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 |
---|---|---|---|---|---|
C0002895 | Anemia, Sickle Cell | SELL | 6402 | selectin L | P14151 |
C0002895 | Anemia, Sickle Cell | SELP | 6403 | selectin P | P16109 |
C0002895 | Anemia, Sickle Cell | SFTPD | 6441 | surfactant protein D | P35247 |
C0002895 | Anemia, Sickle Cell | VCAM1 | 7412 | vascular cell adhesion molecule 1 | P19320 |
C0002895 | Anemia, Sickle Cell | SCD5 | 79966 | stearoyl-CoA desaturase 5 | Q86SK9 |
C0002895 | Anemia, Sickle Cell | LPCAT1 | 79888 | lysophosphatidylcholine acyltransferase 1 | Q8NF37 |
C0002895 | Anemia, Sickle Cell | PLA2G6 | 8398 | phospholipase A2 group VI | O60733 |
C0002895 | Anemia, Sickle Cell | CAT | 847 | catalase | P04040 |
C0002895 | Anemia, Sickle Cell | CD14 | 929 | CD14 molecule | P08571 |
C0002895 | Anemia, Sickle Cell | LIPG | 9388 | lipase G, endothelial type | Q9Y5X9 |
C0002895 | Anemia, Sickle Cell | SLC35A2 | 7355 | solute carrier family 35 member A2 | P78381 |
C0002895 | Anemia, Sickle Cell | PLA2G4A | 5321 | phospholipase A2 group IVA | P47712 |
C0002895 | Anemia, Sickle Cell | TALDO1 | 6888 | transaldolase 1 | P37837 |
C0002895 | Anemia, Sickle Cell | CYP2C19 | 1557 | cytochrome P450 family 2 subfamily C member 19 | P33261 |
C0002895 | Anemia, Sickle Cell | ALOX5 | 240 | arachidonate 5-lipoxygenase | P09917 |
C0002895 | Anemia, Sickle Cell | KLRC3 | 3823 | killer cell lectin like receptor C3 | Q07444 |
C0002895 | Anemia, Sickle Cell | OLR1 | 4973 | oxidized low density lipoprotein receptor 1 | P78380 |
C0002895 | Anemia, Sickle Cell | OXCT1 | 5019 | 3-oxoacid CoA-transferase 1 | P55809 |
C0002895 | Anemia, Sickle Cell | PLA2G1B | 5319 | phospholipase A2 group IB | P04054 |
C0002895 | Anemia, Sickle Cell | PRNP | 5621 | prion protein | F7VJQ1 |
C0002896 | Sideroblastic anemia | CYP2E1 | 1571 | cytochrome P450 family 2 subfamily E member 1 | P05181 |
C0002902 | Anencephaly | B4GAT1 | 11041 | beta-1,4-glucuronyltransferase 1 | O43505 |
C0002902 | Anencephaly | ABO | 28 | ABO, alpha 1-3-N-acetylgalactosaminyltransferase and alpha 1-3-galactosyltransferase | P16442 |
C0002902 | Anencephaly | COMT | 1312 | catechol-O-methyltransferase | P21964 |
C0002902 | Anencephaly | EFNA5 | 1946 | ephrin A5 | P52803 |
GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.
Supported by JST NBDC Grant Number JPMJND2204
Partly supported by NIH Common Fund Grant #1U01GM125267-01
GlyCosmos Portal v4.0.0
Last updated: August 19, 2024