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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:1441 | autosomal dominant cerebellar ataxia | HGNC:31326 | Homo sapiens (human) | 11273 | ATXN2L |
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| DOID:11832 | visual epilepsy | HGNC:5184 | Homo sapiens (human) | 11255 | HRH3 |
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| DOID:10763 | hypertension | HGNC:5184 | Homo sapiens (human) | 11255 | HRH3 |
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| DOID:4195 | hyperglycemia | HGNC:5184 | Homo sapiens (human) | 11255 | HRH3 |
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| DOID:10808 | gastric ulcer | HGNC:5184 | Homo sapiens (human) | 11255 | HRH3 |
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| DOID:11446 | sciatic neuropathy | HGNC:5184 | Homo sapiens (human) | 11255 | HRH3 |
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| DOID:9970 | obesity | HGNC:5184 | Homo sapiens (human) | 11255 | HRH3 |
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| DOID:10914 | amnestic disorder | HGNC:5184 | Homo sapiens (human) | 11255 | HRH3 |
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| DOID:1824 | status epilepticus | HGNC:5184 | Homo sapiens (human) | 11255 | HRH3 |
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| DOID:11723 | Duchenne muscular dystrophy | HGNC:11047 | Homo sapiens (human) | 11254 | SLC6A14 |
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| DOID:9970 | obesity | HGNC:11047 | Homo sapiens (human) | 11254 | SLC6A14 |
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| DOID:0050589 | inflammatory bowel disease | HGNC:11047 | Homo sapiens (human) | 11254 | SLC6A14 |
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| DOID:0081097 | Rafiq syndrome | HGNC:6823 | Homo sapiens (human) | 11253 | MAN1B1 |
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| DOID:1289 | neurodegenerative disease | HGNC:8571 | Homo sapiens (human) | 11252 | PACSIN2 |
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| DOID:12858 | Huntington's disease | HGNC:8571 | Homo sapiens (human) | 11252 | PACSIN2 |
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| DOID:1485 | cystic fibrosis | HGNC:4502 | Homo sapiens (human) | 11251 | PTGDR2 |
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| DOID:4483 | rhinitis | HGNC:4502 | Homo sapiens (human) | 11251 | PTGDR2 |
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| DOID:2841 | asthma | HGNC:4502 | Homo sapiens (human) | 11251 | PTGDR2 |
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| DOID:4450 | renal cell carcinoma | MGI:1932287 | Mus musculus (house mouse) | 112406 | Egln2 |
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| DOID:4450 | renal cell carcinoma | MGI:1932286 | Mus musculus (house mouse) | 112405 | Egln1 |
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| DOID:10763 | hypertension | MGI:1932286 | Mus musculus (house mouse) | 112405 | Egln1 |
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| DOID:5844 | myocardial infarction | MGI:1932286 | Mus musculus (house mouse) | 112405 | Egln1 |
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| DOID:8432 | polycythemia | MGI:1932286 | Mus musculus (house mouse) | 112405 | Egln1 |
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| DOID:0080338 | familial erythrocytosis 3 | MGI:1932286 | Mus musculus (house mouse) | 112405 | Egln1 |
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| DOID:3021 | acute kidney failure | MGI:1932286 | Mus musculus (house mouse) | 112405 | Egln1 |
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