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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:0110197 | Charcot-Marie-Tooth disease dominant intermediate B | MGI:109547 | Mus musculus (house mouse) | 13430 | Dnm2 |
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| DOID:11252 | microcytic anemia | MGI:109547 | Mus musculus (house mouse) | 13430 | Dnm2 |
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| DOID:14717 | centronuclear myopathy | MGI:109547 | Mus musculus (house mouse) | 13430 | Dnm2 |
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| DOID:0111223 | centronuclear myopathy 1 | MGI:109547 | Mus musculus (house mouse) | 13430 | Dnm2 |
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| DOID:0060558 | lethal congenital contracture syndrome | MGI:109547 | Mus musculus (house mouse) | 13430 | Dnm2 |
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| DOID:10652 | Alzheimer's disease | MGI:107384 | Mus musculus (house mouse) | 13429 | Dnm1 |
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| DOID:0112202 | developmental and epileptic encephalopathy | MGI:107384 | Mus musculus (house mouse) | 13429 | Dnm1 |
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| DOID:11252 | microcytic anemia | MGI:107384 | Mus musculus (house mouse) | 13429 | Dnm1 |
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| DOID:1827 | idiopathic generalized epilepsy | MGI:107384 | Mus musculus (house mouse) | 13429 | Dnm1 |
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| DOID:0080437 | developmental and epileptic encephalopathy 31A | MGI:107384 | Mus musculus (house mouse) | 13429 | Dnm1 |
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| DOID:2476 | hereditary spastic paraplegia | MGI:107384 | Mus musculus (house mouse) | 13429 | Dnm1 |
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| DOID:0110197 | Charcot-Marie-Tooth disease dominant intermediate B | MGI:107384 | Mus musculus (house mouse) | 13429 | Dnm1 |
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| DOID:854 | collagen disease | MGI:107384 | Mus musculus (house mouse) | 13429 | Dnm1 |
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| DOID:0111223 | centronuclear myopathy 1 | MGI:107384 | Mus musculus (house mouse) | 13429 | Dnm1 |
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| DOID:0070376 | developmental and epileptic encephalopathy 31B | MGI:107384 | Mus musculus (house mouse) | 13429 | Dnm1 |
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| DOID:1289 | neurodegenerative disease | MGI:103147 | Mus musculus (house mouse) | 13424 | Dync1h1 |
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| DOID:0110175 | Charcot-Marie-Tooth disease axonal type 2O | MGI:103147 | Mus musculus (house mouse) | 13424 | Dync1h1 |
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| DOID:10652 | Alzheimer's disease | MGI:103147 | Mus musculus (house mouse) | 13424 | Dync1h1 |
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| DOID:0070043 | autosomal dominant intellectual developmental disorder 13 | MGI:103147 | Mus musculus (house mouse) | 13424 | Dync1h1 |
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| DOID:0050453 | lissencephaly | MGI:103147 | Mus musculus (house mouse) | 13424 | Dync1h1 |
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| DOID:0070351 | spinal muscular atrophy with lower extremity predominant 1 | MGI:103147 | Mus musculus (house mouse) | 13424 | Dync1h1 |
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| DOID:0050557 | congenital muscular dystrophy | MGI:103147 | Mus musculus (house mouse) | 13424 | Dync1h1 |
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| DOID:1826 | epilepsy | MGI:103147 | Mus musculus (house mouse) | 13424 | Dync1h1 |
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| DOID:7148 | rheumatoid arthritis | MGI:1329019 | Mus musculus (house mouse) | 13423 | Dnase2a |
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| DOID:2048 | autoimmune hepatitis | MGI:103157 | Mus musculus (house mouse) | 13419 | Dnase1 |
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