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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
LM-GlycoRepo
Repository for lectin-assisted multimodality data
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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
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: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:0060767 | autosomal dominant Robinow syndrome 3 | HGNC:3087 | Homo sapiens (human) | 1857 | DVL3 |
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| DOID:0060766 | autosomal dominant Robinow syndrome 1 | WB:WBGene00000858 | Caenorhabditis elegans | 177870 | cwn-2 |
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| DOID:0060766 | autosomal dominant Robinow syndrome 1 | MGI:98958 | Mus musculus (house mouse) | 22418 | Wnt5a |
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| DOID:0060766 | autosomal dominant Robinow syndrome 1 | HGNC:12784 | Homo sapiens (human) | 7474 | WNT5A |
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| DOID:0060766 | autosomal dominant Robinow syndrome 1 | FB:FBgn0010194 | Drosophila melanogaster (fruit fly) | 32838 | Wnt5 |
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| DOID:0060766 | autosomal dominant Robinow syndrome 1 | Xenbase:XB-GENE-6252367 | Xenopus laevis (African clawed frog) | 378689 | wnt5a.S |
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| DOID:0060765 | autosomal dominant Robinow syndrome 2 | MGI:94941 | Mus musculus (house mouse) | 13542 | Dvl1 |
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| DOID:0060765 | autosomal dominant Robinow syndrome 2 | HGNC:3084 | Homo sapiens (human) | 1855 | DVL1 |
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| DOID:0060764 | autosomal recessive Robinow syndrome | HGNC:10257 | Homo sapiens (human) | 4920 | ROR2 |
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| DOID:0060764 | autosomal recessive Robinow syndrome | HGNC:17019 | Homo sapiens (human) | 144165 | PRICKLE1 |
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| DOID:0060764 | autosomal recessive Robinow syndrome | WB:WBGene00000289 | Caenorhabditis elegans | 174473 | cam-1 |
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| DOID:0060764 | autosomal recessive Robinow syndrome | FB:FBgn0010407 | Drosophila melanogaster (fruit fly) | 34367 | Ror |
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| DOID:0060764 | autosomal recessive Robinow syndrome | MGI:1347521 | Mus musculus (house mouse) | 26564 | Ror2 |
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| DOID:0060762 | restrictive dermopathy | MGI:95586 | Mus musculus (house mouse) | 14313 | Fst |
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| DOID:0060762 | restrictive dermopathy | HGNC:3971 | Homo sapiens (human) | 10468 | FST |
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| DOID:0060762 | restrictive dermopathy | ZFIN:ZDB-GENE-990714-11 | Danio rerio (zebrafish) | 100004116 | fsta |
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| DOID:0060762 | restrictive dermopathy | RGD:2633 | Rattus norvegicus (Norway rat) | 24373 | Fst |
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| DOID:0060759 | immunodeficiency with hyper IgM type 5 | MGI:109352 | Mus musculus (house mouse) | 22256 | Ung |
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| DOID:0060759 | immunodeficiency with hyper IgM type 5 | HGNC:12572 | Homo sapiens (human) | 7374 | UNG |
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| DOID:0060759 | immunodeficiency with hyper IgM type 5 | WB:WBGene00013241 | Caenorhabditis elegans | 176633 | ung-1 |
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| DOID:0060759 | immunodeficiency with hyper IgM type 5 | SGD:S000004483 | Saccharomyces cerevisiae S288C | 854987 | UNG1 |
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| DOID:0060757 | sclerosteosis 2 | HGNC:6696 | Homo sapiens (human) | 4038 | LRP4 |
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