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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:332 | amyotrophic lateral sclerosis | HGNC:4617 | Homo sapiens (human) | 2932 | GSK3B |
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| DOID:8725 | vascular dementia | HGNC:4617 | Homo sapiens (human) | 2932 | GSK3B |
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| DOID:1824 | status epilepticus | HGNC:4617 | Homo sapiens (human) | 2932 | GSK3B |
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| DOID:3312 | bipolar disorder | HGNC:4617 | Homo sapiens (human) | 2932 | GSK3B |
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| DOID:10763 | hypertension | HGNC:4617 | Homo sapiens (human) | 2932 | GSK3B |
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| DOID:0050850 | diabetic encephalopathy | HGNC:4617 | Homo sapiens (human) | 2932 | GSK3B |
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| DOID:10652 | Alzheimer's disease | HGNC:4617 | Homo sapiens (human) | 2932 | GSK3B |
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| DOID:5419 | schizophrenia | HGNC:4617 | Homo sapiens (human) | 2932 | GSK3B |
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| DOID:0050861 | colorectal adenocarcinoma | HGNC:4617 | Homo sapiens (human) | 2932 | GSK3B |
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| DOID:14330 | Parkinson's disease | HGNC:4617 | Homo sapiens (human) | 2932 | GSK3B |
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| DOID:114 | heart disease | HGNC:4617 | Homo sapiens (human) | 2932 | GSK3B |
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| DOID:1596 | depressive disorder | HGNC:4617 | Homo sapiens (human) | 2932 | GSK3B |
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| DOID:8283 | peritonitis | HGNC:4696 | Homo sapiens (human) | 2990 | GUSB |
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| DOID:12803 | Sly syndrome | HGNC:4696 | Homo sapiens (human) | 2990 | GUSB |
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| DOID:12798 | mucopolysaccharidosis | HGNC:4696 | Homo sapiens (human) | 2990 | GUSB |
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| DOID:2747 | glycogen storage disease | HGNC:4699 | Homo sapiens (human) | 2992 | GYG1 |
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| DOID:0050579 | glycogen storage disease XV | HGNC:4699 | Homo sapiens (human) | 2992 | GYG1 |
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| DOID:3534 | Lafora disease | HGNC:4706 | Homo sapiens (human) | 2997 | GYS1 |
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| DOID:1287 | cardiovascular system disease | HGNC:4706 | Homo sapiens (human) | 2997 | GYS1 |
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| DOID:3534 | Lafora disease | HGNC:4707 | Homo sapiens (human) | 2998 | GYS2 |
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| DOID:2747 | glycogen storage disease | HGNC:4707 | Homo sapiens (human) | 2998 | GYS2 |
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| DOID:9268 | glycine encephalopathy | HGNC:473 | Homo sapiens (human) | 275 | AMT |
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| DOID:0090141 | cortisone reductase deficiency 1 | HGNC:4795 | Homo sapiens (human) | 9563 | H6PD |
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| DOID:2377 | multiple sclerosis | HGNC:4795 | Homo sapiens (human) | 9563 | H6PD |
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| DOID:0090139 | cortisone reductase deficiency | HGNC:4795 | Homo sapiens (human) | 9563 | H6PD |
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