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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:0110026 | age related macular degeneration 14 | HGNC:1248 | Homo sapiens (human) | 717 | C2 |
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| DOID:10652 | Alzheimer's disease | HGNC:1248 | Homo sapiens (human) | 717 | C2 |
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| DOID:0060295 | complement component 2 deficiency | HGNC:1248 | Homo sapiens (human) | 717 | C2 |
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| DOID:9074 | systemic lupus erythematosus | HGNC:1248 | Homo sapiens (human) | 717 | C2 |
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| DOID:1407 | anterior uveitis | HGNC:1248 | Homo sapiens (human) | 717 | C2 |
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| DOID:0080987 | Ehlers-Danlos syndrome periodontal type 2 | HGNC:1247 | Homo sapiens (human) | 716 | C1S |
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| DOID:0080828 | VEXAS syndrome | HGNC:12469 | Homo sapiens (human) | 7317 | UBA1 |
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| DOID:0111827 | X-linked spinal muscular atrophy 2 | HGNC:12469 | Homo sapiens (human) | 7317 | UBA1 |
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| DOID:0112341 | hereditary spastic paraplegia 80 | HGNC:12461 | Homo sapiens (human) | 51271 | UBAP1 |
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| DOID:0080986 | Ehlers-Danlos syndrome periodontal type 1 | HGNC:1246 | Homo sapiens (human) | 715 | C1R |
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| DOID:1520 | colon carcinoma | HGNC:12458 | Homo sapiens (human) | 7311 | UBA52 |
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| DOID:10123 | pigmentation disease | HGNC:12450 | Homo sapiens (human) | 7306 | TYRP1 |
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| DOID:0050632 | oculocutaneous albinism | HGNC:12450 | Homo sapiens (human) | 7306 | TYRP1 |
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| DOID:0070097 | oculocutaneous albinism type III | HGNC:12450 | Homo sapiens (human) | 7306 | TYRP1 |
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| DOID:0070095 | oculocutaneous albinism type IB | HGNC:12442 | Homo sapiens (human) | 7299 | TYR |
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| DOID:12306 | vitiligo | HGNC:12442 | Homo sapiens (human) | 7299 | TYR |
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| DOID:8465 | retinoschisis | HGNC:12442 | Homo sapiens (human) | 7299 | TYR |
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| DOID:11211 | buphthalmos | HGNC:12442 | Homo sapiens (human) | 7299 | TYR |
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| DOID:10123 | pigmentation disease | HGNC:12442 | Homo sapiens (human) | 7299 | TYR |
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| DOID:0050633 | ocular albinism 1 | HGNC:12442 | Homo sapiens (human) | 7299 | TYR |
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| DOID:1909 | melanoma | HGNC:12442 | Homo sapiens (human) | 7299 | TYR |
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| DOID:13399 | color blindness | HGNC:12442 | Homo sapiens (human) | 7299 | TYR |
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| DOID:8923 | skin melanoma | HGNC:12442 | Homo sapiens (human) | 7299 | TYR |
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| DOID:0070094 | oculocutaneous albinism type IA | HGNC:12442 | Homo sapiens (human) | 7299 | TYR |
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| DOID:0050632 | oculocutaneous albinism | HGNC:12442 | Homo sapiens (human) | 7299 | TYR |
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