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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:13096 | Sneddon syndrome | HGNC:1839 | Homo sapiens (human) | 51816 | ADA2 |
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| DOID:13096 | Sneddon syndrome | Xenbase:XB-GENE-6254244 | Xenopus laevis (African clawed frog) | 779128 | ada2.L |
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| DOID:13096 | Sneddon syndrome | ZFIN:ZDB-GENE-030902-4 | Danio rerio (zebrafish) | 373884 | ada2a |
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| DOID:0081271 | Smith-McCort dysplasia 2 | HGNC:16075 | Homo sapiens (human) | 83452 | RAB33B |
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| DOID:0081270 | Smith-McCort dysplasia 1 | HGNC:21317 | Homo sapiens (human) | 54808 | DYM |
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| DOID:0060247 | Smith-McCort dysplasia | HGNC:30273 | Homo sapiens (human) | 51762 | RAB8B |
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| DOID:0060247 | Smith-McCort dysplasia | MGI:2442982 | Mus musculus (house mouse) | 235442 | Rab8b |
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| DOID:0060247 | Smith-McCort dysplasia | HGNC:21317 | Homo sapiens (human) | 54808 | DYM |
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| DOID:0060768 | Smith-Magenis syndrome | HGNC:7035 | Homo sapiens (human) | 4239 | MFAP4 |
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| DOID:0060768 | Smith-Magenis syndrome | MGI:103291 | Mus musculus (house mouse) | 19377 | Rai1 |
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| DOID:0060768 | Smith-Magenis syndrome | MGI:1342276 | Mus musculus (house mouse) | 76293 | Mfap4 |
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| DOID:0060768 | Smith-Magenis syndrome | HGNC:9834 | Homo sapiens (human) | 10743 | RAI1 |
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| DOID:14692 | Smith-Lemli-Opitz syndrome | HGNC:2860 | Homo sapiens (human) | 1717 | DHCR7 |
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| DOID:12803 | Sly syndrome | MGI:95872 | Mus musculus (house mouse) | 110006 | Gusb |
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| DOID:12803 | Sly syndrome | RGD:2772 | Rattus norvegicus (Norway rat) | 24434 | Gusb |
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| DOID:12803 | Sly syndrome | WB:WBGene00013693 | Caenorhabditis elegans | 173326 | Y105E8B.9 |
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| DOID:12803 | Sly syndrome | HGNC:4696 | Homo sapiens (human) | 2990 | GUSB |
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| DOID:14501 | Sjogren-Larsson syndrome | HGNC:411 | Homo sapiens (human) | 222 | ALDH3B2 |
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| DOID:14501 | Sjogren-Larsson syndrome | HGNC:405 | Homo sapiens (human) | 218 | ALDH3A1 |
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| DOID:14501 | Sjogren-Larsson syndrome | HGNC:3570 | Homo sapiens (human) | 2181 | ACSL3 |
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| DOID:14501 | Sjogren-Larsson syndrome | HGNC:3571 | Homo sapiens (human) | 2182 | ACSL4 |
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| DOID:14501 | Sjogren-Larsson syndrome | MGI:1921455 | Mus musculus (house mouse) | 74205 | Acsl3 |
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| DOID:14501 | Sjogren-Larsson syndrome | HGNC:410 | Homo sapiens (human) | 221 | ALDH3B1 |
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| DOID:14501 | Sjogren-Larsson syndrome | HGNC:403 | Homo sapiens (human) | 224 | ALDH3A2 |
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| DOID:12894 | Sjogren's syndrome | HGNC:6018 | Homo sapiens (human) | 3569 | IL6 |
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