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 |
---|---|---|---|---|---|
C0023895 | Liver diseases | CYP2C9 | 1559 | cytochrome P450 family 2 subfamily C member 9 | P11712 |
C0023895 | Liver diseases | CYP2E1 | 1571 | cytochrome P450 family 2 subfamily E member 1 | P05181 |
C0023895 | Liver diseases | CYP7A1 | 1581 | cytochrome P450 family 7 subfamily A member 1 | P22680 |
C0023895 | Liver diseases | CYP3A4 | 1576 | cytochrome P450 family 3 subfamily A member 4 | P08684 |
C0023895 | Liver diseases | CYP51A1 | 1595 | cytochrome P450 family 51 subfamily A member 1 | Q16850 |
C0023895 | Liver diseases | EHHADH | 1962 | enoyl-CoA hydratase and 3-hydroxyacyl CoA dehydrogenase | Q08426 |
C0023895 | Liver diseases | ALDH1B1 | 219 | aldehyde dehydrogenase 1 family member B1 | P30837 |
C0023895 | Liver diseases | AMACR | 23600 | alpha-methylacyl-CoA racemase | Q9UHK6 |
C0023895 | Liver diseases | HADHA | 3030 | hydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit alpha | P40939 |
C0023895 | Liver diseases | HADH | 3033 | hydroxyacyl-CoA dehydrogenase | Q16836 |
C0023895 | Liver diseases | ACACA | 31 | acetyl-CoA carboxylase alpha | Q13085 |
C0023895 | Liver diseases | HMGCS2 | 3158 | 3-hydroxy-3-methylglutaryl-CoA synthase 2 | P54868 |
C0023895 | Liver diseases | ACADVL | 37 | acyl-CoA dehydrogenase very long chain | P49748 |
C0023895 | Liver diseases | CYP4F3 | 4051 | cytochrome P450 family 4 subfamily F member 3 | Q08477 |
C0023895 | Liver diseases | OLR1 | 4973 | oxidized low density lipoprotein receptor 1 | P78380 |
C0023895 | Liver diseases | ENPP2 | 5168 | ectonucleotide pyrophosphatase/phosphodiesterase 2 | Q13822 |
C0023895 | Liver diseases | PIK3CB | 5291 | phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta | P42338 |
C0023895 | Liver diseases | PIK3CG | 5294 | phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma | P48736 |
C0023895 | Liver diseases | ATP6AP1 | 537 | ATPase H+ transporting accessory protein 1 | Q15904 |
C0023895 | Liver diseases | PLA2G5 | 5322 | phospholipase A2 group V | P39877 |
C0023895 | Liver diseases | PRKAA2 | 5563 | protein kinase AMP-activated catalytic subunit alpha 2 | P54646 |
C0023895 | Liver diseases | MASP1 | 5648 | mannan binding lectin serine peptidase 1 | P48740 |
C0023895 | Liver diseases | PTEN | 5728 | phosphatase and tensin homolog | P60484 |
C0023895 | Liver diseases | PTGS2 | 5743 | prostaglandin-endoperoxide synthase 2 | P35354 |
C0023895 | Liver diseases | GOLPH3 | 64083 | golgi phosphoprotein 3 | Q9H4A6 |
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