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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 |
|---|---|---|---|---|---|
| C0036341 | Schizophrenia | PPT1 | 5538 | palmitoyl-protein thioesterase 1 | P50897 |
| C0036341 | Schizophrenia | CRLS1 | 54675 | cardiolipin synthase 1 | Q9UJA2 |
| C0036341 | Schizophrenia | PRNP | 5621 | prion protein | F7VJQ1 |
| C0036341 | Schizophrenia | PTEN | 5728 | phosphatase and tensin homolog | P60484 |
| C0036341 | Schizophrenia | PTGS2 | 5743 | prostaglandin-endoperoxide synthase 2 | P35354 |
| C0036341 | Schizophrenia | PTGIS | 5740 | prostaglandin I2 synthase | Q16647 |
| C0036341 | Schizophrenia | PTGDS | 5730 | prostaglandin D2 synthase | P41222 |
| C0036341 | Schizophrenia | SDHA | 6389 | succinate dehydrogenase complex flavoprotein subunit A | P31040 |
| C0036341 | Schizophrenia | SHMT1 | 6470 | serine hydroxymethyltransferase 1 | P34896 |
| C0036341 | Schizophrenia | TKT | 7086 | transketolase | P29401 |
| C0036341 | Schizophrenia | SULT1E1 | 6783 | sulfotransferase family 1E member 1 | P49888 |
| C0036341 | Schizophrenia | CNTN2 | 6900 | contactin 2 | Q02246 |
| C0036341 | Schizophrenia | SRD5A2 | 6716 | steroid 5 alpha-reductase 2 | P31213 |
| C0036341 | Schizophrenia | DGKZ | 8525 | diacylglycerol kinase zeta | Q13574 |
| C0036341 | Schizophrenia | PLA2G7 | 7941 | phospholipase A2 group VII | Q13093 |
| C0036341 | Schizophrenia | DGCR2 | 9993 | DiGeorge syndrome critical region gene 2 | P98153 |
| C0036358 | Schizophreniform Disorders | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C0036363 | Schizotypal Personality Disorder | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C0432194 | Schneckenbecken dysplasia | SLC35D1 | 23169 | solute carrier family 35 member D1 | Q9NTN3 |
| C0432194 | Schneckenbecken dysplasia | INPPL1 | 3636 | inositol polyphosphate phosphatase like 1 | O15357 |
| C0036391 | Schwartz-Jampel Syndrome | CHST3 | 9469 | carbohydrate sulfotransferase 3 | Q7LGC8 |
| C0036391 | Schwartz-Jampel Syndrome | SGSH | 6448 | N-sulfoglucosamine sulfohydrolase | P51688 |
| C0036391 | Schwartz-Jampel Syndrome | AKR1B1 | 231 | aldo-keto reductase family 1 member B | P15121 |
| C0036391 | Schwartz-Jampel Syndrome | ACHE | 43 | acetylcholinesterase (Cartwright blood group) | P22303 |
| C0036391 | Schwartz-Jampel Syndrome | HSPG2 | 3339 | heparan sulfate proteoglycan 2 | P98160 |
