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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:0081326 | oxoglutarate dehydrogenase deficiency | HGNC:8124 | Homo sapiens (human) | 4967 | OGDH |
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| DOID:0081326 | oxoglutarate dehydrogenase deficiency | HGNC:25590 | Homo sapiens (human) | 55753 | OGDHL |
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| DOID:0081327 | neurodevelopmental disorder with regression, abnormal movements, loss of speech, and seizures | HGNC:21728 | Homo sapiens (human) | 26145 | IRF2BP1 |
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| DOID:0081327 | neurodevelopmental disorder with regression, abnormal movements, loss of speech, and seizures | MGI:2443921 | Mus musculus (house mouse) | 270110 | Irf2bp2 |
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| DOID:0081327 | neurodevelopmental disorder with regression, abnormal movements, loss of speech, and seizures | HGNC:21729 | Homo sapiens (human) | 359948 | IRF2BP2 |
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| DOID:0081327 | neurodevelopmental disorder with regression, abnormal movements, loss of speech, and seizures | HGNC:14282 | Homo sapiens (human) | 64207 | IRF2BPL |
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| DOID:0081327 | neurodevelopmental disorder with regression, abnormal movements, loss of speech, and seizures | MGI:2442463 | Mus musculus (house mouse) | 238330 | Irf2bpl |
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| DOID:0081328 | familial hyperinsulinemic hypoglycemia 8 | HGNC:29681 | Homo sapiens (human) | 84275 | SLC25A33 |
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| DOID:0081330 | glycogen storage disease Ib | HGNC:4061 | Homo sapiens (human) | 2542 | SLC37A4 |
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| DOID:0081331 | glycogen storage disease Ic | HGNC:4061 | Homo sapiens (human) | 2542 | SLC37A4 |
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| DOID:0081333 | Wiedemann-Rautenstrauch syndrome | HGNC:30074 | Homo sapiens (human) | 11128 | POLR3A |
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| DOID:0081335 | Becker disease | WB:WBGene00000528 | Caenorhabditis elegans | 174821 | clh-1 |
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| DOID:0081336 | Thomsen disease | WB:WBGene00000528 | Caenorhabditis elegans | 174821 | clh-1 |
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| DOID:0081337 | congenital myopathy | MGI:1353592 | Mus musculus (house mouse) | 30963 | Hacd1 |
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| DOID:0081337 | congenital myopathy | MGI:1344412 | Mus musculus (house mouse) | 24131 | Ldb3 |
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| DOID:0081337 | congenital myopathy | FB:FBgn0265991 | Drosophila melanogaster (fruit fly) | 36740 | Zasp52 |
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| DOID:0081337 | congenital myopathy | HGNC:15710 | Homo sapiens (human) | 11155 | LDB3 |
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| DOID:0081337 | congenital myopathy | HGNC:9639 | Homo sapiens (human) | 9200 | HACD1 |
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| DOID:0081337 | congenital myopathy | HGNC:7549 | Homo sapiens (human) | 4604 | MYBPC1 |
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| DOID:0081339 | congenital myopathy 2B | RGD:2025 | Rattus norvegicus (Norway rat) | 29437 | Acta1 |
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| DOID:0081339 | congenital myopathy 2B | MGI:87902 | Mus musculus (house mouse) | 11459 | Acta1 |
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| DOID:0081339 | congenital myopathy 2B | HGNC:129 | Homo sapiens (human) | 58 | ACTA1 |
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| DOID:0081340 | congenital myopathy 2C | MGI:87902 | Mus musculus (house mouse) | 11459 | Acta1 |
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| DOID:0081340 | congenital myopathy 2C | RGD:2025 | Rattus norvegicus (Norway rat) | 29437 | Acta1 |
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| DOID:0081340 | congenital myopathy 2C | HGNC:129 | Homo sapiens (human) | 58 | ACTA1 |
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