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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:0060202 | amyotrophic lateral sclerosis type 11 | HGNC:16873 | Homo sapiens (human) | 9896 | FIG4 |
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| DOID:0080208 | metabolic dysfunction-associated steatotic liver disease | HGNC:6126 | Homo sapiens (human) | 8660 | IRS2 |
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| DOID:1407 | anterior uveitis | HGNC:11850 | Homo sapiens (human) | 7099 | TLR4 |
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| DOID:299 | adenocarcinoma | HGNC:9605 | Homo sapiens (human) | 5743 | PTGS2 |
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| DOID:1485 | cystic fibrosis | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:13544 | low tension glaucoma | HGNC:11998 | Homo sapiens (human) | 7157 | TP53 |
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| DOID:893 | Wilson disease | HGNC:11120 | Homo sapiens (human) | 6609 | SMPD1 |
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| DOID:0110858 | polycystic kidney disease 1 | HGNC:9008 | Homo sapiens (human) | 5310 | PKD1 |
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| DOID:0070255 | congenital disorder of glycosylation type IIc | HGNC:20197 | Homo sapiens (human) | 55343 | SLC35C1 |
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| DOID:8466 | retinal degeneration | HGNC:2422 | Homo sapiens (human) | 1431 | CS |
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| DOID:0050127 | sinusitis | HGNC:11850 | Homo sapiens (human) | 7099 | TLR4 |
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| DOID:7147 | ankylosing spondylitis | HGNC:13633 | Homo sapiens (human) | 9370 | ADIPOQ |
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| DOID:1825 | childhood absence epilepsy | HGNC:11005 | Homo sapiens (human) | 6513 | SLC2A1 |
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| DOID:12206 | dengue hemorrhagic fever | HGNC:1637 | Homo sapiens (human) | 912 | CD1D |
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| DOID:10892 | hypospadias | HGNC:11285 | Homo sapiens (human) | 6716 | SRD5A2 |
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| DOID:0080322 | polycystic kidney disease | HGNC:9008 | Homo sapiens (human) | 5310 | PKD1 |
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| DOID:3322 | GM1 gangliosidosis | HGNC:4298 | Homo sapiens (human) | 2720 | GLB1 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:404 | Homo sapiens (human) | 217 | ALDH2 |
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| DOID:5041 | esophageal cancer | HGNC:4555 | Homo sapiens (human) | 2878 | GPX3 |
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| DOID:5844 | myocardial infarction | HGNC:6623 | Homo sapiens (human) | 9388 | LIPG |
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| DOID:12849 | autistic disorder | HGNC:8978 | Homo sapiens (human) | 5294 | PIK3CG |
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| DOID:5844 | myocardial infarction | HGNC:391 | Homo sapiens (human) | 207 | AKT1 |
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| DOID:9884 | muscular dystrophy | HGNC:2211 | Homo sapiens (human) | 1291 | COL6A1 |
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| DOID:0080208 | metabolic dysfunction-associated steatotic liver disease | HGNC:24865 | Homo sapiens (human) | 57678 | GPAM |
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| DOID:9970 | obesity | HGNC:6922 | Homo sapiens (human) | 4153 | MBL2 |
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