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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:26 | pancreas disease | HGNC:7371 | Homo sapiens (human) | 10232 | MSLN |
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| DOID:2394 | ovarian cancer | HGNC:7371 | Homo sapiens (human) | 10232 | MSLN |
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| DOID:3587 | pancreatic ductal carcinoma | HGNC:7371 | Homo sapiens (human) | 10232 | MSLN |
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| DOID:1793 | pancreatic cancer | HGNC:7371 | Homo sapiens (human) | 10232 | MSLN |
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| DOID:4897 | bile duct carcinoma | HGNC:7371 | Homo sapiens (human) | 10232 | MSLN |
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| DOID:0050570 | congenital disorder of glycosylation type I | HGNC:7216 | Homo sapiens (human) | 4351 | MPI |
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| DOID:0080554 | congenital disorder of glycosylation Ib | HGNC:7216 | Homo sapiens (human) | 4351 | MPI |
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| DOID:2978 | carbohydrate metabolic disorder | HGNC:7216 | Homo sapiens (human) | 4351 | MPI |
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| DOID:0080558 | congenital disorder of glycosylation If | HGNC:7207 | Homo sapiens (human) | 9526 | MPDU1 |
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| DOID:0070254 | congenital disorder of glycosylation type IIb | HGNC:24862 | Homo sapiens (human) | 7841 | MOGS |
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| DOID:0081097 | Rafiq syndrome | SGD:S000003892 | Saccharomyces cerevisiae S288C | 853595 | MNS1 |
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| DOID:1485 | cystic fibrosis | SGD:S000001247 | Saccharomyces cerevisiae S288C | 856611 | MNL1 |
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| DOID:0060740 | methylmalonic aciduria due to methylmalonyl-CoA mutase deficiency | HGNC:7526 | Homo sapiens (human) | 4594 | MMUT |
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| DOID:14749 | methylmalonic acidemia | HGNC:7526 | Homo sapiens (human) | 4594 | MMUT |
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| DOID:0080208 | metabolic dysfunction-associated steatotic liver disease | HGNC:7150 | Homo sapiens (human) | 23417 | MLYCD |
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| DOID:0050700 | cardiomyopathy | HGNC:7150 | Homo sapiens (human) | 23417 | MLYCD |
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| DOID:0112333 | pontocerebellar hypoplasia type 16 | HGNC:7102 | Homo sapiens (human) | 9562 | MINPP1 |
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| DOID:3969 | thyroid gland papillary carcinoma | HGNC:7102 | Homo sapiens (human) | 9562 | MINPP1 |
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| DOID:576 | proteinuria | HGNC:7049 | Homo sapiens (human) | 4249 | MGAT5 |
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| DOID:1793 | pancreatic cancer | HGNC:7047 | Homo sapiens (human) | 11320 | MGAT4A |
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| DOID:0070253 | congenital disorder of glycosylation type IIa | HGNC:7045 | Homo sapiens (human) | 4247 | MGAT2 |
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| DOID:1793 | pancreatic cancer | SGD:S000004007 | Saccharomyces cerevisiae S288C | 850704 | MEU1 |
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| DOID:4608 | common bile duct neoplasm | SGD:S000004007 | Saccharomyces cerevisiae S288C | 850704 | MEU1 |
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| DOID:0080664 | diaphyseal medullary stenosis with malignant fibrous histiocytoma | SGD:S000004007 | Saccharomyces cerevisiae S288C | 850704 | MEU1 |
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| DOID:0050625 | biliary tract benign neoplasm | SGD:S000004007 | Saccharomyces cerevisiae S288C | 850704 | MEU1 |
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