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 |
---|---|---|---|---|---|---|
Sialidosis type II, infantile form
|
NEU1
|
Lysosomal Storage Diseases (LSDs)
|
||||
Sialidosis type II, juvenile form
|
NEU1
|
Lysosomal Storage Diseases (LSDs)
|
||||
Spondyloepimetaphyseal dysplasia, pakistani type
|
PAPSS2
|
|
Congenital Disorders of Glycosylation (CDGs)
|
|||
Spondyloepiphyseal dysplasia with congenital joint dislocations
|
CHST3
|
|
Congenital Disorders of Glycosylation (CDGs)
|
|||
TMEM165-CDG
|
TMEM165
|
|
Congenital Disorders of Glycosylation (CDGs)
|
|||
TUSC3-CDG
|
TUSC3
|
|
Congenital Disorders of Glycosylation (CDGs)
|
|||
Tay-Sachs disease
|
HEXA
|
|
Lysosomal Storage Diseases (LSDs)
|
|||
Tay-Sachs disease, infantile form
|
HEXA
|
|
Lysosomal Storage Diseases (LSDs)
|
|||
Tay-Sachs disease, late-onset forms
|
HEXA
|
|
Lysosomal Storage Diseases (LSDs)
|
|||
Temtamy preaxial brachydactyly syndrome
|
CHSY1
|
|
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