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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:3525 | middle cerebral artery infarction | HGNC:333 | Homo sapiens (human) | 183 | AGT |
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| DOID:1312 | focal segmental glomerulosclerosis | HGNC:333 | Homo sapiens (human) | 183 | AGT |
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| DOID:1936 | atherosclerosis | HGNC:333 | Homo sapiens (human) | 183 | AGT |
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| DOID:13884 | sick sinus syndrome | HGNC:333 | Homo sapiens (human) | 183 | AGT |
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| DOID:0110657 | congenital myasthenic syndrome 8 | HGNC:329 | Homo sapiens (human) | 375790 | AGRN |
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| DOID:2580 | rhizomelic chondrodysplasia punctata | HGNC:327 | Homo sapiens (human) | 8540 | AGPS |
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| DOID:0110853 | rhizomelic chondrodysplasia punctata type 3 | 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:0050741 | alcohol dependence | HGNC:3263 | Homo sapiens (human) | 27161 | AGO2 |
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| DOID:1686 | glaucoma | HGNC:3263 | Homo sapiens (human) | 27161 | AGO2 |
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| DOID:2560 | morphine dependence | HGNC:3263 | Homo sapiens (human) | 27161 | AGO2 |
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| DOID:0060001 | withdrawal disorder | HGNC:3263 | Homo sapiens (human) | 27161 | AGO2 |
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| DOID:0050741 | alcohol dependence | HGNC:3262 | Homo sapiens (human) | 26523 | AGO1 |
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| DOID:4676 | uremia | HGNC:321 | Homo sapiens (human) | 178 | AGL |
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| DOID:2748 | glycogen storage disease III | HGNC:321 | Homo sapiens (human) | 178 | AGL |
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| DOID:0080132 | Sengers syndrome | HGNC:21869 | Homo sapiens (human) | 55750 | AGK |
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| DOID:0110245 | cataract 38 | HGNC:21869 | Homo sapiens (human) | 55750 | AGK |
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| DOID:0070311 | oligoasthenoteratozoospermia | HGNC:5175 | Homo sapiens (human) | 3267 | AGFG1 |
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| DOID:1909 | melanoma | HGNC:320 | Homo sapiens (human) | 177 | AGER |
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| DOID:0050855 | renal fibrosis | HGNC:320 | Homo sapiens (human) | 177 | AGER |
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| DOID:0080832 | mild cognitive impairment | HGNC:320 | Homo sapiens (human) | 177 | AGER |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:320 | Homo sapiens (human) | 177 | AGER |
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| DOID:1891 | optic nerve disease | HGNC:320 | Homo sapiens (human) | 177 | AGER |
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| DOID:2377 | multiple sclerosis | HGNC:320 | Homo sapiens (human) | 177 | AGER |
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