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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 |
|---|---|---|---|---|---|
| C1096184 | West Nile viral infection | GBA3 | 57733 | glucosylceramidase beta 3 (gene/pseudogene) | Q9H227 |
| C1096184 | West Nile viral infection | CD14 | 929 | CD14 molecule | P08571 |
| C1096184 | West Nile viral infection | CD48 | 962 | CD48 molecule | P09326 |
| C1096184 | West Nile viral infection | PIK3CA | 5290 | phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha | P42336 |
| C1096184 | West Nile viral infection | GAD2 | 2572 | glutamate decarboxylase 2 | Q05329 |
| C1096184 | West Nile viral infection | PIK3CB | 5291 | phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta | P42338 |
| C1096184 | West Nile viral infection | PIK3CG | 5294 | phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma | P48736 |
| C1096184 | West Nile viral infection | PLA2G1B | 5319 | phospholipase A2 group IB | P04054 |
| C1096902 | Infantile Sialic Acid Storage Disease | GNE | 10020 | glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase | Q9Y223 |
| C1096902 | Infantile Sialic Acid Storage Disease | SLC17A5 | 26503 | solute carrier family 17 member 5 | Q9NRA2 |
| C1096903 | Sialic Acid Storage Disease, Finnish Type (disorder) | GNE | 10020 | glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase | Q9Y223 |
| C1096903 | Sialic Acid Storage Disease, Finnish Type (disorder) | CHIT1 | 1118 | chitinase 1 | Q13231 |
| C1096903 | Sialic Acid Storage Disease, Finnish Type (disorder) | CEACAM5 | 1048 | CEA cell adhesion molecule 5 | P06731 |
| C1096903 | Sialic Acid Storage Disease, Finnish Type (disorder) | SLC17A5 | 26503 | solute carrier family 17 member 5 | Q9NRA2 |
| C1096903 | Sialic Acid Storage Disease, Finnish Type (disorder) | HPGDS | 27306 | hematopoietic prostaglandin D synthase | O60760 |
| C1096903 | Sialic Acid Storage Disease, Finnish Type (disorder) | PIK3CD | 5293 | phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta | O00329 |
| C1096903 | Sialic Acid Storage Disease, Finnish Type (disorder) | PIK3CA | 5290 | phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha | P42336 |
| C1096903 | Sialic Acid Storage Disease, Finnish Type (disorder) | RENBP | 5973 | renin binding protein | P51606 |
| C1096903 | Sialic Acid Storage Disease, Finnish Type (disorder) | PIK3CB | 5291 | phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta | P42338 |
| C1096903 | Sialic Acid Storage Disease, Finnish Type (disorder) | PIK3CG | 5294 | phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma | P48736 |
| C1112155 | Hereditary non-polyposis colorectal cancer syndrome | MRC1 | 4360 | mannose receptor C-type 1 | P22897 |
| C1112155 | Hereditary non-polyposis colorectal cancer syndrome | PIK3CA | 5290 | phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha | P42336 |
| C1112474 | Small cell carcinoma of esophagus | PARP1 | 142 | poly(ADP-ribose) polymerase 1 | P09874 |
| C1112474 | Small cell carcinoma of esophagus | PTEN | 5728 | phosphatase and tensin homolog | P60484 |
| C1134719 | Invasive Ductal Breast Carcinoma | FUT3 | 2525 | fucosyltransferase 3 (Lewis blood group) | P21217 |
