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 |
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DisGeNET | July 29, 2024 |
Disease ID | Disease Name | Gene Symbol | Gene ID ▲ | Gene Name | UniProt ID |
---|---|---|---|---|---|
C2931132 | Crigler Najjar syndrome, type 2 | UGT1A3 | 54659 | UDP glucuronosyltransferase family 1 member A3 | P35503 |
C0036341 | Schizophrenia | UGT1A3 | 54659 | UDP glucuronosyltransferase family 1 member A3 | P35503 |
C0036572 | Seizures | UGT1A3 | 54659 | UDP glucuronosyltransferase family 1 member A3 | P35503 |
C0011226 | Hepatitis D Infection | UGT1A3 | 54659 | UDP glucuronosyltransferase family 1 member A3 | P35503 |
C1337013 | Differentiated Thyroid Gland Carcinoma | UGT1A3 | 54659 | UDP glucuronosyltransferase family 1 member A3 | P35503 |
C1306459 | Primary malignant neoplasm | UGT1A3 | 54659 | UDP glucuronosyltransferase family 1 member A3 | P35503 |
C0011860 | Diabetes Mellitus, Non-Insulin-Dependent | UGT1A3 | 54659 | UDP glucuronosyltransferase family 1 member A3 | P35503 |
C0152013 | Adenocarcinoma of lung (disorder) | UGT1A3 | 54659 | UDP glucuronosyltransferase family 1 member A3 | P35503 |
C0346647 | Malignant neoplasm of pancreas | UGT1A3 | 54659 | UDP glucuronosyltransferase family 1 member A3 | P35503 |
C0004096 | Asthma | UGT1A3 | 54659 | UDP glucuronosyltransferase family 1 member A3 | P35503 |
C0032580 | Adenomatous Polyposis Coli | UGT1A3 | 54659 | UDP glucuronosyltransferase family 1 member A3 | P35503 |
C0002895 | Anemia, Sickle Cell | UGT1A3 | 54659 | UDP glucuronosyltransferase family 1 member A3 | P35503 |
C0020433 | Hyperbilirubinemia | UGT1A3 | 54659 | UDP glucuronosyltransferase family 1 member A3 | P35503 |
C0334294 | Multiple adenomatous polyps | UGT1A3 | 54659 | UDP glucuronosyltransferase family 1 member A3 | P35503 |
C0271979 | Thalassemia Intermedia | UGT1A3 | 54659 | UDP glucuronosyltransferase family 1 member A3 | P35503 |
C0376358 | Malignant neoplasm of prostate | UGT1A3 | 54659 | UDP glucuronosyltransferase family 1 member A3 | P35503 |
C0010414 | Infection by Cryptococcus neoformans | UGT1A3 | 54659 | UDP glucuronosyltransferase family 1 member A3 | P35503 |
C0005283 | beta Thalassemia | UGT1A3 | 54659 | UDP glucuronosyltransferase family 1 member A3 | P35503 |
C0027651 | Neoplasms | UGT1A3 | 54659 | UDP glucuronosyltransferase family 1 member A3 | P35503 |
C0600139 | Prostate carcinoma | UGT1A3 | 54659 | UDP glucuronosyltransferase family 1 member A3 | P35503 |
C0524620 | Metabolic Syndrome X | UGT1A3 | 54659 | UDP glucuronosyltransferase family 1 member A3 | P35503 |
C0017205 | Gaucher Disease | UGT1A3 | 54659 | UDP glucuronosyltransferase family 1 member A3 | P35503 |
C0268138 | Xeroderma Pigmentosum, Complementation Group D | UGT1A3 | 54659 | UDP glucuronosyltransferase family 1 member A3 | P35503 |
C0006826 | Malignant Neoplasms | UGT1A3 | 54659 | UDP glucuronosyltransferase family 1 member A3 | P35503 |
C0342751 | Generalized glycogen storage disease of infants | UGT1A3 | 54659 | UDP glucuronosyltransferase family 1 member A3 | P35503 |
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Last updated: August 19, 2024