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 |
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DisGeNET | July 29, 2024 |
Disease ID ▲ | Disease Name | Gene Symbol | Gene ID | Gene Name | UniProt ID |
---|---|---|---|---|---|
C0003811 | Cardiac Arrhythmia | CYP19A1 | 1588 | cytochrome P450 family 19 subfamily A member 1 | P11511 |
C0003811 | Cardiac Arrhythmia | EPHX2 | 2053 | epoxide hydrolase 2 | P34913 |
C0003811 | Cardiac Arrhythmia | HADHA | 3030 | hydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit alpha | P40939 |
C0003811 | Cardiac Arrhythmia | HADHB | 3032 | hydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit beta | P55084 |
C0003811 | Cardiac Arrhythmia | ITPKB | 3707 | inositol-trisphosphate 3-kinase B | P27987 |
C0003811 | Cardiac Arrhythmia | PCYT1A | 5130 | phosphate cytidylyltransferase 1, choline, alpha | P49585 |
C0003811 | Cardiac Arrhythmia | PIK3CB | 5291 | phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta | P42338 |
C0003811 | Cardiac Arrhythmia | PIK3CG | 5294 | phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma | P48736 |
C0003811 | Cardiac Arrhythmia | PRKAA2 | 5563 | protein kinase AMP-activated catalytic subunit alpha 2 | P54646 |
C0003811 | Cardiac Arrhythmia | PTGS2 | 5743 | prostaglandin-endoperoxide synthase 2 | P35354 |
C0003811 | Cardiac Arrhythmia | SQLE | 6713 | squalene epoxidase | Q14534 |
C0003811 | Cardiac Arrhythmia | CACNA2D1 | 781 | calcium voltage-gated channel auxiliary subunit alpha2delta 1 | P54289 |
C0003838 | Arterial Occlusive Diseases | IGF2R | 3482 | insulin like growth factor 2 receptor | P11717 |
C0003838 | Arterial Occlusive Diseases | ICAM1 | 3383 | intercellular adhesion molecule 1 | P05362 |
C0003838 | Arterial Occlusive Diseases | STS | 412 | steroid sulfatase | P08842 |
C0003838 | Arterial Occlusive Diseases | SELL | 6402 | selectin L | P14151 |
C0003838 | Arterial Occlusive Diseases | EFNA5 | 1946 | ephrin A5 | P52803 |
C0003850 | Arteriosclerosis | SLC35A1 | 10559 | solute carrier family 35 member A1 | P78382 |
C0003850 | Arteriosclerosis | FUT3 | 2525 | fucosyltransferase 3 (Lewis blood group) | P21217 |
C0003850 | Arteriosclerosis | ABO | 28 | ABO, alpha 1-3-N-acetylgalactosaminyltransferase and alpha 1-3-galactosyltransferase | P16442 |
C0003850 | Arteriosclerosis | FUT8 | 2530 | fucosyltransferase 8 | Q9BYC5 |
C0003850 | Arteriosclerosis | FUT7 | 2529 | fucosyltransferase 7 | Q11130 |
C0003850 | Arteriosclerosis | HAS3 | 3038 | hyaluronan synthase 3 | O00219 |
C0003850 | Arteriosclerosis | HAS2 | 3037 | hyaluronan synthase 2 | Q92819 |
C0003850 | Arteriosclerosis | ST6GAL1 | 6480 | ST6 beta-galactoside alpha-2,6-sialyltransferase 1 | P15907 |
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Last updated: August 19, 2024