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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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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:0050588 | muscular dystrophy-dystroglycanopathy type B1 | WB:WBGene00011554 | Caenorhabditis elegans | 188207 | T07A5.1 |
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| DOID:0050559 | Fukuyama congenital muscular dystrophy | WB:WBGene00020307 | Caenorhabditis elegans | 173469 | T07D3.4 |
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| DOID:0050588 | muscular dystrophy-dystroglycanopathy type B1 | WB:WBGene00020307 | Caenorhabditis elegans | 173469 | T07D3.4 |
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| DOID:0110443 | dilated cardiomyopathy 1B | WB:WBGene00020307 | Caenorhabditis elegans | 173469 | T07D3.4 |
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| DOID:0110296 | autosomal recessive limb-girdle muscular dystrophy type 2M | WB:WBGene00020307 | Caenorhabditis elegans | 173469 | T07D3.4 |
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| DOID:9884 | muscular dystrophy | WB:WBGene00020307 | Caenorhabditis elegans | 173469 | T07D3.4 |
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| DOID:0110284 | autosomal recessive limb-girdle muscular dystrophy type 2L | WB:WBGene00020307 | Caenorhabditis elegans | 173469 | T07D3.4 |
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| DOID:0110444 | dilated cardiomyopathy 1X | WB:WBGene00020307 | Caenorhabditis elegans | 173469 | T07D3.4 |
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| DOID:0112379 | muscular dystrophy-dystroglycanopathy type B4 | WB:WBGene00020307 | Caenorhabditis elegans | 173469 | T07D3.4 |
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| DOID:0050560 | Walker-Warburg syndrome | WB:WBGene00020307 | Caenorhabditis elegans | 173469 | T07D3.4 |
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| DOID:2978 | carbohydrate metabolic disorder | SGD:S000004346 | Saccharomyces cerevisiae S288C | 851068 | TAL1 |
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| DOID:2978 | carbohydrate metabolic disorder | HGNC:11559 | Homo sapiens (human) | 6888 | TALDO1 |
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| DOID:10763 | hypertension | HGNC:11609 | Homo sapiens (human) | 6916 | TBXAS1 |
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| DOID:3526 | cerebral infarction | HGNC:11609 | Homo sapiens (human) | 6916 | TBXAS1 |
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| DOID:0060903 | thrombosis | HGNC:11609 | Homo sapiens (human) | 6916 | TBXAS1 |
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| DOID:0112251 | Ghosal hematodiaphyseal syndrome | HGNC:11609 | Homo sapiens (human) | 6916 | TBXAS1 |
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| DOID:3454 | brain infarction | HGNC:11609 | Homo sapiens (human) | 6916 | TBXAS1 |
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| DOID:10976 | membranous glomerulonephritis | HGNC:11609 | Homo sapiens (human) | 6916 | TBXAS1 |
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| DOID:11111 | hydronephrosis | HGNC:11609 | Homo sapiens (human) | 6916 | TBXAS1 |
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| DOID:0080998 | acute necrotizing pancreatitis | HGNC:11609 | Homo sapiens (human) | 6916 | TBXAS1 |
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| DOID:2349 | arteriosclerosis | HGNC:11609 | Homo sapiens (human) | 6916 | TBXAS1 |
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| DOID:9477 | pulmonary embolism | HGNC:11609 | Homo sapiens (human) | 6916 | TBXAS1 |
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| DOID:2921 | glomerulonephritis | HGNC:11609 | Homo sapiens (human) | 6916 | TBXAS1 |
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| DOID:1826 | epilepsy | SGD:S000003588 | Saccharomyces cerevisiae S288C | 853395 | TDH1 |
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| DOID:0050866 | oral squamous cell carcinoma | SGD:S000003588 | Saccharomyces cerevisiae S288C | 853395 | TDH1 |
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