GDGDB is a database of glycan-related diseases and their responsible genes.
Database | Last Updated |
---|---|
Glyco-Disease Genes Database (GDGDB) | January 25, 2017 |
Concept UI | Disease Name | Gene Symbol | Disease Name Aliases | Disease Type | UniProt ID ▲ | Disease IDs |
---|---|---|---|---|---|---|
Gaucher disease, type I
|
GBA
|
|
Lysosomal Storage Diseases (LSDs)
|
|||
Gaucher disease, type II
|
GBA
|
Lysosomal Storage Diseases (LSDs)
|
||||
Gaucher disease, type II, neuronopathic form, classic type
|
GBA
|
Lysosomal Storage Diseases (LSDs)
|
||||
Gaucher disease, type II, perinatal lethal form
|
GBA
|
Lysosomal Storage Diseases (LSDs)
|
||||
Gaucher disease, type III
|
GBA
|
|
Lysosomal Storage Diseases (LSDs)
|
|||
Gaucher disease, type IIIC
|
GBA
|
|
Lysosomal Storage Diseases (LSDs)
|
|||
Fucosidosis
|
FUCA1
|
Lysosomal Storage Diseases (LSDs)
|
||||
Fabry disease
|
GLA
|
|
Lysosomal Storage Diseases (LSDs)
|
|||
Tay-Sachs disease
|
HEXA
|
|
Lysosomal Storage Diseases (LSDs)
|
|||
Tay-Sachs disease, infantile form
|
HEXA
|
|
Lysosomal Storage Diseases (LSDs)
|
GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.
Supported by JST NBDC Grant Number JPMJND2204
Partly supported by NIH Common Fund Grant #1U01GM125267-01