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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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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:0110339 | osteogenesis imperfecta type 3 | HGNC:2198 | Homo sapiens (human) | 1278 | COL1A2 |
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| DOID:10941 | intracranial aneurysm | HGNC:2198 | Homo sapiens (human) | 1278 | COL1A2 |
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| DOID:5199 | ureteral obstruction | HGNC:2198 | Homo sapiens (human) | 1278 | COL1A2 |
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| DOID:0080728 | Ehlers-Danlos syndrome arthrochalasia type 2 | HGNC:2198 | Homo sapiens (human) | 1278 | COL1A2 |
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| DOID:4079 | heart valve disease | HGNC:2198 | Homo sapiens (human) | 1278 | COL1A2 |
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| DOID:0110341 | osteogenesis imperfecta type 2 | HGNC:2198 | Homo sapiens (human) | 1278 | COL1A2 |
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| DOID:3770 | pulmonary fibrosis | HGNC:2198 | Homo sapiens (human) | 1278 | COL1A2 |
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| DOID:11476 | osteoporosis | HGNC:2198 | Homo sapiens (human) | 1278 | COL1A2 |
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| DOID:12347 | osteogenesis imperfecta | HGNC:2198 | Homo sapiens (human) | 1278 | COL1A2 |
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| DOID:3770 | pulmonary fibrosis | HGNC:2197 | Homo sapiens (human) | 1277 | COL1A1 |
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| DOID:8577 | ulcerative colitis | HGNC:2197 | Homo sapiens (human) | 1277 | COL1A1 |
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| DOID:0110340 | osteogenesis imperfecta type 4 | HGNC:2197 | Homo sapiens (human) | 1277 | COL1A1 |
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| DOID:0080208 | metabolic dysfunction-associated steatotic liver disease | HGNC:2197 | Homo sapiens (human) | 1277 | COL1A1 |
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| DOID:783 | end stage renal disease | HGNC:2197 | Homo sapiens (human) | 1277 | COL1A1 |
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| DOID:8398 | osteoarthritis | HGNC:2197 | Homo sapiens (human) | 1277 | COL1A1 |
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| DOID:12185 | otosclerosis | HGNC:2197 | Homo sapiens (human) | 1277 | COL1A1 |
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| DOID:9970 | obesity | HGNC:2197 | Homo sapiens (human) | 1277 | COL1A1 |
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| DOID:0110341 | osteogenesis imperfecta type 2 | HGNC:2197 | Homo sapiens (human) | 1277 | COL1A1 |
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| DOID:12347 | osteogenesis imperfecta | HGNC:2197 | Homo sapiens (human) | 1277 | COL1A1 |
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| DOID:5199 | ureteral obstruction | HGNC:2197 | Homo sapiens (human) | 1277 | COL1A1 |
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| DOID:0110334 | osteogenesis imperfecta type 1 | HGNC:2197 | Homo sapiens (human) | 1277 | COL1A1 |
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| DOID:9111 | cutaneous leishmaniasis | HGNC:2197 | Homo sapiens (human) | 1277 | COL1A1 |
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| DOID:14004 | thoracic aortic aneurysm | HGNC:2197 | Homo sapiens (human) | 1277 | COL1A1 |
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| DOID:2377 | multiple sclerosis | HGNC:2197 | Homo sapiens (human) | 1277 | COL1A1 |
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| DOID:90 | degenerative disc disease | HGNC:2197 | Homo sapiens (human) | 1277 | COL1A1 |
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