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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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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:1996 | rectum adenocarcinoma | HGNC:11063 | Homo sapiens (human) | 8140 | SLC7A5 |
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| DOID:0050872 | large cell neuroendocrine carcinoma | HGNC:11063 | Homo sapiens (human) | 8140 | SLC7A5 |
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| DOID:9256 | colorectal cancer | HGNC:11063 | Homo sapiens (human) | 8140 | SLC7A5 |
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| DOID:3495 | extrahepatic bile duct adenocarcinoma | HGNC:11063 | Homo sapiens (human) | 8140 | SLC7A5 |
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| DOID:3908 | lung non-small cell carcinoma | HGNC:11063 | Homo sapiens (human) | 8140 | SLC7A5 |
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| DOID:3717 | gastric adenocarcinoma | HGNC:11063 | Homo sapiens (human) | 8140 | SLC7A5 |
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| DOID:0050866 | oral squamous cell carcinoma | HGNC:11063 | Homo sapiens (human) | 8140 | SLC7A5 |
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| DOID:3748 | esophagus squamous cell carcinoma | HGNC:11063 | Homo sapiens (human) | 8140 | SLC7A5 |
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| DOID:4896 | bile duct adenocarcinoma | HGNC:11063 | Homo sapiens (human) | 8140 | SLC7A5 |
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| DOID:3907 | lung squamous cell carcinoma | HGNC:11063 | Homo sapiens (human) | 8140 | SLC7A5 |
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| DOID:11963 | esophagitis | HGNC:11063 | Homo sapiens (human) | 8140 | SLC7A5 |
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| DOID:9455 | lipid storage disease | HGNC:11061 | Homo sapiens (human) | 84889 | SLC7A3 |
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| DOID:0080208 | metabolic dysfunction-associated steatotic liver disease | HGNC:11061 | Homo sapiens (human) | 84889 | SLC7A3 |
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| DOID:3753 | Hermansky-Pudlak syndrome | HGNC:11059 | Homo sapiens (human) | 23657 | SLC7A11 |
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| DOID:2223 | platelet storage pool deficiency | HGNC:11059 | Homo sapiens (human) | 23657 | SLC7A11 |
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| DOID:0050865 | tongue squamous cell carcinoma | HGNC:11059 | Homo sapiens (human) | 23657 | SLC7A11 |
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| DOID:0060250 | idiopathic scoliosis | HGNC:11056 | Homo sapiens (human) | 6536 | SLC6A9 |
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| DOID:9268 | glycine encephalopathy | HGNC:11056 | Homo sapiens (human) | 6536 | SLC6A9 |
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| DOID:0050800 | cerebral creatine deficiency syndrome 1 | HGNC:11055 | Homo sapiens (human) | 6535 | SLC6A8 |
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| DOID:1059 | intellectual disability | HGNC:11055 | Homo sapiens (human) | 6535 | SLC6A8 |
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| DOID:1824 | status epilepticus | HGNC:11055 | Homo sapiens (human) | 6535 | SLC6A8 |
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| DOID:10584 | retinitis pigmentosa | HGNC:11052 | Homo sapiens (human) | 6533 | SLC6A6 |
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| DOID:4752 | multiple system atrophy | HGNC:11052 | Homo sapiens (human) | 6533 | SLC6A6 |
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| DOID:0060698 | hyperekplexia 3 | HGNC:11051 | Homo sapiens (human) | 9152 | SLC6A5 |
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| DOID:11723 | Duchenne muscular dystrophy | HGNC:11051 | Homo sapiens (human) | 9152 | SLC6A5 |
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