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GlyTouCan
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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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
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:13406 | pulmonary sarcoidosis | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:8677 | perinatal necrotizing enterocolitis | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:0060319 | cardiac arrest | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:614 | lymphopenia | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:0080208 | metabolic dysfunction-associated steatotic liver disease | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:10754 | otitis media | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:224 | transient cerebral ischemia | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:3310 | atopic dermatitis | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:11963 | esophagitis | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:12783 | migraine without aura | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:2355 | anemia | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:0060224 | atrial fibrillation | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:1073 | renal hypertension | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:3827 | congenital diaphragmatic hernia | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:633 | myositis | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:3770 | pulmonary fibrosis | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:0050700 | cardiomyopathy | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:12449 | aplastic anemia | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:11832 | visual epilepsy | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:13452 | scleritis | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:9884 | muscular dystrophy | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:2841 | asthma | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:850 | lung disease | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:10283 | prostate cancer | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:8515 | Cor pulmonale | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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