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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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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:2957 | pulmonary tuberculosis | HGNC:4180 | Homo sapiens (human) | 2632 | GBE1 |
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| DOID:2957 | pulmonary tuberculosis | HGNC:10609 | Homo sapiens (human) | 6346 | CCL1 |
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| DOID:4362 | cervical cancer | HGNC:4944 | Homo sapiens (human) | 3119 | HLA-DQB1 |
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| DOID:1324 | lung cancer | HGNC:4553 | Homo sapiens (human) | 2876 | GPX1 |
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| DOID:9538 | multiple myeloma | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:0111222 | centronuclear myopathy 5 | HGNC:16901 | Homo sapiens (human) | 10290 | SPEG |
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| DOID:0111234 | congenital muscular dystrophy-dystroglycanopathy A7 | HGNC:37276 | Homo sapiens (human) | 729920 | CRPPA |
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| DOID:2476 | hereditary spastic paraplegia | HGNC:5261 | Homo sapiens (human) | 3329 | HSPD1 |
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| DOID:0050545 | visceral heterotaxy | HGNC:7865 | Homo sapiens (human) | 4838 | NODAL |
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| DOID:0111069 | congenital bile acid synthesis defect 2 | HGNC:388 | Homo sapiens (human) | 6718 | AKR1D1 |
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| DOID:999 | hypereosinophilic syndrome | HGNC:3542 | Homo sapiens (human) | 2153 | F5 |
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| DOID:12297 | Vogt-Koyanagi-Harada disease | HGNC:4944 | Homo sapiens (human) | 3119 | HLA-DQB1 |
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| DOID:13241 | Behcet's disease | HGNC:11766 | Homo sapiens (human) | 7040 | TGFB1 |
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| DOID:0080652 | calcium oxalate nephrolithiasis | HGNC:6000 | Homo sapiens (human) | 3557 | IL1RN |
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| DOID:0111776 | 46,XY sex reversal 5 | HGNC:1552 | Homo sapiens (human) | 84733 | CBX2 |
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| DOID:9279 | hyperhomocysteinemia | HGNC:7468 | Homo sapiens (human) | 4548 | MTR |
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| DOID:0110801 | hereditary spastic paraplegia 49 | HGNC:19957 | Homo sapiens (human) | 9895 | TECPR2 |
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| DOID:0111354 | arthrogryposis, renal dysfunction, and cholestasis 2 | HGNC:20347 | Homo sapiens (human) | 63894 | VIPAS39 |
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| DOID:10534 | stomach cancer | HGNC:6190 | Homo sapiens (human) | 3716 | JAK1 |
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| DOID:2987 | familial mediterranean fever | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
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| DOID:9074 | systemic lupus erythematosus | HGNC:5962 | Homo sapiens (human) | 3586 | IL10 |
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| DOID:0050866 | oral squamous cell carcinoma | HGNC:12776 | Homo sapiens (human) | 7481 | WNT11 |
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| DOID:0050741 | alcohol dependence | HGNC:4093 | Homo sapiens (human) | 2572 | GAD2 |
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| DOID:3526 | cerebral infarction | HGNC:3788 | Homo sapiens (human) | 2346 | FOLH1 |
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| DOID:2799 | bronchiolitis obliterans | HGNC:5331 | Homo sapiens (human) | 64127 | NOD2 |
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