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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:9744 | type 1 diabetes mellitus | HGNC:11179 | Homo sapiens (human) | 6647 | SOD1 |
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| DOID:224 | transient cerebral ischemia | HGNC:11179 | Homo sapiens (human) | 6647 | SOD1 |
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| DOID:13025 | retinopathy of prematurity | HGNC:11179 | Homo sapiens (human) | 6647 | SOD1 |
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| DOID:5113 | nutritional deficiency disease | HGNC:11179 | Homo sapiens (human) | 6647 | SOD1 |
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| DOID:1459 | hypothyroidism | HGNC:11179 | Homo sapiens (human) | 6647 | SOD1 |
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| DOID:332 | amyotrophic lateral sclerosis | HGNC:11179 | Homo sapiens (human) | 6647 | SOD1 |
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| DOID:0080547 | metabolic dysfunction-associated steatohepatitis | HGNC:11179 | Homo sapiens (human) | 6647 | SOD1 |
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| DOID:231 | motor neuron disease | HGNC:11179 | Homo sapiens (human) | 6647 | SOD1 |
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| DOID:4448 | macular degeneration | HGNC:11179 | Homo sapiens (human) | 6647 | SOD1 |
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| DOID:83 | cataract | HGNC:11179 | Homo sapiens (human) | 6647 | SOD1 |
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| DOID:1574 | alcohol use disorder | HGNC:11179 | Homo sapiens (human) | 6647 | SOD1 |
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| DOID:9282 | ocular hypertension | HGNC:11179 | Homo sapiens (human) | 6647 | SOD1 |
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| DOID:0080322 | polycystic kidney disease | HGNC:11179 | Homo sapiens (human) | 6647 | SOD1 |
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| DOID:10652 | Alzheimer's disease | HGNC:11179 | Homo sapiens (human) | 6647 | SOD1 |
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| DOID:10763 | hypertension | HGNC:11179 | Homo sapiens (human) | 6647 | SOD1 |
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| DOID:649 | prion disease | HGNC:11179 | Homo sapiens (human) | 6647 | SOD1 |
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| DOID:7998 | hyperthyroidism | HGNC:11179 | Homo sapiens (human) | 6647 | SOD1 |
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| DOID:10584 | retinitis pigmentosa | HGNC:11179 | Homo sapiens (human) | 6647 | SOD1 |
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| DOID:4195 | hyperglycemia | HGNC:11179 | Homo sapiens (human) | 6647 | SOD1 |
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| DOID:0060224 | atrial fibrillation | HGNC:11179 | Homo sapiens (human) | 6647 | SOD1 |
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| DOID:11446 | sciatic neuropathy | HGNC:11179 | Homo sapiens (human) | 6647 | SOD1 |
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| DOID:13241 | Behcet's disease | HGNC:11179 | Homo sapiens (human) | 6647 | SOD1 |
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| DOID:10140 | dry eye syndrome | HGNC:11179 | Homo sapiens (human) | 6647 | SOD1 |
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| DOID:3827 | congenital diaphragmatic hernia | HGNC:11179 | Homo sapiens (human) | 6647 | SOD1 |
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| DOID:13544 | low tension glaucoma | HGNC:11179 | Homo sapiens (human) | 6647 | SOD1 |
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