Table Filtering
Submissions
GlyTouCan
Glycan Structure Repository
GlyComb
Glycoconjugate Repository
GlycoPOST
Glycomics MS raw data Repository
UniCarb-DR
Glycomics MS Repository for glycan annotations from GlycoWorkbench
All Resources
Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
Alliance of Genome Resources
Alliance of Genome Resources is a gene dataset, which contains curated genome information essential for the understanding of the genetics and genomic basis of human biology, health and disease. All data is retrieved from six major model organism databases and the Gene Ontology including FlyBase, Mouse Genome Database (MGI), Rat Genome Database (RGD), Saccharomyces Genome Database (SGD), WormBase, Zebrafish Information Network (ZFIN), and the GO Consortium. In GlyCosmos, only glycan-related disease information has been extracted from Alliance of Genome Resources.
| Source | Last Updated |
|---|---|
| Alliance of Genome Resources | July 29, 2024 |
| Disease ID | Disease Name | Alliance of Genome Resources ID | Species | Gene ID ▲ | Gene Symbol | FlyGlycoDB | Evidence Code Names | References |
|---|---|---|---|---|---|---|---|---|
| DOID:893 | Wilson disease | WB:WBGene00000213 | Caenorhabditis elegans | 176879 | asm-3 |
|
||
| DOID:0070111 | Niemann-Pick disease type A | WB:WBGene00000213 | Caenorhabditis elegans | 176879 | asm-3 |
|
||
| DOID:14504 | Niemann-Pick disease | WB:WBGene00000213 | Caenorhabditis elegans | 176879 | asm-3 |
|
||
| DOID:0070112 | Niemann-Pick disease type B | WB:WBGene00000213 | Caenorhabditis elegans | 176879 | asm-3 |
|
||
| DOID:0081326 | oxoglutarate dehydrogenase deficiency | WB:WBGene00020679 | Caenorhabditis elegans | 177235 | ogdh-1 |
|
||
| DOID:0070468 | Yoon-Bellen neurodevelopmental syndrome | WB:WBGene00020679 | Caenorhabditis elegans | 177235 | ogdh-1 |
|
||
| DOID:0110960 | Gaucher's disease perinatal lethal | WB:WBGene00021160 | Caenorhabditis elegans | 177314 | gba-4 |
|
||
| DOID:0112250 | Gaucher's disease type IIIC | WB:WBGene00021160 | Caenorhabditis elegans | 177314 | gba-4 |
|
||
| DOID:0110957 | Gaucher's disease type I | WB:WBGene00021160 | Caenorhabditis elegans | 177314 | gba-4 |
|
||
| DOID:0050474 | Netherton syndrome | WB:WBGene00021160 | Caenorhabditis elegans | 177314 | gba-4 |
|
||
| DOID:1926 | Gaucher's disease | WB:WBGene00021160 | Caenorhabditis elegans | 177314 | gba-4 |
|
||
| DOID:0080855 | Parkinsonism | WB:WBGene00021160 | Caenorhabditis elegans | 177314 | gba-4 |
|
||
| DOID:0110958 | Gaucher's disease type II | WB:WBGene00021160 | Caenorhabditis elegans | 177314 | gba-4 |
|
||
| DOID:8893 | psoriasis | WB:WBGene00021160 | Caenorhabditis elegans | 177314 | gba-4 |
|
||
| DOID:14330 | Parkinson's disease | WB:WBGene00021160 | Caenorhabditis elegans | 177314 | gba-4 |
|
||
| DOID:0110959 | Gaucher's disease type III | WB:WBGene00021160 | Caenorhabditis elegans | 177314 | gba-4 |
|
||
| DOID:0060892 | late onset Parkinson's disease | WB:WBGene00021160 | Caenorhabditis elegans | 177314 | gba-4 |
|
||
| DOID:12217 | Lewy body dementia | WB:WBGene00021160 | Caenorhabditis elegans | 177314 | gba-4 |
|
||
| DOID:2018 | hyperinsulinism | WB:WBGene00019295 | Caenorhabditis elegans | 177363 | pfkb-1.2 |
|
||
| DOID:3827 | congenital diaphragmatic hernia | WB:WBGene00002028 | Caenorhabditis elegans | 177675 | hst-1 |
|
||
| DOID:0081210 | autosomal recessive intellectual developmental disorder 46 | WB:WBGene00002028 | Caenorhabditis elegans | 177675 | hst-1 |
|
||
| DOID:1059 | intellectual disability | WB:WBGene00002028 | Caenorhabditis elegans | 177675 | hst-1 |
|
||
| DOID:12716 | newborn respiratory distress syndrome | WB:WBGene00002028 | Caenorhabditis elegans | 177675 | hst-1 |
|
||
| DOID:0060041 | autism spectrum disorder | WB:WBGene00002028 | Caenorhabditis elegans | 177675 | hst-1 |
|
||
| DOID:11198 | DiGeorge syndrome | WB:WBGene00002028 | Caenorhabditis elegans | 177675 | hst-1 |
|
