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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:10652 | Alzheimer's disease | HGNC:13312 | Homo sapiens (human) | 9446 | GSTO1 |
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| DOID:10652 | Alzheimer's disease | HGNC:23064 | Homo sapiens (human) | 119391 | GSTO2 |
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| DOID:14330 | Parkinson's disease | HGNC:23064 | Homo sapiens (human) | 119391 | GSTO2 |
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| DOID:14330 | Parkinson's disease | HGNC:13312 | Homo sapiens (human) | 9446 | GSTO1 |
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| DOID:5844 | myocardial infarction | HGNC:4553 | Homo sapiens (human) | 2876 | GPX1 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:11850 | Homo sapiens (human) | 7099 | TLR4 |
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| DOID:161 | keratosis | HGNC:1516 | Homo sapiens (human) | 847 | CAT |
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| DOID:1485 | cystic fibrosis | HGNC:2595 | Homo sapiens (human) | 1543 | CYP1A1 |
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| DOID:6132 | bronchitis | HGNC:2595 | Homo sapiens (human) | 1543 | CYP1A1 |
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| DOID:14566 | disease of cellular proliferation | HGNC:9053 | Homo sapiens (human) | 5329 | PLAUR |
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| DOID:224 | transient cerebral ischemia | RGD:621168 | Rattus norvegicus (Norway rat) | 81528 | Ogg1 |
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| DOID:2355 | anemia | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:9120 | amyloidosis | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:557 | kidney disease | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:8398 | osteoarthritis | HGNC:6553 | Homo sapiens (human) | 3952 | LEP |
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| DOID:7998 | hyperthyroidism | RGD:3935 | Rattus norvegicus (Norway rat) | 24861 | Ugt1a1 |
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| DOID:12849 | autistic disorder | HGNC:8978 | Homo sapiens (human) | 5294 | PIK3CG |
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| DOID:0050848 | obstructive sleep apnea | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:2237 | hepatitis | RGD:621168 | Rattus norvegicus (Norway rat) | 81528 | Ogg1 |
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| DOID:13406 | pulmonary sarcoidosis | HGNC:5988 | Homo sapiens (human) | 8809 | IL18R1 |
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| DOID:2352 | hemochromatosis | HGNC:4887 | Homo sapiens (human) | 148738 | HJV |
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| DOID:4450 | renal cell carcinoma | HGNC:429 | Homo sapiens (human) | 239 | ALOX12 |
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| DOID:0110429 | dilated cardiomyopathy 1H | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:6196 | reactive arthritis | HGNC:2595 | Homo sapiens (human) | 1543 | CYP1A1 |
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| DOID:3213 | demyelinating disease | HGNC:9605 | Homo sapiens (human) | 5743 | PTGS2 |
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