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:0060284 | paroxysmal nocturnal hemoglobinuria | HGNC:1331 | Homo sapiens (human) | 727 | C5 |
|
||
| DOID:1227 | neutropenia | HGNC:1331 | Homo sapiens (human) | 727 | C5 |
|
||
| DOID:4724 | brain edema | HGNC:1331 | Homo sapiens (human) | 727 | C5 |
|
||
| DOID:552 | pneumonia | HGNC:1331 | Homo sapiens (human) | 727 | C5 |
|
||
| DOID:12134 | factor VIII deficiency | HGNC:1331 | Homo sapiens (human) | 727 | C5 |
|
||
| DOID:1485 | cystic fibrosis | HGNC:1331 | Homo sapiens (human) | 727 | C5 |
|
||
| DOID:5082 | liver cirrhosis | HGNC:1331 | Homo sapiens (human) | 727 | C5 |
|
||
| DOID:3525 | middle cerebral artery infarction | MGI:1919959 | Mus musculus (house mouse) | 72709 | C1qtnf6 |
|
||
| DOID:3312 | bipolar disorder | HGNC:12401 | Homo sapiens (human) | 7272 | TTK |
|
||
| DOID:684 | hepatocellular carcinoma | HGNC:12401 | Homo sapiens (human) | 7272 | TTK |
|
||
| DOID:0080575 | Larsen-like syndrome B3GAT3 type | MGI:1919977 | Mus musculus (house mouse) | 72727 | B3gat3 |
|
||
| DOID:0110430 | dilated cardiomyopathy 1G | HGNC:12403 | Homo sapiens (human) | 7273 | TTN |
|
||
| DOID:3393 | coronary artery disease | HGNC:12403 | Homo sapiens (human) | 7273 | TTN |
|
||
| DOID:5844 | myocardial infarction | HGNC:12403 | Homo sapiens (human) | 7273 | TTN |
|
||
| DOID:0111078 | tibial muscular dystrophy | HGNC:12403 | Homo sapiens (human) | 7273 | TTN |
|
||
| DOID:0060224 | atrial fibrillation | HGNC:12403 | Homo sapiens (human) | 7273 | TTN |
|
||
| DOID:0111188 | myofibrillar myopathy 9 | HGNC:12403 | Homo sapiens (human) | 7273 | TTN |
|
||
| DOID:0081341 | congenital myopathy 5 | HGNC:12403 | Homo sapiens (human) | 7273 | TTN |
|
||
| DOID:12930 | dilated cardiomyopathy | HGNC:12403 | Homo sapiens (human) | 7273 | TTN |
|
||
| DOID:0110315 | hypertrophic cardiomyopathy 9 | HGNC:12403 | Homo sapiens (human) | 7273 | TTN |
|
||
| DOID:0110283 | autosomal recessive limb-girdle muscular dystrophy type 2J | HGNC:12403 | Homo sapiens (human) | 7273 | TTN |
|
||
| DOID:9970 | obesity | HGNC:12406 | Homo sapiens (human) | 7275 | TUB |
|
||
| DOID:0050933 | ovarian serous carcinoma | MGI:1920004 | Mus musculus (house mouse) | 72754 | Arhgef10l |
|
||
| DOID:6212 | ovarian endometrial cancer | MGI:1920004 | Mus musculus (house mouse) | 72754 | Arhgef10l |
|
||
| DOID:2316 | brain ischemia | HGNC:12405 | Homo sapiens (human) | 7276 | TTR |
|
