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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:3525 | middle cerebral artery infarction | HGNC:30092 | Homo sapiens (human) | 10135 | NAMPT |
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| DOID:0080208 | metabolic dysfunction-associated steatotic liver disease | HGNC:30092 | Homo sapiens (human) | 10135 | NAMPT |
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| DOID:6432 | pulmonary hypertension | HGNC:30092 | Homo sapiens (human) | 10135 | NAMPT |
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| DOID:224 | transient cerebral ischemia | HGNC:30092 | Homo sapiens (human) | 10135 | NAMPT |
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| DOID:9970 | obesity | HGNC:30092 | Homo sapiens (human) | 10135 | NAMPT |
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| DOID:824 | periodontitis | HGNC:30092 | Homo sapiens (human) | 10135 | NAMPT |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:30092 | Homo sapiens (human) | 10135 | NAMPT |
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| DOID:0060227 | Adams-Oliver syndrome | MGI:2141669 | Mus musculus (house mouse) | 101351 | Eogt |
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| DOID:10763 | hypertension | HGNC:18305 | Homo sapiens (human) | 10159 | ATP6AP2 |
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| DOID:0112105 | X-linked parkinsonism-spasticity syndrome | HGNC:18305 | Homo sapiens (human) | 10159 | ATP6AP2 |
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| DOID:0060309 | syndromic X-linked intellectual disability | HGNC:18305 | Homo sapiens (human) | 10159 | ATP6AP2 |
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| DOID:0060806 | syndromic X-linked intellectual disability Hedera type | HGNC:18305 | Homo sapiens (human) | 10159 | ATP6AP2 |
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| DOID:0050571 | congenital disorder of glycosylation type II | HGNC:18305 | Homo sapiens (human) | 10159 | ATP6AP2 |
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| DOID:5212 | congenital disorder of glycosylation | HGNC:18305 | Homo sapiens (human) | 10159 | ATP6AP2 |
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| DOID:0070341 | neonatal-onset type II citrullinemia | HGNC:10983 | Homo sapiens (human) | 10165 | SLC25A13 |
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| DOID:9273 | citrullinemia | HGNC:10983 | Homo sapiens (human) | 10165 | SLC25A13 |
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| DOID:4137 | common bile duct disease | HGNC:10983 | Homo sapiens (human) | 10165 | SLC25A13 |
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| DOID:0070342 | adult-onset type II citrullinemia | HGNC:10983 | Homo sapiens (human) | 10165 | SLC25A13 |
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| DOID:1852 | intrahepatic cholestasis | HGNC:10983 | Homo sapiens (human) | 10165 | SLC25A13 |
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| DOID:0050588 | muscular dystrophy-dystroglycanopathy type B1 | ZFIN:ZDB-GENE-121001-5 | Danio rerio (zebrafish) | 101669768 | b4gat1 |
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| DOID:0050560 | Walker-Warburg syndrome | ZFIN:ZDB-GENE-121001-5 | Danio rerio (zebrafish) | 101669768 | b4gat1 |
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| DOID:0111238 | congenital muscular dystrophy-dystroglycanopathy type A13 | ZFIN:ZDB-GENE-121001-5 | Danio rerio (zebrafish) | 101669768 | b4gat1 |
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| DOID:5212 | congenital disorder of glycosylation | HGNC:23056 | Homo sapiens (human) | 10195 | ALG3 |
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| DOID:0080556 | congenital disorder of glycosylation Id | HGNC:23056 | Homo sapiens (human) | 10195 | ALG3 |
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| DOID:0111041 | glycogen storage disease IXb | MGI:97578 | Mus musculus (house mouse) | 102093 | Phkb |
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