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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:0070273 | hereditary nonpolyposis colorectal cancer type 6 | HGNC:11773 | Homo sapiens (human) | 7048 | TGFBR2 |
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| DOID:0070273 | hereditary nonpolyposis colorectal cancer type 6 | WB:WBGene00000900 | Caenorhabditis elegans | 175781 | daf-4 |
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| DOID:0070273 | hereditary nonpolyposis colorectal cancer type 6 | RGD:69651 | Rattus norvegicus (Norway rat) | 81810 | Tgfbr2 |
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| DOID:0070272 | hereditary nonpolyposis colorectal cancer type 5 | MGI:1343961 | Mus musculus (house mouse) | 17688 | Msh6 |
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| DOID:0070272 | hereditary nonpolyposis colorectal cancer type 5 | HGNC:7329 | Homo sapiens (human) | 2956 | MSH6 |
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| DOID:0070271 | Lynch syndrome 1 | HGNC:7325 | Homo sapiens (human) | 4436 | MSH2 |
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| DOID:0070270 | hereditary nonpolyposis colorectal cancer type 8 | RGD:621365 | Rattus norvegicus (Norway rat) | 171577 | Epcam |
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| DOID:0070270 | hereditary nonpolyposis colorectal cancer type 8 | HGNC:11529 | Homo sapiens (human) | 4072 | EPCAM |
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| DOID:0070270 | hereditary nonpolyposis colorectal cancer type 8 | MGI:106653 | Mus musculus (house mouse) | 17075 | Epcam |
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| DOID:0070270 | hereditary nonpolyposis colorectal cancer type 8 | HGNC:7325 | Homo sapiens (human) | 4436 | MSH2 |
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| DOID:0070269 | congenital disorder of glycosylation type IIq | HGNC:6546 | Homo sapiens (human) | 22796 | COG2 |
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| DOID:0070268 | congenital disorder of glycosylation type IIp | HGNC:18085 | Homo sapiens (human) | 147007 | TMEM199 |
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| DOID:0070267 | congenital disorder of glycosylation type IIo | HGNC:28178 | Homo sapiens (human) | 84317 | CCDC115 |
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| DOID:0070266 | congenital disorder of glycosylation type IIn | HGNC:20862 | Homo sapiens (human) | 64116 | SLC39A8 |
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| DOID:0070266 | congenital disorder of glycosylation type IIn | RGD:1308236 | Rattus norvegicus (Norway rat) | 295455 | Slc39a8 |
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| DOID:0070266 | congenital disorder of glycosylation type IIn | MGI:1914797 | Mus musculus (house mouse) | 67547 | Slc39a8 |
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| DOID:0070265 | congenital disorder of glycosylation type IIm | FB:FBgn0024994 | Drosophila melanogaster (fruit fly) | 31255 | Ugalt | CG2675 |
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| DOID:0070265 | congenital disorder of glycosylation type IIm | HGNC:11022 | Homo sapiens (human) | 7355 | SLC35A2 |
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| DOID:0070264 | congenital disorder of glycosylation type IIl | SGD:S000004986 | Saccharomyces cerevisiae S288C | 855687 | COG6 |
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| DOID:0070264 | congenital disorder of glycosylation type IIl | MGI:1914792 | Mus musculus (house mouse) | 67542 | Cog6 |
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| DOID:0070264 | congenital disorder of glycosylation type IIl | HGNC:18621 | Homo sapiens (human) | 57511 | COG6 |
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| DOID:0070263 | congenital disorder of glycosylation type IIk | HGNC:30760 | Homo sapiens (human) | 55858 | TMEM165 |
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| DOID:0070262 | congenital disorder of glycosylation type IIj | SGD:S000006309 | Saccharomyces cerevisiae S288C | 856220 | COG4 |
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| DOID:0070262 | congenital disorder of glycosylation type IIj | SGD:S000000671 | Saccharomyces cerevisiae S288C | 850438 | ERS1 |
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| DOID:0070262 | congenital disorder of glycosylation type IIj | HGNC:18620 | Homo sapiens (human) | 25839 | COG4 |
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