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GlyTouCan
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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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 | October 9, 2024 |
| Disease ID ▼ | Disease Name | Alliance of Genome Resources ID | Species | Gene ID | Gene Symbol | FlyGlycoDB | Evidence Code Names | References |
|---|---|---|---|---|---|---|---|---|
| DOID:0070483 | Watson syndrome | MGI:97306 | Mus musculus (house mouse) | 18015 | Nf1 |
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| DOID:0070482 | spinal neurofibromatosis | HGNC:7765 | Homo sapiens (human) | 4763 | NF1 |
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| DOID:0070482 | spinal neurofibromatosis | MGI:97306 | Mus musculus (house mouse) | 18015 | Nf1 |
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| DOID:0070480 | schwannomatosis 1 | HGNC:11103 | Homo sapiens (human) | 6598 | SMARCB1 |
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| DOID:0070480 | schwannomatosis 1 | SGD:S000000493 | Saccharomyces cerevisiae S288C | 852592 | SNF5 |
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| DOID:0070478 | diphthamide deficiency syndrome 2 | HGNC:3004 | Homo sapiens (human) | 1802 | DPH2 |
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| DOID:0070478 | diphthamide deficiency syndrome 2 | MGI:1914978 | Mus musculus (house mouse) | 67728 | Dph2 |
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| DOID:0070476 | diphthamide deficiency syndrome | MGI:1914978 | Mus musculus (house mouse) | 67728 | Dph2 |
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| DOID:0070476 | diphthamide deficiency syndrome | HGNC:3004 | Homo sapiens (human) | 1802 | DPH2 |
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| DOID:0070474 | childhood-onset neurodegeneration with brain atrophy | HGNC:12511 | Homo sapiens (human) | 7343 | UBTF |
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| DOID:0070473 | Zaki syndrome | WB:WBGene00003246 | Caenorhabditis elegans | 175020 | mig-14 |
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| DOID:0070473 | Zaki syndrome | FB:FBgn0036141 | Drosophila melanogaster (fruit fly) | 39259 | wls |
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| DOID:0070473 | Zaki syndrome | HGNC:30238 | Homo sapiens (human) | 79971 | WLS |
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| DOID:0070472 | early-onset epilepsy 3 | HGNC:855 | Homo sapiens (human) | 527 | ATP6V0C |
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| DOID:0070471 | early-onset epilepsy 2 | HGNC:29010 | Homo sapiens (human) | 9739 | SETD1A |
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| DOID:0070471 | early-onset epilepsy 2 | MGI:2446244 | Mus musculus (house mouse) | 233904 | Setd1a |
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| DOID:0070469 | neurodevelopmental disorder with dysmorphic facies and thin corpus callosum | HGNC:11465 | Homo sapiens (human) | 11198 | SUPT16H |
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| DOID:0070469 | neurodevelopmental disorder with dysmorphic facies and thin corpus callosum | MGI:1890948 | Mus musculus (house mouse) | 114741 | Supt16 |
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| DOID:0070468 | Yoon-Bellen neurodevelopmental syndrome | WB:WBGene00020679 | Caenorhabditis elegans | 177235 | ogdh-1 |
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| DOID:0070468 | Yoon-Bellen neurodevelopmental syndrome | MGI:1098267 | Mus musculus (house mouse) | 18293 | Ogdh |
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| DOID:0070468 | Yoon-Bellen neurodevelopmental syndrome | HGNC:25590 | Homo sapiens (human) | 55753 | OGDHL |
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| DOID:0070468 | Yoon-Bellen neurodevelopmental syndrome | Xenbase:XB-GENE-984155 | Xenopus laevis (African clawed frog) | 447370 | ogdhl.L |
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| DOID:0070468 | Yoon-Bellen neurodevelopmental syndrome | HGNC:8124 | Homo sapiens (human) | 4967 | OGDH |
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| DOID:0070468 | Yoon-Bellen neurodevelopmental syndrome | RGD:1561359 | Rattus norvegicus (Norway rat) | 360975 | Ogdh |
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| DOID:0070467 | carpal tunnel syndrome 2 | MGI:88469 | Mus musculus (house mouse) | 12845 | Comp |
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