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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:10652 | Alzheimer's disease | HGNC:7734 | Homo sapiens (human) | 4741 | NEFM |
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| DOID:8947 | diabetic retinopathy | HGNC:603 | Homo sapiens (human) | 338 | APOB |
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| DOID:7941 | Barrett's adenocarcinoma | HGNC:4559 | Homo sapiens (human) | 2882 | GPX7 |
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| DOID:5844 | myocardial infarction | HGNC:6169 | Homo sapiens (human) | 3700 | ITIH4 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:5960 | Homo sapiens (human) | 3551 | IKBKB |
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| DOID:224 | transient cerebral ischemia | RGD:3249 | Rattus norvegicus (Norway rat) | 24617 | Serpine1 |
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| DOID:5844 | myocardial infarction | HGNC:2438 | Homo sapiens (human) | 1440 | CSF3 |
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| DOID:3454 | brain infarction | HGNC:4883 | Homo sapiens (human) | 3075 | CFH |
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| DOID:299 | adenocarcinoma | HGNC:30796 | Homo sapiens (human) | 11171 | STRAP |
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| DOID:9206 | Barrett's esophagus | HGNC:4555 | Homo sapiens (human) | 2878 | GPX3 |
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| DOID:1520 | colon carcinoma | HGNC:11913 | Homo sapiens (human) | 608 | TNFRSF17 |
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| DOID:8778 | Crohn's disease | HGNC:8104 | Homo sapiens (human) | 100506658 | OCLN |
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| DOID:865 | vasculitis | HGNC:1515 | Homo sapiens (human) | 831 | CAST |
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| DOID:526 | human immunodeficiency virus infectious disease | HGNC:6006 | Homo sapiens (human) | 50615 | IL21R |
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| DOID:12132 | granulomatosis with polyangiitis | HGNC:12724 | Homo sapiens (human) | 7448 | VTN |
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| DOID:0080855 | Parkinsonism | RGD:619858 | Rattus norvegicus (Norway rat) | 60590 | Grm8 |
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| DOID:9074 | systemic lupus erythematosus | HGNC:11157 | Homo sapiens (human) | 6631 | SNRPC |
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| DOID:1459 | hypothyroidism | RGD:2375 | Rattus norvegicus (Norway rat) | 25412 | Col2a1 |
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| DOID:9538 | multiple myeloma | HGNC:11763 | Homo sapiens (human) | 7037 | TFRC |
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| DOID:2377 | multiple sclerosis | HGNC:7197 | Homo sapiens (human) | 4340 | MOG |
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| DOID:3042 | allergic contact dermatitis | HGNC:5987 | Homo sapiens (human) | 10068 | IL18BP |
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| DOID:11832 | visual epilepsy | RGD:620486 | Rattus norvegicus (Norway rat) | 59323 | Erbb4 |
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| DOID:0050700 | cardiomyopathy | HGNC:6357 | Homo sapiens (human) | 3816 | KLK1 |
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| DOID:11054 | urinary bladder cancer | HGNC:11730 | Homo sapiens (human) | 7015 | TERT |
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| DOID:0050854 | Muckle-Wells syndrome | HGNC:6000 | Homo sapiens (human) | 3557 | IL1RN |
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