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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:423 | myopathy | HGNC:2195 | Homo sapiens (human) | 80781 | COL18A1 |
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| DOID:12930 | dilated cardiomyopathy | HGNC:2195 | Homo sapiens (human) | 80781 | COL18A1 |
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| DOID:684 | hepatocellular carcinoma | HGNC:2195 | Homo sapiens (human) | 80781 | COL18A1 |
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| DOID:699 | mitochondrial myopathy | HGNC:2195 | Homo sapiens (human) | 80781 | COL18A1 |
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| DOID:8577 | ulcerative colitis | HGNC:2195 | Homo sapiens (human) | 80781 | COL18A1 |
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| DOID:0070337 | epithelial recurrent erosion dystrophy | HGNC:2194 | Homo sapiens (human) | 1308 | COL17A1 |
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| DOID:0060738 | junctional epidermolysis bullosa non-Herlitz type | HGNC:2194 | Homo sapiens (human) | 1308 | COL17A1 |
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| DOID:3209 | junctional epidermolysis bullosa | HGNC:2194 | Homo sapiens (human) | 1308 | COL17A1 |
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| DOID:0050700 | cardiomyopathy | HGNC:2192 | Homo sapiens (human) | 1306 | COL15A1 |
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| DOID:699 | mitochondrial myopathy | HGNC:2192 | Homo sapiens (human) | 1306 | COL15A1 |
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| DOID:423 | myopathy | HGNC:2192 | Homo sapiens (human) | 1306 | COL15A1 |
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| DOID:12930 | dilated cardiomyopathy | HGNC:2192 | Homo sapiens (human) | 1306 | COL15A1 |
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| DOID:3748 | esophagus squamous cell carcinoma | HGNC:2191 | Homo sapiens (human) | 7373 | COL14A1 |
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| DOID:0050663 | Bethlem myopathy | HGNC:2188 | Homo sapiens (human) | 1303 | COL12A1 |
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| DOID:674 | cleft palate | HGNC:2187 | Homo sapiens (human) | 1302 | COL11A2 |
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| DOID:0080026 | otospondylomegaepiphyseal dysplasia, autosomal recessive | HGNC:2187 | Homo sapiens (human) | 1302 | COL11A2 |
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| DOID:0110545 | autosomal dominant nonsyndromic deafness 13 | HGNC:2187 | Homo sapiens (human) | 1302 | COL11A2 |
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| DOID:0080673 | fibrochondrogenesis 2 | HGNC:2187 | Homo sapiens (human) | 1302 | COL11A2 |
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| DOID:0080046 | Stickler syndrome | HGNC:2187 | Homo sapiens (human) | 1302 | COL11A2 |
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| DOID:2256 | osteochondrodysplasia | HGNC:2187 | Homo sapiens (human) | 1302 | COL11A2 |
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| DOID:0110509 | autosomal recessive nonsyndromic deafness 53 | HGNC:2187 | Homo sapiens (human) | 1302 | COL11A2 |
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| DOID:0080677 | otospondylomegaepiphyseal dysplasia, autosomal dominant | HGNC:2187 | Homo sapiens (human) | 1302 | COL11A2 |
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| DOID:0050564 | autosomal dominant nonsyndromic deafness | HGNC:2186 | Homo sapiens (human) | 1301 | COL11A1 |
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| DOID:0080672 | fibrochondrogenesis 1 | HGNC:2186 | Homo sapiens (human) | 1301 | COL11A1 |
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| DOID:0111510 | Marshall syndrome | HGNC:2186 | Homo sapiens (human) | 1301 | COL11A1 |
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