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 |
---|---|---|---|---|---|
C0271979 | Thalassemia Intermedia | UGT1A9 | 54600 | UDP glucuronosyltransferase family 1 member A9 | O60656 |
C0023895 | Liver diseases | UGT1A9 | 54600 | UDP glucuronosyltransferase family 1 member A9 | O60656 |
C0024535 | Malaria, Falciparum | UGT1A9 | 54600 | UDP glucuronosyltransferase family 1 member A9 | O60656 |
C0857007 | Hyperbilirubinemia, Neonatal | UGT1A8 | 54576 | UDP glucuronosyltransferase family 1 member A8 | Q9HAW9 |
C0010324 | Crigler Najjar syndrome, type 1 | UGT1A8 | 54576 | UDP glucuronosyltransferase family 1 member A8 | Q9HAW9 |
C1337013 | Differentiated Thyroid Gland Carcinoma | UGT1A8 | 54576 | UDP glucuronosyltransferase family 1 member A8 | Q9HAW9 |
C0008350 | Cholelithiasis | UGT1A8 | 54576 | UDP glucuronosyltransferase family 1 member A8 | Q9HAW9 |
C0271979 | Thalassemia Intermedia | UGT1A8 | 54576 | UDP glucuronosyltransferase family 1 member A8 | Q9HAW9 |
C0270210 | Lucey-Driscoll syndrome (disorder) | UGT1A8 | 54576 | UDP glucuronosyltransferase family 1 member A8 | Q9HAW9 |
C0002875 | Cooley's anemia | UGT1A8 | 54576 | UDP glucuronosyltransferase family 1 member A8 | Q9HAW9 |
C0006826 | Malignant Neoplasms | UGT1A8 | 54576 | UDP glucuronosyltransferase family 1 member A8 | Q9HAW9 |
C0009402 | Colorectal Carcinoma | UGT1A8 | 54576 | UDP glucuronosyltransferase family 1 member A8 | Q9HAW9 |
C0002312 | alpha-Thalassemia | UGT1A8 | 54576 | UDP glucuronosyltransferase family 1 member A8 | Q9HAW9 |
C1306459 | Primary malignant neoplasm | UGT1A8 | 54576 | UDP glucuronosyltransferase family 1 member A8 | Q9HAW9 |
C0600139 | Prostate carcinoma | UGT1A8 | 54576 | UDP glucuronosyltransferase family 1 member A8 | Q9HAW9 |
C0005684 | Malignant neoplasm of urinary bladder | UGT1A8 | 54576 | UDP glucuronosyltransferase family 1 member A8 | Q9HAW9 |
C0524620 | Metabolic Syndrome X | UGT1A8 | 54576 | UDP glucuronosyltransferase family 1 member A8 | Q9HAW9 |
C2939465 | Deficiency of glucose-6-phosphate dehydrogenase | UGT1A8 | 54576 | UDP glucuronosyltransferase family 1 member A8 | Q9HAW9 |
C0017551 | Gilbert Disease (disorder) | UGT1A8 | 54576 | UDP glucuronosyltransferase family 1 member A8 | Q9HAW9 |
C0014859 | Esophageal Neoplasms | UGT1A8 | 54576 | UDP glucuronosyltransferase family 1 member A8 | Q9HAW9 |
C0011226 | Hepatitis D Infection | UGT1A8 | 54576 | UDP glucuronosyltransferase family 1 member A8 | Q9HAW9 |
C0023473 | Myeloid Leukemia, Chronic | UGT1A8 | 54576 | UDP glucuronosyltransferase family 1 member A8 | Q9HAW9 |
C0020433 | Hyperbilirubinemia | UGT1A8 | 54576 | UDP glucuronosyltransferase family 1 member A8 | Q9HAW9 |
C0376358 | Malignant neoplasm of prostate | UGT1A8 | 54576 | UDP glucuronosyltransferase family 1 member A8 | Q9HAW9 |
C0018790 | Cardiac Arrest | UGT1A8 | 54576 | UDP glucuronosyltransferase family 1 member A8 | Q9HAW9 |
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Last updated: August 19, 2024