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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 ▼ |
|---|---|---|---|---|---|
| C0023772 | Lipid Metabolism, Inborn Errors | DGAT1 | 8694 | diacylglycerol O-acyltransferase 1 | O75907 |
| C0022661 | Kidney Failure, Chronic | DGAT1 | 8694 | diacylglycerol O-acyltransferase 1 | O75907 |
| C0024138 | Lupus Erythematosus, Discoid | DGAT1 | 8694 | diacylglycerol O-acyltransferase 1 | O75907 |
| C0018802 | Congestive heart failure | DGAT1 | 8694 | diacylglycerol O-acyltransferase 1 | O75907 |
| C0020757 | Ichthyoses | DGAT1 | 8694 | diacylglycerol O-acyltransferase 1 | O75907 |
| C0011847 | Diabetes | DGAT1 | 8694 | diacylglycerol O-acyltransferase 1 | O75907 |
| C0027651 | Neoplasms | ATRN | 8455 | attractin | O75882 |
| C0028754 | Obesity | ATRN | 8455 | attractin | O75882 |
| C0574083 | 3-Methylglutaconic aciduria type 2 | ATRN | 8455 | attractin | O75882 |
| C0878544 | Cardiomyopathies | ATRN | 8455 | attractin | O75882 |
| C0035258 | Restless Legs Syndrome | ATRN | 8455 | attractin | O75882 |
| C0004114 | Astrocytoma | ATRN | 8455 | attractin | O75882 |
| C0007137 | Squamous cell carcinoma | ATRN | 8455 | attractin | O75882 |
| C0004096 | Asthma | ATRN | 8455 | attractin | O75882 |
| C0007114 | Malignant neoplasm of skin | ATRN | 8455 | attractin | O75882 |
| C0017638 | Glioma | ATRN | 8455 | attractin | O75882 |
| C0574084 | 3-Methylglutaconic aciduria type 3 | ATRN | 8455 | attractin | O75882 |
| C0334579 | Anaplastic astrocytoma | ATRN | 8455 | attractin | O75882 |
| C0023520 | Leukodystrophy | ATRN | 8455 | attractin | O75882 |
| C0205643 | Carcinoma, Cribriform | CYP7B1 | 9420 | cytochrome P450 family 7 subfamily B member 1 | O75881 |
| C0037772 | Spastic Paraplegia | CYP7B1 | 9420 | cytochrome P450 family 7 subfamily B member 1 | O75881 |
| C1849115 | SPASTIC PARAPLEGIA 5A, AUTOSOMAL RECESSIVE (disorder) | CYP7B1 | 9420 | cytochrome P450 family 7 subfamily B member 1 | O75881 |
| C0393559 | Troyer syndrome | CYP7B1 | 9420 | cytochrome P450 family 7 subfamily B member 1 | O75881 |
| C0025517 | Metabolic Diseases | CYP7B1 | 9420 | cytochrome P450 family 7 subfamily B member 1 | O75881 |
| C0235782 | Gallbladder Carcinoma | CYP7B1 | 9420 | cytochrome P450 family 7 subfamily B member 1 | O75881 |
