10 | O95528 |
C3489393 | Hiatal Hernia | SLC2A10 | 81031 | solute carrier family 2 member 10 | O95528 |
C0006142 | Malignant neoplasm of breast | SLC2A10 | 81031 | solute carrier family 2 member 10 | O95528 |
C1275808 | Congenital central hypoventilation | SLC2A10 | 81031 | solute carrier family 2 member 10 | O95528 |
C0018802 | Congestive heart failure | SLC2A10 | 81031 | solute carrier family 2 member 10 | O95528 |
C0020538 | Hypertensive disease | SLC2A10 | 81031 | solute carrier family 2 member 10 | O95528 |
C0022578 | Keratoconus | SLC2A10 | 81031 | solute carrier family 2 member 10 | O95528 |
C0003504 | Aortic Valve Insufficiency | SLC2A10 | 81031 | solute carrier family 2 member 10 | O95528 |
C0004096 | Asthma | SLC2A10 | 81031 | solute carrier family 2 member 10 | O95528 |
C0026654 | Moyamoya Disease | SLC2A10 | 81031 | solute carrier family 2 member 10 | O95528 |
C1704436 | Peripheral Arterial Diseases | SLC2A10 | 81031 | solute carrier family 2 member 10 | O95528 |
C4721509 | Usual Interstitial Pneumonia | SLC2A10 | 81031 | solute carrier family 2 member 10 | O95528 |
C1442965 | Avascular necrosis of the capital femoral epiphysis | SLC2A10 | 81031 | solute carrier family 2 member 10 | O95528 |
C0035222 | Respiratory Distress Syndrome, Adult | SLC2A10 | 81031 | solute carrier family 2 member 10 | O95528 |
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Last updated: August 19, 2024