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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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MIRAGE
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:0080941 | acquired angioedema | HGNC:3530 | Homo sapiens (human) | 2161 | F12 |
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| DOID:224 | transient cerebral ischemia | HGNC:3530 | Homo sapiens (human) | 2161 | F12 |
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| DOID:3525 | middle cerebral artery infarction | HGNC:3530 | Homo sapiens (human) | 2161 | F12 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:3530 | Homo sapiens (human) | 2161 | F12 |
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| DOID:9279 | hyperhomocysteinemia | HGNC:3530 | Homo sapiens (human) | 2161 | F12 |
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| DOID:2231 | factor XII deficiency | HGNC:3530 | Homo sapiens (human) | 2161 | F12 |
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| DOID:0080940 | hereditary angioedema type III | HGNC:3530 | Homo sapiens (human) | 2161 | F12 |
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| DOID:5844 | myocardial infarction | HGNC:3530 | Homo sapiens (human) | 2161 | F12 |
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| DOID:3490 | Noonan syndrome | HGNC:3529 | Homo sapiens (human) | 2160 | F11 |
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| DOID:0060903 | thrombosis | HGNC:3529 | Homo sapiens (human) | 2160 | F11 |
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| DOID:2229 | factor XI deficiency | HGNC:3529 | Homo sapiens (human) | 2160 | F11 |
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| DOID:2222 | factor X deficiency | HGNC:3528 | Homo sapiens (human) | 2159 | F10 |
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| DOID:1612 | breast cancer | HGNC:3528 | Homo sapiens (human) | 2159 | F10 |
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| DOID:9279 | hyperhomocysteinemia | HGNC:3528 | Homo sapiens (human) | 2159 | F10 |
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| DOID:0111899 | X-linked thrombophilia due to factor IX defect | HGNC:3551 | Homo sapiens (human) | 2158 | F9 |
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| DOID:12259 | hemophilia B | HGNC:3551 | Homo sapiens (human) | 2158 | F9 |
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| DOID:0080839 | X-linked warfarin sensitivity | HGNC:3551 | Homo sapiens (human) | 2158 | F9 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:3551 | Homo sapiens (human) | 2158 | F9 |
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| DOID:12134 | factor VIII deficiency | HGNC:3546 | Homo sapiens (human) | 2157 | F8 |
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| DOID:0060574 | von Willebrand's disease 2 | HGNC:3546 | Homo sapiens (human) | 2157 | F8 |
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| DOID:9279 | hyperhomocysteinemia | HGNC:3546 | Homo sapiens (human) | 2157 | F8 |
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| DOID:801 | hemarthrosis | HGNC:3546 | Homo sapiens (human) | 2157 | F8 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:3546 | Homo sapiens (human) | 2157 | F8 |
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| DOID:9351 | diabetes mellitus | HGNC:3544 | Homo sapiens (human) | 2155 | F7 |
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| DOID:1588 | thrombocytopenia | HGNC:3544 | Homo sapiens (human) | 2155 | F7 |
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