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 |
---|---|---|---|---|---|---|
Alpha-mannosidosis, type II (later-onset)
|
MAN2B1
|
Lysosomal Storage Diseases (LSDs)
|
||||
Sialidosis type II, congenital form
|
NEU1
|
Lysosomal Storage Diseases (LSDs)
|
||||
Sialidosis type II, infantile form
|
NEU1
|
Lysosomal Storage Diseases (LSDs)
|
||||
Sialidosis type II, juvenile form
|
NEU1
|
Lysosomal Storage Diseases (LSDs)
|
||||
Maroteaux-Lamy syndrome, severe form
|
ARSB
|
Lysosomal Storage Diseases (LSDs)
|
||||
Maroteaux-Lamy syndrome, mild form
|
ARSB
|
Lysosomal Storage Diseases (LSDs)
|
||||
Maroteaux-Lamy syndrome, intermediate form
|
ARSB
|
Lysosomal Storage Diseases (LSDs)
|
||||
Sandhoff disease, infantile form
|
HEXB
|
Lysosomal Storage Diseases (LSDs)
|
||||
Sandhoff disease, juvenile form
|
HEXB
|
Lysosomal Storage Diseases (LSDs)
|
||||
Sandhoff disease, adult form
|
HEXB
|
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