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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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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:9884 | muscular dystrophy | RGD:1586427 | Rattus norvegicus (Norway rat) | 688673 | Pomt2 |
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| DOID:0112380 | muscular dystrophy-dystroglycanopathy type B2 | RGD:1586427 | Rattus norvegicus (Norway rat) | 688673 | Pomt2 |
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| DOID:2978 | carbohydrate metabolic disorder | HGNC:11559 | Homo sapiens (human) | 6888 | TALDO1 |
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| DOID:5082 | liver cirrhosis | MGI:1916211 | Mus musculus (house mouse) | 68961 | Phkg2 |
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| DOID:2747 | glycogen storage disease | MGI:1916211 | Mus musculus (house mouse) | 68961 | Phkg2 |
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| DOID:0111043 | glycogen storage disease IXc | MGI:1916211 | Mus musculus (house mouse) | 68961 | Phkg2 |
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| DOID:0080201 | Peters plus syndrome | RGD:1588723 | Rattus norvegicus (Norway rat) | 689765 | B3glct |
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| DOID:3070 | high grade glioma | HGNC:2172 | Homo sapiens (human) | 6900 | CNTN2 |
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| DOID:850 | lung disease | HGNC:2172 | Homo sapiens (human) | 6900 | CNTN2 |
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| DOID:0111691 | familial adult myoclonic epilepsy 5 | HGNC:2172 | Homo sapiens (human) | 6900 | CNTN2 |
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| DOID:1287 | cardiovascular system disease | RGD:1589798 | Rattus norvegicus (Norway rat) | 690987 | Gys1 |
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| DOID:3534 | Lafora disease | RGD:1589798 | Rattus norvegicus (Norway rat) | 690987 | Gys1 |
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| DOID:0080736 | Ehlers-Danlos syndrome musculocontractural type 1 | RGD:1585023 | Rattus norvegicus (Norway rat) | 691394 | Chst14 |
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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:0110544 | autosomal dominant nonsyndromic deafness 12 | HGNC:11720 | Homo sapiens (human) | 7007 | TECTA |
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