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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:10763 | hypertension | HGNC:11048 | Homo sapiens (human) | 6530 | SLC6A2 |
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| DOID:11569 | neurocirculatory asthenia | HGNC:11048 | Homo sapiens (human) | 6530 | SLC6A2 |
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| DOID:1596 | depressive disorder | HGNC:11048 | Homo sapiens (human) | 6530 | SLC6A2 |
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| DOID:0070489 | classic dopamine transporter deficiency syndrome | HGNC:11048 | Homo sapiens (human) | 6530 | SLC6A2 |
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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:11832 | visual epilepsy | HGNC:11044 | Homo sapiens (human) | 6538 | SLC6A11 |
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| DOID:3526 | cerebral infarction | HGNC:11042 | Homo sapiens (human) | 6529 | SLC6A1 |
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| DOID:0060475 | myoclonic-atonic epilepsy | HGNC:11042 | Homo sapiens (human) | 6529 | SLC6A1 |
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| DOID:3328 | temporal lobe epilepsy | HGNC:11042 | Homo sapiens (human) | 6529 | SLC6A1 |
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| DOID:1826 | epilepsy | HGNC:11042 | Homo sapiens (human) | 6529 | SLC6A1 |
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| DOID:0060001 | withdrawal disorder | HGNC:11042 | Homo sapiens (human) | 6529 | SLC6A1 |
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| DOID:2316 | brain ischemia | HGNC:11042 | Homo sapiens (human) | 6529 | SLC6A1 |
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| DOID:5419 | schizophrenia | HGNC:11042 | Homo sapiens (human) | 6529 | SLC6A1 |
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| DOID:0050741 | alcohol dependence | HGNC:11042 | Homo sapiens (human) | 6529 | SLC6A1 |
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| DOID:0050718 | vitamin metabolic disorder | HGNC:11041 | Homo sapiens (human) | 8884 | SLC5A6 |
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| DOID:0050718 | vitamin metabolic disorder | HGNC:11040 | Homo sapiens (human) | 6528 | SLC5A5 |
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| DOID:0050328 | congenital hypothyroidism | HGNC:11040 | Homo sapiens (human) | 6528 | SLC5A5 |
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| DOID:0112185 | thyroid dyshormonogenesis 1 | HGNC:11040 | Homo sapiens (human) | 6528 | SLC5A5 |
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| DOID:10763 | hypertension | HGNC:11037 | Homo sapiens (human) | 6524 | SLC5A2 |
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| DOID:9432 | renal glycosuria | HGNC:11037 | Homo sapiens (human) | 6524 | SLC5A2 |
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| DOID:2355 | anemia | HGNC:11035 | Homo sapiens (human) | 83697 | SLC4A9 |
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| DOID:2355 | anemia | HGNC:11034 | Homo sapiens (human) | 9498 | SLC4A8 |
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| DOID:11716 | prediabetes syndrome | HGNC:11034 | Homo sapiens (human) | 9498 | SLC4A8 |
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