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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
LM-GlycoRepo
Repository for lectin-assisted multimodality data
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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:2018 | hyperinsulinism | MGI:1270854 | Mus musculus (house mouse) | 103988 | Gck |
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| DOID:9351 | diabetes mellitus | MGI:1270854 | Mus musculus (house mouse) | 103988 | Gck |
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| DOID:0111100 | maturity-onset diabetes of the young type 2 | MGI:1270854 | Mus musculus (house mouse) | 103988 | Gck |
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| DOID:10763 | hypertension | MGI:1270854 | Mus musculus (house mouse) | 103988 | Gck |
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| DOID:0060639 | permanent neonatal diabetes mellitus | MGI:1270854 | Mus musculus (house mouse) | 103988 | Gck |
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| DOID:9970 | obesity | MGI:1270854 | Mus musculus (house mouse) | 103988 | Gck |
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| DOID:9352 | type 2 diabetes mellitus | MGI:1270854 | Mus musculus (house mouse) | 103988 | Gck |
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| DOID:0060610 | megacystis-microcolon-intestinal hypoperistalsis syndrome | HGNC:15754 | Homo sapiens (human) | 10398 | MYL9 |
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| DOID:0080326 | familial hypertrophic cardiomyopathy | HGNC:15754 | Homo sapiens (human) | 10398 | MYL9 |
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| DOID:0110186 | Charcot-Marie-Tooth disease type 4D | HGNC:7679 | Homo sapiens (human) | 10397 | NDRG1 |
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| DOID:0070205 | familial partial lipodystrophy type 4 | MGI:1890505 | Mus musculus (house mouse) | 103968 | Plin1 |
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| DOID:0080208 | metabolic dysfunction-associated steatotic liver disease | MGI:1890505 | Mus musculus (house mouse) | 103968 | Plin1 |
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| DOID:9970 | obesity | MGI:1890505 | Mus musculus (house mouse) | 103968 | Plin1 |
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| DOID:0111223 | centronuclear myopathy 1 | MGI:1341299 | Mus musculus (house mouse) | 103967 | Dnm3 |
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| DOID:2476 | hereditary spastic paraplegia | MGI:1341299 | Mus musculus (house mouse) | 103967 | Dnm3 |
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| DOID:0110197 | Charcot-Marie-Tooth disease dominant intermediate B | MGI:1341299 | Mus musculus (house mouse) | 103967 | Dnm3 |
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| DOID:854 | collagen disease | MGI:1341299 | Mus musculus (house mouse) | 103967 | Dnm3 |
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| DOID:0112202 | developmental and epileptic encephalopathy | MGI:1341299 | Mus musculus (house mouse) | 103967 | Dnm3 |
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| DOID:11252 | microcytic anemia | MGI:1341299 | Mus musculus (house mouse) | 103967 | Dnm3 |
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| DOID:14447 | gonadal dysgenesis | HGNC:2897 | Homo sapiens (human) | 10395 | DLC1 |
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| DOID:9256 | colorectal cancer | HGNC:2897 | Homo sapiens (human) | 10395 | DLC1 |
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| DOID:5679 | retinal disease | HGNC:24289 | Homo sapiens (human) | 10390 | CEPT1 |
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| DOID:14452 | hypokalemic periodic paralysis | HGNC:20771 | Homo sapiens (human) | 10383 | TUBB4B |
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| DOID:0090132 | complex cortical dysplasia with other brain malformations 7 | HGNC:20771 | Homo sapiens (human) | 10383 | TUBB4B |
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| DOID:0060260 | ptosis | HGNC:20771 | Homo sapiens (human) | 10383 | TUBB4B |
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