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 |
---|---|---|---|---|---|
C0004763 | Barrett Esophagus | KLRC1 | 3821 | killer cell lectin like receptor C1 | P26715 |
C0004763 | Barrett Esophagus | PTGS1 | 5742 | prostaglandin-endoperoxide synthase 1 | P23219 |
C0004763 | Barrett Esophagus | SI | 6476 | sucrase-isomaltase | P14410 |
C0004763 | Barrett Esophagus | VCAM1 | 7412 | vascular cell adhesion molecule 1 | P19320 |
C0004763 | Barrett Esophagus | CAT | 847 | catalase | P04040 |
C0004763 | Barrett Esophagus | PTGES | 9536 | prostaglandin E synthase | O14684 |
C0004763 | Barrett Esophagus | CD44 | 960 | CD44 molecule (Indian blood group) | P16070 |
C0004763 | Barrett Esophagus | AKR1C2 | 1646 | aldo-keto reductase family 1 member C2 | P52895 |
C0004763 | Barrett Esophagus | DAD1 | 1603 | defender against cell death 1 | P61803 |
C0004763 | Barrett Esophagus | MTAP | 4507 | methylthioadenosine phosphorylase | Q13126 |
C0004763 | Barrett Esophagus | PIK3CA | 5290 | phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha | P42336 |
C0004763 | Barrett Esophagus | CDH13 | 1012 | cadherin 13 | P55290 |
C0004763 | Barrett Esophagus | MICA | 100507436 | MHC class I polypeptide-related sequence A | Q29983 |
C0004763 | Barrett Esophagus | FASN | 2194 | fatty acid synthase | P49327 |
C0004763 | Barrett Esophagus | AMACR | 23600 | alpha-methylacyl-CoA racemase | Q9UHK6 |
C0004763 | Barrett Esophagus | GPX3 | 2878 | glutathione peroxidase 3 | P22352 |
C0004763 | Barrett Esophagus | GPX2 | 2877 | glutathione peroxidase 2 | P18283 |
C0004763 | Barrett Esophagus | CEACAM6 | 4680 | CEA cell adhesion molecule 6 | P40199 |
C0004763 | Barrett Esophagus | PIK3CB | 5291 | phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta | P42338 |
C0004763 | Barrett Esophagus | PTGS2 | 5743 | prostaglandin-endoperoxide synthase 2 | P35354 |
C0004763 | Barrett Esophagus | GOLPH3 | 64083 | golgi phosphoprotein 3 | Q9H4A6 |
C0004763 | Barrett Esophagus | SOAT1 | 6646 | sterol O-acyltransferase 1 | P35610 |
C0004775 | Bartter Disease | CYP17A1 | 1586 | cytochrome P450 family 17 subfamily A member 1 | P05093 |
C0004775 | Bartter Disease | CYP11B1 | 1584 | cytochrome P450 family 11 subfamily B member 1 | P15538 |
C0004775 | Bartter Disease | HSD11B2 | 3291 | hydroxysteroid 11-beta dehydrogenase 2 | P80365 |
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