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 |
---|---|---|---|---|---|
C0025517 | Metabolic Diseases | TALDO1 | 6888 | transaldolase 1 | P37837 |
C0043346 | Xeroderma Pigmentosum | TALDO1 | 6888 | transaldolase 1 | P37837 |
C0239946 | Fibrosis, Liver | TALDO1 | 6888 | transaldolase 1 | P37837 |
C0011847 | Diabetes | TALDO1 | 6888 | transaldolase 1 | P37837 |
C0011053 | Deafness | TALDO1 | 6888 | transaldolase 1 | P37837 |
C0016522 | Foramen Ovale, Patent | TALDO1 | 6888 | transaldolase 1 | P37837 |
C0002895 | Anemia, Sickle Cell | TALDO1 | 6888 | transaldolase 1 | P37837 |
C0011849 | Diabetes Mellitus | TALDO1 | 6888 | transaldolase 1 | P37837 |
C0018818 | Ventricular Septal Defects | TALDO1 | 6888 | transaldolase 1 | P37837 |
C0268419 | Acatalasia | TALDO1 | 6888 | transaldolase 1 | P37837 |
C2931868 | Catalase deficiency | TALDO1 | 6888 | transaldolase 1 | P37837 |
C0006142 | Malignant neoplasm of breast | SYNJ2 | 8871 | synaptojanin 2 | O15056 |
C0086132 | Depressive Symptoms | SYNJ2 | 8871 | synaptojanin 2 | O15056 |
C0684249 | Carcinoma of lung | SYNJ2 | 8871 | synaptojanin 2 | O15056 |
C0699790 | Colon Carcinoma | SYNJ2 | 8871 | synaptojanin 2 | O15056 |
C0431399 | Familial aplasia of the vermis | SYNJ2 | 8871 | synaptojanin 2 | O15056 |
C0007102 | Malignant tumor of colon | SYNJ2 | 8871 | synaptojanin 2 | O15056 |
C0026850 | Muscular Dystrophy | SYNJ2 | 8871 | synaptojanin 2 | O15056 |
C0002736 | Amyotrophic Lateral Sclerosis | SYNJ2 | 8871 | synaptojanin 2 | O15056 |
C0278878 | Adult Glioblastoma | SYNJ2 | 8871 | synaptojanin 2 | O15056 |
C0017636 | Glioblastoma | SYNJ2 | 8871 | synaptojanin 2 | O15056 |
C0013080 | Down Syndrome | SYNJ1 | 8867 | synaptojanin 1 | O43426 |
C0005586 | Bipolar Disorder | SYNJ1 | 8867 | synaptojanin 1 | O43426 |
C3809824 | PARKINSON DISEASE 20, EARLY-ONSET | SYNJ1 | 8867 | synaptojanin 1 | O43426 |
C0025958 | Microcephaly | SYNJ1 | 8867 | synaptojanin 1 | O43426 |
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Last updated: August 19, 2024