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
Displaying entries 2376 - 2400 of 62743 in total
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