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GlyTouCan
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
LM-GlycoRepo
Repository for lectin-assisted multimodality data
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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 | October 9, 2024 |
| Disease ID | Disease Name | Alliance of Genome Resources ID | Species | Gene ID | Gene Symbol ▼ | FlyGlycoDB | Evidence Code Names | References |
|---|---|---|---|---|---|---|---|---|
| DOID:1459 | hypothyroidism | HGNC:17288 | Homo sapiens (human) | 116519 | APOA5 |
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| DOID:3393 | coronary artery disease | HGNC:17288 | Homo sapiens (human) | 116519 | APOA5 |
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| DOID:1172 | hyperlipoproteinemia type IV | HGNC:17288 | Homo sapiens (human) | 116519 | APOA5 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:17288 | Homo sapiens (human) | 116519 | APOA5 |
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| DOID:1171 | hyperlipoproteinemia type V | HGNC:17288 | Homo sapiens (human) | 116519 | APOA5 |
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| DOID:0111421 | familial apolipoprotein A5 deficiency | HGNC:17288 | Homo sapiens (human) | 116519 | APOA5 |
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| DOID:3526 | cerebral infarction | HGNC:17288 | Homo sapiens (human) | 116519 | APOA5 |
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| DOID:5419 | schizophrenia | HGNC:602 | Homo sapiens (human) | 337 | APOA4 |
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| DOID:784 | chronic kidney disease | HGNC:602 | Homo sapiens (human) | 337 | APOA4 |
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| DOID:684 | hepatocellular carcinoma | HGNC:602 | Homo sapiens (human) | 337 | APOA4 |
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| DOID:12858 | Huntington's disease | HGNC:602 | Homo sapiens (human) | 337 | APOA4 |
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| DOID:0081267 | graft-versus-host disease | HGNC:602 | Homo sapiens (human) | 337 | APOA4 |
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| DOID:8805 | intermediate coronary syndrome | HGNC:602 | Homo sapiens (human) | 337 | APOA4 |
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| DOID:1287 | cardiovascular system disease | HGNC:602 | Homo sapiens (human) | 337 | APOA4 |
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| DOID:9719 | neovascular inflammatory vitreoretinopathy | HGNC:602 | Homo sapiens (human) | 337 | APOA4 |
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| DOID:7148 | rheumatoid arthritis | HGNC:602 | Homo sapiens (human) | 337 | APOA4 |
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| DOID:705 | Leber hereditary optic neuropathy | HGNC:602 | Homo sapiens (human) | 337 | APOA4 |
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| DOID:12842 | Guillain-Barre syndrome | HGNC:602 | Homo sapiens (human) | 337 | APOA4 |
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| DOID:1470 | major depressive disorder | HGNC:602 | Homo sapiens (human) | 337 | APOA4 |
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| DOID:8778 | Crohn's disease | HGNC:602 | Homo sapiens (human) | 337 | APOA4 |
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| DOID:5327 | retinal detachment | HGNC:602 | Homo sapiens (human) | 337 | APOA4 |
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| DOID:1686 | glaucoma | HGNC:602 | Homo sapiens (human) | 337 | APOA4 |
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| DOID:8947 | diabetic retinopathy | HGNC:602 | Homo sapiens (human) | 337 | APOA4 |
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| DOID:5844 | myocardial infarction | HGNC:602 | Homo sapiens (human) | 337 | APOA4 |
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| DOID:8577 | ulcerative colitis | HGNC:602 | Homo sapiens (human) | 337 | APOA4 |
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