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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:8398 | osteoarthritis | HGNC:14899 | Homo sapiens (human) | 140766 | ADAMTS14 |
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| DOID:0110971 | brachydactyly type D | HGNC:5136 | Homo sapiens (human) | 3239 | HOXD13 |
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| DOID:3526 | cerebral infarction | HGNC:11784 | Homo sapiens (human) | 7056 | THBD |
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| DOID:8947 | diabetic retinopathy | HGNC:12762 | Homo sapiens (human) | 7466 | WFS1 |
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| DOID:0111907 | thrombophilia due to thrombin defect | HGNC:4798 | Homo sapiens (human) | 3026 | HABP2 |
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| DOID:1115 | sarcoma | HGNC:11290 | Homo sapiens (human) | 6721 | SREBF2 |
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| DOID:0111917 | spermatogenic failure 43 | HGNC:26293 | Homo sapiens (human) | 79925 | SPEF2 |
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| DOID:1682 | congenital heart disease | HGNC:4214 | Homo sapiens (human) | 2657 | GDF1 |
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| DOID:0111502 | combined oxidative phosphorylation deficiency 6 | HGNC:8768 | Homo sapiens (human) | 9131 | AIFM1 |
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| DOID:0110014 | age related macular degeneration 1 | HGNC:16980 | Homo sapiens (human) | 10878 | CFHR3 |
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| DOID:9261 | nasopharynx carcinoma | HGNC:2631 | Homo sapiens (human) | 1571 | CYP2E1 |
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| DOID:5517 | stomach carcinoma | HGNC:7230 | Homo sapiens (human) | 4361 | MRE11 |
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| DOID:0081120 | Graves ophthalmopathy | HGNC:19100 | Homo sapiens (human) | 149233 | IL23R |
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| DOID:5419 | schizophrenia | HGNC:13759 | Homo sapiens (human) | 23191 | CYFIP1 |
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| DOID:2018 | hyperinsulinism | HGNC:333 | Homo sapiens (human) | 183 | AGT |
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| DOID:10140 | dry eye syndrome | HGNC:6018 | Homo sapiens (human) | 3569 | IL6 |
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| DOID:0111883 | Diamond-Blackfan anemia 5 | HGNC:10345 | Homo sapiens (human) | 6165 | RPL35A |
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| DOID:234 | colon adenocarcinoma | HGNC:11366 | Homo sapiens (human) | 6776 | STAT5A |
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| DOID:2938 | Epstein-Barr virus infectious disease | HGNC:3689 | Homo sapiens (human) | 2263 | FGFR2 |
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| DOID:0110663 | congenital myasthenic syndrome 1A | HGNC:1955 | Homo sapiens (human) | 1134 | CHRNA1 |
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| DOID:1380 | endometrial cancer | HGNC:7230 | Homo sapiens (human) | 4361 | MRE11 |
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| DOID:3910 | lung adenocarcinoma | HGNC:3229 | Homo sapiens (human) | 1950 | EGF |
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| DOID:0111730 | familial episodic pain syndrome 2 | HGNC:10582 | Homo sapiens (human) | 6336 | SCN10A |
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| DOID:1749 | squamous cell carcinoma | HGNC:8101 | Homo sapiens (human) | 4948 | OCA2 |
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| DOID:0070123 | congenital nongoitrous hypothyroidism 4 | HGNC:12372 | Homo sapiens (human) | 7252 | TSHB |
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