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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
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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 | July 29, 2024 |
| Disease ID | Disease Name | Alliance of Genome Resources ID | Species | Gene ID | Gene Symbol ▲ | FlyGlycoDB | Evidence Code Names | References |
|---|---|---|---|---|---|---|---|---|
| DOID:9253 | gastrointestinal stromal tumor | HGNC:10681 | Homo sapiens (human) | 6390 | SDHB |
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| DOID:9253 | gastrointestinal stromal tumor | HGNC:10682 | Homo sapiens (human) | 6391 | SDHC |
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| DOID:3652 | Leigh disease | HGNC:10682 | Homo sapiens (human) | 6391 | SDHC |
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| DOID:0050773 | paraganglioma | HGNC:10682 | Homo sapiens (human) | 6391 | SDHC |
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| DOID:0080533 | Carney-Stratakis syndrome | HGNC:10682 | Homo sapiens (human) | 6391 | SDHC |
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| DOID:3908 | lung non-small cell carcinoma | HGNC:10682 | Homo sapiens (human) | 6391 | SDHC |
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| DOID:0080533 | Carney-Stratakis syndrome | HGNC:10683 | Homo sapiens (human) | 6392 | SDHD |
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| DOID:0050773 | paraganglioma | HGNC:10683 | Homo sapiens (human) | 6392 | SDHD |
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| DOID:11984 | hypertrophic cardiomyopathy | HGNC:10683 | Homo sapiens (human) | 6392 | SDHD |
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| DOID:0060537 | mitochondrial complex II deficiency | HGNC:10683 | Homo sapiens (human) | 6392 | SDHD |
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| DOID:0050570 | congenital disorder of glycosylation type I | SGD:S000001849 | Saccharomyces cerevisiae S288C | 850499 | SEC53 |
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| DOID:5212 | congenital disorder of glycosylation | SGD:S000001849 | Saccharomyces cerevisiae S288C | 850499 | SEC53 |
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| DOID:0080552 | congenital disorder of glycosylation Ia | SGD:S000001849 | Saccharomyces cerevisiae S288C | 850499 | SEC53 |
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| DOID:2316 | brain ischemia | HGNC:10718 | Homo sapiens (human) | 6401 | SELE |
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| DOID:6713 | cerebrovascular disease | HGNC:10718 | Homo sapiens (human) | 6401 | SELE |
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| DOID:9744 | type 1 diabetes mellitus | HGNC:10718 | Homo sapiens (human) | 6401 | SELE |
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| DOID:0080600 | COVID-19 | HGNC:10718 | Homo sapiens (human) | 6401 | SELE |
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| DOID:3393 | coronary artery disease | HGNC:10718 | Homo sapiens (human) | 6401 | SELE |
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| DOID:2986 | IgA glomerulonephritis | HGNC:10718 | Homo sapiens (human) | 6401 | SELE |
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| DOID:8481 | rheumatic myocarditis | HGNC:10718 | Homo sapiens (human) | 6401 | SELE |
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| DOID:0112349 | hereditary spastic paraplegia 81 | HGNC:29361 | Homo sapiens (human) | 85465 | SELENOI |
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| DOID:341 | peripheral vascular disease | HGNC:10720 | Homo sapiens (human) | 6402 | SELL |
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| DOID:2986 | IgA glomerulonephritis | HGNC:10720 | Homo sapiens (human) | 6402 | SELL |
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| DOID:8778 | Crohn's disease | HGNC:10720 | Homo sapiens (human) | 6402 | SELL |
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| DOID:14115 | toxic shock syndrome | HGNC:10720 | Homo sapiens (human) | 6402 | SELL |
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