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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:1612 | breast cancer | HGNC:11766 | Homo sapiens (human) | 7040 | TGFB1 |
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| DOID:9351 | diabetes mellitus | HGNC:11766 | Homo sapiens (human) | 7040 | TGFB1 |
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| DOID:1793 | pancreatic cancer | HGNC:11766 | Homo sapiens (human) | 7040 | TGFB1 |
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| DOID:8893 | psoriasis | HGNC:11766 | Homo sapiens (human) | 7040 | TGFB1 |
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| DOID:4450 | renal cell carcinoma | HGNC:11766 | Homo sapiens (human) | 7040 | TGFB1 |
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| DOID:5773 | oral submucous fibrosis | HGNC:11766 | Homo sapiens (human) | 7040 | TGFB1 |
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| DOID:13406 | pulmonary sarcoidosis | HGNC:11766 | Homo sapiens (human) | 7040 | TGFB1 |
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| DOID:4997 | Camurati-Engelmann disease | HGNC:11766 | Homo sapiens (human) | 7040 | TGFB1 |
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| DOID:12894 | Sjogren's syndrome | HGNC:11766 | Homo sapiens (human) | 7040 | TGFB1 |
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| DOID:234 | colon adenocarcinoma | HGNC:11766 | Homo sapiens (human) | 7040 | TGFB1 |
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| DOID:1168 | familial hyperlipidemia | HGNC:11766 | Homo sapiens (human) | 7040 | TGFB1 |
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| DOID:5844 | myocardial infarction | HGNC:11766 | Homo sapiens (human) | 7040 | TGFB1 |
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| DOID:8472 | localized scleroderma | HGNC:11766 | Homo sapiens (human) | 7040 | TGFB1 |
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| DOID:2256 | osteochondrodysplasia | HGNC:11766 | Homo sapiens (human) | 7040 | TGFB1 |
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| DOID:1270 | hereditary hemorrhagic telangiectasia | HGNC:11766 | Homo sapiens (human) | 7040 | TGFB1 |
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| DOID:10923 | sickle cell anemia | HGNC:11766 | Homo sapiens (human) | 7040 | TGFB1 |
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| DOID:1875 | impotence | HGNC:11766 | Homo sapiens (human) | 7040 | TGFB1 |
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| DOID:12134 | factor VIII deficiency | HGNC:11766 | Homo sapiens (human) | 7040 | TGFB1 |
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| DOID:0050589 | inflammatory bowel disease | HGNC:11766 | Homo sapiens (human) | 7040 | TGFB1 |
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| DOID:8924 | autoimmune thrombocytopenic purpura | HGNC:11766 | Homo sapiens (human) | 7040 | TGFB1 |
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| DOID:0081292 | traumatic brain injury | HGNC:11766 | Homo sapiens (human) | 7040 | TGFB1 |
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| DOID:13608 | biliary atresia | HGNC:11766 | Homo sapiens (human) | 7040 | TGFB1 |
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| DOID:1520 | colon carcinoma | HGNC:11766 | Homo sapiens (human) | 7040 | TGFB1 |
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| DOID:114 | heart disease | HGNC:11766 | Homo sapiens (human) | 7040 | TGFB1 |
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| DOID:4483 | rhinitis | HGNC:11766 | Homo sapiens (human) | 7040 | TGFB1 |
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