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
LM-GlycoRepo
Repository for lectin-assisted multimodality data
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 | October 9, 2024 |
| Disease ID | Disease Name | Alliance of Genome Resources ID ▲ | Species | Gene ID | Gene Symbol | FlyGlycoDB | Evidence Code Names | References |
|---|---|---|---|---|---|---|---|---|
| DOID:0080555 | congenital disorder of glycosylation Ic | WB:WBGene00007435 | Caenorhabditis elegans | 182392 | algn-6 |
|
||
| DOID:7998 | hyperthyroidism | WB:WBGene00007455 | Caenorhabditis elegans | 178330 | ugt-22 |
|
||
| DOID:9352 | type 2 diabetes mellitus | WB:WBGene00007455 | Caenorhabditis elegans | 178330 | ugt-22 |
|
||
| DOID:9744 | type 1 diabetes mellitus | WB:WBGene00007455 | Caenorhabditis elegans | 178330 | ugt-22 |
|
||
| DOID:3803 | Crigler-Najjar syndrome | WB:WBGene00007455 | Caenorhabditis elegans | 178330 | ugt-22 |
|
||
| DOID:2741 | bilirubin metabolic disorder | WB:WBGene00007455 | Caenorhabditis elegans | 178330 | ugt-22 |
|
||
| DOID:0050570 | congenital disorder of glycosylation type I | WB:WBGene00007464 | Caenorhabditis elegans | 174542 | algn-8 |
|
||
| DOID:0080560 | congenital disorder of glycosylation Ih | WB:WBGene00007464 | Caenorhabditis elegans | 174542 | algn-8 |
|
||
| DOID:0111576 | dehydrated hereditary stomatocytosis 1 | WB:WBGene00007505 | Caenorhabditis elegans | 182492 | pezo-1 |
|
||
| DOID:0050580 | hereditary lymphedema | WB:WBGene00007505 | Caenorhabditis elegans | 182492 | pezo-1 |
|
||
| DOID:0111607 | distal arthrogryposis type 3 | WB:WBGene00007505 | Caenorhabditis elegans | 182492 | pezo-1 |
|
||
| DOID:0111608 | distal arthrogryposis type 5 | WB:WBGene00007505 | Caenorhabditis elegans | 182492 | pezo-1 |
|
||
| DOID:8725 | vascular dementia | WB:WBGene00007516 | Caenorhabditis elegans | 181178 | gpx-5 |
|
||
| DOID:2870 | endometrial adenocarcinoma | WB:WBGene00007516 | Caenorhabditis elegans | 181178 | gpx-5 |
|
||
| DOID:0050083 | Keshan disease | WB:WBGene00007516 | Caenorhabditis elegans | 181178 | gpx-5 |
|
||
| DOID:9261 | nasopharynx carcinoma | WB:WBGene00007516 | Caenorhabditis elegans | 181178 | gpx-5 |
|
||
| DOID:285 | hairy cell leukemia | WB:WBGene00007516 | Caenorhabditis elegans | 181178 | gpx-5 |
|
||
| DOID:12858 | Huntington's disease | WB:WBGene00007516 | Caenorhabditis elegans | 181178 | gpx-5 |
|
||
| DOID:1936 | atherosclerosis | WB:WBGene00007516 | Caenorhabditis elegans | 181178 | gpx-5 |
|
||
| DOID:9256 | colorectal cancer | WB:WBGene00007516 | Caenorhabditis elegans | 181178 | gpx-5 |
|
||
| DOID:11713 | diabetic angiopathy | WB:WBGene00007516 | Caenorhabditis elegans | 181178 | gpx-5 |
|
||
| DOID:10763 | hypertension | WB:WBGene00007516 | Caenorhabditis elegans | 181178 | gpx-5 |
|
||
| DOID:0050731 | vitamin B12 deficiency | WB:WBGene00007516 | Caenorhabditis elegans | 181178 | gpx-5 |
|
||
| DOID:7998 | hyperthyroidism | WB:WBGene00007516 | Caenorhabditis elegans | 181178 | gpx-5 |
|
||
| DOID:0080199 | colorectal carcinoma | WB:WBGene00007516 | Caenorhabditis elegans | 181178 | gpx-5 |
|
