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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:2862 | glucosephosphate dehydrogenase deficiency | HGNC:11027 | Homo sapiens (human) | 6521 | SLC4A1 |
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| DOID:3910 | lung adenocarcinoma | HGNC:11026 | Homo sapiens (human) | 6520 | SLC3A2 |
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| DOID:0050865 | tongue squamous cell carcinoma | HGNC:11026 | Homo sapiens (human) | 6520 | SLC3A2 |
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| DOID:0080899 | lung pleomorphic carcinoma | HGNC:11026 | Homo sapiens (human) | 6520 | SLC3A2 |
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| DOID:3908 | lung non-small cell carcinoma | HGNC:11026 | Homo sapiens (human) | 6520 | SLC3A2 |
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| DOID:2671 | transitional cell carcinoma | HGNC:11026 | Homo sapiens (human) | 6520 | SLC3A2 |
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| DOID:0080202 | adenoid cystic carcinoma | HGNC:11026 | Homo sapiens (human) | 6520 | SLC3A2 |
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| DOID:5517 | stomach carcinoma | HGNC:11026 | Homo sapiens (human) | 6520 | SLC3A2 |
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| DOID:9266 | cystinuria | HGNC:11025 | Homo sapiens (human) | 6519 | SLC3A1 |
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| DOID:0070265 | congenital disorder of glycosylation type IIm | HGNC:11022 | Homo sapiens (human) | 7355 | SLC35A2 |
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| DOID:104 | bacterial infectious disease | HGNC:11022 | Homo sapiens (human) | 7355 | SLC35A2 |
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| DOID:0070258 | congenital disorder of glycosylation type IIf | HGNC:11021 | Homo sapiens (human) | 10559 | SLC35A1 |
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| DOID:12117 | pulmonary alveolar microlithiasis | HGNC:11020 | Homo sapiens (human) | 10568 | SLC34A2 |
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| DOID:3312 | bipolar disorder | HGNC:1102 | Homo sapiens (human) | 23774 | BRD1 |
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| DOID:5419 | schizophrenia | HGNC:1102 | Homo sapiens (human) | 23774 | BRD1 |
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| DOID:11832 | visual epilepsy | HGNC:1102 | Homo sapiens (human) | 23774 | BRD1 |
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| DOID:0050336 | hypophosphatemia | HGNC:11019 | Homo sapiens (human) | 6569 | SLC34A1 |
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| DOID:0080758 | Fanconi renotubular syndrome 2 | HGNC:11019 | Homo sapiens (human) | 6569 | SLC34A1 |
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| DOID:0080077 | hypophosphatemic nephrolithiasis/osteoporosis 1 | HGNC:11019 | Homo sapiens (human) | 6569 | SLC34A1 |
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| DOID:0050947 | hereditary hypophosphatemic rickets with hypercalciuria | HGNC:11019 | Homo sapiens (human) | 6569 | SLC34A1 |
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| DOID:12678 | hypercalcemia | HGNC:11019 | Homo sapiens (human) | 6569 | SLC34A1 |
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| DOID:7998 | hyperthyroidism | HGNC:11019 | Homo sapiens (human) | 6569 | SLC34A1 |
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| DOID:898 | autosomal dominant polycystic kidney disease | HGNC:11019 | Homo sapiens (human) | 6569 | SLC34A1 |
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| DOID:1062 | Fanconi syndrome | HGNC:11019 | Homo sapiens (human) | 6569 | SLC34A1 |
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| DOID:783 | end stage renal disease | HGNC:11019 | Homo sapiens (human) | 6569 | SLC34A1 |
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