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.

Database Last Updated
DisGeNET February 14, 2024
Disease ID ▼ Disease Name Gene Symbol Gene ID Gene Name UniProt ID
Glomerulosclerosis (disorder)
RAP1B, member of RAS oncogene family
Prion Diseases
prion protein
Prion Diseases
prion protein
Migraine with Aura
insulin receptor
Congenital heart disease
histone deacetylase 3
Esophageal carcinoma
phosphatase and tensin homolog
Esophageal carcinoma
fragile histidine triad diadenosine triphosphatase
Esophageal carcinoma
phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha
Esophageal carcinoma
phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma
Esophageal carcinoma
phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta
Displaying entries 531 - 540 of 1194 in total

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