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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
LM-GlycoRepo
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:3454 | brain infarction | HGNC:11609 | Homo sapiens (human) | 6916 | TBXAS1 |
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| DOID:1588 | thrombocytopenia | HGNC:11608 | Homo sapiens (human) | 6915 | TBXA2R |
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| DOID:2841 | asthma | HGNC:11608 | Homo sapiens (human) | 6915 | TBXA2R |
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| DOID:1074 | kidney failure | HGNC:11608 | Homo sapiens (human) | 6915 | TBXA2R |
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| DOID:11394 | adult respiratory distress syndrome | HGNC:11608 | Homo sapiens (human) | 6915 | TBXA2R |
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| DOID:0080822 | aspirin-induced respiratory disease | HGNC:11608 | Homo sapiens (human) | 6915 | TBXA2R |
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| DOID:2218 | blood platelet disease | HGNC:11608 | Homo sapiens (human) | 6915 | TBXA2R |
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| DOID:14115 | toxic shock syndrome | HGNC:11608 | Homo sapiens (human) | 6915 | TBXA2R |
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| DOID:0060249 | scoliosis | HGNC:11605 | Homo sapiens (human) | 6911 | TBX6 |
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| DOID:0070515 | chromosome 16p11.2 deletion syndrome, 593-kb | HGNC:11605 | Homo sapiens (human) | 6911 | TBX6 |
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| DOID:0112363 | spondylocostal dysostosis 5 | HGNC:11605 | Homo sapiens (human) | 6911 | TBX6 |
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| DOID:684 | hepatocellular carcinoma | HGNC:11602 | Homo sapiens (human) | 6926 | TBX3 |
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| DOID:2394 | ovarian cancer | HGNC:11602 | Homo sapiens (human) | 6926 | TBX3 |
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| DOID:10534 | stomach cancer | HGNC:11602 | Homo sapiens (human) | 6926 | TBX3 |
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| DOID:5844 | myocardial infarction | HGNC:11602 | Homo sapiens (human) | 6926 | TBX3 |
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| DOID:0060614 | ulnar-mammary syndrome | HGNC:11602 | Homo sapiens (human) | 6926 | TBX3 |
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| DOID:9256 | colorectal cancer | HGNC:11602 | Homo sapiens (human) | 6926 | TBX3 |
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| DOID:162 | cancer | HGNC:11602 | Homo sapiens (human) | 6926 | TBX3 |
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| DOID:162 | cancer | HGNC:11597 | Homo sapiens (human) | 6909 | TBX2 |
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| DOID:0070345 | vertebral anomalies and variable endocrine and T-cell dysfunction | HGNC:11597 | Homo sapiens (human) | 6909 | TBX2 |
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| DOID:1882 | atrial heart septal defect | HGNC:11597 | Homo sapiens (human) | 6909 | TBX2 |
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| DOID:1681 | heart septal defect | HGNC:11597 | Homo sapiens (human) | 6909 | TBX2 |
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| DOID:0060041 | autism spectrum disorder | HGNC:11590 | Homo sapiens (human) | 10716 | TBR1 |
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| DOID:0060892 | late onset Parkinson's disease | HGNC:11588 | Homo sapiens (human) | 6908 | TBP |
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| DOID:0050967 | spinocerebellar ataxia type 17 | HGNC:11588 | Homo sapiens (human) | 6908 | TBP |
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