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
MYELODYSPLASTIC SYNDROME
glutathione peroxidase 3
MYELODYSPLASTIC SYNDROME
phospholipase A2 receptor 1
Lynch Syndrome
mannose receptor C-type 1
Lymphoma, T-Cell, Cutaneous
methylthioadenosine phosphorylase
Lymphoma, Non-Hodgkin, Familial
phosphatase and tensin homolog
Lymphoma, Follicular
activation induced cytidine deaminase
Lymphoma, Follicular
960
CD44 molecule (Indian blood group)
Lymphoma, Diffuse
ALG1 chitobiosyldiphosphodolichol beta-mannosyltransferase
Lymphoma
142
poly(ADP-ribose) polymerase 1
Lymphoma
143
poly(ADP-ribose) polymerase family member 4
Displaying entries 611 - 620 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