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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:11722 | myotonic dystrophy type 1 | HGNC:16746 | Homo sapiens (human) | 10150 | MBNL2 |
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| DOID:0111863 | X-linked congenital bilateral absence of vas deferens | HGNC:4516 | Homo sapiens (human) | 10149 | ADGRG2 |
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| DOID:1793 | pancreatic cancer | MGI:1351872 | Mus musculus (house mouse) | 101488 | Slco2b1 |
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| DOID:3571 | liver cancer | MGI:1351872 | Mus musculus (house mouse) | 101488 | Slco2b1 |
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| DOID:10591 | pre-eclampsia | HGNC:3129 | Homo sapiens (human) | 10148 | EBI3 |
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| DOID:0110652 | long QT syndrome 11 | HGNC:379 | Homo sapiens (human) | 10142 | AKAP9 |
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| DOID:1781 | thyroid cancer | HGNC:1755 | Homo sapiens (human) | 1014 | CDH16 |
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| DOID:0080281 | schizophrenia 19 | HGNC:9898 | Homo sapiens (human) | 10137 | RBM12 |
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| DOID:0060227 | Adams-Oliver syndrome | MGI:2141669 | Mus musculus (house mouse) | 101351 | Eogt |
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| DOID:1074 | kidney failure | HGNC:30092 | Homo sapiens (human) | 10135 | NAMPT |
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| DOID:3525 | middle cerebral artery infarction | 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:3407 | carotid artery disease | 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:9970 | obesity | HGNC:30092 | Homo sapiens (human) | 10135 | NAMPT |
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| DOID:3393 | coronary artery disease | HGNC:30092 | Homo sapiens (human) | 10135 | NAMPT |
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| DOID:8893 | psoriasis | 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:824 | periodontitis | HGNC:30092 | Homo sapiens (human) | 10135 | NAMPT |
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| DOID:0060203 | amyotrophic lateral sclerosis type 12 | HGNC:17142 | Homo sapiens (human) | 10133 | OPTN |
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| DOID:891 | progressive myoclonus epilepsy | HGNC:17142 | Homo sapiens (human) | 10133 | OPTN |
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| DOID:332 | amyotrophic lateral sclerosis | HGNC:17142 | Homo sapiens (human) | 10133 | OPTN |
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| DOID:224 | transient cerebral ischemia | HGNC:17142 | Homo sapiens (human) | 10133 | OPTN |
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| DOID:13641 | exfoliation syndrome | HGNC:17142 | Homo sapiens (human) | 10133 | OPTN |
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