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Glycan Structure 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:0050571 | congenital disorder of glycosylation type II | MGI:1928483 | Mus musculus (house mouse) | 56389 | Stx5a |
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| DOID:0050571 | congenital disorder of glycosylation type II | Xenbase:XB-GENE-5811512 | Xenopus laevis (African clawed frog) | 443907 | edem3.L |
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| DOID:0050571 | congenital disorder of glycosylation type II | FB:FBgn0032480 | Drosophila melanogaster (fruit fly) | 34714 | Edem2 | CG5682 |
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| DOID:0050571 | congenital disorder of glycosylation type II | FB:FBgn0265351 | Drosophila melanogaster (fruit fly) | 40981 | nac | CG9620 |
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| DOID:0050571 | congenital disorder of glycosylation type II | RGD:1310692 | Rattus norvegicus (Norway rat) | 292090 | Galnt2 |
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| DOID:0050571 | congenital disorder of glycosylation type II | HGNC:4124 | Homo sapiens (human) | 2590 | GALNT2 |
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| DOID:0050571 | congenital disorder of glycosylation type II | WB:WBGene00001629 | Caenorhabditis elegans | 180302 | gly-4 |
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| DOID:0050571 | congenital disorder of glycosylation type II | Xenbase:XB-GENE-6486521 | Xenopus laevis (African clawed frog) | 101027298 | galnt2.S |
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| DOID:0050570 | congenital disorder of glycosylation type I | ZFIN:ZDB-GENE-030131-5812 | Danio rerio (zebrafish) | 327601 | alg8 |
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| DOID:0050570 | congenital disorder of glycosylation type I | MGI:1913498 | Mus musculus (house mouse) | 66248 | Alg5 |
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| DOID:0050570 | congenital disorder of glycosylation type I | FB:FBgn0037743 | Drosophila melanogaster (fruit fly) | 41191 | Alg12 | CG8412 |
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| DOID:0050570 | congenital disorder of glycosylation type I | HGNC:3005 | Homo sapiens (human) | 8813 | DPM1 |
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| DOID:0050570 | congenital disorder of glycosylation type I | MGI:2444031 | Mus musculus (house mouse) | 320438 | Alg6 |
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| DOID:0050570 | congenital disorder of glycosylation type I | SGD:S000005593 | Saccharomyces cerevisiae S288C | 854233 | ALG8 |
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| DOID:0050570 | congenital disorder of glycosylation type I | HGNC:37258 | Homo sapiens (human) | 644974 | ALG1L2 |
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| DOID:0050570 | congenital disorder of glycosylation type I | SGD:S000005163 | Saccharomyces cerevisiae S288C | 855502 | ALG9 |
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| DOID:0050570 | congenital disorder of glycosylation type I | Xenbase:XB-GENE-967047 | Xenopus tropicalis (tropical clawed frog) | 548388 | alg8 |
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| DOID:0050570 | congenital disorder of glycosylation type I | HGNC:23157 | Homo sapiens (human) | 29929 | ALG6 |
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| DOID:0050570 | congenital disorder of glycosylation type I | MGI:1330239 | Mus musculus (house mouse) | 13480 | Dpm1 |
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| DOID:0050570 | congenital disorder of glycosylation type I | WB:WBGene00007556 | Caenorhabditis elegans | 174633 | algn-9 |
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| DOID:0050570 | congenital disorder of glycosylation type I | HGNC:18294 | Homo sapiens (human) | 56052 | ALG1 |
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| DOID:0050570 | congenital disorder of glycosylation type I | RGD:1310120 | Rattus norvegicus (Norway rat) | 296394 | Dpm1 |
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| DOID:0050570 | congenital disorder of glycosylation type I | RGD:1308900 | Rattus norvegicus (Norway rat) | 295051 | Alg5 |
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| DOID:0050570 | congenital disorder of glycosylation type I | HGNC:7216 | Homo sapiens (human) | 4351 | MPI |
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| DOID:0050570 | congenital disorder of glycosylation type I | MGI:1330238 | Mus musculus (house mouse) | 13481 | Dpm2 |
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