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 |
---|---|---|---|---|---|
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 |
C0006826 | Malignant Neoplasms | UGT1A6 | 54578 | UDP glucuronosyltransferase family 1 member A6 | P19224 |
C0019163 | Hepatitis B | UGT1A6 | 54578 | UDP glucuronosyltransferase family 1 member A6 | P19224 |
C0027651 | Neoplasms | UGT1A6 | 54578 | UDP glucuronosyltransferase family 1 member A6 | P19224 |
C0008370 | Cholestasis | UGT1A6 | 54578 | UDP glucuronosyltransferase family 1 member A6 | P19224 |
C0010414 | Infection by Cryptococcus neoformans | UGT1A6 | 54578 | UDP glucuronosyltransferase family 1 member A6 | P19224 |
C0011991 | Diarrhea | UGT1A6 | 54578 | UDP glucuronosyltransferase family 1 member A6 | P19224 |
C0151744 | Myocardial Ischemia | UGT1A6 | 54578 | UDP glucuronosyltransferase family 1 member A6 | P19224 |
C0023895 | Liver diseases | UGT1A6 | 54578 | UDP glucuronosyltransferase family 1 member A6 | P19224 |
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Last updated: August 19, 2024