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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
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:0080046 | Stickler syndrome | 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:0111508 | Torrance type platyspondylic dysplasia | HGNC:2200 | Homo sapiens (human) | 1280 | COL2A1 |
|
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| DOID:10159 | osteonecrosis | 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:0080028 | spondyloepimetaphyseal dysplasia, Strudwick type | HGNC:2200 | Homo sapiens (human) | 1280 | COL2A1 |
|
||
| DOID:11830 | myopia | 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:0080676 | Stickler syndrome 1 | 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:0050827 | rheumatic heart disease | HGNC:2201 | Homo sapiens (human) | 1281 | COL3A1 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:2201 | Homo sapiens (human) | 1281 | COL3A1 |
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| DOID:9970 | obesity | HGNC:2201 | Homo sapiens (human) | 1281 | COL3A1 |
|
||
| DOID:13948 | bladder neck obstruction | HGNC:2201 | Homo sapiens (human) | 1281 | COL3A1 |
|
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| DOID:418 | systemic scleroderma | HGNC:2201 | Homo sapiens (human) | 1281 | COL3A1 |
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| DOID:5844 | myocardial infarction | HGNC:2201 | Homo sapiens (human) | 1281 | COL3A1 |
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| DOID:783 | end stage renal disease | HGNC:2201 | Homo sapiens (human) | 1281 | COL3A1 |
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| DOID:13359 | Ehlers-Danlos syndrome | HGNC:2201 | Homo sapiens (human) | 1281 | COL3A1 |
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| DOID:14756 | vascular type Ehlers-Danlos syndrome | HGNC:2201 | Homo sapiens (human) | 1281 | COL3A1 |
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| DOID:0050851 | glomerulosclerosis | HGNC:2201 | Homo sapiens (human) | 1281 | COL3A1 |
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| DOID:14757 | Ehlers-Danlos syndrome hypermobility type | HGNC:2201 | Homo sapiens (human) | 1281 | COL3A1 |
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| DOID:0090125 | brain small vessel disease 1 | HGNC:2202 | Homo sapiens (human) | 1282 | COL4A1 |
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| DOID:0111547 | retinal arterial tortuosity | HGNC:2202 | Homo sapiens (human) | 1282 | COL4A1 |
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| DOID:0060263 | porencephaly | HGNC:2202 | Homo sapiens (human) | 1282 | COL4A1 |
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| DOID:9970 | obesity | HGNC:2202 | Homo sapiens (human) | 1282 | COL4A1 |
|
