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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 |
|---|---|---|---|---|---|
| C0024419 | Waldenstrom Macroglobulinemia | COLEC10 | 10584 | collectin subfamily member 10 | Q9Y6Z7 |
| C0024419 | Waldenstrom Macroglobulinemia | CLEC12A | 160364 | C-type lectin domain family 12 member A | Q5QGZ9 |
| C0024419 | Waldenstrom Macroglobulinemia | ACSBG1 | 23205 | acyl-CoA synthetase bubblegum family member 1 | Q96GR2 |
| C0024419 | Waldenstrom Macroglobulinemia | ANXA5 | 308 | annexin A5 | P08758 |
| C0024419 | Waldenstrom Macroglobulinemia | HMMR | 3161 | hyaluronan mediated motility receptor | O75330 |
| C0024419 | Waldenstrom Macroglobulinemia | LPL | 4023 | lipoprotein lipase | P06858 |
| C0024419 | Waldenstrom Macroglobulinemia | NCAM1 | 4684 | neural cell adhesion molecule 1 | P13591 |
| C0024419 | Waldenstrom Macroglobulinemia | PIK3CD | 5293 | phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta | O00329 |
| C0024419 | Waldenstrom Macroglobulinemia | PLCG2 | 5336 | phospholipase C gamma 2 | P16885 |
| C0024419 | Waldenstrom Macroglobulinemia | CD22 | 933 | CD22 molecule | P20273 |
| C0024419 | Waldenstrom Macroglobulinemia | NAMPT | 10135 | nicotinamide phosphoribosyltransferase | P43490 |
| C0024419 | Waldenstrom Macroglobulinemia | PIK3CA | 5290 | phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha | P42336 |
| C0024419 | Waldenstrom Macroglobulinemia | PIK3CB | 5291 | phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta | P42338 |
| C0024419 | Waldenstrom Macroglobulinemia | PIK3CG | 5294 | phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma | P48736 |
| C0024419 | Waldenstrom Macroglobulinemia | SOAT1 | 6646 | sterol O-acyltransferase 1 | P35610 |
| C0265221 | Walker-Warburg congenital muscular dystrophy | POMT1 | 10585 | protein O-mannosyltransferase 1 | Q9Y6A1 |
| C0265221 | Walker-Warburg congenital muscular dystrophy | B3GALNT2 | 148789 | beta-1,3-N-acetylgalactosaminyltransferase 2 | Q8NCR0 |
| C0265221 | Walker-Warburg congenital muscular dystrophy | B4GAT1 | 11041 | beta-1,4-glucuronyltransferase 1 | O43505 |
| C0265221 | Walker-Warburg congenital muscular dystrophy | B3GNT2 | 10678 | UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 2 | Q9NY97 |
| C0265221 | Walker-Warburg congenital muscular dystrophy | FKTN | 2218 | fukutin | O75072 |
| C0265221 | Walker-Warburg congenital muscular dystrophy | POMT2 | 29954 | protein O-mannosyltransferase 2 | Q9UKY4 |
| C0265221 | Walker-Warburg congenital muscular dystrophy | POMGNT1 | 55624 | protein O-linked mannose N-acetylglucosaminyltransferase 1 (beta 1,2-) | Q8WZA1 |
| C0265221 | Walker-Warburg congenital muscular dystrophy | ALG1 | 56052 | ALG1 chitobiosyldiphosphodolichol beta-mannosyltransferase | Q9BT22 |
| C0265221 | Walker-Warburg congenital muscular dystrophy | FKRP | 79147 | fukutin related protein | Q9H9S5 |
| C0265221 | Walker-Warburg congenital muscular dystrophy | POMGNT2 | 84892 | protein O-linked mannose N-acetylglucosaminyltransferase 2 (beta 1,4-) | Q8NAT1 |
