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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:0050882 | spinocerebellar ataxia type 5 | HGNC:11276 | Homo sapiens (human) | 6712 | SPTBN2 |
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| DOID:0050882 | spinocerebellar ataxia type 5 | HGNC:11274 | Homo sapiens (human) | 6710 | SPTB |
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| DOID:0050882 | spinocerebellar ataxia type 5 | MGI:98388 | Mus musculus (house mouse) | 20742 | Sptbn1 |
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| DOID:0050882 | spinocerebellar ataxia type 5 | HGNC:14896 | Homo sapiens (human) | 57731 | SPTBN4 |
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| DOID:0050881 | inclusion body myopathy with Paget disease of bone and frontotemporal dementia | MGI:105047 | Mus musculus (house mouse) | 19184 | Psmc5 |
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| DOID:0050881 | inclusion body myopathy with Paget disease of bone and frontotemporal dementia | HGNC:9552 | Homo sapiens (human) | 5705 | PSMC5 |
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| DOID:0050881 | inclusion body myopathy with Paget disease of bone and frontotemporal dementia | RGD:2542 | Rattus norvegicus (Norway rat) | 25313 | Egf |
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| DOID:0050881 | inclusion body myopathy with Paget disease of bone and frontotemporal dementia | MGI:95290 | Mus musculus (house mouse) | 13645 | Egf |
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| DOID:0050881 | inclusion body myopathy with Paget disease of bone and frontotemporal dementia | HGNC:5033 | Homo sapiens (human) | 3181 | HNRNPA2B1 |
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| DOID:0050881 | inclusion body myopathy with Paget disease of bone and frontotemporal dementia | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:0050881 | inclusion body myopathy with Paget disease of bone and frontotemporal dementia | HGNC:12666 | Homo sapiens (human) | 7415 | VCP |
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| DOID:0050881 | inclusion body myopathy with Paget disease of bone and frontotemporal dementia | MGI:104798 | Mus musculus (house mouse) | 21926 | Tnf |
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| DOID:0050881 | inclusion body myopathy with Paget disease of bone and frontotemporal dementia | RGD:3876 | Rattus norvegicus (Norway rat) | 24835 | Tnf |
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| DOID:0050881 | inclusion body myopathy with Paget disease of bone and frontotemporal dementia | HGNC:3229 | Homo sapiens (human) | 1950 | EGF |
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| DOID:0050880 | Koolen de Vries syndrome | HGNC:24565 | Homo sapiens (human) | 284058 | KANSL1 |
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| DOID:0050880 | Koolen de Vries syndrome | MGI:1923969 | Mus musculus (house mouse) | 76719 | Kansl1 |
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| DOID:0050879 | fragile X-associated tremor/ataxia syndrome | HGNC:3775 | Homo sapiens (human) | 2332 | FMR1 |
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| DOID:0050877 | pancreatic agenesis | MGI:102851 | Mus musculus (house mouse) | 18609 | Pdx1 |
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| DOID:0050877 | pancreatic agenesis | HGNC:6107 | Homo sapiens (human) | 3651 | PDX1 |
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| DOID:0050877 | pancreatic agenesis | RGD:62387 | Rattus norvegicus (Norway rat) | 29535 | Pdx1 |
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| DOID:0050876 | Caroli disease | RGD:621861 | Rattus norvegicus (Norway rat) | 89805 | Angpt2 |
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| DOID:0050876 | Caroli disease | WB:WBGene00012782 | Caenorhabditis elegans | 177911 | Y43C5A.2 |
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| DOID:0050876 | Caroli disease | HGNC:485 | Homo sapiens (human) | 285 | ANGPT2 |
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| DOID:0050876 | Caroli disease | WB:WBGene00016769 | Caenorhabditis elegans | 177668 | C49C8.5 |
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| DOID:0050876 | Caroli disease | MGI:1202890 | Mus musculus (house mouse) | 11601 | Angpt2 |
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