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DisGeNET
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 |
|---|---|---|---|---|---|
| C0024141 | Lupus Erythematosus, Systemic | CYP2C19 | 1557 | cytochrome P450 family 2 subfamily C member 19 | P33261 |
| C0042384 | Vasculitis | CYP2C19 | 1557 | cytochrome P450 family 2 subfamily C member 19 | P33261 |
| C3489393 | Hiatal Hernia | CYP2C19 | 1557 | cytochrome P450 family 2 subfamily C member 19 | P33261 |
| C0085096 | Peripheral Vascular Diseases | CYP2C19 | 1557 | cytochrome P450 family 2 subfamily C member 19 | P33261 |
| C0392164 | Pulmonary Cystic Fibrosis | CYP2C19 | 1557 | cytochrome P450 family 2 subfamily C member 19 | P33261 |
| C0685938 | Malignant neoplasm of gastrointestinal tract | CYP2C19 | 1557 | cytochrome P450 family 2 subfamily C member 19 | P33261 |
| C0027726 | Nephrotic Syndrome | CYP2C19 | 1557 | cytochrome P450 family 2 subfamily C member 19 | P33261 |
| C1853926 | NONAKA MYOPATHY | CYP2C19 | 1557 | cytochrome P450 family 2 subfamily C member 19 | P33261 |
| C0004153 | Atherosclerosis | CYP2C19 | 1557 | cytochrome P450 family 2 subfamily C member 19 | P33261 |
| C4552079 | Premature Ovarian Failure 1 | CYP2C19 | 1557 | cytochrome P450 family 2 subfamily C member 19 | P33261 |
| C0917805 | Transient Cerebral Ischemia | CYP2C19 | 1557 | cytochrome P450 family 2 subfamily C member 19 | P33261 |
| C0004364 | Autoimmune Diseases | CYP2C19 | 1557 | cytochrome P450 family 2 subfamily C member 19 | P33261 |
| C0038358 | Gastric ulcer | CYP2C19 | 1557 | cytochrome P450 family 2 subfamily C member 19 | P33261 |
| 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 |
