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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:3526 | cerebral infarction | RGD:3876 | Rattus norvegicus (Norway rat) | 24835 | Tnf |
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| DOID:3526 | cerebral infarction | HGNC:6623 | Homo sapiens (human) | 9388 | LIPG |
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| DOID:3526 | cerebral infarction | HGNC:4555 | Homo sapiens (human) | 2878 | GPX3 |
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| DOID:3526 | cerebral infarction | MGI:104798 | Mus musculus (house mouse) | 21926 | Tnf |
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| DOID:3526 | cerebral infarction | MGI:96113 | Mus musculus (house mouse) | 15289 | Hmgb1 |
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| DOID:0050719 | cerebral folate receptor alpha deficiency | HGNC:3791 | Homo sapiens (human) | 2348 | FOLR1 |
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| DOID:0080491 | cerebral cavernous malformation 1 | HGNC:9603 | Homo sapiens (human) | 5740 | PTGIS |
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| DOID:0060669 | cerebral cavernous malformation | MGI:1206581 | Mus musculus (house mouse) | 18706 | Pik3ca |
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| DOID:0060669 | cerebral cavernous malformation | RGD:620916 | Rattus norvegicus (Norway rat) | 170911 | Pik3ca |
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| DOID:0060669 | cerebral cavernous malformation | HGNC:8975 | Homo sapiens (human) | 5290 | PIK3CA |
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| DOID:0060669 | cerebral cavernous malformation | HGNC:9588 | Homo sapiens (human) | 5728 | PTEN |
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| DOID:9246 | cerebral amyloid angiopathy | HGNC:8133 | Homo sapiens (human) | 4973 | OLR1 |
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| DOID:0050753 | cerebellar ataxia | HGNC:16268 | Homo sapiens (human) | 10908 | PNPLA6 |
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| DOID:0050753 | cerebellar ataxia | HGNC:24768 | Homo sapiens (human) | 375775 | PNPLA7 |
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| DOID:0050753 | cerebellar ataxia | FB:FBgn0032729 | Drosophila melanogaster (fruit fly) | 35156 | L2HGDH |
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| DOID:0050753 | cerebellar ataxia | HGNC:20499 | Homo sapiens (human) | 79944 | L2HGDH |
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| DOID:0111225 | centronuclear myopathy X-linked | HGNC:7451 | Homo sapiens (human) | 8897 | MTMR3 |
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| DOID:0111225 | centronuclear myopathy X-linked | HGNC:7452 | Homo sapiens (human) | 9110 | MTMR4 |
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| DOID:0111225 | centronuclear myopathy X-linked | HGNC:16825 | Homo sapiens (human) | 55613 | MTMR8 |
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| DOID:0111225 | centronuclear myopathy X-linked | HGNC:7449 | Homo sapiens (human) | 8776 | MTMR1 |
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| DOID:0111225 | centronuclear myopathy X-linked | HGNC:7454 | Homo sapiens (human) | 9108 | MTMR7 |
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| DOID:0111225 | centronuclear myopathy X-linked | HGNC:7450 | Homo sapiens (human) | 8898 | MTMR2 |
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| DOID:0111225 | centronuclear myopathy X-linked | HGNC:7448 | Homo sapiens (human) | 4534 | MTM1 |
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| DOID:0111225 | centronuclear myopathy X-linked | HGNC:7453 | Homo sapiens (human) | 9107 | MTMR6 |
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| DOID:0111223 | centronuclear myopathy 1 | HGNC:26190 | Homo sapiens (human) | 64419 | MTMR14 |
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