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 |
---|---|---|---|---|---|---|
Niemann-Pick disease, type C2
|
NPC2
|
Lysosomal Storage Diseases (LSDs)
|
||||
Farber Lipogranulomatosis, type 1
|
ASAH1
|
Lysosomal Storage Diseases (LSDs)
|
||||
Farber Lipogranulomatosis, type 2
|
ASAH1
|
Lysosomal Storage Diseases (LSDs)
|
||||
Farber Lipogranulomatosis, type 3
|
ASAH1
|
Lysosomal Storage Diseases (LSDs)
|
||||
Farber Lipogranulomatosis, type 4
|
ASAH1
|
Lysosomal Storage Diseases (LSDs)
|
||||
Farber Lipogranulomatosis, type 5
|
ASAH1
|
Lysosomal Storage Diseases (LSDs)
|
||||
Pompe disease, infantile-onset form
|
GAA
|
Lysosomal Storage Diseases (LSDs)
|
||||
Pompe disease, late-onset form
|
GAA
|
Lysosomal Storage Diseases (LSDs)
|
||||
PMM2-CDG, infantile multisystem stage
|
PMM2
|
Congenital Disorders of Glycosylation (CDGs)
|
||||
PMM2-CDG, late-infantile and childhood ataxia-intellectual disability stage
|
PMM2
|
Congenital Disorders of Glycosylation (CDGs)
|
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