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 |
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DisGeNET | July 29, 2024 |
Disease ID | Disease Name | Gene Symbol | Gene ID | Gene Name | UniProt ID ▲ |
---|---|---|---|---|---|
C0029463 | Osteosarcoma | ALDOA | 226 | aldolase, fructose-bisphosphate A | P04075 |
C0152013 | Adenocarcinoma of lung (disorder) | ALDOA | 226 | aldolase, fructose-bisphosphate A | P04075 |
C0002878 | Anemia, Hemolytic | ALDOA | 226 | aldolase, fructose-bisphosphate A | P04075 |
C0013336 | Dwarfism | ALDOA | 226 | aldolase, fructose-bisphosphate A | P04075 |
C0740277 | Bile duct carcinoma | ALDOA | 226 | aldolase, fructose-bisphosphate A | P04075 |
C0002881 | Anemia, Hemolytic, Congenital | ALDOA | 226 | aldolase, fructose-bisphosphate A | P04075 |
C0029408 | Degenerative polyarthritis | ALDOA | 226 | aldolase, fructose-bisphosphate A | P04075 |
C1257931 | Mammary Neoplasms, Human | ALDOA | 226 | aldolase, fructose-bisphosphate A | P04075 |
C0206698 | Cholangiocarcinoma | ALDOA | 226 | aldolase, fructose-bisphosphate A | P04075 |
C0151744 | Myocardial Ischemia | ALDOA | 226 | aldolase, fructose-bisphosphate A | P04075 |
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 |
C0376358 | Malignant neoplasm of prostate | PRNP | 5621 | prion protein | P04156 |
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Last updated: August 19, 2024