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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:9970 | obesity | HGNC:2843 | Homo sapiens (human) | 8694 | DGAT1 |
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| DOID:0060778 | congenital diarrhea 7 with exudative enteropathy | HGNC:2843 | Homo sapiens (human) | 8694 | DGAT1 |
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| DOID:0080721 | calvarial doughnut lesions with bone fragility | HGNC:28395 | Homo sapiens (human) | 166929 | SGMS2 |
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| DOID:0014667 | disease of metabolism | HGNC:28335 | Homo sapiens (human) | 160287 | LDHAL6A |
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| DOID:0110658 | congenital myasthenic syndrome 15 | HGNC:28287 | Homo sapiens (human) | 199857 | ALG14 |
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| DOID:0070437 | hyperphosphatasia with impaired intellectual development syndrome 6 | HGNC:28213 | Homo sapiens (human) | 84992 | PIGY |
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| DOID:0070267 | congenital disorder of glycosylation type IIo | HGNC:28178 | Homo sapiens (human) | 84317 | CCDC115 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:27301 | Homo sapiens (human) | 200186 | CRTC2 |
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| DOID:0111263 | combined malonic and methylmalonic acidemia | HGNC:27288 | Homo sapiens (human) | 197322 | ACSF3 |
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| DOID:0080569 | congenital disorder of glycosylation Ir | HGNC:2728 | Homo sapiens (human) | 1650 | DDOST |
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| DOID:2841 | asthma | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
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| DOID:3526 | cerebral infarction | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
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| DOID:576 | proteinuria | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
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| DOID:3393 | coronary artery disease | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
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| DOID:12932 | endomyocardial fibrosis | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
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| DOID:9970 | obesity | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
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| DOID:10534 | stomach cancer | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
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| DOID:0050864 | non-arteritic anterior ischemic optic neuropathy | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
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| DOID:9538 | multiple myeloma | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
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| DOID:1205 | allergic disease | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
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| DOID:0080600 | COVID-19 | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
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| DOID:3500 | gallbladder adenocarcinoma | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
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| DOID:0080599 | Coronavirus infectious disease | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
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| DOID:11400 | pyelonephritis | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
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| DOID:1591 | renovascular hypertension | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
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