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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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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:0080027 | spondyloepimetaphyseal dysplasia | HGNC:2200 | Homo sapiens (human) | 1280 | COL2A1 |
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| DOID:8398 | osteoarthritis | HGNC:2200 | Homo sapiens (human) | 1280 | COL2A1 |
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| DOID:0080046 | Stickler syndrome | HGNC:2200 | Homo sapiens (human) | 1280 | COL2A1 |
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| DOID:0080045 | Kniest dysplasia | HGNC:2200 | Homo sapiens (human) | 1280 | COL2A1 |
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| DOID:3371 | chondrosarcoma | HGNC:2200 | Homo sapiens (human) | 1280 | COL2A1 |
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| DOID:5327 | retinal detachment | HGNC:2200 | Homo sapiens (human) | 1280 | COL2A1 |
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| DOID:8886 | chorioretinitis | HGNC:2200 | Homo sapiens (human) | 1280 | COL2A1 |
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| DOID:1123 | spondyloarthropathy | HGNC:2200 | Homo sapiens (human) | 1280 | COL2A1 |
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| DOID:14415 | Legg-Calve-Perthes disease | HGNC:2200 | Homo sapiens (human) | 1280 | COL2A1 |
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| DOID:90 | degenerative disc disease | HGNC:2200 | Homo sapiens (human) | 1280 | COL2A1 |
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| DOID:0080044 | hypochondrogenesis | HGNC:2200 | Homo sapiens (human) | 1280 | COL2A1 |
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| DOID:2256 | osteochondrodysplasia | HGNC:2200 | Homo sapiens (human) | 1280 | COL2A1 |
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| DOID:1459 | hypothyroidism | HGNC:2200 | Homo sapiens (human) | 1280 | COL2A1 |
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| DOID:0112195 | spondyloperipheral dysplasia | HGNC:2200 | Homo sapiens (human) | 1280 | COL2A1 |
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| DOID:5614 | eye disease | HGNC:2200 | Homo sapiens (human) | 1280 | COL2A1 |
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| DOID:0080056 | achondrogenesis type II | HGNC:2200 | Homo sapiens (human) | 1280 | COL2A1 |
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| DOID:0080028 | spondyloepimetaphyseal dysplasia, Strudwick type | HGNC:2200 | Homo sapiens (human) | 1280 | COL2A1 |
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| DOID:0081020 | congenital fibrosis of the extraocular muscles 5 | HGNC:18603 | Homo sapiens (human) | 84570 | COL25A1 |
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| DOID:10941 | intracranial aneurysm | HGNC:22989 | Homo sapiens (human) | 169044 | COL22A1 |
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| DOID:9975 | cocaine dependence | HGNC:17025 | Homo sapiens (human) | 81578 | COL21A1 |
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| DOID:13359 | Ehlers-Danlos syndrome | HGNC:2198 | Homo sapiens (human) | 1278 | COL1A2 |
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| DOID:1459 | hypothyroidism | HGNC:2198 | Homo sapiens (human) | 1278 | COL1A2 |
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| DOID:0080730 | Ehlers-Danlos syndrome cardiac valvular type | HGNC:2198 | Homo sapiens (human) | 1278 | COL1A2 |
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| DOID:767 | muscular atrophy | HGNC:2198 | Homo sapiens (human) | 1278 | COL1A2 |
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| DOID:0110340 | osteogenesis imperfecta type 4 | HGNC:2198 | Homo sapiens (human) | 1278 | COL1A2 |
|
