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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 |
|---|---|---|---|---|---|
| C0032460 | Polycystic Ovary Syndrome | ITLN1 | 55600 | intelectin 1 | Q8WWA0 |
| C0024623 | Malignant neoplasm of stomach | ITLN1 | 55600 | intelectin 1 | Q8WWA0 |
| C0026769 | Multiple Sclerosis | ITLN1 | 55600 | intelectin 1 | Q8WWA0 |
| C0025500 | Mesothelioma | ITLN1 | 55600 | intelectin 1 | Q8WWA0 |
| C0862312 | Epithelioid mesothelioma, malignant | ITLN1 | 55600 | intelectin 1 | Q8WWA0 |
| C0011615 | Dermatitis, Atopic | ITLN1 | 55600 | intelectin 1 | Q8WWA0 |
| C0010068 | Coronary heart disease | ITLN1 | 55600 | intelectin 1 | Q8WWA0 |
| C0029458 | Osteoporosis, Postmenopausal | ITLN1 | 55600 | intelectin 1 | Q8WWA0 |
| C0011860 | Diabetes Mellitus, Non-Insulin-Dependent | ITLN1 | 55600 | intelectin 1 | Q8WWA0 |
| C1956346 | Coronary Artery Disease | ITLN1 | 55600 | intelectin 1 | Q8WWA0 |
| C0011849 | Diabetes Mellitus | ITLN1 | 55600 | intelectin 1 | Q8WWA0 |
| C0007097 | Carcinoma | ITLN1 | 55600 | intelectin 1 | Q8WWA0 |
| C0033860 | Psoriasis | ITLN1 | 55600 | intelectin 1 | Q8WWA0 |
| C0151744 | Myocardial Ischemia | ITLN1 | 55600 | intelectin 1 | Q8WWA0 |
| C0001418 | Adenocarcinoma | ITLN1 | 55600 | intelectin 1 | Q8WWA0 |
| C0006142 | Malignant neoplasm of breast | MTMR8 | 55613 | myotubularin related protein 8 | Q96EF0 |
| C3150417 | MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 3 | POMGNT1 | 55624 | protein O-linked mannose N-acetylglucosaminyltransferase 1 (beta 1,2-) | Q8WZA1 |
| C0265221 | Walker-Warburg congenital muscular dystrophy | POMGNT1 | 55624 | protein O-linked mannose N-acetylglucosaminyltransferase 1 (beta 1,2-) | Q8WZA1 |
| C0010417 | Cryptorchidism | POMGNT1 | 55624 | protein O-linked mannose N-acetylglucosaminyltransferase 1 (beta 1,2-) | Q8WZA1 |
| C3150412 | MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 3 | POMGNT1 | 55624 | protein O-linked mannose N-acetylglucosaminyltransferase 1 (beta 1,2-) | Q8WZA1 |
| C0035334 | Retinitis Pigmentosa | POMGNT1 | 55624 | protein O-linked mannose N-acetylglucosaminyltransferase 1 (beta 1,2-) | Q8WZA1 |
| C3714756 | Intellectual Disability | POMGNT1 | 55624 | protein O-linked mannose N-acetylglucosaminyltransferase 1 (beta 1,2-) | Q8WZA1 |
| C0241005 | Creatine phosphokinase serum increased | POMGNT1 | 55624 | protein O-linked mannose N-acetylglucosaminyltransferase 1 (beta 1,2-) | Q8WZA1 |
| C0206157 | Myopathies, Nemaline | POMGNT1 | 55624 | protein O-linked mannose N-acetylglucosaminyltransferase 1 (beta 1,2-) | Q8WZA1 |
| C0026850 | Muscular Dystrophy | POMGNT1 | 55624 | protein O-linked mannose N-acetylglucosaminyltransferase 1 (beta 1,2-) | Q8WZA1 |
