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 |
|---|---|---|---|---|---|
|
Essential Hypertension
|
methylenetetrahydrofolate dehydrogenase, cyclohydrolase and formyltetrahydrofolate synthetase 1
|
||||
|
Essential Hypertension
|
serine hydroxymethyltransferase 1
|
||||
|
Exophthalmos
|
intercellular adhesion molecule 1
|
||||
|
FANCONI ANEMIA, COMPLEMENTATION GROUP A (disorder)
|
insulin receptor
|
||||
|
Fanconi Anemia
|
insulin receptor
|
||||
|
Fetal Growth Retardation
|
hydroxysteroid 11-beta dehydrogenase 2
|
||||
|
Fibroid Tumor
|
fumarate hydratase
|
||||
|
Fibroid Tumor
|
cytochrome P450 family 19 subfamily A member 1
|
||||
|
Fibrosarcoma
|
steroid sulfatase
|
||||
|
Follicular adenoma
|
phosphatase and tensin homolog
|
Displaying entries 411 - 420 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
