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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 |
|---|---|---|---|---|---|
| C1851584 | Childhood Ependymoma | CD44 | 960 | CD44 molecule (Indian blood group) | P16070 |
| C1851584 | Childhood Ependymoma | PIK3CA | 5290 | phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha | P42336 |
| C1851584 | Childhood Ependymoma | L1CAM | 3897 | L1 cell adhesion molecule | P32004 |
| C1851584 | Childhood Ependymoma | PIK3CB | 5291 | phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta | P42338 |
| C1851584 | Childhood Ependymoma | PIK3CG | 5294 | phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma | P48736 |
| C1851584 | Childhood Ependymoma | PTEN | 5728 | phosphatase and tensin homolog | P60484 |
| C1851585 | MYELOPROLIFERATIVE DISORDER, CHRONIC, WITH EOSINOPHILIA | B3GAT1 | 27087 | beta-1,3-glucuronyltransferase 1 | Q9P2W7 |
| C1851585 | MYELOPROLIFERATIVE DISORDER, CHRONIC, WITH EOSINOPHILIA | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C1851585 | MYELOPROLIFERATIVE DISORDER, CHRONIC, WITH EOSINOPHILIA | ENO2 | 2026 | enolase 2 | P09104 |
| C1851585 | MYELOPROLIFERATIVE DISORDER, CHRONIC, WITH EOSINOPHILIA | SMUG1 | 23583 | single-strand-selective monofunctional uracil-DNA glycosylase 1 | Q53HV7 |
| C1851585 | MYELOPROLIFERATIVE DISORDER, CHRONIC, WITH EOSINOPHILIA | PKM | 5315 | pyruvate kinase M1/2 | P14618 |
| C1851585 | MYELOPROLIFERATIVE DISORDER, CHRONIC, WITH EOSINOPHILIA | CEACAM5 | 1048 | CEA cell adhesion molecule 5 | P06731 |
| C1851585 | MYELOPROLIFERATIVE DISORDER, CHRONIC, WITH EOSINOPHILIA | DCN | 1634 | decorin | P07585 |
| C1851585 | MYELOPROLIFERATIVE DISORDER, CHRONIC, WITH EOSINOPHILIA | FCGR3B | 2215 | Fc fragment of IgG receptor IIIb | O75015 |
| C1851585 | MYELOPROLIFERATIVE DISORDER, CHRONIC, WITH EOSINOPHILIA | ALPP | 250 | alkaline phosphatase, placental | P05187 |
| C1851585 | MYELOPROLIFERATIVE DISORDER, CHRONIC, WITH EOSINOPHILIA | ATRNL1 | 26033 | attractin like 1 | Q5VV63 |
| C1851585 | MYELOPROLIFERATIVE DISORDER, CHRONIC, WITH EOSINOPHILIA | ANXA5 | 308 | annexin A5 | P08758 |
| C1851585 | MYELOPROLIFERATIVE DISORDER, CHRONIC, WITH EOSINOPHILIA | ICAM1 | 3383 | intercellular adhesion molecule 1 | P05362 |
| C1851585 | MYELOPROLIFERATIVE DISORDER, CHRONIC, WITH EOSINOPHILIA | LTA4H | 4048 | leukotriene A4 hydrolase | P09960 |
| C1851585 | MYELOPROLIFERATIVE DISORDER, CHRONIC, WITH EOSINOPHILIA | NCAM1 | 4684 | neural cell adhesion molecule 1 | P13591 |
| C1851585 | MYELOPROLIFERATIVE DISORDER, CHRONIC, WITH EOSINOPHILIA | SCD | 6319 | stearoyl-CoA desaturase | O00767 |
| C1851585 | MYELOPROLIFERATIVE DISORDER, CHRONIC, WITH EOSINOPHILIA | VTCN1 | 79679 | V-set domain containing T cell activation inhibitor 1 | Q7Z7D3 |
| C1851585 | MYELOPROLIFERATIVE DISORDER, CHRONIC, WITH EOSINOPHILIA | CEACAM7 | 1087 | CEA cell adhesion molecule 7 | Q14002 |
| C1851585 | MYELOPROLIFERATIVE DISORDER, CHRONIC, WITH EOSINOPHILIA | TKT | 7086 | transketolase | P29401 |
| C1851710 | LATERAL MENINGOCELE SYNDROME | COMT | 1312 | catechol-O-methyltransferase | P21964 |
