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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:289 | endometriosis | HGNC:10610 | Homo sapiens (human) | 6356 | CCL11 |
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| DOID:11204 | allergic conjunctivitis | HGNC:10610 | Homo sapiens (human) | 6356 | CCL11 |
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| DOID:2921 | glomerulonephritis | HGNC:10609 | Homo sapiens (human) | 6346 | CCL1 |
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| DOID:2377 | multiple sclerosis | HGNC:10609 | Homo sapiens (human) | 6346 | CCL1 |
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| DOID:399 | tuberculosis | HGNC:10609 | Homo sapiens (human) | 6346 | CCL1 |
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| DOID:2527 | nephrosis | HGNC:10609 | Homo sapiens (human) | 6346 | CCL1 |
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| DOID:3083 | chronic obstructive pulmonary disease | HGNC:10609 | Homo sapiens (human) | 6346 | CCL1 |
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| DOID:4483 | rhinitis | HGNC:10609 | Homo sapiens (human) | 6346 | CCL1 |
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| DOID:2841 | asthma | HGNC:10609 | Homo sapiens (human) | 6346 | CCL1 |
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| DOID:2957 | pulmonary tuberculosis | HGNC:10609 | Homo sapiens (human) | 6346 | CCL1 |
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| DOID:9970 | obesity | HGNC:10606 | Homo sapiens (human) | 6342 | SCP2 |
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| DOID:905 | Zellweger syndrome | HGNC:10606 | Homo sapiens (human) | 6342 | SCP2 |
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| DOID:326 | ischemia | HGNC:10602 | Homo sapiens (human) | 6340 | SCNN1G |
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| DOID:14452 | hypokalemic periodic paralysis | HGNC:10602 | Homo sapiens (human) | 6340 | SCNN1G |
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| DOID:0050477 | Liddle syndrome | HGNC:10602 | Homo sapiens (human) | 6340 | SCNN1G |
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| DOID:0060854 | autosomal recessive pseudohypoaldosteronism type 1 | HGNC:10602 | Homo sapiens (human) | 6340 | SCNN1G |
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| DOID:1289 | neurodegenerative disease | HGNC:10602 | Homo sapiens (human) | 6340 | SCNN1G |
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| DOID:0080528 | bronchiectasis 3 | HGNC:10602 | Homo sapiens (human) | 6340 | SCNN1G |
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| DOID:4479 | pseudohypoaldosteronism | HGNC:10602 | Homo sapiens (human) | 6340 | SCNN1G |
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| DOID:1289 | neurodegenerative disease | HGNC:10601 | Homo sapiens (human) | 6339 | SCNN1D |
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| DOID:14452 | hypokalemic periodic paralysis | HGNC:10601 | Homo sapiens (human) | 6339 | SCNN1D |
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| DOID:326 | ischemia | HGNC:10601 | Homo sapiens (human) | 6339 | SCNN1D |
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| DOID:326 | ischemia | HGNC:10600 | Homo sapiens (human) | 6338 | SCNN1B |
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| DOID:0050477 | Liddle syndrome | HGNC:10600 | Homo sapiens (human) | 6338 | SCNN1B |
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| DOID:0060854 | autosomal recessive pseudohypoaldosteronism type 1 | HGNC:10600 | Homo sapiens (human) | 6338 | SCNN1B |
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