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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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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 | July 29, 2024 |
| Disease ID | Disease Name | Alliance of Genome Resources ID | Species | Gene ID | Gene Symbol | FlyGlycoDB | Evidence Code Names ▼ | References |
|---|---|---|---|---|---|---|---|---|
| DOID:5419 | schizophrenia | HGNC:6470 | Homo sapiens (human) | 3897 | L1CAM |
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| DOID:1588 | thrombocytopenia | HGNC:6922 | Homo sapiens (human) | 4153 | MBL2 |
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| DOID:3146 | lipid metabolism disorder | HGNC:2330 | Homo sapiens (human) | 1376 | CPT2 |
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| DOID:1612 | breast cancer | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
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| DOID:3393 | coronary artery disease | HGNC:11998 | Homo sapiens (human) | 7157 | TP53 |
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| DOID:3649 | pyruvate decarboxylase deficiency | HGNC:21350 | Homo sapiens (human) | 8050 | PDHX |
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| DOID:6364 | migraine | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:0060448 | Fleck corneal dystrophy | HGNC:23785 | Homo sapiens (human) | 200576 | PIKFYVE |
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| DOID:2349 | arteriosclerosis | HGNC:435 | Homo sapiens (human) | 240 | ALOX5 |
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| DOID:13544 | low tension glaucoma | HGNC:11998 | Homo sapiens (human) | 7157 | TP53 |
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| DOID:1825 | childhood absence epilepsy | HGNC:11005 | Homo sapiens (human) | 6513 | SLC2A1 |
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| DOID:10892 | hypospadias | HGNC:11285 | Homo sapiens (human) | 6716 | SRD5A2 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:404 | Homo sapiens (human) | 217 | ALDH2 |
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| DOID:5844 | myocardial infarction | HGNC:6623 | Homo sapiens (human) | 9388 | LIPG |
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| DOID:12849 | autistic disorder | HGNC:8978 | Homo sapiens (human) | 5294 | PIK3CG |
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| DOID:9970 | obesity | HGNC:6922 | Homo sapiens (human) | 4153 | MBL2 |
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| DOID:10923 | sickle cell anemia | HGNC:2621 | Homo sapiens (human) | 1557 | CYP2C19 |
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| DOID:8778 | Crohn's disease | HGNC:5344 | Homo sapiens (human) | 3383 | ICAM1 |
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| DOID:2738 | pseudoxanthoma elasticum | HGNC:15517 | Homo sapiens (human) | 64132 | XYLT2 |
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| DOID:552 | pneumonia | HGNC:2631 | Homo sapiens (human) | 1571 | CYP2E1 |
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| DOID:2747 | glycogen storage disease | HGNC:9725 | Homo sapiens (human) | 5836 | PYGL |
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| DOID:3393 | coronary artery disease | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:1612 | breast cancer | HGNC:11850 | Homo sapiens (human) | 7099 | TLR4 |
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| DOID:0111582 | hereditary arterial and articular multiple calcification syndrome | HGNC:8021 | Homo sapiens (human) | 4907 | NT5E |
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| DOID:6543 | acne | HGNC:11850 | Homo sapiens (human) | 7099 | TLR4 |
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