GDGDB is a database of glycan-related diseases and their responsible genes.
Source | 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 ▲ |
---|---|---|---|---|---|---|
CON00376 | POMT1/POMT2-CDG (cong. muscular dystrophy spectrum) | POMT1,POMT2 |
|
Congenital Disorders of Glycosylation (CDGs) | ||
CON00389 | EXT1/EXT2-CDG | EXT1,EXT2 |
|
Congenital Disorders of Glycosylation (CDGs) | ||
CON00409 | Lysyl hydroxylase 3 deficiency | PLOD3 |
|
Congenital Disorders of Glycosylation (CDGs) | O60568 | |
CON00415 | PIGM-CDG | PIGM |
|
Congenital Disorders of Glycosylation (CDGs) | Q9H3S5 | |
CON00620 | DPM3-CDG | DPM3 |
|
Congenital Disorders of Glycosylation (CDGs) | Q9P2X0 | |
CON00078 | Multiple sulfatase deficiency | SUMF1 |
|
Lysosomal Storage Diseases (LSDs) | Q8NBK3 | |
CON00005 | Aspartylglucosaminuria | AGA |
|
Lysosomal Storage Diseases (LSDs) | P20933 | |
CON00091 | Farber Lipogranulomatosis | ASAH1 |
|
Lysosomal Storage Diseases (LSDs) | Q13510 | |
CON00092 | Farber Lipogranulomatosis, type 1 | ASAH1 |
|
Lysosomal Storage Diseases (LSDs) | Q13510 | |
CON00093 | Farber Lipogranulomatosis, type 2 | ASAH1 |
|
Lysosomal Storage Diseases (LSDs) | Q13510 | |
CON00094 | Farber Lipogranulomatosis, type 3 | ASAH1 |
|
Lysosomal Storage Diseases (LSDs) | Q13510 | |
CON00095 | Farber Lipogranulomatosis, type 4 | ASAH1 |
|
Lysosomal Storage Diseases (LSDs) | Q13510 | |
CON00096 | Farber Lipogranulomatosis, type 5 | ASAH1 |
|
Lysosomal Storage Diseases (LSDs) | Q13510 | |
CON00378 | Fukuyama congenital muscular dystrophy | FKTN |
|
Congenital Disorders of Glycosylation (CDGs) | O75072 | |
CON00377 | POMGNT1-CDG (cong. muscular dystrophy spectrum) | POMGNT1 |
|
Congenital Disorders of Glycosylation (CDGs) | Q8WZA1 | |
CON00351 | ALG2-CDG | ALG2 |
|
Congenital Disorders of Glycosylation (CDGs) | Q9H553 | |
CON00397 | Neonatal osseous dysplasia I | SLC26A2 |
|
Congenital Disorders of Glycosylation (CDGs) | P50443 | |
CON00399 | SLC35D1-CDG | SLC35D1 |
|
Congenital Disorders of Glycosylation (CDGs) | Q9NTN3 | |
CON00393 | Spondyloepimetaphyseal dysplasia, pakistani type | PAPSS2 |
|
Congenital Disorders of Glycosylation (CDGs) | O95340 | |
CON00633 | Spondyloepiphyseal dysplasia with congenital joint dislocations | CHST3 |
|
Congenital Disorders of Glycosylation (CDGs) | Q7LGC8 | |
CON00632 | Temtamy preaxial brachydactyly syndrome | CHSY1 |
|
Congenital Disorders of Glycosylation (CDGs) | Q86X52 | |
CON00031 | Scheie syndrome | IDUA |
|
Lysosomal Storage Diseases (LSDs) | P35475 | |
CON00408 | Bruck syndrome 2 | PLOD2 |
|
Congenital Disorders of Glycosylation (CDGs) | O00469 | |
CON00414 | Paroxysmal nocturnal hemoglobinuria, somatic (SOMATIC MUTATION) | PIGA |
|
Congenital Disorders of Glycosylation (CDGs) | P37287 | |
CON00412 | ST3GAL5-CDG | SIAT9 |
|
Congenital Disorders of Glycosylation (CDGs) | Q9UNP4 |
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
GlyCosmos Portal v4.0.0
Last updated: August 19, 2024