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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:423 | myopathy | HGNC:7448 | Homo sapiens (human) | 4534 | MTM1 |
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| DOID:14717 | centronuclear myopathy | HGNC:7448 | Homo sapiens (human) | 4534 | MTM1 |
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| DOID:0111225 | centronuclear myopathy X-linked | HGNC:7449 | Homo sapiens (human) | 8776 | MTMR1 |
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| DOID:10595 | Charcot-Marie-Tooth disease | HGNC:7449 | Homo sapiens (human) | 8776 | MTMR1 |
|
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| DOID:423 | myopathy | HGNC:7449 | Homo sapiens (human) | 8776 | MTMR1 |
|
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| DOID:10595 | Charcot-Marie-Tooth disease | HGNC:7450 | Homo sapiens (human) | 8898 | MTMR2 |
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| DOID:0110191 | Charcot-Marie-Tooth disease type 4B1 | HGNC:7450 | Homo sapiens (human) | 8898 | MTMR2 |
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| DOID:0111225 | centronuclear myopathy X-linked | HGNC:7450 | Homo sapiens (human) | 8898 | MTMR2 |
|
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| DOID:423 | myopathy | HGNC:7450 | Homo sapiens (human) | 8898 | MTMR2 |
|
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| DOID:0111225 | centronuclear myopathy X-linked | HGNC:7451 | Homo sapiens (human) | 8897 | MTMR3 |
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| DOID:10595 | Charcot-Marie-Tooth disease | 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:10595 | Charcot-Marie-Tooth disease | HGNC:7452 | Homo sapiens (human) | 9110 | MTMR4 |
|
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| DOID:767 | muscular atrophy | HGNC:7452 | Homo sapiens (human) | 9110 | MTMR4 |
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| DOID:10595 | Charcot-Marie-Tooth disease | HGNC:7453 | Homo sapiens (human) | 9107 | MTMR6 |
|
||
| DOID:14717 | centronuclear myopathy | HGNC:7453 | Homo sapiens (human) | 9107 | MTMR6 |
|
||
| DOID:0111225 | centronuclear myopathy X-linked | HGNC:7453 | Homo sapiens (human) | 9107 | MTMR6 |
|
||
| DOID:0111225 | centronuclear myopathy X-linked | HGNC:7454 | Homo sapiens (human) | 9108 | MTMR7 |
|
||
| DOID:10595 | Charcot-Marie-Tooth disease | HGNC:7454 | Homo sapiens (human) | 9108 | MTMR7 |
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| DOID:14717 | centronuclear myopathy | HGNC:7454 | Homo sapiens (human) | 9108 | MTMR7 |
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| DOID:0060740 | methylmalonic aciduria due to methylmalonyl-CoA mutase deficiency | HGNC:7526 | Homo sapiens (human) | 4594 | MMUT |
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| DOID:14749 | methylmalonic acidemia | HGNC:7526 | Homo sapiens (human) | 4594 | MMUT |
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| DOID:5517 | stomach carcinoma | HGNC:7527 | Homo sapiens (human) | 4595 | MUTYH |
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| DOID:0080410 | familial adenomatous polyposis 2 | HGNC:7527 | Homo sapiens (human) | 4595 | MUTYH |
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| DOID:0050424 | familial adenomatous polyposis | HGNC:7527 | Homo sapiens (human) | 4595 | MUTYH |
|
