GDGDB is a database of glycan-related diseases and their responsible genes.
Database | Last Updated |
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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, congenital form
|
NEU1
|
Lysosomal Storage Diseases (LSDs)
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Sialidosis type II, infantile form
|
NEU1
|
Lysosomal Storage Diseases (LSDs)
|
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Sialidosis type II, juvenile form
|
NEU1
|
Lysosomal Storage Diseases (LSDs)
|
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COG8-CDG
|
COG8
|
|
Congenital Disorders of Glycosylation (CDGs)
|
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Tn polyagglutination syndrome, somatic (SOMATIC MUTATION)
|
C1GALT1C1
|
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Congenital Disorders of Glycosylation (CDGs)
|
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RFT1-CDG
|
RFT1
|
|
Congenital Disorders of Glycosylation (CDGs)
|
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SLC35C1-CDG
|
SLC35C1
|
|
Congenital Disorders of Glycosylation (CDGs)
|
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ALG3-CDG
|
ALG3
|
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Congenital Disorders of Glycosylation (CDGs)
|
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POMGNT1-CDG (cong. muscular dystrophy spectrum)
|
POMGNT1
|
|
Congenital Disorders of Glycosylation (CDGs)
|
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COG1-CDG
|
COG1
|
|
Congenital Disorders of Glycosylation (CDGs)
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Supported by JST NBDC Grant Number JPMJND2204
Partly supported by NIH Common Fund Grant #1U01GM125267-01