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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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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:224 | transient cerebral ischemia | RGD:631365 | Rattus norvegicus (Norway rat) | 297508 | Nampt |
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| DOID:2367 | neuroaxonal dystrophy | RGD:1306025 | Rattus norvegicus (Norway rat) | 315165 | Naga |
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| DOID:0112319 | Kanzaki disease | MGI:1261422 | Mus musculus (house mouse) | 17939 | Naga |
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| DOID:479 | angiokeratoma | RGD:1306025 | Rattus norvegicus (Norway rat) | 315165 | Naga |
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| DOID:2367 | neuroaxonal dystrophy | MGI:1261422 | Mus musculus (house mouse) | 17939 | Naga |
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| DOID:0112318 | Schindler disease type 1 | RGD:1306025 | Rattus norvegicus (Norway rat) | 315165 | Naga |
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| DOID:0112319 | Kanzaki disease | RGD:1306025 | Rattus norvegicus (Norway rat) | 315165 | Naga |
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| DOID:14499 | Fabry disease | RGD:1306025 | Rattus norvegicus (Norway rat) | 315165 | Naga |
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| DOID:479 | angiokeratoma | MGI:1261422 | Mus musculus (house mouse) | 17939 | Naga |
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| DOID:0112318 | Schindler disease type 1 | MGI:1261422 | Mus musculus (house mouse) | 17939 | Naga |
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| DOID:14499 | Fabry disease | MGI:1261422 | Mus musculus (house mouse) | 17939 | Naga |
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| DOID:0110870 | congenital stationary night blindness 1A | HGNC:8082 | Homo sapiens (human) | 60506 | NYX |
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| DOID:8499 | night blindness | HGNC:8082 | Homo sapiens (human) | 60506 | NYX |
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| DOID:0050534 | congenital stationary night blindness | HGNC:8082 | Homo sapiens (human) | 60506 | NYX |
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| DOID:0080411 | familial adenomatous polyposis 3 | HGNC:8028 | Homo sapiens (human) | 4913 | NTHL1 |
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| DOID:0080411 | familial adenomatous polyposis 3 | SGD:S000005403 | Saccharomyces cerevisiae S288C | 854114 | NTG2 |
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| DOID:0080411 | familial adenomatous polyposis 3 | SGD:S000000013 | Saccharomyces cerevisiae S288C | 851218 | NTG1 |
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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: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:10762 | portal hypertension | HGNC:7962 | Homo sapiens (human) | 9572 | NR1D1 |
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