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GlyTouCan
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
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:321 | tropical spastic paraparesis | HGNC:11914 | Homo sapiens (human) | 8784 | TNFRSF18 |
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| DOID:1520 | colon carcinoma | HGNC:11913 | Homo sapiens (human) | 608 | TNFRSF17 |
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| DOID:9538 | multiple myeloma | HGNC:11913 | Homo sapiens (human) | 608 | TNFRSF17 |
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| DOID:5844 | myocardial infarction | HGNC:11912 | Homo sapiens (human) | 8764 | TNFRSF14 |
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| DOID:2349 | arteriosclerosis | HGNC:11912 | Homo sapiens (human) | 8764 | TNFRSF14 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:11909 | Homo sapiens (human) | 4982 | TNFRSF11B |
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| DOID:1712 | aortic valve stenosis | HGNC:11909 | Homo sapiens (human) | 4982 | TNFRSF11B |
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| DOID:8398 | osteoarthritis | HGNC:11909 | Homo sapiens (human) | 4982 | TNFRSF11B |
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| DOID:10595 | Charcot-Marie-Tooth disease | HGNC:11909 | Homo sapiens (human) | 4982 | TNFRSF11B |
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| DOID:0081368 | Paget's disease of bone 5 | HGNC:11909 | Homo sapiens (human) | 4982 | TNFRSF11B |
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| DOID:341 | peripheral vascular disease | HGNC:11909 | Homo sapiens (human) | 4982 | TNFRSF11B |
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| DOID:3407 | carotid artery disease | HGNC:11909 | Homo sapiens (human) | 4982 | TNFRSF11B |
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| DOID:1184 | nephrotic syndrome | HGNC:11909 | Homo sapiens (human) | 4982 | TNFRSF11B |
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| DOID:823 | periapical periodontitis | HGNC:11909 | Homo sapiens (human) | 4982 | TNFRSF11B |
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| DOID:10763 | hypertension | HGNC:11909 | Homo sapiens (human) | 4982 | TNFRSF11B |
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| DOID:11476 | osteoporosis | HGNC:11909 | Homo sapiens (human) | 4982 | TNFRSF11B |
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| DOID:5419 | schizophrenia | HGNC:11909 | Homo sapiens (human) | 4982 | TNFRSF11B |
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| DOID:3393 | coronary artery disease | HGNC:11909 | Homo sapiens (human) | 4982 | TNFRSF11B |
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| DOID:4248 | coronary stenosis | HGNC:11909 | Homo sapiens (human) | 4982 | TNFRSF11B |
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| DOID:820 | myocarditis | HGNC:11909 | Homo sapiens (human) | 4982 | TNFRSF11B |
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| DOID:0111582 | hereditary arterial and articular multiple calcification syndrome | HGNC:11909 | Homo sapiens (human) | 4982 | TNFRSF11B |
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| DOID:12466 | secondary hyperparathyroidism | HGNC:11909 | Homo sapiens (human) | 4982 | TNFRSF11B |
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| DOID:3526 | cerebral infarction | HGNC:11909 | Homo sapiens (human) | 4982 | TNFRSF11B |
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| DOID:0080162 | lupus nephritis | HGNC:11909 | Homo sapiens (human) | 4982 | TNFRSF11B |
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| DOID:6000 | congestive heart failure | HGNC:11909 | Homo sapiens (human) | 4982 | TNFRSF11B |
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