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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:0050600 | ABCD syndrome | HGNC:3180 | Homo sapiens (human) | 1910 | EDNRB |
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| DOID:8923 | skin melanoma | HGNC:13723 | Homo sapiens (human) | 10664 | CTCF |
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| DOID:9432 | renal glycosuria | HGNC:11037 | Homo sapiens (human) | 6524 | SLC5A2 |
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| DOID:2236 | congenital afibrinogenemia | HGNC:3662 | Homo sapiens (human) | 2244 | FGB |
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| DOID:0060652 | familial erythrocytosis 1 | HGNC:3416 | Homo sapiens (human) | 2057 | EPOR |
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| DOID:0070054 | Vulto-van Silfout-de Vries syndrome | HGNC:14677 | Homo sapiens (human) | 10522 | DEAF1 |
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| DOID:0050700 | cardiomyopathy | HGNC:6207 | Homo sapiens (human) | 3728 | JUP |
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| DOID:0050745 | diffuse large B-cell lymphoma | HGNC:11919 | Homo sapiens (human) | 958 | CD40 |
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| DOID:10763 | hypertension | HGNC:5208 | Homo sapiens (human) | 3290 | HSD11B1 |
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| DOID:4362 | cervical cancer | HGNC:43 | Homo sapiens (human) | 6890 | TAP1 |
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| DOID:0080726 | Ehlers-Danlos syndrome classic type 2 | HGNC:2210 | Homo sapiens (human) | 1290 | COL5A2 |
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| DOID:0060577 | 3MC syndrome 3 | HGNC:2220 | Homo sapiens (human) | 10584 | COLEC10 |
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| DOID:0111976 | immunodeficiency 9 | HGNC:25896 | Homo sapiens (human) | 84876 | ORAI1 |
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| DOID:526 | human immunodeficiency virus infectious disease | HGNC:4942 | Homo sapiens (human) | 3117 | HLA-DQA1 |
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| DOID:0080922 | bilateral frontoparietal polymicrogyria | HGNC:4512 | Homo sapiens (human) | 9289 | ADGRG1 |
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| DOID:1389 | polyneuropathy | HGNC:4948 | Homo sapiens (human) | 3123 | HLA-DRB1 |
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| DOID:0080846 | latent autoimmune diabetes in adults | HGNC:2505 | Homo sapiens (human) | 1493 | CTLA4 |
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| DOID:0050633 | ocular albinism 1 | HGNC:12442 | Homo sapiens (human) | 7299 | TYR |
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| DOID:2741 | bilirubin metabolic disorder | HGNC:11180 | Homo sapiens (human) | 6648 | SOD2 |
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| DOID:10283 | prostate cancer | HGNC:2595 | Homo sapiens (human) | 1543 | CYP1A1 |
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| DOID:1612 | breast cancer | HGNC:5331 | Homo sapiens (human) | 64127 | NOD2 |
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| DOID:0111903 | thrombophilia due to HRG deficiency | HGNC:5181 | Homo sapiens (human) | 3273 | HRG |
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| DOID:11569 | neurocirculatory asthenia | HGNC:11048 | Homo sapiens (human) | 6530 | SLC6A2 |
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| DOID:3393 | coronary artery disease | HGNC:6547 | Homo sapiens (human) | 3949 | LDLR |
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| DOID:10126 | keratoconus | HGNC:5991 | Homo sapiens (human) | 3552 | IL1A |
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