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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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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 | July 29, 2024 |
| Disease ID | Disease Name | Alliance of Genome Resources ID ▼ | Species | Gene ID | Gene Symbol | FlyGlycoDB | Evidence Code Names | References |
|---|---|---|---|---|---|---|---|---|
| DOID:14115 | toxic shock syndrome | HGNC:3353 | Homo sapiens (human) | 2026 | ENO2 |
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| DOID:11054 | urinary bladder cancer | HGNC:3353 | Homo sapiens (human) | 2026 | ENO2 |
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| DOID:10763 | hypertension | HGNC:3353 | Homo sapiens (human) | 2026 | ENO2 |
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| DOID:3459 | breast carcinoma | HGNC:3353 | Homo sapiens (human) | 2026 | ENO2 |
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| DOID:1800 | neuroendocrine carcinoma | HGNC:3353 | Homo sapiens (human) | 2026 | ENO2 |
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| DOID:11832 | visual epilepsy | HGNC:3353 | Homo sapiens (human) | 2026 | ENO2 |
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| DOID:936 | brain disease | HGNC:3353 | Homo sapiens (human) | 2026 | ENO2 |
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| DOID:12783 | migraine without aura | HGNC:3353 | Homo sapiens (human) | 2026 | ENO2 |
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| DOID:10283 | prostate cancer | HGNC:3353 | Homo sapiens (human) | 2026 | ENO2 |
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| DOID:10652 | Alzheimer's disease | HGNC:3350 | Homo sapiens (human) | 2023 | ENO1 |
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| DOID:10763 | hypertension | HGNC:3350 | Homo sapiens (human) | 2023 | ENO1 |
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| DOID:0110657 | congenital myasthenic syndrome 8 | HGNC:329 | Homo sapiens (human) | 375790 | AGRN |
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| DOID:0110853 | rhizomelic chondrodysplasia punctata type 3 | HGNC:327 | Homo sapiens (human) | 8540 | AGPS |
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| DOID:2580 | rhizomelic chondrodysplasia punctata | HGNC:327 | Homo sapiens (human) | 8540 | AGPS |
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| DOID:811 | lipodystrophy | HGNC:325 | Homo sapiens (human) | 10555 | AGPAT2 |
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| DOID:0111135 | congenital generalized lipodystrophy type 1 | HGNC:325 | Homo sapiens (human) | 10555 | AGPAT2 |
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| DOID:0080759 | Fanconi renotubular syndrome 3 | HGNC:3247 | Homo sapiens (human) | 1962 | EHHADH |
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| DOID:0080567 | congenital disorder of glycosylation Ip | HGNC:32456 | Homo sapiens (human) | 440138 | ALG11 |
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| DOID:0060668 | anencephaly | HGNC:3225 | Homo sapiens (human) | 1946 | EFNA5 |
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| DOID:2748 | glycogen storage disease III | HGNC:321 | Homo sapiens (human) | 178 | AGL |
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| DOID:4676 | uremia | HGNC:321 | Homo sapiens (human) | 178 | AGL |
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| DOID:8398 | osteoarthritis | HGNC:319 | Homo sapiens (human) | 176 | ACAN |
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| DOID:2377 | multiple sclerosis | HGNC:319 | Homo sapiens (human) | 176 | ACAN |
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| DOID:6000 | congestive heart failure | HGNC:319 | Homo sapiens (human) | 176 | ACAN |
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| DOID:1824 | status epilepticus | HGNC:319 | Homo sapiens (human) | 176 | ACAN |
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