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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 |
|---|---|---|---|---|---|
| C1306459 | Primary malignant neoplasm | MPG | 4350 | N-methylpurine DNA glycosylase | P29372 |
| C0021390 | Inflammatory Bowel Diseases | MPG | 4350 | N-methylpurine DNA glycosylase | P29372 |
| C0302592 | Cervix carcinoma | MPG | 4350 | N-methylpurine DNA glycosylase | P29372 |
| C0242379 | Malignant neoplasm of lung | MPG | 4350 | N-methylpurine DNA glycosylase | P29372 |
| C0017661 | IGA Glomerulonephritis | MPG | 4350 | N-methylpurine DNA glycosylase | P29372 |
| C4048328 | cervical cancer | MPG | 4350 | N-methylpurine DNA glycosylase | P29372 |
| C0023903 | Liver neoplasms | MPG | 4350 | N-methylpurine DNA glycosylase | P29372 |
| C0011570 | Mental Depression | MPG | 4350 | N-methylpurine DNA glycosylase | P29372 |
| C0001430 | Adenoma | MPG | 4350 | N-methylpurine DNA glycosylase | P29372 |
| C0009404 | Colorectal Neoplasms | MPG | 4350 | N-methylpurine DNA glycosylase | P29372 |
| C0026764 | Multiple Myeloma | MPG | 4350 | N-methylpurine DNA glycosylase | P29372 |
| C0041296 | Tuberculosis | MPG | 4350 | N-methylpurine DNA glycosylase | P29372 |
| C0003507 | Aortic Valve Stenosis | MPG | 4350 | N-methylpurine DNA glycosylase | P29372 |
| C0020456 | Hyperglycemia | MPG | 4350 | N-methylpurine DNA glycosylase | P29372 |
| C0002871 | Anemia | MPG | 4350 | N-methylpurine DNA glycosylase | P29372 |
| C0004763 | Barrett Esophagus | MPG | 4350 | N-methylpurine DNA glycosylase | P29372 |
| C0034069 | Pulmonary Fibrosis | MPG | 4350 | N-methylpurine DNA glycosylase | P29372 |
| C0002395 | Alzheimer's Disease | MPG | 4350 | N-methylpurine DNA glycosylase | P29372 |
| C0851140 | Carcinoma in situ of uterine cervix | MPG | 4350 | N-methylpurine DNA glycosylase | P29372 |
| C0235946 | Cerebral atrophy | NGLY1 | 55768 | N-glycanase 1 | Q96IV0 |
| C0026650 | Movement Disorders | NGLY1 | 55768 | N-glycanase 1 | Q96IV0 |
| C3808991 | NGLY1 deficiency | NGLY1 | 55768 | N-glycanase 1 | Q96IV0 |
| C0008489 | Chorea | NGLY1 | 55768 | N-glycanase 1 | Q96IV0 |
| C0235991 | Small for gestational age (disorder) | NGLY1 | 55768 | N-glycanase 1 | Q96IV0 |
| C0036572 | Seizures | NGLY1 | 55768 | N-glycanase 1 | Q96IV0 |
