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 |
---|---|---|---|---|---|
C0162351 | Contact hypersensitivity | UGT1A6 | 54578 | UDP glucuronosyltransferase family 1 member A6 | P19224 |
C0242379 | Malignant neoplasm of lung | UGT1A6 | 54578 | UDP glucuronosyltransferase family 1 member A6 | P19224 |
C0342751 | Generalized glycogen storage disease of infants | UGT1A6 | 54578 | UDP glucuronosyltransferase family 1 member A6 | P19224 |
C0007222 | Cardiovascular Diseases | UGT1A6 | 54578 | UDP glucuronosyltransferase family 1 member A6 | P19224 |
C0271979 | Thalassemia Intermedia | UGT1A6 | 54578 | UDP glucuronosyltransferase family 1 member A6 | P19224 |
C0010054 | Coronary Arteriosclerosis | UGT1A6 | 54578 | UDP glucuronosyltransferase family 1 member A6 | P19224 |
C1337013 | Differentiated Thyroid Gland Carcinoma | UGT1A6 | 54578 | UDP glucuronosyltransferase family 1 member A6 | P19224 |
C0039730 | Thalassemia | UGT1A6 | 54578 | UDP glucuronosyltransferase family 1 member A6 | P19224 |
C0018790 | Cardiac Arrest | UGT1A6 | 54578 | UDP glucuronosyltransferase family 1 member A6 | P19224 |
C0003873 | Rheumatoid Arthritis | UGT1A6 | 54578 | UDP glucuronosyltransferase family 1 member A6 | P19224 |
C0009404 | Colorectal Neoplasms | UGT1A6 | 54578 | UDP glucuronosyltransferase family 1 member A6 | P19224 |
C3887461 | Head and Neck Carcinoma | UGT1A6 | 54578 | UDP glucuronosyltransferase family 1 member A6 | P19224 |
C0038220 | Status Epilepticus | UGT1A6 | 54578 | UDP glucuronosyltransferase family 1 member A6 | P19224 |
C0023452 | Childhood Acute Lymphoblastic Leukemia | UGT1A6 | 54578 | UDP glucuronosyltransferase family 1 member A6 | P19224 |
C0005684 | Malignant neoplasm of urinary bladder | UGT1A6 | 54578 | UDP glucuronosyltransferase family 1 member A6 | P19224 |
C0024623 | Malignant neoplasm of stomach | UGT1A6 | 54578 | UDP glucuronosyltransferase family 1 member A6 | P19224 |
C0002312 | alpha-Thalassemia | UGT1A6 | 54578 | UDP glucuronosyltransferase family 1 member A6 | P19224 |
C0600139 | Prostate carcinoma | UGT1A5 | 54579 | UDP glucuronosyltransferase family 1 member A5 | P35504 |
C0008350 | Cholelithiasis | UGT1A5 | 54579 | UDP glucuronosyltransferase family 1 member A5 | P35504 |
C0524620 | Metabolic Syndrome X | UGT1A5 | 54579 | UDP glucuronosyltransferase family 1 member A5 | P35504 |
C0010324 | Crigler Najjar syndrome, type 1 | UGT1A5 | 54579 | UDP glucuronosyltransferase family 1 member A5 | P35504 |
C0017205 | Gaucher Disease | UGT1A5 | 54579 | UDP glucuronosyltransferase family 1 member A5 | P35504 |
C1306459 | Primary malignant neoplasm | UGT1A5 | 54579 | UDP glucuronosyltransferase family 1 member A5 | P35504 |
C0376358 | Malignant neoplasm of prostate | UGT1A5 | 54579 | UDP glucuronosyltransferase family 1 member A5 | P35504 |
C0028754 | Obesity | UGT1A5 | 54579 | UDP glucuronosyltransferase family 1 member A5 | P35504 |
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Last updated: August 19, 2024