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 |
---|---|---|---|---|---|
C0034494 | Rabies (disorder) | HPSE | 10855 | heparanase | Q9Y251 |
C0034494 | Rabies (disorder) | ENOSF1 | 55556 | enolase superfamily member 1 | Q7L5Y1 |
C0034494 | Rabies (disorder) | CYP1A2 | 1544 | cytochrome P450 family 1 subfamily A member 2 | P05177 |
C0034494 | Rabies (disorder) | PIP5K1C | 23396 | phosphatidylinositol-4-phosphate 5-kinase type 1 gamma | O60331 |
C0034494 | Rabies (disorder) | PIK3CD | 5293 | phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta | O00329 |
C0034494 | Rabies (disorder) | CH25H | 9023 | cholesterol 25-hydroxylase | O95992 |
C0034494 | Rabies (disorder) | PIK3CA | 5290 | phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha | P42336 |
C0034494 | Rabies (disorder) | CYP2C9 | 1559 | cytochrome P450 family 2 subfamily C member 9 | P11712 |
C0034494 | Rabies (disorder) | CYP3A4 | 1576 | cytochrome P450 family 3 subfamily A member 4 | P08684 |
C0034494 | Rabies (disorder) | GAS1 | 2619 | growth arrest specific 1 | P54826 |
C0034494 | Rabies (disorder) | MTM1 | 4534 | myotubularin 1 | Q13496 |
C0034494 | Rabies (disorder) | PIK3CB | 5291 | phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta | P42338 |
C0034494 | Rabies (disorder) | PIK3CG | 5294 | phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma | P48736 |
C0034494 | Rabies (disorder) | SOAT1 | 6646 | sterol O-acyltransferase 1 | P35610 |
C0266508 | Rachischisis | CHKA | 1119 | choline kinase alpha | P35790 |
C0266508 | Rachischisis | PCYT1A | 5130 | phosphate cytidylyltransferase 1, choline, alpha | P49585 |
C1306600 | Radial nerve palsy | PRNP | 5621 | prion protein | P04156 |
C1306600 | Radial nerve palsy | PRNP | 5621 | prion protein | F7VJQ1 |
C0700594 | Radiculopathy | APRT | 353 | adenine phosphoribosyltransferase | P07741 |
C0158761 | Radioulnar Synostosis | B4GALT7 | 11285 | beta-1,4-galactosyltransferase 7 | Q9UBV7 |
C0158761 | Radioulnar Synostosis | B3GAT3 | 26229 | beta-1,3-glucuronyltransferase 3 | O94766 |
C0158761 | Radioulnar Synostosis | XYLT1 | 64131 | xylosyltransferase 1 | Q86Y38 |
C0158761 | Radioulnar Synostosis | CHST3 | 9469 | carbohydrate sulfotransferase 3 | Q7LGC8 |
C0158761 | Radioulnar Synostosis | SMC3 | 9126 | structural maintenance of chromosomes 3 | Q9UQE7 |
C0158761 | Radioulnar Synostosis | COLEC10 | 10584 | collectin subfamily member 10 | Q9Y6Z7 |
GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.
Supported by JST NBDC Grant Number JPMJND2204
Partly supported by NIH Common Fund Grant #1U01GM125267-01
GlyCosmos Portal v4.0.0
Last updated: August 19, 2024