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 |
|---|---|---|---|---|---|
|
Lipodystrophy
|
stearoyl-CoA desaturase
|
||||
|
Leishmaniasis
|
sphingosine kinase 1
|
||||
|
Glioma
|
sphingosine kinase 1
|
||||
|
Hypotonia-Cystinuria Syndrome
|
solute carrier family 3 member 1
|
||||
|
Periodontal Diseases
|
solute carrier family 2 member 4
|
||||
|
Central neuroblastoma
|
solute carrier family 2 member 3
|
||||
|
Neuroblastoma
|
solute carrier family 2 member 3
|
||||
|
Arthritis, Psoriatic
|
sirtuin 6
|
||||
|
Neurodegenerative Disorders
|
sirtuin 2
|
||||
|
Malignant neoplasm of prostate
|
serine protease 8
|
Displaying entries 91 - 100 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
