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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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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:1324 | lung cancer | RGD:69062 | Rattus norvegicus (Norway rat) | 83571 | Cdkn1b |
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| DOID:8991 | cervix uteri carcinoma in situ | RGD:69062 | Rattus norvegicus (Norway rat) | 83571 | Cdkn1b |
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| DOID:7693 | abdominal aortic aneurysm | RGD:619999 | Rattus norvegicus (Norway rat) | 83576 | Sort1 |
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| DOID:3827 | congenital diaphragmatic hernia | HGNC:18196 | Homo sapiens (human) | 83595 | SOX7 |
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| DOID:10155 | intestinal cancer | HGNC:18196 | Homo sapiens (human) | 83595 | SOX7 |
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| DOID:0050981 | spinocerebellar ataxia type 34 | MGI:1933331 | Mus musculus (house mouse) | 83603 | Elovl4 |
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| DOID:0050817 | Stargardt disease | MGI:1933331 | Mus musculus (house mouse) | 83603 | Elovl4 |
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| DOID:2566 | corneal dystrophy | MGI:1933331 | Mus musculus (house mouse) | 83603 | Elovl4 |
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| DOID:0060669 | cerebral cavernous malformation | HGNC:21708 | Homo sapiens (human) | 83605 | CCM2 |
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| DOID:0060670 | cerebral cavernous malformation 2 | HGNC:21708 | Homo sapiens (human) | 83605 | CCM2 |
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| DOID:0110165 | Charcot-Marie-Tooth disease type 2E | RGD:621458 | Rattus norvegicus (Norway rat) | 83613 | Nefl |
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| DOID:3008 | invasive ductal carcinoma | RGD:621458 | Rattus norvegicus (Norway rat) | 83613 | Nefl |
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| DOID:4166 | syphilis | RGD:621458 | Rattus norvegicus (Norway rat) | 83613 | Nefl |
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| DOID:0080832 | mild cognitive impairment | RGD:621458 | Rattus norvegicus (Norway rat) | 83613 | Nefl |
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| DOID:8869 | neuromyelitis optica | RGD:621458 | Rattus norvegicus (Norway rat) | 83613 | Nefl |
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| DOID:10652 | Alzheimer's disease | RGD:621458 | Rattus norvegicus (Norway rat) | 83613 | Nefl |
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| DOID:11949 | Creutzfeldt-Jakob disease | RGD:621458 | Rattus norvegicus (Norway rat) | 83613 | Nefl |
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| DOID:224 | transient cerebral ischemia | RGD:621458 | Rattus norvegicus (Norway rat) | 83613 | Nefl |
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| DOID:12894 | Sjogren's syndrome | RGD:621458 | Rattus norvegicus (Norway rat) | 83613 | Nefl |
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| DOID:0080600 | COVID-19 | RGD:621458 | Rattus norvegicus (Norway rat) | 83613 | Nefl |
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| DOID:2378 | relapsing-remitting multiple sclerosis | RGD:621458 | Rattus norvegicus (Norway rat) | 83613 | Nefl |
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| DOID:8725 | vascular dementia | RGD:621458 | Rattus norvegicus (Norway rat) | 83613 | Nefl |
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| DOID:0050328 | congenital hypothyroidism | RGD:621458 | Rattus norvegicus (Norway rat) | 83613 | Nefl |
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| DOID:0050433 | fatal familial insomnia | RGD:621458 | Rattus norvegicus (Norway rat) | 83613 | Nefl |
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| DOID:3213 | demyelinating disease | RGD:621458 | Rattus norvegicus (Norway rat) | 83613 | Nefl |
|
