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 |
---|---|---|---|---|---|
C0031117 | Peripheral Neuropathy | CYP2C8 | 1558 | cytochrome P450 family 2 subfamily C member 8 | P10632 |
C1458155 | Mammary Neoplasms | CYP2C8 | 1558 | cytochrome P450 family 2 subfamily C member 8 | P10632 |
C1961102 | Precursor Cell Lymphoblastic Leukemia Lymphoma | CYP2C8 | 1558 | cytochrome P450 family 2 subfamily C member 8 | P10632 |
C0023453 | L2 Acute Lymphoblastic Leukemia | CYP2C8 | 1558 | cytochrome P450 family 2 subfamily C member 8 | P10632 |
C0023452 | Childhood Acute Lymphoblastic Leukemia | CYP2C8 | 1558 | cytochrome P450 family 2 subfamily C member 8 | P10632 |
C0027765 | nervous system disorder | CYP2C8 | 1558 | cytochrome P450 family 2 subfamily C member 8 | P10632 |
C0007137 | Squamous cell carcinoma | CYP2C8 | 1558 | cytochrome P450 family 2 subfamily C member 8 | P10632 |
C0006826 | Malignant Neoplasms | CYP2C8 | 1558 | cytochrome P450 family 2 subfamily C member 8 | P10632 |
C0238198 | Gastrointestinal Stromal Tumors | CYP2C8 | 1558 | cytochrome P450 family 2 subfamily C member 8 | P10632 |
C0029445 | Bone necrosis | CYP2C8 | 1558 | cytochrome P450 family 2 subfamily C member 8 | P10632 |
C0019189 | Hepatitis, Chronic | CYP2C19 | 1557 | cytochrome P450 family 2 subfamily C member 19 | P33261 |
C0010054 | Coronary Arteriosclerosis | CYP2C19 | 1557 | cytochrome P450 family 2 subfamily C member 19 | P33261 |
C0024623 | Malignant neoplasm of stomach | CYP2C19 | 1557 | cytochrome P450 family 2 subfamily C member 19 | P33261 |
C0038454 | Cerebrovascular accident | CYP2C19 | 1557 | cytochrome P450 family 2 subfamily C member 19 | P33261 |
C1956346 | Coronary Artery Disease | CYP2C19 | 1557 | cytochrome P450 family 2 subfamily C member 19 | P33261 |
C0027051 | Myocardial Infarction | CYP2C19 | 1557 | cytochrome P450 family 2 subfamily C member 19 | P33261 |
C0011847 | Diabetes | CYP2C19 | 1557 | cytochrome P450 family 2 subfamily C member 19 | P33261 |
C0011849 | Diabetes Mellitus | CYP2C19 | 1557 | cytochrome P450 family 2 subfamily C member 19 | P33261 |
C0003850 | Arteriosclerosis | CYP2C19 | 1557 | cytochrome P450 family 2 subfamily C member 19 | P33261 |
C0339573 | Glaucoma, Primary Open Angle | CYP2C19 | 1557 | cytochrome P450 family 2 subfamily C member 19 | P33261 |
C0003872 | Arthritis, Psoriatic | CYP2C19 | 1557 | cytochrome P450 family 2 subfamily C member 19 | P33261 |
C0006142 | Malignant neoplasm of breast | CYP2C19 | 1557 | cytochrome P450 family 2 subfamily C member 19 | P33261 |
C0011570 | Mental Depression | CYP2C19 | 1557 | cytochrome P450 family 2 subfamily C member 19 | P33261 |
C0948008 | Ischemic stroke | CYP2C19 | 1557 | cytochrome P450 family 2 subfamily C member 19 | P33261 |
C0007787 | Transient Ischemic Attack | CYP2C19 | 1557 | cytochrome P450 family 2 subfamily C member 19 | P33261 |
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Last updated: August 19, 2024