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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:0050589 | inflammatory bowel disease | HGNC:3236 | Homo sapiens (human) | 1956 | EGFR |
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| DOID:0111261 | fumarase deficiency | HGNC:3700 | Homo sapiens (human) | 2271 | FH |
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| DOID:0112127 | HRPT-related hyperuricemia | HGNC:5157 | Homo sapiens (human) | 3251 | HPRT1 |
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| DOID:0080061 | autosomal recessive spinocerebellar ataxia 2 | HGNC:18667 | Homo sapiens (human) | 23203 | PMPCA |
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| DOID:12554 | hemolytic-uremic syndrome | HGNC:9040 | Homo sapiens (human) | 7941 | PLA2G7 |
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| DOID:12361 | Graves' disease | HGNC:1142 | Homo sapiens (human) | 56244 | BTNL2 |
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| DOID:0060224 | atrial fibrillation | HGNC:30689 | Homo sapiens (human) | 23066 | CAND2 |
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| DOID:8725 | vascular dementia | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:0081155 | common variable immunodeficiency 13 | HGNC:13176 | Homo sapiens (human) | 10320 | IKZF1 |
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| DOID:399 | tuberculosis | HGNC:7782 | Homo sapiens (human) | 4780 | NFE2L2 |
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| DOID:0070390 | developmental and epileptic encephalopathy 104 | HGNC:865 | Homo sapiens (human) | 535 | ATP6V0A1 |
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| DOID:4448 | macular degeneration | HGNC:1037 | Homo sapiens (human) | 629 | CFB |
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| DOID:2228 | thrombocytosis | HGNC:1455 | Homo sapiens (human) | 811 | CALR |
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| DOID:4450 | renal cell carcinoma | HGNC:6015 | Homo sapiens (human) | 3566 | IL4R |
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| DOID:0060010 | Omenn syndrome | HGNC:17642 | Homo sapiens (human) | 64421 | DCLRE1C |
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| DOID:2377 | multiple sclerosis | HGNC:16636 | Homo sapiens (human) | 23095 | KIF1B |
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| DOID:0110960 | Gaucher's disease perinatal lethal | HGNC:4177 | Homo sapiens (human) | 2629 | GBA1 |
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| DOID:12347 | osteogenesis imperfecta | HGNC:23697 | Homo sapiens (human) | 23187 | PHLDB1 |
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| DOID:0080766 | erythrokeratodermia variabilis et progressiva 6 | HGNC:17993 | Homo sapiens (human) | 54795 | TRPM4 |
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| DOID:9074 | systemic lupus erythematosus | HGNC:2336 | Homo sapiens (human) | 1380 | CR2 |
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| DOID:0050827 | rheumatic heart disease | HGNC:5962 | Homo sapiens (human) | 3586 | IL10 |
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| DOID:8924 | autoimmune thrombocytopenic purpura | HGNC:6000 | Homo sapiens (human) | 3557 | IL1RN |
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| DOID:0111127 | nephronophthisis 20 | HGNC:29536 | Homo sapiens (human) | 23005 | MAPKBP1 |
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| DOID:8577 | ulcerative colitis | HGNC:4944 | Homo sapiens (human) | 3119 | HLA-DQB1 |
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| DOID:12449 | aplastic anemia | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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