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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:2256 | osteochondrodysplasia | HGNC:2217 | Homo sapiens (human) | 1297 | COL9A1 |
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| DOID:0080046 | Stickler syndrome | HGNC:2217 | Homo sapiens (human) | 1297 | COL9A1 |
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| DOID:8398 | osteoarthritis | HGNC:2217 | Homo sapiens (human) | 1297 | COL9A1 |
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| DOID:0070301 | multiple epiphyseal dysplasia 6 | HGNC:2217 | Homo sapiens (human) | 1297 | COL9A1 |
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| DOID:11555 | Fuchs' endothelial dystrophy | HGNC:2216 | Homo sapiens (human) | 1296 | COL8A2 |
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| DOID:0110856 | posterior polymorphous corneal dystrophy 2 | HGNC:2216 | Homo sapiens (human) | 1296 | COL8A2 |
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| DOID:0080224 | autosomal dominant dystrophic epidermolysis bullosa | HGNC:2214 | Homo sapiens (human) | 1294 | COL7A1 |
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| DOID:0080086 | nonsyndromic congenital nail disorder 8 | HGNC:2214 | Homo sapiens (human) | 1294 | COL7A1 |
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| DOID:4959 | epidermolysis bullosa dystrophica | HGNC:2214 | Homo sapiens (human) | 1294 | COL7A1 |
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| DOID:0111345 | transient bullous dermolysis of the newborn | HGNC:2214 | Homo sapiens (human) | 1294 | COL7A1 |
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| DOID:0060642 | recessive dystrophic epidermolysis bullosa | HGNC:2214 | Homo sapiens (human) | 1294 | COL7A1 |
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| DOID:0111347 | epidermolysis bullosa with congenital localized absence of skin and deformity of nails | HGNC:2214 | Homo sapiens (human) | 1294 | COL7A1 |
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| DOID:0080988 | pretibial dystrophic epidermolysis bullosa | HGNC:2214 | Homo sapiens (human) | 1294 | COL7A1 |
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| DOID:9884 | muscular dystrophy | HGNC:2213 | Homo sapiens (human) | 1293 | COL6A3 |
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| DOID:0050558 | Ullrich congenital muscular dystrophy | HGNC:2213 | Homo sapiens (human) | 1293 | COL6A3 |
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| DOID:0090050 | dystonia 27 | HGNC:2213 | Homo sapiens (human) | 1293 | COL6A3 |
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| DOID:5844 | myocardial infarction | HGNC:2213 | Homo sapiens (human) | 1293 | COL6A3 |
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| DOID:13207 | proliferative diabetic retinopathy | HGNC:2213 | Homo sapiens (human) | 1293 | COL6A3 |
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| DOID:14004 | thoracic aortic aneurysm | HGNC:2213 | Homo sapiens (human) | 1293 | COL6A3 |
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| DOID:219 | colon cancer | HGNC:2213 | Homo sapiens (human) | 1293 | COL6A3 |
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| DOID:8778 | Crohn's disease | HGNC:2213 | Homo sapiens (human) | 1293 | COL6A3 |
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| DOID:784 | chronic kidney disease | HGNC:2213 | Homo sapiens (human) | 1293 | COL6A3 |
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| DOID:2033 | communication disorder | HGNC:2213 | Homo sapiens (human) | 1293 | COL6A3 |
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| DOID:1070 | primary open angle glaucoma | HGNC:2213 | Homo sapiens (human) | 1293 | COL6A3 |
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| DOID:10534 | stomach cancer | HGNC:2213 | Homo sapiens (human) | 1293 | COL6A3 |
|
