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 |
|---|---|---|---|---|---|
|
ANOPHTHALMIA AND PULMONARY HYPOPLASIA
|
L1 cell adhesion molecule
|
||||
|
ANOPHTHALMIA AND PULMONARY HYPOPLASIA
|
pyruvate kinase M1/2
|
||||
|
Hypotonia-Cystinuria Syndrome
|
solute carrier family 3 member 1
|
||||
|
Dopa-Responsive Dystonia
|
GTP cyclohydrolase 1
|
||||
|
Childhood Ataxia with Central Nervous System Hypomyelinization
|
eukaryotic translation initiation factor 2 subunit gamma
|
||||
|
Venous Thromboembolism
|
actin beta
|
||||
|
TARSAL-CARPAL COALITION SYNDROME
|
ABO, alpha 1-3-N-acetylgalactosaminyltransferase and alpha 1-3-galactosyltransferase
|
||||
|
TARSAL-CARPAL COALITION SYNDROME
|
cadherin 13
|
||||
|
Coronary Artery Disease
|
polypeptide N-acetylgalactosaminyltransferase 2
|
||||
|
Coronary Artery Disease
|
phospholipase A2 group VII
|
Displaying entries 1111 - 1120 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
