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 |
---|---|---|---|---|---|
C0279000 | Liver and Intrahepatic Biliary Tract Carcinoma | CYP2C9 | 1559 | cytochrome P450 family 2 subfamily C member 9 | P11712 |
C0013336 | Dwarfism | CYP2C9 | 1559 | cytochrome P450 family 2 subfamily C member 9 | P11712 |
C0011991 | Diarrhea | CYP2C9 | 1559 | cytochrome P450 family 2 subfamily C member 9 | P11712 |
C0496899 | Benign neoplasm of brain, unspecified | CYP2C9 | 1559 | cytochrome P450 family 2 subfamily C member 9 | P11712 |
C0027651 | Neoplasms | CYP2C8 | 1558 | cytochrome P450 family 2 subfamily C member 8 | P10632 |
C0024530 | Malaria | CYP2C8 | 1558 | cytochrome P450 family 2 subfamily C member 8 | P10632 |
C0006142 | Malignant neoplasm of breast | CYP2C8 | 1558 | cytochrome P450 family 2 subfamily C member 8 | P10632 |
C0678222 | Breast Carcinoma | CYP2C8 | 1558 | cytochrome P450 family 2 subfamily C member 8 | P10632 |
C1956346 | Coronary Artery Disease | CYP2C8 | 1558 | cytochrome P450 family 2 subfamily C member 8 | P10632 |
C4721453 | Peripheral Nervous System Diseases | CYP2C8 | 1558 | cytochrome P450 family 2 subfamily C member 8 | P10632 |
C0442874 | Neuropathy | CYP2C8 | 1558 | cytochrome P450 family 2 subfamily C member 8 | P10632 |
C0007131 | Non-Small Cell Lung Carcinoma | CYP2C8 | 1558 | cytochrome P450 family 2 subfamily C member 8 | P10632 |
C0020538 | Hypertensive disease | CYP2C8 | 1558 | cytochrome P450 family 2 subfamily C member 8 | P10632 |
C4721610 | Carcinoma, Ovarian Epithelial | CYP2C8 | 1558 | cytochrome P450 family 2 subfamily C member 8 | P10632 |
C0024535 | Malaria, Falciparum | CYP2C8 | 1558 | cytochrome P450 family 2 subfamily C member 8 | P10632 |
C2239176 | Liver carcinoma | CYP2C8 | 1558 | cytochrome P450 family 2 subfamily C member 8 | P10632 |
C0027051 | Myocardial Infarction | CYP2C8 | 1558 | cytochrome P450 family 2 subfamily C member 8 | P10632 |
C0002871 | Anemia | CYP2C8 | 1558 | cytochrome P450 family 2 subfamily C member 8 | P10632 |
C1140680 | Malignant neoplasm of ovary | CYP2C8 | 1558 | cytochrome P450 family 2 subfamily C member 8 | P10632 |
C0023473 | Myeloid Leukemia, Chronic | CYP2C8 | 1558 | cytochrome P450 family 2 subfamily C member 8 | P10632 |
C0023530 | Leukopenia | CYP2C8 | 1558 | cytochrome P450 family 2 subfamily C member 8 | P10632 |
C0022658 | Kidney Diseases | CYP2C8 | 1558 | cytochrome P450 family 2 subfamily C member 8 | P10632 |
C0919267 | ovarian neoplasm | CYP2C8 | 1558 | cytochrome P450 family 2 subfamily C member 8 | P10632 |
C0010068 | Coronary heart disease | CYP2C8 | 1558 | cytochrome P450 family 2 subfamily C member 8 | P10632 |
C0010054 | Coronary Arteriosclerosis | CYP2C8 | 1558 | cytochrome P450 family 2 subfamily C member 8 | P10632 |
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Last updated: August 19, 2024