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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:0080572 | congenital disorder of glycosylation Iw | FB:FBgn0031149 | Drosophila melanogaster (fruit fly) | 33082 | Stt3A | CG1518 |
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| DOID:0080572 | congenital disorder of glycosylation Iw | ZFIN:ZDB-GENE-021015-3 | Danio rerio (zebrafish) | 266797 | stt3a |
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| DOID:0080572 | congenital disorder of glycosylation Iw | MGI:105124 | Mus musculus (house mouse) | 16430 | Stt3a |
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| DOID:0080572 | congenital disorder of glycosylation Iw | Xenbase:XB-GENE-973644 | Xenopus laevis (African clawed frog) | 399234 | stt3a.L |
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| DOID:0080572 | congenital disorder of glycosylation Iw | RGD:1311563 | Rattus norvegicus (Norway rat) | 363160 | Stt3b |
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| DOID:0080572 | congenital disorder of glycosylation Iw | WB:WBGene00020437 | Caenorhabditis elegans | 175886 | stt-3 |
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| DOID:0080572 | congenital disorder of glycosylation Iw | Xenbase:XB-GENE-17338795 | Xenopus laevis (African clawed frog) | 779022 | stt3a.S |
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| DOID:0080573 | congenital disorder of glycosylation Ix | HGNC:30611 | Homo sapiens (human) | 201595 | STT3B |
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| DOID:0080573 | congenital disorder of glycosylation Ix | RGD:1311563 | Rattus norvegicus (Norway rat) | 363160 | Stt3b |
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| DOID:0080573 | congenital disorder of glycosylation Ix | Xenbase:XB-GENE-969897 | Xenopus laevis (African clawed frog) | 100380973 | stt3b.S |
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| DOID:0080573 | congenital disorder of glycosylation Ix | Xenbase:XB-GENE-17341012 | Xenopus laevis (African clawed frog) | 108718938 | stt3b.L |
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| DOID:0080573 | congenital disorder of glycosylation Ix | WB:WBGene00020437 | Caenorhabditis elegans | 175886 | stt-3 |
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| DOID:0080573 | congenital disorder of glycosylation Ix | MGI:1915542 | Mus musculus (house mouse) | 68292 | Stt3b |
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| DOID:0080573 | congenital disorder of glycosylation Ix | ZFIN:ZDB-GENE-030131-2638 | Danio rerio (zebrafish) | 323918 | stt3b |
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| DOID:0080573 | congenital disorder of glycosylation Ix | FB:FBgn0011336 | Drosophila melanogaster (fruit fly) | 43005 | Stt3B | CG7748 |
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| DOID:0080573 | congenital disorder of glycosylation Ix | SGD:S000002990 | Saccharomyces cerevisiae S288C | 852862 | STT3 |
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| DOID:0050570 | congenital disorder of glycosylation type I | MGI:2384774 | Mus musculus (house mouse) | 208211 | Alg1 |
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| DOID:0050570 | congenital disorder of glycosylation type I | Xenbase:XB-GENE-6036140 | Xenopus tropicalis (tropical clawed frog) | 100497477 | alg9 |
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| DOID:0050570 | congenital disorder of glycosylation type I | HGNC:19358 | Homo sapiens (human) | 79087 | ALG12 |
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| DOID:0050570 | congenital disorder of glycosylation type I | HGNC:3007 | Homo sapiens (human) | 54344 | DPM3 |
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| DOID:0050570 | congenital disorder of glycosylation type I | WB:WBGene00009925 | Caenorhabditis elegans | 178364 | F52B11.2 |
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| DOID:0050570 | congenital disorder of glycosylation type I | SGD:S000001849 | Saccharomyces cerevisiae S288C | 850499 | SEC53 |
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| DOID:0050570 | congenital disorder of glycosylation type I | SGD:S000005313 | Saccharomyces cerevisiae S288C | 855764 | ALG12 |
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| DOID:0050570 | congenital disorder of glycosylation type I | SGD:S000005528 | Saccharomyces cerevisiae S288C | 854163 | ALG6 |
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| DOID:0050570 | congenital disorder of glycosylation type I | HGNC:20266 | Homo sapiens (human) | 29880 | ALG5 |
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