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 |
---|---|---|---|---|---|
C0524620 | Metabolic Syndrome X | DAG1 | 1605 | dystroglycan 1 | Q14118 |
C0524620 | Metabolic Syndrome X | GCK | 2645 | glucokinase | P35557 |
C0524620 | Metabolic Syndrome X | HSPG2 | 3339 | heparan sulfate proteoglycan 2 | P98160 |
C0524620 | Metabolic Syndrome X | PCK1 | 5105 | phosphoenolpyruvate carboxykinase 1 | P35558 |
C0524620 | Metabolic Syndrome X | ACOX1 | 51 | acyl-CoA oxidase 1 | Q15067 |
C0524620 | Metabolic Syndrome X | PCK2 | 5106 | phosphoenolpyruvate carboxykinase 2, mitochondrial | Q16822 |
C0524620 | Metabolic Syndrome X | PIK3CA | 5290 | phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha | P42336 |
C0524620 | Metabolic Syndrome X | PLA2G4A | 5321 | phospholipase A2 group IVA | P47712 |
C0524620 | Metabolic Syndrome X | RENBP | 5973 | renin binding protein | P51606 |
C0524620 | Metabolic Syndrome X | AKR1C3 | 8644 | aldo-keto reductase family 1 member C3 | P42330 |
C0524620 | Metabolic Syndrome X | CDH13 | 1012 | cadherin 13 | P55290 |
C0524620 | Metabolic Syndrome X | ACSM1 | 116285 | acyl-CoA synthetase medium chain family member 1 | Q08AH1 |
C0524620 | Metabolic Syndrome X | SLC27A5 | 10998 | solute carrier family 27 member 5 | Q9Y2P5 |
C0524620 | Metabolic Syndrome X | CYP2C19 | 1557 | cytochrome P450 family 2 subfamily C member 19 | P33261 |
C0524620 | Metabolic Syndrome X | CYP3A4 | 1576 | cytochrome P450 family 3 subfamily A member 4 | P08684 |
C0524620 | Metabolic Syndrome X | CYP11B2 | 1585 | cytochrome P450 family 11 subfamily B member 2 | P19099 |
C0524620 | Metabolic Syndrome X | CYP19A1 | 1588 | cytochrome P450 family 19 subfamily A member 1 | P11511 |
C0524620 | Metabolic Syndrome X | CYP24A1 | 1591 | cytochrome P450 family 24 subfamily A member 1 | Q07973 |
C0524620 | Metabolic Syndrome X | CYP21A2 | 1589 | cytochrome P450 family 21 subfamily A member 2 | P08686 |
C0524620 | Metabolic Syndrome X | EPHX2 | 2053 | epoxide hydrolase 2 | P34913 |
C0524620 | Metabolic Syndrome X | ACSL1 | 2180 | acyl-CoA synthetase long chain family member 1 | P33121 |
C0524620 | Metabolic Syndrome X | CLEC16A | 23274 | C-type lectin domain containing 16A | Q2KHT3 |
C0524620 | Metabolic Syndrome X | LPIN1 | 23175 | lipin 1 | Q14693 |
C0524620 | Metabolic Syndrome X | ALOX5 | 240 | arachidonate 5-lipoxygenase | P09917 |
C0524620 | Metabolic Syndrome X | NAAA | 27163 | N-acylethanolamine acid amidase | Q02083 |
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