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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:3652 | Leigh disease | HGNC:10682 | Homo sapiens (human) | 6391 | SDHC |
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| DOID:9408 | acute myocardial infarction | HGNC:10681 | Homo sapiens (human) | 6390 | SDHB |
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| DOID:0050773 | paraganglioma | HGNC:10681 | Homo sapiens (human) | 6390 | SDHB |
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| DOID:890 | mitochondrial encephalomyopathy | HGNC:10681 | Homo sapiens (human) | 6390 | SDHB |
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| DOID:0080533 | Carney-Stratakis syndrome | HGNC:10681 | Homo sapiens (human) | 6390 | SDHB |
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| DOID:0050771 | pheochromocytoma | HGNC:10681 | Homo sapiens (human) | 6390 | SDHB |
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| DOID:9253 | gastrointestinal stromal tumor | HGNC:10681 | Homo sapiens (human) | 6390 | SDHB |
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| DOID:0060537 | mitochondrial complex II deficiency | HGNC:10681 | Homo sapiens (human) | 6390 | SDHB |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:10681 | Homo sapiens (human) | 6390 | SDHB |
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| DOID:1289 | neurodegenerative disease | HGNC:10680 | Homo sapiens (human) | 6389 | SDHA |
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| DOID:0050771 | pheochromocytoma | HGNC:10680 | Homo sapiens (human) | 6389 | SDHA |
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| DOID:14330 | Parkinson's disease | HGNC:10680 | Homo sapiens (human) | 6389 | SDHA |
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| DOID:10579 | leukodystrophy | HGNC:10680 | Homo sapiens (human) | 6389 | SDHA |
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| DOID:9253 | gastrointestinal stromal tumor | HGNC:10680 | Homo sapiens (human) | 6389 | SDHA |
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| DOID:0050700 | cardiomyopathy | HGNC:10680 | Homo sapiens (human) | 6389 | SDHA |
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| DOID:3652 | Leigh disease | HGNC:10680 | Homo sapiens (human) | 6389 | SDHA |
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| DOID:0050773 | paraganglioma | HGNC:10680 | Homo sapiens (human) | 6389 | SDHA |
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| DOID:3829 | pituitary adenoma | HGNC:10680 | Homo sapiens (human) | 6389 | SDHA |
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| DOID:0060537 | mitochondrial complex II deficiency | HGNC:10680 | Homo sapiens (human) | 6389 | SDHA |
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| DOID:0110435 | dilated cardiomyopathy 1GG | HGNC:10680 | Homo sapiens (human) | 6389 | SDHA |
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| DOID:3908 | lung non-small cell carcinoma | HGNC:10680 | Homo sapiens (human) | 6389 | SDHA |
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| DOID:5426 | primary ovarian insufficiency | HGNC:1068 | Homo sapiens (human) | 9210 | BMP15 |
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| DOID:0080494 | ovarian dysgenesis 2 | HGNC:1068 | Homo sapiens (human) | 9210 | BMP15 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:10676 | Homo sapiens (human) | 23753 | SDF2L1 |
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| DOID:12347 | osteogenesis imperfecta | HGNC:1067 | Homo sapiens (human) | 649 | BMP1 |
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