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 |
|---|---|---|---|---|---|
|
Hodgkin Disease
|
opioid binding protein/cell adhesion molecule like
|
||||
|
Histiocytic sarcoma
|
phosphatase and tensin homolog
|
||||
|
Hirschsprung Disease
|
GDNF family receptor alpha 4
|
||||
|
Hereditary Nonpolyposis Colorectal Cancer
|
mannose receptor C-type 1
|
||||
|
Hereditary Multiple Exostoses
|
exostosin glycosyltransferase 1
|
||||
|
Hepatitis C
|
eukaryotic translation initiation factor 2 subunit gamma
|
||||
|
Hepatitis C
|
mannose receptor C-type 1
|
||||
|
Hepatitis C
|
prostaglandin-endoperoxide synthase 2
|
||||
|
Hepatitis B
|
SAM and HD domain containing deoxynucleoside triphosphate triphosphohydrolase 1
|
||||
|
Hepatitis B
|
killer cell lectin like receptor K1
|
Displaying entries 701 - 710 of 1194 in total
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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
