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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 |
|---|---|---|---|---|---|
| C0678222 | Breast Carcinoma | PGAP3 | 93210 | post-GPI attachment to proteins phospholipase 3 | Q96FM1 |
| C0020295 | Hydronephrosis | PGAP3 | 93210 | post-GPI attachment to proteins phospholipase 3 | Q96FM1 |
| C0005586 | Bipolar Disorder | PGAP3 | 93210 | post-GPI attachment to proteins phospholipase 3 | Q96FM1 |
| C0036572 | Seizures | PGAP3 | 93210 | post-GPI attachment to proteins phospholipase 3 | Q96FM1 |
| C0006325 | Bruxism | PGAP3 | 93210 | post-GPI attachment to proteins phospholipase 3 | Q96FM1 |
| C0036857 | Severe intellectual disability | PGAP3 | 93210 | post-GPI attachment to proteins phospholipase 3 | Q96FM1 |
| C0021390 | Inflammatory Bowel Diseases | PGAP3 | 93210 | post-GPI attachment to proteins phospholipase 3 | Q96FM1 |
| C0024623 | Malignant neoplasm of stomach | PGAP3 | 93210 | post-GPI attachment to proteins phospholipase 3 | Q96FM1 |
| C0036439 | Scoliosis, unspecified | PGAP3 | 93210 | post-GPI attachment to proteins phospholipase 3 | Q96FM1 |
| C0006142 | Malignant neoplasm of breast | PGAP3 | 93210 | post-GPI attachment to proteins phospholipase 3 | Q96FM1 |
| C0038356 | Stomach Neoplasms | PGAP3 | 93210 | post-GPI attachment to proteins phospholipase 3 | Q96FM1 |
| C0020490 | Hyperopia | PGAP3 | 93210 | post-GPI attachment to proteins phospholipase 3 | Q96FM1 |
| C0221356 | Brachycephaly | PGAP3 | 93210 | post-GPI attachment to proteins phospholipase 3 | Q96FM1 |
| C0039446 | Telangiectasis | PGAP3 | 93210 | post-GPI attachment to proteins phospholipase 3 | Q96FM1 |
| C0019569 | Hirschsprung Disease | PGAP3 | 93210 | post-GPI attachment to proteins phospholipase 3 | Q96FM1 |
| C0524851 | Neurodegenerative Disorders | PRNP | 5621 | prion protein | P04156 |
| C1852467 | Creutzfeldt-Jakob Disease, Sporadic | PRNP | 5621 | prion protein | P04156 |
| C0162534 | Prion Diseases | PRNP | 5621 | prion protein | P04156 |
| C0002395 | Alzheimer's Disease | PRNP | 5621 | prion protein | P04156 |
| C0006142 | Malignant neoplasm of breast | PRNP | 5621 | prion protein | P04156 |
| C0017495 | Gerstmann-Straussler-Scheinker Disease | PRNP | 5621 | prion protein | P04156 |
| C0026650 | Movement Disorders | PRNP | 5621 | prion protein | P04156 |
| C0206042 | Fatal Familial Insomnia | PRNP | 5621 | prion protein | P04156 |
| C0022336 | Creutzfeldt-Jakob disease | PRNP | 5621 | prion protein | P04156 |
| C0002726 | Amyloidosis | PRNP | 5621 | prion protein | P04156 |
