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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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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:585 | nephrolithiasis | HGNC:11078 | Homo sapiens (human) | 6553 | SLC9A5 |
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| DOID:783 | end stage renal disease | HGNC:11078 | Homo sapiens (human) | 6553 | SLC9A5 |
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| DOID:585 | nephrolithiasis | HGNC:11077 | Homo sapiens (human) | 389015 | SLC9A4 |
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| DOID:0060777 | congenital secretory sodium diarrhea 8 | HGNC:11073 | Homo sapiens (human) | 6550 | SLC9A3 |
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| DOID:585 | nephrolithiasis | HGNC:11073 | Homo sapiens (human) | 6550 | SLC9A3 |
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| DOID:9970 | obesity | HGNC:11073 | Homo sapiens (human) | 6550 | SLC9A3 |
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| DOID:10763 | hypertension | HGNC:11073 | Homo sapiens (human) | 6550 | SLC9A3 |
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| DOID:1591 | renovascular hypertension | HGNC:11073 | Homo sapiens (human) | 6550 | SLC9A3 |
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| DOID:585 | nephrolithiasis | HGNC:11072 | Homo sapiens (human) | 6549 | SLC9A2 |
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| DOID:83 | cataract | HGNC:11071 | Homo sapiens (human) | 6548 | SLC9A1 |
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| DOID:6000 | congestive heart failure | HGNC:11071 | Homo sapiens (human) | 6548 | SLC9A1 |
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| DOID:1459 | hypothyroidism | HGNC:11071 | Homo sapiens (human) | 6548 | SLC9A1 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:11071 | Homo sapiens (human) | 6548 | SLC9A1 |
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| DOID:0080065 | autosomal recessive spinocerebellar ataxia 19 | HGNC:11071 | Homo sapiens (human) | 6548 | SLC9A1 |
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| DOID:7998 | hyperthyroidism | HGNC:11071 | Homo sapiens (human) | 6548 | SLC9A1 |
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| DOID:576 | proteinuria | HGNC:11071 | Homo sapiens (human) | 6548 | SLC9A1 |
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| DOID:1591 | renovascular hypertension | HGNC:11071 | Homo sapiens (human) | 6548 | SLC9A1 |
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| DOID:585 | nephrolithiasis | HGNC:11071 | Homo sapiens (human) | 6548 | SLC9A1 |
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| DOID:3525 | middle cerebral artery infarction | HGNC:11071 | Homo sapiens (human) | 6548 | SLC9A1 |
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| DOID:1824 | status epilepticus | HGNC:11070 | Homo sapiens (human) | 6547 | SLC8A3 |
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| DOID:10652 | Alzheimer's disease | HGNC:11070 | Homo sapiens (human) | 6547 | SLC8A3 |
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| DOID:2316 | brain ischemia | HGNC:11070 | Homo sapiens (human) | 6547 | SLC8A3 |
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| DOID:2316 | brain ischemia | HGNC:11069 | Homo sapiens (human) | 6543 | SLC8A2 |
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| DOID:1824 | status epilepticus | HGNC:11069 | Homo sapiens (human) | 6543 | SLC8A2 |
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| DOID:10652 | Alzheimer's disease | HGNC:11069 | Homo sapiens (human) | 6543 | SLC8A2 |
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