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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:0110245 | cataract 38 | HGNC:21869 | Homo sapiens (human) | 55750 | AGK |
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| DOID:0080132 | Sengers syndrome | HGNC:21869 | Homo sapiens (human) | 55750 | AGK |
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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: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: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:0110657 | congenital myasthenic syndrome 8 | HGNC:329 | Homo sapiens (human) | 375790 | AGRN |
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| DOID:0111670 | primary hyperoxaluria type 1 | HGNC:341 | Homo sapiens (human) | 189 | AGXT |
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| DOID:2977 | primary hyperoxaluria | HGNC:341 | Homo sapiens (human) | 189 | AGXT |
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| DOID:3910 | lung adenocarcinoma | HGNC:380 | Homo sapiens (human) | 10327 | AKR1A1 |
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| DOID:1612 | breast cancer | HGNC:380 | Homo sapiens (human) | 10327 | AKR1A1 |
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| DOID:2349 | arteriosclerosis | HGNC:381 | Homo sapiens (human) | 231 | AKR1B1 |
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| DOID:4500 | hypokalemia | HGNC:381 | Homo sapiens (human) | 231 | AKR1B1 |
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| DOID:1205 | allergic disease | HGNC:381 | Homo sapiens (human) | 231 | AKR1B1 |
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| DOID:10534 | stomach cancer | HGNC:381 | Homo sapiens (human) | 231 | AKR1B1 |
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| DOID:9743 | diabetic neuropathy | HGNC:381 | Homo sapiens (human) | 231 | AKR1B1 |
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| DOID:9870 | galactosemia | HGNC:381 | Homo sapiens (human) | 231 | AKR1B1 |
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| DOID:4195 | hyperglycemia | HGNC:381 | Homo sapiens (human) | 231 | AKR1B1 |
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| DOID:83 | cataract | HGNC:381 | Homo sapiens (human) | 231 | AKR1B1 |
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| DOID:8947 | diabetic retinopathy | HGNC:381 | Homo sapiens (human) | 231 | AKR1B1 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:381 | Homo sapiens (human) | 231 | AKR1B1 |
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| DOID:684 | hepatocellular carcinoma | HGNC:381 | Homo sapiens (human) | 231 | AKR1B1 |
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| DOID:9970 | obesity | HGNC:384 | Homo sapiens (human) | 1645 | AKR1C1 |
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