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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 |
|---|---|---|---|---|---|
| C0023470 | Myeloid Leukemia | CYP3A5 | 1577 | cytochrome P450 family 3 subfamily A member 5 | P20815 |
| C0027720 | Nephrosis | CYP3A5 | 1577 | cytochrome P450 family 3 subfamily A member 5 | P20815 |
| C0027726 | Nephrotic Syndrome | CYP3A5 | 1577 | cytochrome P450 family 3 subfamily A member 5 | P20815 |
| C0027651 | Neoplasms | CYP3A5 | 1577 | cytochrome P450 family 3 subfamily A member 5 | P20815 |
| C0036341 | Schizophrenia | CYP3A5 | 1577 | cytochrome P450 family 3 subfamily A member 5 | P20815 |
| C0024141 | Lupus Erythematosus, Systemic | CYP3A5 | 1577 | cytochrome P450 family 3 subfamily A member 5 | P20815 |
| C0009782 | Connective Tissue Diseases | CYP3A5 | 1577 | cytochrome P450 family 3 subfamily A member 5 | P20815 |
| C0279702 | Conventional (Clear Cell) Renal Cell Carcinoma | CYP3A5 | 1577 | cytochrome P450 family 3 subfamily A member 5 | P20815 |
| C1565489 | Renal Insufficiency | CYP3A5 | 1577 | cytochrome P450 family 3 subfamily A member 5 | P20815 |
| C0751606 | Adult Acute Lymphocytic Leukemia | CYP3A5 | 1577 | cytochrome P450 family 3 subfamily A member 5 | P20815 |
| C0024620 | Primary Malignant Liver Neoplasm | CYP3A5 | 1577 | cytochrome P450 family 3 subfamily A member 5 | P20815 |
| C1561643 | Chronic Kidney Diseases | CYP3A5 | 1577 | cytochrome P450 family 3 subfamily A member 5 | P20815 |
| C0022661 | Kidney Failure, Chronic | CYP3A5 | 1577 | cytochrome P450 family 3 subfamily A member 5 | P20815 |
| C0278510 | Childhood Medulloblastoma | CYP3A5 | 1577 | cytochrome P450 family 3 subfamily A member 5 | P20815 |
| C0678222 | Breast Carcinoma | CYP3A5 | 1577 | cytochrome P450 family 3 subfamily A member 5 | P20815 |
| C0004936 | Mental disorders | CYP3A5 | 1577 | cytochrome P450 family 3 subfamily A member 5 | P20815 |
| C0948008 | Ischemic stroke | CYP3A5 | 1577 | cytochrome P450 family 3 subfamily A member 5 | P20815 |
| C0600139 | Prostate carcinoma | CYP3A5 | 1577 | cytochrome P450 family 3 subfamily A member 5 | P20815 |
| C0033578 | Prostatic Neoplasms | CYP3A5 | 1577 | cytochrome P450 family 3 subfamily A member 5 | P20815 |
| C0524620 | Metabolic Syndrome X | CYP3A5 | 1577 | cytochrome P450 family 3 subfamily A member 5 | P20815 |
| C0010054 | Coronary Arteriosclerosis | CYP3A5 | 1577 | cytochrome P450 family 3 subfamily A member 5 | P20815 |
| C0022650 | Kidney Calculi | CYP3A5 | 1577 | cytochrome P450 family 3 subfamily A member 5 | P20815 |
| C0004364 | Autoimmune Diseases | CYP3A5 | 1577 | cytochrome P450 family 3 subfamily A member 5 | P20815 |
| C0684249 | Carcinoma of lung | CYP3A5 | 1577 | cytochrome P450 family 3 subfamily A member 5 | P20815 |
| C0008370 | Cholestasis | CYP3A5 | 1577 | cytochrome P450 family 3 subfamily A member 5 | P20815 |
