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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:14540 | Homo sapiens (human) | 65125 | WNK1 |
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| DOID:0070155 | hereditary sensory and autonomic neuropathy type 2A | HGNC:14540 | Homo sapiens (human) | 65125 | WNK1 |
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| DOID:4479 | pseudohypoaldosteronism | HGNC:14540 | Homo sapiens (human) | 65125 | WNK1 |
|
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| DOID:224 | transient cerebral ischemia | HGNC:14542 | Homo sapiens (human) | 65268 | WNK2 |
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| DOID:4479 | pseudohypoaldosteronism | HGNC:14542 | Homo sapiens (human) | 65268 | WNK2 |
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| DOID:4479 | pseudohypoaldosteronism | HGNC:14543 | Homo sapiens (human) | 65267 | WNK3 |
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| DOID:0060805 | Prieto syndrome | HGNC:14543 | Homo sapiens (human) | 65267 | WNK3 |
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| DOID:0110347 | osteogenesis imperfecta type 15 | HGNC:12774 | Homo sapiens (human) | 7471 | WNT1 |
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| DOID:1612 | breast cancer | HGNC:12774 | Homo sapiens (human) | 7471 | WNT1 |
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| DOID:9970 | obesity | HGNC:12774 | Homo sapiens (human) | 7471 | WNT1 |
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| DOID:0111647 | Schopf-Schulz-Passarge syndrome | HGNC:13829 | Homo sapiens (human) | 80326 | WNT10A |
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| DOID:0050591 | tooth agenesis | HGNC:13829 | Homo sapiens (human) | 80326 | WNT10A |
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| DOID:2121 | ectodermal dysplasia | HGNC:13829 | Homo sapiens (human) | 80326 | WNT10A |
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| DOID:0090026 | split hand-foot malformation 6 | HGNC:12775 | Homo sapiens (human) | 7480 | WNT10B |
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| DOID:0050591 | tooth agenesis | HGNC:12775 | Homo sapiens (human) | 7480 | WNT10B |
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| DOID:9970 | obesity | HGNC:12775 | Homo sapiens (human) | 7480 | WNT10B |
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| DOID:4450 | renal cell carcinoma | HGNC:12776 | Homo sapiens (human) | 7481 | WNT11 |
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| DOID:0050866 | oral squamous cell carcinoma | HGNC:12776 | Homo sapiens (human) | 7481 | WNT11 |
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| DOID:3459 | breast carcinoma | HGNC:12780 | Homo sapiens (human) | 7472 | WNT2 |
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| DOID:11832 | visual epilepsy | HGNC:12780 | Homo sapiens (human) | 7472 | WNT2 |
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| DOID:10283 | prostate cancer | HGNC:12780 | Homo sapiens (human) | 7472 | WNT2 |
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| DOID:684 | hepatocellular carcinoma | HGNC:12780 | Homo sapiens (human) | 7472 | WNT2 |
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| DOID:2871 | endometrial carcinoma | HGNC:12780 | Homo sapiens (human) | 7472 | WNT2 |
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| DOID:3996 | urinary system cancer | HGNC:12780 | Homo sapiens (human) | 7472 | WNT2 |
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| DOID:1612 | breast cancer | HGNC:12780 | Homo sapiens (human) | 7472 | WNT2 |
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