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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: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: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: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:0111223 | centronuclear myopathy 1 | HGNC:26190 | Homo sapiens (human) | 64419 | MTMR14 |
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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:7448 | Homo sapiens (human) | 4534 | MTM1 |
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| DOID:422 | congenital structural myopathy | HGNC:7448 | Homo sapiens (human) | 4534 | MTM1 |
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| DOID:0111225 | centronuclear myopathy X-linked | HGNC:7448 | Homo sapiens (human) | 4534 | MTM1 |
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| DOID:423 | myopathy | HGNC:7448 | Homo sapiens (human) | 4534 | MTM1 |
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| DOID:1289 | neurodegenerative disease | SGD:S000003489 | Saccharomyces cerevisiae S288C | 853173 | MTM1 |
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| DOID:14717 | centronuclear myopathy | HGNC:7448 | Homo sapiens (human) | 4534 | MTM1 |
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| DOID:4608 | common bile duct neoplasm | HGNC:7413 | Homo sapiens (human) | 4507 | MTAP |
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| DOID:0080664 | diaphyseal medullary stenosis with malignant fibrous histiocytoma | HGNC:7413 | Homo sapiens (human) | 4507 | MTAP |
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| DOID:0050625 | biliary tract benign neoplasm | HGNC:7413 | Homo sapiens (human) | 4507 | MTAP |
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| DOID:1793 | pancreatic cancer | HGNC:7413 | Homo sapiens (human) | 4507 | MTAP |
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| DOID:2581 | chondrodysplasia punctata | HGNC:10545 | Homo sapiens (human) | 6307 | MSMO1 |
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| DOID:4608 | common bile duct neoplasm | HGNC:7371 | Homo sapiens (human) | 10232 | MSLN |
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