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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 ▼ |
|---|---|---|---|---|---|
| C0036572 | Seizures | UGCG | 7357 | UDP-glucose ceramide glucosyltransferase | Q16739 |
| C1961835 | Gaucher Disease, Type 1 | UGCG | 7357 | UDP-glucose ceramide glucosyltransferase | Q16739 |
| C0206663 | Neuroectodermal Tumor, Primitive | UGCG | 7357 | UDP-glucose ceramide glucosyltransferase | Q16739 |
| C0220756 | Niemann-Pick Disease, Type C | UGCG | 7357 | UDP-glucose ceramide glucosyltransferase | Q16739 |
| C0038220 | Status Epilepticus | UGCG | 7357 | UDP-glucose ceramide glucosyltransferase | Q16739 |
| C3887461 | Head and Neck Carcinoma | UGCG | 7357 | UDP-glucose ceramide glucosyltransferase | Q16739 |
| C0497327 | Dementia | UGCG | 7357 | UDP-glucose ceramide glucosyltransferase | Q16739 |
| C0011880 | Diabetic Ketoacidosis | UGCG | 7357 | UDP-glucose ceramide glucosyltransferase | Q16739 |
| C0024117 | Chronic Obstructive Airway Disease | UGCG | 7357 | UDP-glucose ceramide glucosyltransferase | Q16739 |
| C4048328 | cervical cancer | UGCG | 7357 | UDP-glucose ceramide glucosyltransferase | Q16739 |
| C0020456 | Hyperglycemia | UGCG | 7357 | UDP-glucose ceramide glucosyltransferase | Q16739 |
| C0011581 | Depressive disorder | UGCG | 7357 | UDP-glucose ceramide glucosyltransferase | Q16739 |
| C0677886 | Epithelial ovarian cancer | UGCG | 7357 | UDP-glucose ceramide glucosyltransferase | Q16739 |
| C0025312 | Meningomyelocele | UGCG | 7357 | UDP-glucose ceramide glucosyltransferase | Q16739 |
| C0018790 | Cardiac Arrest | UGCG | 7357 | UDP-glucose ceramide glucosyltransferase | Q16739 |
| C0004364 | Autoimmune Diseases | MAN2A1 | 4124 | mannosidase alpha class 2A member 1 | Q16706 |
| C0024141 | Lupus Erythematosus, Systemic | MAN2A1 | 4124 | mannosidase alpha class 2A member 1 | Q16706 |
| C1306459 | Primary malignant neoplasm | MAN2A1 | 4124 | mannosidase alpha class 2A member 1 | Q16706 |
| C0036341 | Schizophrenia | MAN2A1 | 4124 | mannosidase alpha class 2A member 1 | Q16706 |
| C2239176 | Liver carcinoma | MAN2A1 | 4124 | mannosidase alpha class 2A member 1 | Q16706 |
| C1621958 | Glioblastoma Multiforme | MAN2A1 | 4124 | mannosidase alpha class 2A member 1 | Q16706 |
| C0002876 | Congenital dyserythropoietic anemia | MAN2A1 | 4124 | mannosidase alpha class 2A member 1 | Q16706 |
| C0027651 | Neoplasms | MAN2A1 | 4124 | mannosidase alpha class 2A member 1 | Q16706 |
| C0600139 | Prostate carcinoma | MAN2A1 | 4124 | mannosidase alpha class 2A member 1 | Q16706 |
| C0376358 | Malignant neoplasm of prostate | MAN2A1 | 4124 | mannosidase alpha class 2A member 1 | Q16706 |
