DisGeNET

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
Displaying entries 3626 - 3650 of 62743 in total
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

About Release Notes Help Feedback

International Collaboration

GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


Logo License Policies Site Map

Contact: support@glycosmos.org

This work is licensed under Creative Commons Attribution 4.0 International


GlyCosmos Portal v4.0.0

Last updated: August 19, 2024