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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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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:1394 | urinary schistosomiasis | HGNC:1637 | Homo sapiens (human) | 912 | CD1D |
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| DOID:0050741 | alcohol dependence | HGNC:18596 | Homo sapiens (human) | 91227 | GGTLC2 |
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| DOID:5022 | aflatoxins-related hepatocellular carcinoma | HGNC:18596 | Homo sapiens (human) | 91227 | GGTLC2 |
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| DOID:0080507 | Cornelia de Lange syndrome 3 | HGNC:2468 | Homo sapiens (human) | 9126 | SMC3 |
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| DOID:11725 | Cornelia de Lange syndrome | HGNC:2468 | Homo sapiens (human) | 9126 | SMC3 |
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| DOID:1059 | intellectual disability | HGNC:2468 | Homo sapiens (human) | 9126 | SMC3 |
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| DOID:684 | hepatocellular carcinoma | HGNC:2468 | Homo sapiens (human) | 9126 | SMC3 |
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| DOID:1059 | intellectual disability | HGNC:25114 | Homo sapiens (human) | 91272 | BOD1 |
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| DOID:0110392 | retinitis pigmentosa 70 | HGNC:17349 | Homo sapiens (human) | 9128 | PRPF4 |
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| DOID:10584 | retinitis pigmentosa | HGNC:17349 | Homo sapiens (human) | 9128 | PRPF4 |
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| DOID:10584 | retinitis pigmentosa | HGNC:17348 | Homo sapiens (human) | 9129 | PRPF3 |
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| DOID:0110356 | retinitis pigmentosa 18 | HGNC:17348 | Homo sapiens (human) | 9129 | PRPF3 |
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| DOID:10584 | retinitis pigmentosa | HGNC:8768 | Homo sapiens (human) | 9131 | AIFM1 |
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| DOID:0110429 | dilated cardiomyopathy 1H | HGNC:8768 | Homo sapiens (human) | 9131 | AIFM1 |
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| DOID:0110212 | Charcot-Marie-Tooth disease X-linked recessive 4 | HGNC:8768 | Homo sapiens (human) | 9131 | AIFM1 |
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| DOID:0111502 | combined oxidative phosphorylation deficiency 6 | HGNC:8768 | Homo sapiens (human) | 9131 | AIFM1 |
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| DOID:5327 | retinal detachment | HGNC:8768 | Homo sapiens (human) | 9131 | AIFM1 |
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| DOID:0111741 | X-linked deafness 5 | HGNC:8768 | Homo sapiens (human) | 9131 | AIFM1 |
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| DOID:0060536 | mitochondrial complex I deficiency | HGNC:8768 | Homo sapiens (human) | 9131 | AIFM1 |
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| DOID:3525 | middle cerebral artery infarction | HGNC:8768 | Homo sapiens (human) | 9131 | AIFM1 |
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| DOID:224 | transient cerebral ischemia | HGNC:8768 | Homo sapiens (human) | 9131 | AIFM1 |
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| DOID:10652 | Alzheimer's disease | HGNC:8768 | Homo sapiens (human) | 9131 | AIFM1 |
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| DOID:10283 | prostate cancer | HGNC:1590 | Homo sapiens (human) | 9134 | CCNE2 |
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| DOID:162 | cancer | HGNC:1590 | Homo sapiens (human) | 9134 | CCNE2 |
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| DOID:0080909 | castration-resistant prostate carcinoma | HGNC:1590 | Homo sapiens (human) | 9134 | CCNE2 |
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