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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:10652 | Alzheimer's disease | HGNC:23 | Homo sapiens (human) | 18 | ABAT |
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| DOID:2548 | reflex epilepsy | HGNC:23 | Homo sapiens (human) | 18 | ABAT |
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| DOID:0050562 | West syndrome | HGNC:23 | Homo sapiens (human) | 18 | ABAT |
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| DOID:12858 | Huntington's disease | HGNC:23 | Homo sapiens (human) | 18 | ABAT |
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| DOID:1824 | status epilepticus | HGNC:23 | Homo sapiens (human) | 18 | ABAT |
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| DOID:1596 | depressive disorder | HGNC:23 | Homo sapiens (human) | 18 | ABAT |
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| DOID:326 | ischemia | HGNC:23 | Homo sapiens (human) | 18 | ABAT |
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| DOID:3343 | glycoproteinosis | HGNC:23026 | Homo sapiens (human) | 84572 | GNPTG |
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| DOID:0080678 | mucolipidosis III gamma | HGNC:23026 | Homo sapiens (human) | 84572 | GNPTG |
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| DOID:5212 | congenital disorder of glycosylation | HGNC:23056 | Homo sapiens (human) | 10195 | ALG3 |
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| DOID:0080556 | congenital disorder of glycosylation Id | HGNC:23056 | Homo sapiens (human) | 10195 | ALG3 |
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| DOID:10584 | retinitis pigmentosa | HGNC:23059 | Homo sapiens (human) | 63827 | BCAN |
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| DOID:3525 | middle cerebral artery infarction | HGNC:23059 | Homo sapiens (human) | 63827 | BCAN |
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| DOID:3070 | high grade glioma | HGNC:23059 | Homo sapiens (human) | 63827 | BCAN |
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| DOID:14330 | Parkinson's disease | HGNC:23064 | Homo sapiens (human) | 119391 | GSTO2 |
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| DOID:10652 | Alzheimer's disease | HGNC:23064 | Homo sapiens (human) | 119391 | GSTO2 |
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| DOID:1574 | alcohol use disorder | HGNC:23064 | Homo sapiens (human) | 119391 | GSTO2 |
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| DOID:2841 | asthma | HGNC:23064 | Homo sapiens (human) | 119391 | GSTO2 |
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| DOID:0080555 | congenital disorder of glycosylation Ic | HGNC:23157 | Homo sapiens (human) | 29929 | ALG6 |
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| DOID:0050570 | congenital disorder of glycosylation type I | HGNC:23157 | Homo sapiens (human) | 29929 | ALG6 |
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| DOID:0080561 | congenital disorder of glycosylation Ii | HGNC:23159 | Homo sapiens (human) | 85365 | ALG2 |
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| DOID:0110669 | congenital myasthenic syndrome 14 | HGNC:23159 | Homo sapiens (human) | 85365 | ALG2 |
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| DOID:0080560 | congenital disorder of glycosylation Ih | HGNC:23161 | Homo sapiens (human) | 79053 | ALG8 |
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| DOID:0050770 | polycystic liver disease | HGNC:23161 | Homo sapiens (human) | 79053 | ALG8 |
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| DOID:0050570 | congenital disorder of glycosylation type I | HGNC:23161 | Homo sapiens (human) | 79053 | ALG8 |
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