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 ▲ |
|---|---|---|---|---|---|
|
Status Epilepticus
|
dynamin 1 like
|
||||
|
Optic Atrophy 1
|
dynamin 1 like
|
||||
|
Sepsis
|
dynamin 1 like
|
||||
|
Alzheimer's Disease
|
dynamin 1 like
|
||||
|
Pancreatic carcinoma
|
dynamin 1 like
|
||||
|
Ischemic stroke
|
dynamin 1 like
|
||||
|
Lipodystrophy
|
stearoyl-CoA desaturase
|
||||
|
Aortic valve disorder
|
phospholipid phosphatase 3
|
||||
|
Chondrosarcoma
|
heparan sulfate-glucosamine 3-sulfotransferase 1
|
||||
|
Malignant mesothelioma
|
TNF receptor superfamily member 10c
|
Displaying entries 31 - 40 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
