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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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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 | July 29, 2024 |
| Disease ID | Disease Name | Alliance of Genome Resources ID | Species | Gene ID | Gene Symbol ▲ | FlyGlycoDB | Evidence Code Names | References |
|---|---|---|---|---|---|---|---|---|
| DOID:2030 | anxiety disorder | HGNC:7956 | Homo sapiens (human) | 4886 | NPY1R |
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| DOID:11832 | visual epilepsy | HGNC:7956 | Homo sapiens (human) | 4886 | NPY1R |
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| DOID:1596 | depressive disorder | HGNC:7956 | Homo sapiens (human) | 4886 | NPY1R |
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| DOID:2559 | opiate dependence | HGNC:7956 | Homo sapiens (human) | 4886 | NPY1R |
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| DOID:9970 | obesity | HGNC:7956 | Homo sapiens (human) | 4886 | NPY1R |
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| DOID:1825 | childhood absence epilepsy | HGNC:7956 | Homo sapiens (human) | 4886 | NPY1R |
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| DOID:670 | amphetamine abuse | HGNC:7956 | Homo sapiens (human) | 4886 | NPY1R |
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| DOID:10763 | hypertension | HGNC:7956 | Homo sapiens (human) | 4886 | NPY1R |
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| DOID:3328 | temporal lobe epilepsy | HGNC:7956 | Homo sapiens (human) | 4886 | NPY1R |
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| DOID:809 | cocaine abuse | HGNC:7956 | Homo sapiens (human) | 4886 | NPY1R |
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| DOID:2978 | carbohydrate metabolic disorder | SGD:S000003275 | Saccharomyces cerevisiae S288C | 852934 | NQM1 |
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| DOID:10762 | portal hypertension | HGNC:7962 | Homo sapiens (human) | 9572 | NR1D1 |
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| DOID:1459 | hypothyroidism | HGNC:7962 | Homo sapiens (human) | 9572 | NR1D1 |
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| DOID:0112313 | brain small vessel disease | HGNC:7962 | Homo sapiens (human) | 9572 | NR1D1 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:7962 | Homo sapiens (human) | 9572 | NR1D1 |
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| DOID:7998 | hyperthyroidism | HGNC:7962 | Homo sapiens (human) | 9572 | NR1D1 |
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| DOID:14018 | alcoholic liver cirrhosis | HGNC:7962 | Homo sapiens (human) | 9572 | NR1D1 |
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| DOID:0060292 | X-linked chondrodysplasia punctata 1 | HGNC:13398 | Homo sapiens (human) | 50814 | NSDHL |
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| DOID:0111822 | CHILD syndrome | HGNC:13398 | Homo sapiens (human) | 50814 | NSDHL |
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| DOID:0111898 | CK syndrome | HGNC:13398 | Homo sapiens (human) | 50814 | NSDHL |
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| DOID:12305 | Bloch-Sulzberger syndrome | HGNC:13398 | Homo sapiens (human) | 50814 | NSDHL |
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| DOID:162 | cancer | HGNC:13398 | Homo sapiens (human) | 50814 | NSDHL |
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| DOID:1824 | status epilepticus | HGNC:8021 | Homo sapiens (human) | 4907 | NT5E |
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| DOID:0111582 | hereditary arterial and articular multiple calcification syndrome | HGNC:8021 | Homo sapiens (human) | 4907 | NT5E |
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| DOID:0080411 | familial adenomatous polyposis 3 | SGD:S000000013 | Saccharomyces cerevisiae S288C | 851218 | NTG1 |
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