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 |
---|---|---|---|---|---|
C2973529 | Leukocytoclastic vasculitis | CYP19A1 | 1588 | cytochrome P450 family 19 subfamily A member 1 | P11511 |
C2973527 | Dentinogenesis imperfecta without osteogenesis imperfecta | AKR1C2 | 1646 | aldo-keto reductase family 1 member C2 | P52895 |
C2955673 | Urate nephropathy | PTGS2 | 5743 | prostaglandin-endoperoxide synthase 2 | P35354 |
C2939465 | Deficiency of glucose-6-phosphate dehydrogenase | ABO | 28 | ABO, alpha 1-3-N-acetylgalactosaminyltransferase and alpha 1-3-galactosyltransferase | P16442 |
C2939465 | Deficiency of glucose-6-phosphate dehydrogenase | GLA | 2717 | galactosidase alpha | P06280 |
C2939465 | Deficiency of glucose-6-phosphate dehydrogenase | MPDU1 | 9526 | mannose-P-dolichol utilization defect 1 | O75352 |
C2939465 | Deficiency of glucose-6-phosphate dehydrogenase | G6PD | 2539 | glucose-6-phosphate dehydrogenase | P11413 |
C2939465 | Deficiency of glucose-6-phosphate dehydrogenase | GPI | 2821 | glucose-6-phosphate isomerase | P06744 |
C2939465 | Deficiency of glucose-6-phosphate dehydrogenase | HK1 | 3098 | hexokinase 1 | P19367 |
C2939465 | Deficiency of glucose-6-phosphate dehydrogenase | UGT1A6 | 54578 | UDP glucuronosyltransferase family 1 member A6 | P19224 |
C2939465 | Deficiency of glucose-6-phosphate dehydrogenase | UGT1A8 | 54576 | UDP glucuronosyltransferase family 1 member A8 | Q9HAW9 |
C2939465 | Deficiency of glucose-6-phosphate dehydrogenase | UGT1A7 | 54577 | UDP glucuronosyltransferase family 1 member A7 | Q9HAW7 |
C2939465 | Deficiency of glucose-6-phosphate dehydrogenase | UGT1A10 | 54575 | UDP glucuronosyltransferase family 1 member A10 | Q9HAW8 |
C2939465 | Deficiency of glucose-6-phosphate dehydrogenase | UGT1A1 | 54658 | UDP glucuronosyltransferase family 1 member A1 | P22309 |
C2939465 | Deficiency of glucose-6-phosphate dehydrogenase | UGT1A4 | 54657 | UDP glucuronosyltransferase family 1 member A4 | P22310 |
C2939465 | Deficiency of glucose-6-phosphate dehydrogenase | HPGDS | 27306 | hematopoietic prostaglandin D synthase | O60760 |
C2939465 | Deficiency of glucose-6-phosphate dehydrogenase | ICAM1 | 3383 | intercellular adhesion molecule 1 | P05362 |
C2939465 | Deficiency of glucose-6-phosphate dehydrogenase | NDUFAB1 | 4706 | NADH:ubiquinone oxidoreductase subunit AB1 | O14561 |
C2939465 | Deficiency of glucose-6-phosphate dehydrogenase | VCAM1 | 7412 | vascular cell adhesion molecule 1 | P19320 |
C2939465 | Deficiency of glucose-6-phosphate dehydrogenase | SLC35A2 | 7355 | solute carrier family 35 member A2 | P78381 |
C2939465 | Deficiency of glucose-6-phosphate dehydrogenase | CYP4F3 | 4051 | cytochrome P450 family 4 subfamily F member 3 | Q08477 |
C2939465 | Deficiency of glucose-6-phosphate dehydrogenase | MTM1 | 4534 | myotubularin 1 | Q13496 |
C2939465 | Deficiency of glucose-6-phosphate dehydrogenase | TKT | 7086 | transketolase | P29401 |
C2939447 | Right ventricular failure | ACE | 1636 | angiotensin I converting enzyme | P12821 |
C2939447 | Right ventricular failure | SDHD | 6392 | succinate dehydrogenase complex subunit D | O14521 |
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Last updated: August 19, 2024