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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:0080555 | congenital disorder of glycosylation Ic | WB:WBGene00007435 | Caenorhabditis elegans | 182392 | algn-6 |
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| DOID:0080555 | congenital disorder of glycosylation Ic | Xenbase:XB-GENE-998193 | Xenopus laevis (African clawed frog) | 100049135 | alg6.L |
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| DOID:0080555 | congenital disorder of glycosylation Ic | ZFIN:ZDB-GENE-040808-45 | Danio rerio (zebrafish) | 445327 | alg6 |
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| DOID:0080555 | congenital disorder of glycosylation Ic | SGD:S000005528 | Saccharomyces cerevisiae S288C | 854163 | ALG6 |
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| DOID:0080554 | congenital disorder of glycosylation Ib | WB:WBGene00014013 | Caenorhabditis elegans | 176388 | ZK632.4 |
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| DOID:0080554 | congenital disorder of glycosylation Ib | RGD:3107 | Rattus norvegicus (Norway rat) | 300741 | Mpi |
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| DOID:0080554 | congenital disorder of glycosylation Ib | HGNC:7216 | Homo sapiens (human) | 4351 | MPI |
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| DOID:0080554 | congenital disorder of glycosylation Ib | SGD:S000000805 | Saccharomyces cerevisiae S288C | 856720 | PMI40 |
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| DOID:0080554 | congenital disorder of glycosylation Ib | MGI:97075 | Mus musculus (house mouse) | 110119 | Mpi |
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| DOID:0080552 | congenital disorder of glycosylation Ia | FB:FBgn0036300 | Drosophila melanogaster (fruit fly) | 39436 | Pmm2 |
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| DOID:0080552 | congenital disorder of glycosylation Ia | HGNC:9115 | Homo sapiens (human) | 5373 | PMM2 |
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| DOID:0080552 | congenital disorder of glycosylation Ia | HGNC:9114 | Homo sapiens (human) | 5372 | PMM1 |
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| DOID:0080552 | congenital disorder of glycosylation Ia | HGNC:5466 | Homo sapiens (human) | 3481 | IGF2 |
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| DOID:0080552 | congenital disorder of glycosylation Ia | MGI:96434 | Mus musculus (house mouse) | 16002 | Igf2 |
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| DOID:0080552 | congenital disorder of glycosylation Ia | MGI:1859214 | Mus musculus (house mouse) | 54128 | Pmm2 |
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| DOID:0080552 | congenital disorder of glycosylation Ia | RGD:2870 | Rattus norvegicus (Norway rat) | 24483 | Igf2 |
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| DOID:0080552 | congenital disorder of glycosylation Ia | MGI:1353418 | Mus musculus (house mouse) | 29858 | Pmm1 |
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| DOID:0080552 | congenital disorder of glycosylation Ia | WB:WBGene00009925 | Caenorhabditis elegans | 178364 | F52B11.2 |
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| DOID:0080552 | congenital disorder of glycosylation Ia | SGD:S000001849 | Saccharomyces cerevisiae S288C | 850499 | SEC53 |
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| DOID:0080550 | Noonan syndrome with multiple lentigines 3 | HGNC:1097 | Homo sapiens (human) | 673 | BRAF |
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| DOID:0080550 | Noonan syndrome with multiple lentigines 3 | MGI:88190 | Mus musculus (house mouse) | 109880 | Braf |
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| DOID:0080547 | metabolic dysfunction-associated steatohepatitis | RGD:3267 | Rattus norvegicus (Norway rat) | 362282 | Pck1 |
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| DOID:0080547 | metabolic dysfunction-associated steatohepatitis | HGNC:8724 | Homo sapiens (human) | 5105 | PCK1 |
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| DOID:0080547 | metabolic dysfunction-associated steatohepatitis | RGD:2396 | Rattus norvegicus (Norway rat) | 25757 | Cpt1a |
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| DOID:0080547 | metabolic dysfunction-associated steatohepatitis | HGNC:10571 | Homo sapiens (human) | 6319 | SCD |
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