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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:13603 | obstructive jaundice | HGNC:1628 | Homo sapiens (human) | 929 | CD14 |
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| DOID:9744 | type 1 diabetes mellitus | HGNC:1628 | Homo sapiens (human) | 929 | CD14 |
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| DOID:11335 | sarcoidosis | HGNC:1628 | Homo sapiens (human) | 929 | CD14 |
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| DOID:1205 | allergic disease | HGNC:1628 | Homo sapiens (human) | 929 | CD14 |
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| DOID:2957 | pulmonary tuberculosis | HGNC:1628 | Homo sapiens (human) | 929 | CD14 |
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| DOID:13580 | cholestasis | HGNC:1628 | Homo sapiens (human) | 929 | CD14 |
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| DOID:13608 | biliary atresia | HGNC:1628 | Homo sapiens (human) | 929 | CD14 |
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| DOID:4483 | rhinitis | HGNC:1628 | Homo sapiens (human) | 929 | CD14 |
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| DOID:2986 | IgA glomerulonephritis | HGNC:1628 | Homo sapiens (human) | 929 | CD14 |
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| DOID:10487 | Hirschsprung's disease | HGNC:1628 | Homo sapiens (human) | 929 | CD14 |
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| DOID:5844 | myocardial infarction | HGNC:1628 | Homo sapiens (human) | 929 | CD14 |
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| DOID:3407 | carotid artery disease | HGNC:1628 | Homo sapiens (human) | 929 | CD14 |
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| DOID:824 | periodontitis | HGNC:1628 | Homo sapiens (human) | 929 | CD14 |
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| DOID:10763 | hypertension | HGNC:1628 | Homo sapiens (human) | 929 | CD14 |
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| DOID:1574 | alcohol use disorder | HGNC:4508 | Homo sapiens (human) | 9293 | GPR52 |
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| DOID:0050855 | renal fibrosis | HGNC:4508 | Homo sapiens (human) | 9293 | GPR52 |
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| DOID:700 | mitochondrial metabolism disease | HGNC:25133 | Homo sapiens (human) | 92935 | MARS2 |
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| DOID:0050942 | spastic ataxia 3 | HGNC:25133 | Homo sapiens (human) | 92935 | MARS2 |
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| DOID:1289 | neurodegenerative disease | HGNC:25133 | Homo sapiens (human) | 92935 | MARS2 |
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| DOID:0111468 | combined oxidative phosphorylation deficiency 25 | HGNC:25133 | Homo sapiens (human) | 92935 | MARS2 |
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| DOID:305 | carcinoma | HGNC:3169 | Homo sapiens (human) | 9294 | S1PR2 |
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| DOID:0060060 | non-Hodgkin lymphoma | HGNC:3169 | Homo sapiens (human) | 9294 | S1PR2 |
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| DOID:0110519 | autosomal recessive nonsyndromic deafness 68 | HGNC:3169 | Homo sapiens (human) | 9294 | S1PR2 |
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| DOID:0050908 | myelodysplastic syndrome | HGNC:10782 | Homo sapiens (human) | 9295 | SRSF11 |
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| DOID:0060041 | autism spectrum disorder | HGNC:10782 | Homo sapiens (human) | 9295 | SRSF11 |
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