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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:0060589 | Yunis-Varon syndrome | HGNC:16873 | Homo sapiens (human) | 9896 | FIG4 |
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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:0070187 | Y-linked spermatogenic failure 2 | FB:FBgn0005632 | Drosophila melanogaster (fruit fly) | 43749 | faf |
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| DOID:0070187 | Y-linked spermatogenic failure 2 | HGNC:12633 | Homo sapiens (human) | 8287 | USP9Y |
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| DOID:0111758 | Y-linked deafness 2 | MGI:1336172 | Mus musculus (house mouse) | 21372 | Tbl1x |
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| DOID:0111758 | Y-linked deafness 2 | HGNC:18502 | Homo sapiens (human) | 90665 | TBL1Y |
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| DOID:0070055 | Xia-Gibbs Syndrome | MGI:2444218 | Mus musculus (house mouse) | 230793 | Ahdc1 |
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| DOID:0070055 | Xia-Gibbs Syndrome | HGNC:25230 | Homo sapiens (human) | 27245 | AHDC1 |
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| DOID:0080839 | X-linked warfarin sensitivity | HGNC:3551 | Homo sapiens (human) | 2158 | F9 |
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| DOID:0080839 | X-linked warfarin sensitivity | MGI:88384 | Mus musculus (house mouse) | 14071 | F9 |
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| DOID:0080839 | X-linked warfarin sensitivity | RGD:2589 | Rattus norvegicus (Norway rat) | 24946 | F9 |
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| DOID:0111899 | X-linked thrombophilia due to factor IX defect | RGD:2589 | Rattus norvegicus (Norway rat) | 24946 | F9 |
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| DOID:0111899 | X-linked thrombophilia due to factor IX defect | MGI:88384 | Mus musculus (house mouse) | 14071 | F9 |
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| DOID:0111899 | X-linked thrombophilia due to factor IX defect | HGNC:3551 | Homo sapiens (human) | 2158 | F9 |
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| DOID:0112150 | X-linked spondyloepimetaphyseal dysplasia | MGI:88158 | Mus musculus (house mouse) | 12111 | Bgn |
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| DOID:0112150 | X-linked spondyloepimetaphyseal dysplasia | HGNC:1044 | Homo sapiens (human) | 633 | BGN |
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| DOID:0112150 | X-linked spondyloepimetaphyseal dysplasia | RGD:2207 | Rattus norvegicus (Norway rat) | 25181 | Bgn |
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| DOID:0111827 | X-linked spinal muscular atrophy 2 | MGI:98890 | Mus musculus (house mouse) | 22201 | Uba1 |
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| DOID:0111827 | X-linked spinal muscular atrophy 2 | HGNC:12469 | Homo sapiens (human) | 7317 | UBA1 |
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| DOID:0112274 | X-linked spermatogenic failure 3 | HGNC:26708 | Homo sapiens (human) | 286464 | CFAP47 |
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