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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 |
|---|---|---|---|---|---|
| C2675481 | COLORECTAL CANCER, SUSCEPTIBILITY TO, 10 | ELOVL5 | 60481 | ELOVL fatty acid elongase 5 | Q9NYP7 |
| C2675481 | COLORECTAL CANCER, SUSCEPTIBILITY TO, 10 | FADS2 | 9415 | fatty acid desaturase 2 | O95864 |
| C2675481 | COLORECTAL CANCER, SUSCEPTIBILITY TO, 10 | CLEC3A | 10143 | C-type lectin domain family 3 member A | O75596 |
| C1837315 | COLORECTAL CANCER, SUSCEPTIBILITY TO, 1 | PIGU | 128869 | phosphatidylinositol glycan anchor biosynthesis class U | Q9H490 |
| C1837315 | COLORECTAL CANCER, SUSCEPTIBILITY TO, 1 | GALNT12 | 79695 | polypeptide N-acetylgalactosaminyltransferase 12 | Q8IXK2 |
| C1837315 | COLORECTAL CANCER, SUSCEPTIBILITY TO, 1 | TMTC1 | 83857 | transmembrane O-mannosyltransferase targeting cadherins 1 | Q8IUR5 |
| C1837315 | COLORECTAL CANCER, SUSCEPTIBILITY TO, 1 | CYP17A1 | 1586 | cytochrome P450 family 17 subfamily A member 1 | P05093 |
| C1837315 | COLORECTAL CANCER, SUSCEPTIBILITY TO, 1 | ELOVL5 | 60481 | ELOVL fatty acid elongase 5 | Q9NYP7 |
| C1837315 | COLORECTAL CANCER, SUSCEPTIBILITY TO, 1 | FADS2 | 9415 | fatty acid desaturase 2 | O95864 |
| C1837315 | COLORECTAL CANCER, SUSCEPTIBILITY TO, 1 | CLEC3A | 10143 | C-type lectin domain family 3 member A | O75596 |
| C3150876 | COG5 congenital disorder of glycosylation | COG5 | 10466 | component of oligomeric golgi complex 5 | Q9UP83 |
| C0007682 | CNS disorder | MGAT1 | 4245 | alpha-1,3-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyltransferase | P26572 |
| C0007682 | CNS disorder | GLB1 | 2720 | galactosidase beta 1 | P16278 |
| C0007682 | CNS disorder | IDS | 3423 | iduronate 2-sulfatase | P22304 |
| C0007682 | CNS disorder | IDUA | 3425 | alpha-L-iduronidase | P35475 |
| C0007682 | CNS disorder | ARSB | 411 | arylsulfatase B | P15848 |
| C0007682 | CNS disorder | SGSH | 6448 | N-sulfoglucosamine sulfohydrolase | P51688 |
| C0007682 | CNS disorder | PARP1 | 142 | poly(ADP-ribose) polymerase 1 | P09874 |
| C0007682 | CNS disorder | CD38 | 952 | CD38 molecule | P28907 |
| C0007682 | CNS disorder | CHAT | 1103 | choline O-acetyltransferase | P28329 |
| C0007682 | CNS disorder | MGLL | 11343 | monoglyceride lipase | Q99685 |
| C0007682 | CNS disorder | CYP1A2 | 1544 | cytochrome P450 family 1 subfamily A member 2 | P05177 |
| C0007682 | CNS disorder | ACE | 1636 | angiotensin I converting enzyme | P12821 |
| C0007682 | CNS disorder | ICAM1 | 3383 | intercellular adhesion molecule 1 | P05362 |
| C0007682 | CNS disorder | MBL2 | 4153 | mannose binding lectin 2 | P11226 |
