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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
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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:14004 | thoracic aortic aneurysm | HGNC:144 | Homo sapiens (human) | 71 | ACTG1 |
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| DOID:13099 | Moyamoya disease | HGNC:144 | Homo sapiens (human) | 71 | ACTG1 |
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| DOID:898 | autosomal dominant polycystic kidney disease | HGNC:1228 | Homo sapiens (human) | 710 | SERPING1 |
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| DOID:0080939 | hereditary angioedema type I | HGNC:1228 | Homo sapiens (human) | 710 | SERPING1 |
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| DOID:4989 | pancreatitis | HGNC:1228 | Homo sapiens (human) | 710 | SERPING1 |
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| DOID:14115 | toxic shock syndrome | HGNC:1228 | Homo sapiens (human) | 710 | SERPING1 |
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| DOID:0080600 | COVID-19 | HGNC:1228 | Homo sapiens (human) | 710 | SERPING1 |
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| DOID:14735 | hereditary angioedema | HGNC:1228 | Homo sapiens (human) | 710 | SERPING1 |
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| DOID:0080998 | acute necrotizing pancreatitis | HGNC:1228 | Homo sapiens (human) | 710 | SERPING1 |
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| DOID:3526 | cerebral infarction | HGNC:1228 | Homo sapiens (human) | 710 | SERPING1 |
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| DOID:1558 | angioedema | HGNC:1228 | Homo sapiens (human) | 710 | SERPING1 |
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| DOID:3068 | glioblastoma | HGNC:1228 | Homo sapiens (human) | 710 | SERPING1 |
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| DOID:4448 | macular degeneration | HGNC:1228 | Homo sapiens (human) | 710 | SERPING1 |
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| DOID:9408 | acute myocardial infarction | HGNC:1228 | Homo sapiens (human) | 710 | SERPING1 |
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| DOID:3265 | chronic granulomatous disease | HGNC:11851 | Homo sapiens (human) | 7100 | TLR5 |
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| DOID:8677 | perinatal necrotizing enterocolitis | HGNC:11851 | Homo sapiens (human) | 7100 | TLR5 |
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| DOID:612 | primary immunodeficiency disease | HGNC:11851 | Homo sapiens (human) | 7100 | TLR5 |
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| DOID:4194 | glucose metabolism disease | HGNC:11851 | Homo sapiens (human) | 7100 | TLR5 |
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| DOID:7147 | ankylosing spondylitis | HGNC:11851 | Homo sapiens (human) | 7100 | TLR5 |
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| DOID:1679 | cystitis | HGNC:11851 | Homo sapiens (human) | 7100 | TLR5 |
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| DOID:1485 | cystic fibrosis | HGNC:11851 | Homo sapiens (human) | 7100 | TLR5 |
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| DOID:5052 | melioidosis | HGNC:11851 | Homo sapiens (human) | 7100 | TLR5 |
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| DOID:9074 | systemic lupus erythematosus | HGNC:11851 | Homo sapiens (human) | 7100 | TLR5 |
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| DOID:854 | collagen disease | HGNC:11851 | Homo sapiens (human) | 7100 | TLR5 |
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| DOID:10457 | Legionnaires' disease | HGNC:11851 | Homo sapiens (human) | 7100 | TLR5 |
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