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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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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:0050557 | congenital muscular dystrophy | HGNC:2213 | Homo sapiens (human) | 1293 | COL6A3 |
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| DOID:13223 | uterine fibroid | HGNC:2213 | Homo sapiens (human) | 1293 | COL6A3 |
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| DOID:10763 | hypertension | HGNC:2213 | Homo sapiens (human) | 1293 | COL6A3 |
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| DOID:0050663 | Bethlem myopathy | HGNC:2213 | Homo sapiens (human) | 1293 | COL6A3 |
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| DOID:8577 | ulcerative colitis | HGNC:2213 | Homo sapiens (human) | 1293 | COL6A3 |
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| DOID:11054 | urinary bladder cancer | HGNC:2213 | Homo sapiens (human) | 1293 | COL6A3 |
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| DOID:0050663 | Bethlem myopathy | HGNC:2212 | Homo sapiens (human) | 1292 | COL6A2 |
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| DOID:0050663 | Bethlem myopathy | HGNC:2211 | Homo sapiens (human) | 1291 | COL6A1 |
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| DOID:0050558 | Ullrich congenital muscular dystrophy | HGNC:2211 | Homo sapiens (human) | 1291 | COL6A1 |
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| DOID:0050557 | congenital muscular dystrophy | HGNC:2211 | Homo sapiens (human) | 1291 | COL6A1 |
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| DOID:9884 | muscular dystrophy | HGNC:2211 | Homo sapiens (human) | 1291 | COL6A1 |
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| DOID:0080726 | Ehlers-Danlos syndrome classic type 2 | HGNC:2210 | Homo sapiens (human) | 1290 | COL5A2 |
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| DOID:14720 | Ehlers-Danlos syndrome classic type 1 | HGNC:2210 | Homo sapiens (human) | 1290 | COL5A2 |
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| DOID:13207 | proliferative diabetic retinopathy | HGNC:2210 | Homo sapiens (human) | 1290 | COL5A2 |
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| DOID:13359 | Ehlers-Danlos syndrome | HGNC:2210 | Homo sapiens (human) | 1290 | COL5A2 |
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| DOID:850 | lung disease | HGNC:2210 | Homo sapiens (human) | 1290 | COL5A2 |
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| DOID:13359 | Ehlers-Danlos syndrome | HGNC:2209 | Homo sapiens (human) | 1289 | COL5A1 |
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| DOID:14720 | Ehlers-Danlos syndrome classic type 1 | HGNC:2209 | Homo sapiens (human) | 1289 | COL5A1 |
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| DOID:423 | myopathy | HGNC:2208 | Homo sapiens (human) | 1288 | COL4A6 |
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| DOID:854 | collagen disease | HGNC:2208 | Homo sapiens (human) | 1288 | COL4A6 |
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| DOID:0111740 | X-linked deafness 6 | HGNC:2208 | Homo sapiens (human) | 1288 | COL4A6 |
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| DOID:576 | proteinuria | HGNC:2207 | Homo sapiens (human) | 1287 | COL4A5 |
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| DOID:0110034 | X-linked Alport syndrome | HGNC:2207 | Homo sapiens (human) | 1287 | COL4A5 |
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| DOID:10983 | Alport syndrome | HGNC:2207 | Homo sapiens (human) | 1287 | COL4A5 |
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| DOID:423 | myopathy | HGNC:2207 | Homo sapiens (human) | 1287 | COL4A5 |
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