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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:10652 | Alzheimer's disease | HGNC:6547 | Homo sapiens (human) | 3949 | LDLR |
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| DOID:2030 | anxiety disorder | HGNC:2516 | Homo sapiens (human) | 1501 | CTNND2 |
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| DOID:2841 | asthma | HGNC:5988 | Homo sapiens (human) | 8809 | IL18R1 |
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| DOID:13922 | eosinophilic esophagitis | HGNC:2621 | Homo sapiens (human) | 1557 | CYP2C19 |
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| DOID:0110065 | amelogenesis imperfecta type 1F | HGNC:452 | Homo sapiens (human) | 258 | AMBN |
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| DOID:5082 | liver cirrhosis | HGNC:4938 | Homo sapiens (human) | 3113 | HLA-DPA1 |
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| DOID:6270 | gastric cardia carcinoma | HGNC:12828 | Homo sapiens (human) | 7515 | XRCC1 |
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| DOID:0060372 | Parkinson's disease 15 | HGNC:13586 | Homo sapiens (human) | 25793 | FBXO7 |
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| DOID:0060438 | Cole-Carpenter syndrome | HGNC:10706 | Homo sapiens (human) | 9871 | SEC24D |
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| DOID:0070065 | autosomal dominant intellectual developmental disorder 35 | HGNC:9312 | Homo sapiens (human) | 5528 | PPP2R5D |
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| DOID:1825 | childhood absence epilepsy | HGNC:4579 | Homo sapiens (human) | 2897 | GRIK1 |
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| DOID:824 | periodontitis | HGNC:2595 | Homo sapiens (human) | 1543 | CYP1A1 |
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| DOID:0070422 | syndromic X-linked intellectual disability Pilorge type | HGNC:4327 | Homo sapiens (human) | 2742 | GLRA2 |
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| DOID:0081330 | glycogen storage disease Ib | HGNC:4061 | Homo sapiens (human) | 2542 | SLC37A4 |
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| DOID:11123 | Henoch-Schoenlein purpura | HGNC:6000 | Homo sapiens (human) | 3557 | IL1RN |
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| DOID:0110264 | cataract 33 | HGNC:1040 | Homo sapiens (human) | 631 | BFSP1 |
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| DOID:0111839 | congenital disorder of glycosylation Icc | HGNC:28880 | Homo sapiens (human) | 84061 | MAGT1 |
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| DOID:635 | acquired immunodeficiency syndrome | HGNC:1641 | Homo sapiens (human) | 30835 | CD209 |
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| DOID:12894 | Sjogren's syndrome | HGNC:4942 | Homo sapiens (human) | 3117 | HLA-DQA1 |
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| DOID:5041 | esophageal cancer | HGNC:12828 | Homo sapiens (human) | 7515 | XRCC1 |
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| DOID:10871 | age related macular degeneration | HGNC:3602 | Homo sapiens (human) | 10516 | FBLN5 |
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| DOID:0080822 | aspirin-induced respiratory disease | HGNC:18274 | Homo sapiens (human) | 57105 | CYSLTR2 |
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| DOID:0070266 | congenital disorder of glycosylation type IIn | HGNC:20862 | Homo sapiens (human) | 64116 | SLC39A8 |
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| DOID:8552 | chronic myeloid leukemia | HGNC:12828 | Homo sapiens (human) | 7515 | XRCC1 |
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| DOID:0080059 | autosomal recessive spinocerebellar ataxia 7 | HGNC:2073 | Homo sapiens (human) | 1200 | TPP1 |
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