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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:9402 | epididymitis | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:9452 | steatotic liver disease | HGNC:438 | Homo sapiens (human) | 249 | ALPL |
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| DOID:0080611 | anterior segment dysgenesis 6 | HGNC:2597 | Homo sapiens (human) | 1545 | CYP1B1 |
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| DOID:0090122 | aromatase excess syndrome | HGNC:2594 | Homo sapiens (human) | 1588 | CYP19A1 |
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| DOID:11446 | sciatic neuropathy | HGNC:5217 | Homo sapiens (human) | 3283 | HSD3B1 |
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| DOID:824 | periodontitis | HGNC:1628 | Homo sapiens (human) | 929 | CD14 |
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| DOID:0080491 | cerebral cavernous malformation 1 | HGNC:9603 | Homo sapiens (human) | 5740 | PTGIS |
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| DOID:1287 | cardiovascular system disease | HGNC:4706 | Homo sapiens (human) | 2997 | GYS1 |
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| DOID:0050700 | cardiomyopathy | HGNC:7150 | Homo sapiens (human) | 23417 | MLYCD |
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| DOID:0080489 | GM1 gangliosidosis type 3 | HGNC:4298 | Homo sapiens (human) | 2720 | GLB1 |
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| DOID:0081385 | ataxia-telangiectasia-like disorder-2 | HGNC:8729 | Homo sapiens (human) | 5111 | PCNA |
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| DOID:114 | heart disease | HGNC:4617 | Homo sapiens (human) | 2932 | GSK3B |
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| DOID:0081326 | oxoglutarate dehydrogenase deficiency | HGNC:25590 | Homo sapiens (human) | 55753 | OGDHL |
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| DOID:1324 | lung cancer | HGNC:2595 | Homo sapiens (human) | 1543 | CYP1A1 |
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| DOID:1824 | status epilepticus | HGNC:23 | Homo sapiens (human) | 18 | ABAT |
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| DOID:0070436 | hyperphosphatasia with impaired intellectual development syndrome 4 | HGNC:23719 | Homo sapiens (human) | 93210 | PGAP3 |
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| DOID:5844 | myocardial infarction | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:4195 | hyperglycemia | HGNC:4923 | Homo sapiens (human) | 3099 | HK2 |
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| DOID:2367 | neuroaxonal dystrophy | HGNC:7631 | Homo sapiens (human) | 4668 | NAGA |
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| DOID:0050560 | Walker-Warburg syndrome | HGNC:9202 | Homo sapiens (human) | 10585 | POMT1 |
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| DOID:1612 | breast cancer | HGNC:2594 | Homo sapiens (human) | 1588 | CYP19A1 |
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| DOID:9406 | hypopituitarism | HGNC:14240 | Homo sapiens (human) | 55512 | SMPD3 |
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| DOID:224 | transient cerebral ischemia | HGNC:14240 | Homo sapiens (human) | 55512 | SMPD3 |
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| DOID:4194 | glucose metabolism disease | HGNC:4195 | Homo sapiens (human) | 2645 | GCK |
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| DOID:8432 | polycythemia | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
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