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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:14330 | Parkinson's disease | HGNC:23064 | Homo sapiens (human) | 119391 | GSTO2 |
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| DOID:10534 | stomach cancer | HGNC:6848 | Homo sapiens (human) | 4214 | MAP3K1 |
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| DOID:13714 | anodontia | HGNC:4319 | Homo sapiens (human) | 2737 | GLI3 |
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| DOID:11054 | urinary bladder cancer | HGNC:6027 | Homo sapiens (human) | 3579 | CXCR2 |
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| DOID:0111162 | epidermal nevus | HGNC:8975 | Homo sapiens (human) | 5290 | PIK3CA |
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| DOID:1574 | alcohol use disorder | HGNC:11813 | Homo sapiens (human) | 8914 | TIMELESS |
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| DOID:0111004 | Joubert syndrome 9 | HGNC:29253 | Homo sapiens (human) | 57545 | CC2D2A |
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| DOID:0110110 | atrial heart septal defect 5 | HGNC:143 | Homo sapiens (human) | 70 | ACTC1 |
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| DOID:1070 | primary open angle glaucoma | HGNC:30696 | Homo sapiens (human) | 134430 | WDR36 |
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| DOID:3407 | carotid artery disease | HGNC:4886 | Homo sapiens (human) | 3077 | HFE |
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| DOID:3083 | chronic obstructive pulmonary disease | HGNC:2631 | Homo sapiens (human) | 1571 | CYP2E1 |
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| DOID:14400 | capillary leak syndrome | HGNC:9204 | Homo sapiens (human) | 5444 | PON1 |
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| DOID:12930 | dilated cardiomyopathy | HGNC:12949 | Homo sapiens (human) | 7716 | VEZF1 |
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| DOID:13406 | pulmonary sarcoidosis | HGNC:1884 | Homo sapiens (human) | 1080 | CFTR |
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| DOID:0111982 | immunodeficiency 56 | HGNC:6006 | Homo sapiens (human) | 50615 | IL21R |
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| DOID:3393 | coronary artery disease | HGNC:9205 | Homo sapiens (human) | 5445 | PON2 |
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| DOID:0050012 | chikungunya | HGNC:4944 | Homo sapiens (human) | 3119 | HLA-DQB1 |
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| DOID:0050827 | rheumatic heart disease | HGNC:4942 | Homo sapiens (human) | 3117 | HLA-DQA1 |
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| DOID:11832 | visual epilepsy | HGNC:20499 | Homo sapiens (human) | 79944 | L2HGDH |
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| DOID:0090070 | hypogonadotropic hypogonadism | HGNC:26256 | Homo sapiens (human) | 79625 | NDNF |
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| DOID:14004 | thoracic aortic aneurysm | HGNC:9414 | Homo sapiens (human) | 5592 | PRKG1 |
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| DOID:10652 | Alzheimer's disease | HGNC:277 | Homo sapiens (human) | 148 | ADRA1A |
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| DOID:670 | amphetamine abuse | HGNC:2228 | Homo sapiens (human) | 1312 | COMT |
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| DOID:0080413 | developmental and epileptic encephalopathy 18 | HGNC:29040 | Homo sapiens (human) | 23334 | SZT2 |
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| DOID:3652 | Leigh disease | HGNC:15714 | Homo sapiens (human) | 10128 | LRPPRC |
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