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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 |
|---|---|---|---|---|---|
| C0001815 | Primary Myelofibrosis | LGALS3 | 3958 | galectin 3 | P17931 |
| C0001815 | Primary Myelofibrosis | LGALS1 | 3956 | galectin 1 | P09382 |
| C0001815 | Primary Myelofibrosis | STS | 412 | steroid sulfatase | P08842 |
| C0001815 | Primary Myelofibrosis | PIK3CD | 5293 | phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta | O00329 |
| C0001815 | Primary Myelofibrosis | PRG2 | 5553 | proteoglycan 2, pro eosinophil major basic protein | P13727 |
| C0001815 | Primary Myelofibrosis | CD177 | 57126 | CD177 molecule | Q8N6Q3 |
| C0001815 | Primary Myelofibrosis | TBXAS1 | 6916 | thromboxane A synthase 1 | P24557 |
| C0001815 | Primary Myelofibrosis | CAT | 847 | catalase | P04040 |
| C0001815 | Primary Myelofibrosis | IDH2 | 3418 | isocitrate dehydrogenase (NADP(+)) 2 | P48735 |
| C0001815 | Primary Myelofibrosis | PIK3CA | 5290 | phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha | P42336 |
| C0001815 | Primary Myelofibrosis | IL18R1 | 8809 | interleukin 18 receptor 1 | Q13478 |
| C0001815 | Primary Myelofibrosis | CEACAM6 | 4680 | CEA cell adhesion molecule 6 | P40199 |
| C0001815 | Primary Myelofibrosis | PIK3CB | 5291 | phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta | P42338 |
| C0001815 | Primary Myelofibrosis | PIK3CG | 5294 | phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma | P48736 |
| C0001815 | Primary Myelofibrosis | SOAT1 | 6646 | sterol O-acyltransferase 1 | P35610 |
| C0282513 | Primary Progressive Aphasia (disorder) | GBA | 2629 | glucosylceramidase beta | P04062 |
| C0282513 | Primary Progressive Aphasia (disorder) | CHI3L1 | 1116 | chitinase 3 like 1 | P36222 |
| C0282513 | Primary Progressive Aphasia (disorder) | SMUG1 | 23583 | single-strand-selective monofunctional uracil-DNA glycosylase 1 | Q53HV7 |
| C0282513 | Primary Progressive Aphasia (disorder) | SIGLEC7 | 27036 | sialic acid binding Ig like lectin 7 | Q9Y286 |
| C0282513 | Primary Progressive Aphasia (disorder) | ACHE | 43 | acetylcholinesterase (Cartwright blood group) | P22303 |
| C0282513 | Primary Progressive Aphasia (disorder) | PRNP | 5621 | prion protein | P04156 |
| C0282513 | Primary Progressive Aphasia (disorder) | CAT | 847 | catalase | P04040 |
| C0282513 | Primary Progressive Aphasia (disorder) | ABAT | 18 | 4-aminobutyrate aminotransferase | P80404 |
| C0282513 | Primary Progressive Aphasia (disorder) | ALOX5 | 240 | arachidonate 5-lipoxygenase | P09917 |
| C0282513 | Primary Progressive Aphasia (disorder) | PRNP | 5621 | prion protein | F7VJQ1 |
