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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 |
|---|---|---|---|---|---|
| C0004238 | Atrial Fibrillation | SLC35F1 | 222553 | solute carrier family 35 member F1 | Q5T1Q4 |
| C0004238 | Atrial Fibrillation | AMACR | 23600 | alpha-methylacyl-CoA racemase | Q9UHK6 |
| C0004238 | Atrial Fibrillation | HSD11B2 | 3291 | hydroxysteroid 11-beta dehydrogenase 2 | P80365 |
| C0004238 | Atrial Fibrillation | ITPK1 | 3705 | inositol-tetrakisphosphate 1-kinase | Q13572 |
| C0004238 | Atrial Fibrillation | OLR1 | 4973 | oxidized low density lipoprotein receptor 1 | P78380 |
| C0004238 | Atrial Fibrillation | PCYT1A | 5130 | phosphate cytidylyltransferase 1, choline, alpha | P49585 |
| C0004238 | Atrial Fibrillation | PIK3CB | 5291 | phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta | P42338 |
| C0004238 | Atrial Fibrillation | PIK3CG | 5294 | phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma | P48736 |
| C0004238 | Atrial Fibrillation | PKD2 | 5311 | polycystin 2, transient receptor potential cation channel | Q13563 |
| C0004238 | Atrial Fibrillation | PTGS2 | 5743 | prostaglandin-endoperoxide synthase 2 | P35354 |
| C0004238 | Atrial Fibrillation | SOAT1 | 6646 | sterol O-acyltransferase 1 | P35610 |
| C0004238 | Atrial Fibrillation | CNTN2 | 6900 | contactin 2 | Q02246 |
| C0004238 | Atrial Fibrillation | CACNA2D1 | 781 | calcium voltage-gated channel auxiliary subunit alpha2delta 1 | P54289 |
| C0004238 | Atrial Fibrillation | PLA2G7 | 7941 | phospholipase A2 group VII | Q13093 |
| C0004238 | Atrial Fibrillation | CYP4F2 | 8529 | cytochrome P450 family 4 subfamily F member 2 | P78329 |
| C0796206 | Atkin syndrome | IL1RAPL1 | 11141 | interleukin 1 receptor accessory protein like 1 | Q9NZN1 |
| C0796206 | Atkin syndrome | EPM2A | 7957 | EPM2A glucan phosphatase, laforin | O95278 |
| C0155733 | Atherosclerosis of aorta | CHGA | 1113 | chromogranin A | P10645 |
| C0155733 | Atherosclerosis of aorta | ACE | 1636 | angiotensin I converting enzyme | P12821 |
| C0155733 | Atherosclerosis of aorta | LCAT | 3931 | lecithin-cholesterol acyltransferase | P04180 |
| C0155733 | Atherosclerosis of aorta | LPL | 4023 | lipoprotein lipase | P06858 |
| C0155733 | Atherosclerosis of aorta | LIPG | 9388 | lipase G, endothelial type | Q9Y5X9 |
| C0155733 | Atherosclerosis of aorta | PTGS2 | 5743 | prostaglandin-endoperoxide synthase 2 | P35354 |
| C0004153 | Atherosclerosis | SLC35A1 | 10559 | solute carrier family 35 member A1 | P78382 |
| C0004153 | Atherosclerosis | FUT3 | 2525 | fucosyltransferase 3 (Lewis blood group) | P21217 |
