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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:0050560 | Walker-Warburg syndrome | HGNC:9202 | Homo sapiens (human) | 10585 | POMT1 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:1667 | Homo sapiens (human) | 952 | CD38 |
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| DOID:5844 | myocardial infarction | HGNC:543 | Homo sapiens (human) | 308 | ANXA5 |
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| DOID:9655 | oral mucosa leukoplakia | RGD:3889 | Rattus norvegicus (Norway rat) | 24842 | Tp53 |
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| DOID:5844 | myocardial infarction | HGNC:10721 | Homo sapiens (human) | 6403 | SELP |
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| DOID:684 | hepatocellular carcinoma | HGNC:9588 | Homo sapiens (human) | 5728 | PTEN |
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| DOID:9206 | Barrett's esophagus | HGNC:9605 | Homo sapiens (human) | 5743 | PTGS2 |
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| DOID:12918 | thromboangiitis obliterans | HGNC:12663 | Homo sapiens (human) | 7412 | VCAM1 |
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| DOID:0080119 | mitochondrial DNA depletion syndrome 1 | MGI:1920212 | Mus musculus (house mouse) | 72962 | Tymp |
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| DOID:10763 | hypertension | HGNC:5217 | Homo sapiens (human) | 3283 | HSD3B1 |
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| DOID:2842 | Jervell-Lange Nielsen syndrome | HGNC:6294 | Homo sapiens (human) | 3784 | KCNQ1 |
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| DOID:6432 | pulmonary hypertension | HGNC:9603 | Homo sapiens (human) | 5740 | PTGIS |
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| DOID:1926 | Gaucher's disease | MGI:95665 | Mus musculus (house mouse) | 14466 | Gba1 |
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| DOID:784 | chronic kidney disease | RGD:620396 | Rattus norvegicus (Norway rat) | 83504 | Kl |
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| DOID:0060849 | osteoporosis-pseudoglioma syndrome | MGI:1278315 | Mus musculus (house mouse) | 16973 | Lrp5 |
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| DOID:2749 | glycogen storage disease Ia | HGNC:4056 | Homo sapiens (human) | 2538 | G6PC1 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:8976 | Homo sapiens (human) | 5291 | PIK3CB |
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| DOID:0070253 | congenital disorder of glycosylation type IIa | MGI:2384966 | Mus musculus (house mouse) | 217664 | Mgat2 |
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| DOID:10763 | hypertension | RGD:2168 | Rattus norvegicus (Norway rat) | 24212 | Atp1a2 |
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| DOID:9256 | colorectal cancer | RGD:2082 | Rattus norvegicus (Norway rat) | 25233 | Akt2 |
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| DOID:9256 | colorectal cancer | HGNC:392 | Homo sapiens (human) | 208 | AKT2 |
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| DOID:384 | Wolff-Parkinson-White syndrome | HGNC:9386 | Homo sapiens (human) | 51422 | PRKAG2 |
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| DOID:0110299 | autosomal recessive limb-girdle muscular dystrophy type 2I | HGNC:17997 | Homo sapiens (human) | 79147 | FKRP |
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| DOID:0060849 | osteoporosis-pseudoglioma syndrome | HGNC:6697 | Homo sapiens (human) | 4041 | LRP5 |
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| DOID:0050560 | Walker-Warburg syndrome | HGNC:19139 | Homo sapiens (human) | 55624 | POMGNT1 |
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