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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 |
|---|---|---|---|---|---|
| C0855197 | Malignant Testicular Germ Cell Tumor | CYP3A5 | 1577 | cytochrome P450 family 3 subfamily A member 5 | P20815 |
| C0855197 | Malignant Testicular Germ Cell Tumor | HPGDS | 27306 | hematopoietic prostaglandin D synthase | O60760 |
| C0855197 | Malignant Testicular Germ Cell Tumor | PSMD10 | 5716 | proteasome 26S subunit, non-ATPase 10 | O75832 |
| C0855197 | Malignant Testicular Germ Cell Tumor | CYP2B6 | 1555 | cytochrome P450 family 2 subfamily B member 6 | P20813 |
| C0855197 | Malignant Testicular Germ Cell Tumor | CYP3A7 | 1551 | cytochrome P450 family 3 subfamily A member 7 | P24462 |
| C0856761 | Budd-Chiari Syndrome | CALR | 811 | calreticulin | P27797 |
| C0856761 | Budd-Chiari Syndrome | CD55 | 1604 | CD55 molecule (Cromer blood group) | P08174 |
| C0856761 | Budd-Chiari Syndrome | CYP2C9 | 1559 | cytochrome P450 family 2 subfamily C member 9 | P11712 |
| C0856761 | Budd-Chiari Syndrome | GPLD1 | 2822 | glycosylphosphatidylinositol specific phospholipase D1 | P80108 |
| C0856830 | Calcium pyrophosphate arthropathy | ENPP1 | 5167 | ectonucleotide pyrophosphatase/phosphodiesterase 1 | P22413 |
| C0857007 | Hyperbilirubinemia, Neonatal | UGGT1 | 56886 | UDP-glucose glycoprotein glucosyltransferase 1 | Q9NYU2 |
| C0857007 | Hyperbilirubinemia, Neonatal | FBP1 | 2203 | fructose-bisphosphatase 1 | P09467 |
| C0857007 | Hyperbilirubinemia, Neonatal | G6PD | 2539 | glucose-6-phosphate dehydrogenase | P11413 |
| C0857007 | Hyperbilirubinemia, Neonatal | UGT1A8 | 54576 | UDP glucuronosyltransferase family 1 member A8 | Q9HAW9 |
| C0857007 | Hyperbilirubinemia, Neonatal | UGT1A6 | 54578 | UDP glucuronosyltransferase family 1 member A6 | P19224 |
| C0857007 | Hyperbilirubinemia, Neonatal | UGT1A7 | 54577 | UDP glucuronosyltransferase family 1 member A7 | Q9HAW7 |
| C0857007 | Hyperbilirubinemia, Neonatal | UGT1A10 | 54575 | UDP glucuronosyltransferase family 1 member A10 | Q9HAW8 |
| C0857007 | Hyperbilirubinemia, Neonatal | UGT1A1 | 54658 | UDP glucuronosyltransferase family 1 member A1 | P22309 |
| C0857007 | Hyperbilirubinemia, Neonatal | UGT1A9 | 54600 | UDP glucuronosyltransferase family 1 member A9 | O60656 |
| C0857007 | Hyperbilirubinemia, Neonatal | UGT1A4 | 54657 | UDP glucuronosyltransferase family 1 member A4 | P22310 |
| C0857007 | Hyperbilirubinemia, Neonatal | UGT1A5 | 54579 | UDP glucuronosyltransferase family 1 member A5 | P35504 |
| C0857007 | Hyperbilirubinemia, Neonatal | UGT1A3 | 54659 | UDP glucuronosyltransferase family 1 member A3 | P35503 |
| C0857007 | Hyperbilirubinemia, Neonatal | HPGDS | 27306 | hematopoietic prostaglandin D synthase | O60760 |
| C0857007 | Hyperbilirubinemia, Neonatal | GPX1 | 2876 | glutathione peroxidase 1 | P07203 |
| C0857007 | Hyperbilirubinemia, Neonatal | CAT | 847 | catalase | P04040 |
