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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 |
|---|---|---|---|---|---|
| C0027092 | Myopia | PSMD10 | 5716 | proteasome 26S subunit, non-ATPase 10 | O75832 |
| C0036341 | Schizophrenia | PSMD10 | 5716 | proteasome 26S subunit, non-ATPase 10 | O75832 |
| C0019196 | Hepatitis C | PSMD10 | 5716 | proteasome 26S subunit, non-ATPase 10 | O75832 |
| C0279702 | Conventional (Clear Cell) Renal Cell Carcinoma | PSMD10 | 5716 | proteasome 26S subunit, non-ATPase 10 | O75832 |
| C2711227 | Steatohepatitis | PSMD10 | 5716 | proteasome 26S subunit, non-ATPase 10 | O75832 |
| C0011849 | Diabetes Mellitus | PSMD10 | 5716 | proteasome 26S subunit, non-ATPase 10 | O75832 |
| C0026769 | Multiple Sclerosis | PSMD10 | 5716 | proteasome 26S subunit, non-ATPase 10 | O75832 |
| C0025202 | melanoma | PSMD10 | 5716 | proteasome 26S subunit, non-ATPase 10 | O75832 |
| C0011847 | Diabetes | PSMD10 | 5716 | proteasome 26S subunit, non-ATPase 10 | O75832 |
| C1332986 | Childhood Osteosarcoma | PSMD10 | 5716 | proteasome 26S subunit, non-ATPase 10 | O75832 |
| C0079731 | B-Cell Lymphomas | PSMD10 | 5716 | proteasome 26S subunit, non-ATPase 10 | O75832 |
| C0600139 | Prostate carcinoma | PSMD10 | 5716 | proteasome 26S subunit, non-ATPase 10 | O75832 |
| C0155490 | Middle Ear Cholesteatoma | PSMD10 | 5716 | proteasome 26S subunit, non-ATPase 10 | O75832 |
| C1336708 | Testicular Germ Cell Tumor | PSMD10 | 5716 | proteasome 26S subunit, non-ATPase 10 | O75832 |
| C0007137 | Squamous cell carcinoma | PSMD10 | 5716 | proteasome 26S subunit, non-ATPase 10 | O75832 |
| C0007124 | Noninfiltrating Intraductal Carcinoma | PSMD10 | 5716 | proteasome 26S subunit, non-ATPase 10 | O75832 |
| C0003493 | Aortic Diseases | PTDSS1 | 9791 | phosphatidylserine synthase 1 | P48651 |
| C0003507 | Aortic Valve Stenosis | PTDSS1 | 9791 | phosphatidylserine synthase 1 | P48651 |
| C0432269 | Lenz Majewski hyperostotic dwarfism | PTDSS1 | 9791 | phosphatidylserine synthase 1 | P48651 |
| C1851710 | LATERAL MENINGOCELE SYNDROME | PTDSS1 | 9791 | phosphatidylserine synthase 1 | P48651 |
| C0036439 | Scoliosis, unspecified | PTDSS1 | 9791 | phosphatidylserine synthase 1 | P48651 |
| C0010495 | Cutis Laxa | PTDSS1 | 9791 | phosphatidylserine synthase 1 | P48651 |
| C0039075 | Syndactyly | PTDSS1 | 9791 | phosphatidylserine synthase 1 | P48651 |
| C0015934 | Fetal Growth Retardation | PTDSS1 | 9791 | phosphatidylserine synthase 1 | P48651 |
| C0008297 | Choanal Atresia | PTDSS1 | 9791 | phosphatidylserine synthase 1 | P48651 |
