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 |
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C0007820 | Cerebrovascular Disorders | KL | 9365 | klotho | Q9UEF7 |
C0007820 | Cerebrovascular Disorders | CYP46A1 | 10858 | cytochrome P450 family 46 subfamily A member 1 | Q9Y6A2 |
C0007820 | Cerebrovascular Disorders | ACOT7 | 11332 | acyl-CoA thioesterase 7 | O00154 |
C0007820 | Cerebrovascular Disorders | DCN | 1634 | decorin | P07585 |
C0007820 | Cerebrovascular Disorders | ACE | 1636 | angiotensin I converting enzyme | P12821 |
C0007820 | Cerebrovascular Disorders | HPGDS | 27306 | hematopoietic prostaglandin D synthase | O60760 |
C0007820 | Cerebrovascular Disorders | ICAM1 | 3383 | intercellular adhesion molecule 1 | P05362 |
C0007820 | Cerebrovascular Disorders | LGALS3 | 3958 | galectin 3 | P17931 |
C0007820 | Cerebrovascular Disorders | LIPC | 3990 | lipase C, hepatic type | P11150 |
C0007820 | Cerebrovascular Disorders | LPL | 4023 | lipoprotein lipase | P06858 |
C0007820 | Cerebrovascular Disorders | VCAM1 | 7412 | vascular cell adhesion molecule 1 | P19320 |
C0007820 | Cerebrovascular Disorders | CD14 | 929 | CD14 molecule | P08571 |
C0007820 | Cerebrovascular Disorders | CYP2C19 | 1557 | cytochrome P450 family 2 subfamily C member 19 | P33261 |
C0007820 | Cerebrovascular Disorders | CYP2C9 | 1559 | cytochrome P450 family 2 subfamily C member 9 | P11712 |
C0007820 | Cerebrovascular Disorders | CYP4A11 | 1579 | cytochrome P450 family 4 subfamily A member 11 | Q02928 |
C0007820 | Cerebrovascular Disorders | LTC4S | 4056 | leukotriene C4 synthase | Q16873 |
C0007820 | Cerebrovascular Disorders | OLR1 | 4973 | oxidized low density lipoprotein receptor 1 | P78380 |
C0007820 | Cerebrovascular Disorders | PTGS2 | 5743 | prostaglandin-endoperoxide synthase 2 | P35354 |
C0007820 | Cerebrovascular Disorders | PLA2G7 | 7941 | phospholipase A2 group VII | Q13093 |
C0007820 | Cerebrovascular Disorders | CYP4F2 | 8529 | cytochrome P450 family 4 subfamily F member 2 | P78329 |
C0007789 | Cerebral Palsy | ST3GAL5 | 8869 | ST3 beta-galactoside alpha-2,3-sialyltransferase 5 | Q9UNP4 |
C0007789 | Cerebral Palsy | IDUA | 3425 | alpha-L-iduronidase | P35475 |
C0007789 | Cerebral Palsy | ARSA | 410 | arylsulfatase A | P15289 |
C0007789 | Cerebral Palsy | PMM2 | 5373 | phosphomannomutase 2 | O15305 |
C0007789 | Cerebral Palsy | HPRT1 | 3251 | hypoxanthine phosphoribosyltransferase 1 | P00492 |
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Last updated: August 19, 2024