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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 |
|---|---|---|---|---|---|
| C0600260 | Lung Diseases, Obstructive | SLC2A10 | 81031 | solute carrier family 2 member 10 | O95528 |
| C0034194 | Pyloric Stenosis | SLC2A10 | 81031 | solute carrier family 2 member 10 | O95528 |
| C0003486 | Aortic Aneurysm | SLC2A10 | 81031 | solute carrier family 2 member 10 | O95528 |
| C1306503 | Congenital exomphalos | SLC2A10 | 81031 | solute carrier family 2 member 10 | O95528 |
| C0085096 | Peripheral Vascular Diseases | SLC2A10 | 81031 | solute carrier family 2 member 10 | O95528 |
| C0038379 | Strabismus | SLC2A10 | 81031 | solute carrier family 2 member 10 | O95528 |
| C0005744 | Blepharophimosis | SLC2A10 | 81031 | solute carrier family 2 member 10 | O95528 |
| C0264408 | Childhood asthma | SLC2A10 | 81031 | solute carrier family 2 member 10 | O95528 |
| C1800706 | Idiopathic Pulmonary Fibrosis | SLC2A10 | 81031 | solute carrier family 2 member 10 | O95528 |
| C0010495 | Cutis Laxa | SLC2A10 | 81031 | solute carrier family 2 member 10 | O95528 |
| C0034067 | Pulmonary Emphysema | SLC2A10 | 81031 | solute carrier family 2 member 10 | O95528 |
| C0036439 | Scoliosis, unspecified | SLC2A10 | 81031 | solute carrier family 2 member 10 | O95528 |
| C0270850 | Idiopathic generalized epilepsy | NPL | 80896 | N-acetylneuraminate pyruvate lyase | Q9BXD5 |
| C0021390 | Inflammatory Bowel Diseases | NPL | 80896 | N-acetylneuraminate pyruvate lyase | Q9BXD5 |
| C0033975 | Psychotic Disorders | NPL | 80896 | N-acetylneuraminate pyruvate lyase | Q9BXD5 |
| C0020538 | Hypertensive disease | NPL | 80896 | N-acetylneuraminate pyruvate lyase | Q9BXD5 |
| C0021400 | Influenza | NPL | 80896 | N-acetylneuraminate pyruvate lyase | Q9BXD5 |
| C1691779 | Sensory hearing loss | NPL | 80896 | N-acetylneuraminate pyruvate lyase | Q9BXD5 |
| C1852197 | MAJOR AFFECTIVE DISORDER 1 | NPL | 80896 | N-acetylneuraminate pyruvate lyase | Q9BXD5 |
| C0005586 | Bipolar Disorder | NPL | 80896 | N-acetylneuraminate pyruvate lyase | Q9BXD5 |
| C0494475 | Tonic - clonic seizures | NPL | 80896 | N-acetylneuraminate pyruvate lyase | Q9BXD5 |
| C0036341 | Schizophrenia | NPL | 80896 | N-acetylneuraminate pyruvate lyase | Q9BXD5 |
| C0030319 | Panic Disorder | NPL | 80896 | N-acetylneuraminate pyruvate lyase | Q9BXD5 |
| C0600139 | Prostate carcinoma | NPL | 80896 | N-acetylneuraminate pyruvate lyase | Q9BXD5 |
| C0376358 | Malignant neoplasm of prostate | NPL | 80896 | N-acetylneuraminate pyruvate lyase | Q9BXD5 |
