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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 |
|---|---|---|---|---|---|
| C0022336 | Creutzfeldt-Jakob disease | ALG1 | 56052 | ALG1 chitobiosyldiphosphodolichol beta-mannosyltransferase | Q9BT22 |
| C0015300 | Exophthalmos | ALG1 | 56052 | ALG1 chitobiosyldiphosphodolichol beta-mannosyltransferase | Q9BT22 |
| C1862939 | AMYOTROPHIC LATERAL SCLEROSIS 1 | ALG1 | 56052 | ALG1 chitobiosyldiphosphodolichol beta-mannosyltransferase | Q9BT22 |
| C0020619 | Hypogonadism | ALG1 | 56052 | ALG1 chitobiosyldiphosphodolichol beta-mannosyltransferase | Q9BT22 |
| C0751495 | Seizures, Focal | ALG1 | 56052 | ALG1 chitobiosyldiphosphodolichol beta-mannosyltransferase | Q9BT22 |
| C0242379 | Malignant neoplasm of lung | ALG1 | 56052 | ALG1 chitobiosyldiphosphodolichol beta-mannosyltransferase | Q9BT22 |
| C0006826 | Malignant Neoplasms | ALG1 | 56052 | ALG1 chitobiosyldiphosphodolichol beta-mannosyltransferase | Q9BT22 |
| C0206650 | Fibroadenoma | ALG1 | 56052 | ALG1 chitobiosyldiphosphodolichol beta-mannosyltransferase | Q9BT22 |
| C0015934 | Fetal Growth Retardation | ALG1 | 56052 | ALG1 chitobiosyldiphosphodolichol beta-mannosyltransferase | Q9BT22 |
| C0684249 | Carcinoma of lung | ALG1 | 56052 | ALG1 chitobiosyldiphosphodolichol beta-mannosyltransferase | Q9BT22 |
| C0019829 | Hodgkin Disease | ALG1 | 56052 | ALG1 chitobiosyldiphosphodolichol beta-mannosyltransferase | Q9BT22 |
| 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 |
| C0027888 | Hereditary Motor and Sensory Neuropathies | PRNP | 5621 | prion protein | P04156 |
| C1864112 | HUNTINGTON DISEASE-LIKE 1 | PRNP | 5621 | prion protein | P04156 |
| C0376329 | New Variant Creutzfeldt-Jakob Disease | PRNP | 5621 | prion protein | P04156 |
| C0007758 | Cerebellar Ataxia | PRNP | 5621 | prion protein | P04156 |
