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Glycan Structure Repository
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Glycoconjugate Repository
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Glycomics MS raw data Repository
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Glycomics MS Repository for glycan annotations from GlycoWorkbench
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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:13099 | Moyamoya disease | HGNC:144 | Homo sapiens (human) | 71 | ACTG1 |
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| DOID:0060224 | atrial fibrillation | HGNC:14388 | Homo sapiens (human) | 51206 | GP6 |
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| DOID:0111057 | platelet-type bleeding disorder 11 | HGNC:14388 | Homo sapiens (human) | 51206 | GP6 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:14388 | Homo sapiens (human) | 51206 | GP6 |
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| DOID:2218 | blood platelet disease | HGNC:14388 | Homo sapiens (human) | 51206 | GP6 |
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| DOID:6000 | congestive heart failure | HGNC:14388 | Homo sapiens (human) | 51206 | GP6 |
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| DOID:11847 | coronary thrombosis | HGNC:14388 | Homo sapiens (human) | 51206 | GP6 |
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| DOID:11247 | disseminated intravascular coagulation | HGNC:14388 | Homo sapiens (human) | 51206 | GP6 |
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| DOID:5844 | myocardial infarction | HGNC:14388 | Homo sapiens (human) | 51206 | GP6 |
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| DOID:3393 | coronary artery disease | HGNC:14388 | Homo sapiens (human) | 51206 | GP6 |
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| DOID:9408 | acute myocardial infarction | HGNC:14388 | Homo sapiens (human) | 51206 | GP6 |
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| DOID:0080953 | amelogenesis imperfecta type 1J | HGNC:14376 | Homo sapiens (human) | 93650 | ACP4 |
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| DOID:2316 | brain ischemia | HGNC:14375 | Homo sapiens (human) | 23645 | PPP1R15A |
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| DOID:224 | transient cerebral ischemia | HGNC:14375 | Homo sapiens (human) | 23645 | PPP1R15A |
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| DOID:10241 | thalassemia | HGNC:14375 | Homo sapiens (human) | 23645 | PPP1R15A |
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| DOID:2436 | glomangioma | HGNC:14373 | Homo sapiens (human) | 11146 | GLMN |
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| DOID:11294 | arteriovenous malformation | HGNC:14373 | Homo sapiens (human) | 11146 | GLMN |
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| DOID:2431 | glomus tumor | HGNC:14373 | Homo sapiens (human) | 11146 | GLMN |
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| DOID:0111155 | autosomal recessive spinocerebellar ataxia 21 | HGNC:14372 | Homo sapiens (human) | 57410 | SCYL1 |
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| DOID:0050951 | hereditary ataxia | HGNC:14372 | Homo sapiens (human) | 57410 | SCYL1 |
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| DOID:326 | ischemia | HGNC:1437 | Homo sapiens (human) | 796 | CALCA |
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| DOID:11400 | pyelonephritis | HGNC:1437 | Homo sapiens (human) | 796 | CALCA |
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| DOID:11476 | osteoporosis | HGNC:1437 | Homo sapiens (human) | 796 | CALCA |
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| DOID:0080998 | acute necrotizing pancreatitis | HGNC:1437 | Homo sapiens (human) | 796 | CALCA |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:1437 | Homo sapiens (human) | 796 | CALCA |
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