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 |
---|---|---|---|---|---|
C0742343 | Acute Chest Syndrome | CD14 | 929 | CD14 molecule | P08571 |
C0742343 | Acute Chest Syndrome | LIPG | 9388 | lipase G, endothelial type | Q9Y5X9 |
C0742343 | Acute Chest Syndrome | CD44 | 960 | CD44 molecule (Indian blood group) | P16070 |
C0742343 | Acute Chest Syndrome | GCK | 2645 | glucokinase | P35557 |
C0742343 | Acute Chest Syndrome | PLA2G4A | 5321 | phospholipase A2 group IVA | P47712 |
C0742343 | Acute Chest Syndrome | CYP2C19 | 1557 | cytochrome P450 family 2 subfamily C member 19 | P33261 |
C0742343 | Acute Chest Syndrome | CYP3A4 | 1576 | cytochrome P450 family 3 subfamily A member 4 | P08684 |
C0742343 | Acute Chest Syndrome | EPHX2 | 2053 | epoxide hydrolase 2 | P34913 |
C0742343 | Acute Chest Syndrome | FASN | 2194 | fatty acid synthase | P49327 |
C0742343 | Acute Chest Syndrome | ALOX5 | 240 | arachidonate 5-lipoxygenase | P09917 |
C0742343 | Acute Chest Syndrome | ACSL6 | 23305 | acyl-CoA synthetase long chain family member 6 | Q9UKU0 |
C0742343 | Acute Chest Syndrome | ACACA | 31 | acetyl-CoA carboxylase alpha | Q13085 |
C0742343 | Acute Chest Syndrome | L1CAM | 3897 | L1 cell adhesion molecule | P32004 |
C0742343 | Acute Chest Syndrome | OLR1 | 4973 | oxidized low density lipoprotein receptor 1 | P78380 |
C0742343 | Acute Chest Syndrome | PCYT1A | 5130 | phosphate cytidylyltransferase 1, choline, alpha | P49585 |
C0742343 | Acute Chest Syndrome | PLCB4 | 5332 | phospholipase C beta 4 | Q15147 |
C0742343 | Acute Chest Syndrome | PTGS2 | 5743 | prostaglandin-endoperoxide synthase 2 | P35354 |
C0742343 | Acute Chest Syndrome | PLA2G7 | 7941 | phospholipase A2 group VII | Q13093 |
C0740858 | Substance abuse problem | XYLT1 | 64131 | xylosyltransferase 1 | Q86Y38 |
C0740858 | Substance abuse problem | COMT | 1312 | catechol-O-methyltransferase | P21964 |
C0740858 | Substance abuse problem | PARP9 | 83666 | poly(ADP-ribose) polymerase family member 9 | Q8IXQ6 |
C0740858 | Substance abuse problem | CERS6 | 253782 | ceramide synthase 6 | Q6ZMG9 |
C0740858 | Substance abuse problem | MAG | 4099 | myelin associated glycoprotein | P20916 |
C0740858 | Substance abuse problem | GBA3 | 57733 | glucosylceramidase beta 3 (gene/pseudogene) | Q9H227 |
C0740858 | Substance abuse problem | COLEC12 | 81035 | collectin subfamily member 12 | Q5KU26 |
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