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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 |
|---|---|---|---|---|---|
| C0007121 | Bronchogenic Carcinoma | HPGDS | 27306 | hematopoietic prostaglandin D synthase | O60760 |
| C0007121 | Bronchogenic Carcinoma | GPX1 | 2876 | glutathione peroxidase 1 | P07203 |
| C1857941 | Brooke-Spiegler syndrome | XYLT1 | 64131 | xylosyltransferase 1 | Q86Y38 |
| C1857941 | Brooke-Spiegler syndrome | PNPLA6 | 10908 | patatin like phospholipase domain containing 6 | Q8IY17 |
| C0302362 | Brucella melitensis infection | APRT | 353 | adenine phosphoribosyltransferase | P07741 |
| C0302362 | Brucella melitensis infection | OXSM | 54995 | 3-oxoacyl-ACP synthase, mitochondrial | Q9NWU1 |
| C0302362 | Brucella melitensis infection | CD14 | 929 | CD14 molecule | P08571 |
| C0302362 | Brucella melitensis infection | MICA | 100507436 | MHC class I polypeptide-related sequence A | Q29983 |
| C0006309 | Brucellosis | GLA | 2717 | galactosidase alpha | P06280 |
| C0006309 | Brucellosis | SELE | 6401 | selectin E | P16581 |
| C0006309 | Brucellosis | SELL | 6402 | selectin L | P14151 |
| C0006309 | Brucellosis | CD14 | 929 | CD14 molecule | P08571 |
| C0006309 | Brucellosis | MDH2 | 4191 | malate dehydrogenase 2 | P40926 |
| C0006309 | Brucellosis | MICA | 100507436 | MHC class I polypeptide-related sequence A | Q29983 |
| C0006309 | Brucellosis | IL18R1 | 8809 | interleukin 18 receptor 1 | Q13478 |
| C0006309 | Brucellosis | SOAT1 | 6646 | sterol O-acyltransferase 1 | P35610 |
| C1142166 | Brugada Syndrome (disorder) | IDS | 3423 | iduronate 2-sulfatase | P22304 |
| C1142166 | Brugada Syndrome (disorder) | GPD1L | 23171 | glycerol-3-phosphate dehydrogenase 1 like | Q8N335 |
| C1142166 | Brugada Syndrome (disorder) | APRT | 353 | adenine phosphoribosyltransferase | P07741 |
| C1142166 | Brugada Syndrome (disorder) | SCD | 6319 | stearoyl-CoA desaturase | O00767 |
| C1142166 | Brugada Syndrome (disorder) | CACNA2D1 | 781 | calcium voltage-gated channel auxiliary subunit alpha2delta 1 | P54289 |
| C4551804 | Brugada Syndrome 1 | GPD1L | 23171 | glycerol-3-phosphate dehydrogenase 1 like | Q8N335 |
| C4551804 | Brugada Syndrome 1 | CACNA2D1 | 781 | calcium voltage-gated channel auxiliary subunit alpha2delta 1 | P54289 |
| C2673193 | Brugada Syndrome 2 | GPD1L | 23171 | glycerol-3-phosphate dehydrogenase 1 like | Q8N335 |
| C0006325 | Bruxism | PGAP3 | 93210 | post-GPI attachment to proteins phospholipase 3 | Q96FM1 |
