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 |
---|---|---|---|---|---|---|
Combined saposin deficiency
|
PSAP
|
|
Lysosomal Storage Diseases (LSDs)
|
|||
Wolman disease
|
LIPA
|
|
Lysosomal Storage Diseases (LSDs)
|
|||
Pompe disease
|
GAA
|
|
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
|
PMM2
|
|
Congenital Disorders of Glycosylation (CDGs)
|
|||
MPI-CDG
|
MPI
|
|
Congenital Disorders of Glycosylation (CDGs)
|
|||
ALG6-CDG
|
ALG6
|
|
Congenital Disorders of Glycosylation (CDGs)
|
|||
ALG3-CDG
|
ALG3
|
|
Congenital Disorders of Glycosylation (CDGs)
|
|||
DPM1-CDG
|
DPM1
|
|
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