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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 |
|---|---|---|---|---|---|
| C0206754 | Neuroendocrine Tumors | CD33 | 945 | CD33 molecule | P20138 |
| C0002726 | Amyloidosis | CD33 | 945 | CD33 molecule | P20138 |
| C0007137 | Squamous cell carcinoma | CD33 | 945 | CD33 molecule | P20138 |
| C0524851 | Neurodegenerative Disorders | CD33 | 945 | CD33 molecule | P20138 |
| C0699791 | Stomach Carcinoma | CD33 | 945 | CD33 molecule | P20138 |
| C1168401 | Squamous cell carcinoma of the head and neck | CD33 | 945 | CD33 molecule | P20138 |
| C0032463 | Polycythemia Vera | CD33 | 945 | CD33 molecule | P20138 |
| C0015625 | Fanconi Anemia | CD33 | 945 | CD33 molecule | P20138 |
| C0009324 | Ulcerative Colitis | CHST2 | 9435 | carbohydrate sulfotransferase 2 | Q9Y4C5 |
| C0029463 | Osteosarcoma | CHST2 | 9435 | carbohydrate sulfotransferase 2 | Q9Y4C5 |
| C1850900 | Familial primary gastric lymphoma | CHST2 | 9435 | carbohydrate sulfotransferase 2 | Q9Y4C5 |
| C0002736 | Amyotrophic Lateral Sclerosis | CHST2 | 9435 | carbohydrate sulfotransferase 2 | Q9Y4C5 |
| C0585442 | Osteosarcoma of bone | CHST2 | 9435 | carbohydrate sulfotransferase 2 | Q9Y4C5 |
| C0027651 | Neoplasms | CHST2 | 9435 | carbohydrate sulfotransferase 2 | Q9Y4C5 |
| C0205643 | Carcinoma, Cribriform | CYP7B1 | 9420 | cytochrome P450 family 7 subfamily B member 1 | O75881 |
| C0037772 | Spastic Paraplegia | CYP7B1 | 9420 | cytochrome P450 family 7 subfamily B member 1 | O75881 |
| C1849115 | SPASTIC PARAPLEGIA 5A, AUTOSOMAL RECESSIVE (disorder) | CYP7B1 | 9420 | cytochrome P450 family 7 subfamily B member 1 | O75881 |
| C0393559 | Troyer syndrome | CYP7B1 | 9420 | cytochrome P450 family 7 subfamily B member 1 | O75881 |
| C0025517 | Metabolic Diseases | CYP7B1 | 9420 | cytochrome P450 family 7 subfamily B member 1 | O75881 |
| C0235782 | Gallbladder Carcinoma | CYP7B1 | 9420 | cytochrome P450 family 7 subfamily B member 1 | O75881 |
| C0034152 | Henoch-Schoenlein Purpura | CYP7B1 | 9420 | cytochrome P450 family 7 subfamily B member 1 | O75881 |
| C0023772 | Lipid Metabolism, Inborn Errors | CYP7B1 | 9420 | cytochrome P450 family 7 subfamily B member 1 | O75881 |
| C0029408 | Degenerative polyarthritis | CYP7B1 | 9420 | cytochrome P450 family 7 subfamily B member 1 | O75881 |
| C0011849 | Diabetes Mellitus | CYP7B1 | 9420 | cytochrome P450 family 7 subfamily B member 1 | O75881 |
| C3151147 | Bile Acid Synthesis Defect, Congenital, 3 | CYP7B1 | 9420 | cytochrome P450 family 7 subfamily B member 1 | O75881 |
