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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 |
|---|---|---|---|---|---|
| C0085409 | Polyendocrinopathies, Autoimmune | NT5E | 4907 | 5'-nucleotidase ecto | P21589 |
| C0003467 | Anxiety | NT5E | 4907 | 5'-nucleotidase ecto | P21589 |
| C0750974 | Brain Tumor, Primary | NT5E | 4907 | 5'-nucleotidase ecto | P21589 |
| C0085110 | Severe Combined Immunodeficiency | NT5E | 4907 | 5'-nucleotidase ecto | P21589 |
| C0007103 | Malignant neoplasm of endometrium | NT5E | 4907 | 5'-nucleotidase ecto | P21589 |
| C1859726 | ARTERIAL TORTUOSITY SYNDROME | NT5E | 4907 | 5'-nucleotidase ecto | P21589 |
| C0017152 | Gastritis | NT5E | 4907 | 5'-nucleotidase ecto | P21589 |
| C0020179 | Huntington Disease | NT5E | 4907 | 5'-nucleotidase ecto | P21589 |
| C2242813 | Ranula (disorder) | NT5E | 4907 | 5'-nucleotidase ecto | P21589 |
| C0392607 | Severe combined immunodeficiency due to adenosine deaminase deficiency | NT5E | 4907 | 5'-nucleotidase ecto | P21589 |
| C0031099 | Periodontitis | NT5E | 4907 | 5'-nucleotidase ecto | P21589 |
| C0013080 | Down Syndrome | NT5E | 4907 | 5'-nucleotidase ecto | P21589 |
| C0014544 | Epilepsy | NT5E | 4907 | 5'-nucleotidase ecto | P21589 |
| C0024959 | Maxillary Sinusitis | NT5E | 4907 | 5'-nucleotidase ecto | P21589 |
| C0026703 | Mucopolysaccharidoses | NT5E | 4907 | 5'-nucleotidase ecto | P21589 |
| C0010054 | Coronary Arteriosclerosis | NT5E | 4907 | 5'-nucleotidase ecto | P21589 |
| C0024904 | Mastoiditis | NT5E | 4907 | 5'-nucleotidase ecto | P21589 |
| C0038356 | Stomach Neoplasms | PFKFB1 | 5207 | 6-phosphofructo-2-kinase/fructose-2,6-biphosphatase 1 | P16118 |
| C0020459 | Hyperinsulinism | PFKFB1 | 5207 | 6-phosphofructo-2-kinase/fructose-2,6-biphosphatase 1 | P16118 |
| C0027651 | Neoplasms | PFKFB1 | 5207 | 6-phosphofructo-2-kinase/fructose-2,6-biphosphatase 1 | P16118 |
| C0006826 | Malignant Neoplasms | PFKFB2 | 5208 | 6-phosphofructo-2-kinase/fructose-2,6-biphosphatase 2 | O60825 |
| C1621958 | Glioblastoma Multiforme | PFKFB2 | 5208 | 6-phosphofructo-2-kinase/fructose-2,6-biphosphatase 2 | O60825 |
| C0038356 | Stomach Neoplasms | PFKFB2 | 5208 | 6-phosphofructo-2-kinase/fructose-2,6-biphosphatase 2 | O60825 |
| C0017636 | Glioblastoma | PFKFB2 | 5208 | 6-phosphofructo-2-kinase/fructose-2,6-biphosphatase 2 | O60825 |
| C0015934 | Fetal Growth Retardation | PFKFB2 | 5208 | 6-phosphofructo-2-kinase/fructose-2,6-biphosphatase 2 | O60825 |
