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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 |
|---|---|---|---|---|---|
| C1269683 | Major Depressive Disorder | MDGA1 | 266727 | MAM domain containing glycosylphosphatidylinositol anchor 1 | Q8NFP4 |
| C0026691 | Mucocutaneous Lymph Node Syndrome | MDGA1 | 266727 | MAM domain containing glycosylphosphatidylinositol anchor 1 | Q8NFP4 |
| C0041696 | Unipolar Depression | MDGA1 | 266727 | MAM domain containing glycosylphosphatidylinositol anchor 1 | Q8NFP4 |
| C0005586 | Bipolar Disorder | MDGA1 | 266727 | MAM domain containing glycosylphosphatidylinositol anchor 1 | Q8NFP4 |
| C0011884 | Diabetic Retinopathy | HS6ST3 | 266722 | heparan sulfate 6-O-sulfotransferase 3 | Q8IZP7 |
| C0027651 | Neoplasms | HS6ST3 | 266722 | heparan sulfate 6-O-sulfotransferase 3 | Q8IZP7 |
| C0019163 | Hepatitis B | HS6ST3 | 266722 | heparan sulfate 6-O-sulfotransferase 3 | Q8IZP7 |
| C0011860 | Diabetes Mellitus, Non-Insulin-Dependent | HS6ST3 | 266722 | heparan sulfate 6-O-sulfotransferase 3 | Q8IZP7 |
| C0028754 | Obesity | HS6ST3 | 266722 | heparan sulfate 6-O-sulfotransferase 3 | Q8IZP7 |
| C0678222 | Breast Carcinoma | HS6ST3 | 266722 | heparan sulfate 6-O-sulfotransferase 3 | Q8IZP7 |
| C0037369 | Smoking | HS6ST3 | 266722 | heparan sulfate 6-O-sulfotransferase 3 | Q8IZP7 |
| C0011847 | Diabetes | HS6ST3 | 266722 | heparan sulfate 6-O-sulfotransferase 3 | Q8IZP7 |
| C0011849 | Diabetes Mellitus | HS6ST3 | 266722 | heparan sulfate 6-O-sulfotransferase 3 | Q8IZP7 |
| C0006142 | Malignant neoplasm of breast | HS6ST3 | 266722 | heparan sulfate 6-O-sulfotransferase 3 | Q8IZP7 |
| C0027404 | Narcolepsy | HS6ST3 | 266722 | heparan sulfate 6-O-sulfotransferase 3 | Q8IZP7 |
| C0751748 | Nonketotic Hyperglycinemia | GCSH | 2653 | glycine cleavage system protein H | P23434 |
| C3714756 | Intellectual Disability | GCSH | 2653 | glycine cleavage system protein H | P23434 |
| C0006826 | Malignant Neoplasms | GCSH | 2653 | glycine cleavage system protein H | P23434 |
| C0175693 | Russell-Silver syndrome | GCSH | 2653 | glycine cleavage system protein H | P23434 |
| C0268560 | Hyperglycinemia, Transient Neonatal | GCSH | 2653 | glycine cleavage system protein H | P23434 |
| C0678222 | Breast Carcinoma | GCSH | 2653 | glycine cleavage system protein H | P23434 |
| C0006142 | Malignant neoplasm of breast | GCSH | 2653 | glycine cleavage system protein H | P23434 |
| C0024299 | Lymphoma | GCSH | 2653 | glycine cleavage system protein H | P23434 |
| C0036341 | Schizophrenia | GCSH | 2653 | glycine cleavage system protein H | P23434 |
| C0036572 | Seizures | GCSH | 2653 | glycine cleavage system protein H | P23434 |
