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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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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 | October 9, 2024 |
| Disease ID | Disease Name | Alliance of Genome Resources ID ▼ | Species | Gene ID | Gene Symbol | FlyGlycoDB | Evidence Code Names | References |
|---|---|---|---|---|---|---|---|---|
| DOID:3407 | carotid artery disease | HGNC:11766 | Homo sapiens (human) | 7040 | TGFB1 |
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| DOID:5082 | liver cirrhosis | HGNC:11766 | Homo sapiens (human) | 7040 | TGFB1 |
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| DOID:4947 | cholangiocarcinoma | HGNC:11766 | Homo sapiens (human) | 7040 | TGFB1 |
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| DOID:9538 | multiple myeloma | HGNC:11766 | Homo sapiens (human) | 7040 | TGFB1 |
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| DOID:3892 | insulinoma | HGNC:11766 | Homo sapiens (human) | 7040 | TGFB1 |
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| DOID:0050697 | chorioamnionitis | HGNC:11766 | Homo sapiens (human) | 7040 | TGFB1 |
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| DOID:2945 | severe acute respiratory syndrome | HGNC:11766 | Homo sapiens (human) | 7040 | TGFB1 |
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| DOID:585 | nephrolithiasis | HGNC:11766 | Homo sapiens (human) | 7040 | TGFB1 |
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| DOID:13141 | uveitis | HGNC:11766 | Homo sapiens (human) | 7040 | TGFB1 |
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| DOID:12449 | aplastic anemia | HGNC:11766 | Homo sapiens (human) | 7040 | TGFB1 |
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| DOID:3227 | tracheal stenosis | HGNC:11766 | Homo sapiens (human) | 7040 | TGFB1 |
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| DOID:9675 | pulmonary emphysema | HGNC:11766 | Homo sapiens (human) | 7040 | TGFB1 |
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| DOID:8866 | actinic keratosis | HGNC:11766 | Homo sapiens (human) | 7040 | TGFB1 |
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| DOID:6432 | pulmonary hypertension | HGNC:11766 | Homo sapiens (human) | 7040 | TGFB1 |
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| DOID:9256 | colorectal cancer | HGNC:11766 | Homo sapiens (human) | 7040 | TGFB1 |
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| DOID:13241 | Behcet's disease | HGNC:11766 | Homo sapiens (human) | 7040 | TGFB1 |
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| DOID:3021 | acute kidney failure | HGNC:11765 | Homo sapiens (human) | 7039 | TGFA |
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| DOID:684 | hepatocellular carcinoma | HGNC:11765 | Homo sapiens (human) | 7039 | TGFA |
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| DOID:1793 | pancreatic cancer | HGNC:11765 | Homo sapiens (human) | 7039 | TGFA |
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| DOID:4948 | gallbladder carcinoma | HGNC:11765 | Homo sapiens (human) | 7039 | TGFA |
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| DOID:3892 | insulinoma | HGNC:11765 | Homo sapiens (human) | 7039 | TGFA |
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| DOID:2326 | gastroenteritis | HGNC:11765 | Homo sapiens (human) | 7039 | TGFA |
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| DOID:0080208 | metabolic dysfunction-associated steatotic liver disease | HGNC:11764 | Homo sapiens (human) | 7038 | TG |
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| DOID:0060870 | isolated growth hormone deficiency | HGNC:11764 | Homo sapiens (human) | 7038 | TG |
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| DOID:0050328 | congenital hypothyroidism | HGNC:11764 | Homo sapiens (human) | 7038 | TG |
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