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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 |
|---|---|---|---|---|---|
| C0948896 | Primary hypogonadism | SCP2 | 6342 | sterol carrier protein 2 | P22307 |
| C0206686 | Adrenocortical carcinoma | SCP2 | 6342 | sterol carrier protein 2 | P22307 |
| C0678222 | Breast Carcinoma | SCP2 | 6342 | sterol carrier protein 2 | P22307 |
| C0393593 | Dystonia Disorders | SCP2 | 6342 | sterol carrier protein 2 | P22307 |
| C0393588 | Dystonia, Paroxysmal | SCP2 | 6342 | sterol carrier protein 2 | P22307 |
| C0042384 | Vasculitis | SCP2 | 6342 | sterol carrier protein 2 | P22307 |
| C0235025 | Peripheral motor neuropathy | SCP2 | 6342 | sterol carrier protein 2 | P22307 |
| C0034960 | Refsum Disease | SCP2 | 6342 | sterol carrier protein 2 | P22307 |
| C0524851 | Neurodegenerative Disorders | SCP2 | 6342 | sterol carrier protein 2 | P22307 |
| C1858991 | Childhood Ataxia with Central Nervous System Hypomyelinization | SCP2 | 6342 | sterol carrier protein 2 | P22307 |
| C0020456 | Hyperglycemia | SCP2 | 6342 | sterol carrier protein 2 | P22307 |
| C0220668 | Congenital contractural arachnodactyly | SCP2 | 6342 | sterol carrier protein 2 | P22307 |
| C0393851 | Polyneuropathy, Critical Illness | SCP2 | 6342 | sterol carrier protein 2 | P22307 |
| C0024141 | Lupus Erythematosus, Systemic | SCD5 | 79966 | stearoyl-CoA desaturase 5 | Q86SK9 |
| C0023903 | Liver neoplasms | SCD5 | 79966 | stearoyl-CoA desaturase 5 | Q86SK9 |
| C1306459 | Primary malignant neoplasm | SCD5 | 79966 | stearoyl-CoA desaturase 5 | Q86SK9 |
| C0002895 | Anemia, Sickle Cell | SCD5 | 79966 | stearoyl-CoA desaturase 5 | Q86SK9 |
| C0002395 | Alzheimer's Disease | SCD5 | 79966 | stearoyl-CoA desaturase 5 | Q86SK9 |
| C0025202 | melanoma | SCD5 | 79966 | stearoyl-CoA desaturase 5 | Q86SK9 |
| C1961099 | Precursor T-Cell Lymphoblastic Leukemia-Lymphoma | SCD5 | 79966 | stearoyl-CoA desaturase 5 | Q86SK9 |
| C0242383 | Age related macular degeneration | SCD5 | 79966 | stearoyl-CoA desaturase 5 | Q86SK9 |
| C0029408 | Degenerative polyarthritis | SCD5 | 79966 | stearoyl-CoA desaturase 5 | Q86SK9 |
| C0011860 | Diabetes Mellitus, Non-Insulin-Dependent | SCD5 | 79966 | stearoyl-CoA desaturase 5 | Q86SK9 |
| C4551720 | Primary Ciliary Dyskinesia | SCD5 | 79966 | stearoyl-CoA desaturase 5 | Q86SK9 |
| C0003873 | Rheumatoid Arthritis | SCD5 | 79966 | stearoyl-CoA desaturase 5 | Q86SK9 |
