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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:3312 | bipolar disorder | HGNC:10934 | Homo sapiens (human) | 6570 | SLC18A1 |
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| DOID:670 | amphetamine abuse | HGNC:10934 | Homo sapiens (human) | 6570 | SLC18A1 |
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| DOID:5419 | schizophrenia | HGNC:10934 | Homo sapiens (human) | 6570 | SLC18A1 |
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| DOID:14175 | von Hippel-Lindau disease | HGNC:10934 | Homo sapiens (human) | 6570 | SLC18A1 |
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| DOID:3659 | sialuria | HGNC:10933 | Homo sapiens (human) | 26503 | SLC17A5 |
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| DOID:3211 | lysosomal storage disease | HGNC:10933 | Homo sapiens (human) | 26503 | SLC17A5 |
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| DOID:13189 | gout | HGNC:10931 | Homo sapiens (human) | 10786 | SLC17A3 |
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| DOID:0111630 | familial erythrocytosis 8 | HGNC:1093 | Homo sapiens (human) | 669 | BPGM |
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| DOID:9970 | obesity | HGNC:10921 | Homo sapiens (human) | 6565 | SLC15A2 |
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| DOID:9970 | obesity | HGNC:10920 | Homo sapiens (human) | 6564 | SLC15A1 |
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| DOID:3908 | lung non-small cell carcinoma | HGNC:1092 | Homo sapiens (human) | 668 | FOXL2 |
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| DOID:0080860 | primary ovarian insufficiency 3 | HGNC:1092 | Homo sapiens (human) | 668 | FOXL2 |
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| DOID:14778 | blepharophimosis, ptosis, and epicanthus inversus syndrome | HGNC:1092 | Homo sapiens (human) | 668 | FOXL2 |
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| DOID:2876 | laryngeal squamous cell carcinoma | HGNC:1092 | Homo sapiens (human) | 668 | FOXL2 |
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| DOID:0111668 | Kohlschutter-Tonz syndrome | HGNC:10916 | Homo sapiens (human) | 6561 | SLC13A1 |
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| DOID:1826 | epilepsy | HGNC:10916 | Homo sapiens (human) | 6561 | SLC13A1 |
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| DOID:0050667 | alcohol-related neurodevelopmental disorder | HGNC:10916 | Homo sapiens (human) | 6561 | SLC13A1 |
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| DOID:1826 | epilepsy | HGNC:10915 | Homo sapiens (human) | 10723 | SLC12A7 |
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| DOID:0090003 | agenesis of the corpus callosum with peripheral neuropathy | HGNC:10914 | Homo sapiens (human) | 9990 | SLC12A6 |
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| DOID:10595 | Charcot-Marie-Tooth disease | HGNC:10914 | Homo sapiens (human) | 9990 | SLC12A6 |
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| DOID:1826 | epilepsy | HGNC:10914 | Homo sapiens (human) | 9990 | SLC12A6 |
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| DOID:2477 | motor peripheral neuropathy | HGNC:10914 | Homo sapiens (human) | 9990 | SLC12A6 |
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| DOID:1826 | epilepsy | HGNC:10913 | Homo sapiens (human) | 6560 | SLC12A4 |
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| DOID:10825 | essential hypertension | HGNC:10912 | Homo sapiens (human) | 6559 | SLC12A3 |
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| DOID:1826 | epilepsy | HGNC:10912 | Homo sapiens (human) | 6559 | SLC12A3 |
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