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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 |
|---|---|---|---|---|---|
| C0268138 | Xeroderma Pigmentosum, Complementation Group D | UGT1A5 | 54579 | UDP glucuronosyltransferase family 1 member A5 | P35504 |
| C0005695 | Bladder Neoplasm | UGT1A6 | 54578 | UDP glucuronosyltransferase family 1 member A6 | P19224 |
| C0020433 | Hyperbilirubinemia | UGT1A6 | 54578 | UDP glucuronosyltransferase family 1 member A6 | P19224 |
| C0017551 | Gilbert Disease (disorder) | UGT1A6 | 54578 | UDP glucuronosyltransferase family 1 member A6 | P19224 |
| C0011616 | Contact Dermatitis | UGT1A6 | 54578 | UDP glucuronosyltransferase family 1 member A6 | P19224 |
| C0009402 | Colorectal Carcinoma | UGT1A6 | 54578 | UDP glucuronosyltransferase family 1 member A6 | P19224 |
| C0684249 | Carcinoma of lung | UGT1A6 | 54578 | UDP glucuronosyltransferase family 1 member A6 | P19224 |
| C0857007 | Hyperbilirubinemia, Neonatal | UGT1A6 | 54578 | UDP glucuronosyltransferase family 1 member A6 | P19224 |
| C0021400 | Influenza | UGT1A6 | 54578 | UDP glucuronosyltransferase family 1 member A6 | P19224 |
| C0011860 | Diabetes Mellitus, Non-Insulin-Dependent | UGT1A6 | 54578 | UDP glucuronosyltransferase family 1 member A6 | P19224 |
| C0010324 | Crigler Najjar syndrome, type 1 | UGT1A6 | 54578 | UDP glucuronosyltransferase family 1 member A6 | P19224 |
| C0008350 | Cholelithiasis | UGT1A6 | 54578 | UDP glucuronosyltransferase family 1 member A6 | P19224 |
| C0004096 | Asthma | UGT1A6 | 54578 | UDP glucuronosyltransferase family 1 member A6 | P19224 |
| C2939465 | Deficiency of glucose-6-phosphate dehydrogenase | UGT1A6 | 54578 | UDP glucuronosyltransferase family 1 member A6 | P19224 |
| C0400966 | Non-alcoholic Fatty Liver Disease | UGT1A6 | 54578 | UDP glucuronosyltransferase family 1 member A6 | P19224 |
| C0023530 | Leukopenia | UGT1A6 | 54578 | UDP glucuronosyltransferase family 1 member A6 | P19224 |
| C0278996 | Malignant Head and Neck Neoplasm | UGT1A6 | 54578 | UDP glucuronosyltransferase family 1 member A6 | P19224 |
| C0017152 | Gastritis | UGT1A6 | 54578 | UDP glucuronosyltransferase family 1 member A6 | P19224 |
| C0037889 | Hereditary spherocytosis | UGT1A6 | 54578 | UDP glucuronosyltransferase family 1 member A6 | P19224 |
| C0007097 | Carcinoma | UGT1A6 | 54578 | UDP glucuronosyltransferase family 1 member A6 | P19224 |
| C0947622 | Cholecystolithiasis | UGT1A6 | 54578 | UDP glucuronosyltransferase family 1 member A6 | P19224 |
| C0699889 | Malignant Female Reproductive System Neoplasm | UGT1A6 | 54578 | UDP glucuronosyltransferase family 1 member A6 | P19224 |
| C2931132 | Crigler Najjar syndrome, type 2 | UGT1A6 | 54578 | UDP glucuronosyltransferase family 1 member A6 | P19224 |
| C0027947 | Neutropenia | UGT1A6 | 54578 | UDP glucuronosyltransferase family 1 member A6 | P19224 |
| C0017205 | Gaucher Disease | UGT1A6 | 54578 | UDP glucuronosyltransferase family 1 member A6 | P19224 |
