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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:0080282 | developmental and epileptic encephalopathy 56 | HGNC:12852 | Homo sapiens (human) | 7532 | YWHAG |
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| DOID:0080281 | schizophrenia 19 | HGNC:9898 | Homo sapiens (human) | 10137 | RBM12 |
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| DOID:0080281 | schizophrenia 19 | MGI:1922960 | Mus musculus (house mouse) | 75710 | Rbm12 |
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| DOID:0080280 | gingival fibromatosis 5 | MGI:104897 | Mus musculus (house mouse) | 19712 | Rest |
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| DOID:0080280 | gingival fibromatosis 5 | HGNC:9966 | Homo sapiens (human) | 5978 | REST |
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| DOID:0080272 | nephrotic syndrome type 16 | RGD:2320289 | Rattus norvegicus (Norway rat) | 100361376 | Kank2 |
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| DOID:0080272 | nephrotic syndrome type 16 | HGNC:29300 | Homo sapiens (human) | 25959 | KANK2 |
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| DOID:0080272 | nephrotic syndrome type 16 | MGI:2384568 | Mus musculus (house mouse) | 235041 | Kank2 |
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| DOID:0080269 | autosomal dominant nonsyndromic deafness 73 | RGD:620779 | Rattus norvegicus (Norway rat) | 360417 | Ptprq |
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| DOID:0080269 | autosomal dominant nonsyndromic deafness 73 | MGI:1096349 | Mus musculus (house mouse) | 237523 | Ptprq |
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| DOID:0080269 | autosomal dominant nonsyndromic deafness 73 | FB:FBgn0043903 | Drosophila melanogaster (fruit fly) | 32976 | dome |
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| DOID:0080268 | autosomal dominant nonsyndromic deafness 72 | Xenbase:XB-GENE-865528 | Xenopus laevis (African clawed frog) | 444429 | slc44a4.L |
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| DOID:0080268 | autosomal dominant nonsyndromic deafness 72 | HGNC:13941 | Homo sapiens (human) | 80736 | SLC44A4 |
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| DOID:0080268 | autosomal dominant nonsyndromic deafness 72 | RGD:1303167 | Rattus norvegicus (Norway rat) | 294255 | Slc44a4 |
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| DOID:0080268 | autosomal dominant nonsyndromic deafness 72 | MGI:1917379 | Mus musculus (house mouse) | 70129 | Slc44a4 |
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| DOID:0080268 | autosomal dominant nonsyndromic deafness 72 | FB:FBgn0039637 | Drosophila melanogaster (fruit fly) | 43440 | Ctl2 |
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| DOID:0080268 | autosomal dominant nonsyndromic deafness 72 | WB:WBGene00018037 | Caenorhabditis elegans | 180809 | chtl-1 |
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| DOID:0080268 | autosomal dominant nonsyndromic deafness 72 | ZFIN:ZDB-GENE-040426-1371 | Danio rerio (zebrafish) | 393385 | slc44a4 |
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| DOID:0080267 | autosomal dominant nonsyndromic deafness 71 | HGNC:2938 | Homo sapiens (human) | 23312 | DMXL2 |
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| DOID:0080267 | autosomal dominant nonsyndromic deafness 71 | MGI:2444630 | Mus musculus (house mouse) | 235380 | Dmxl2 |
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| DOID:0080266 | primary ciliary dyskinesia 37 | HGNC:2940 | Homo sapiens (human) | 25981 | DNAH1 |
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| DOID:0080265 | nephrotic syndrome type 14 | SGD:S000002702 | Saccharomyces cerevisiae S288C | 851888 | DPL1 |
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| DOID:0080265 | nephrotic syndrome type 14 | HGNC:10817 | Homo sapiens (human) | 8879 | SGPL1 |
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| DOID:0080264 | exudative vitreoretinopathy 7 | MGI:88276 | Mus musculus (house mouse) | 12387 | Ctnnb1 |
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| DOID:0080264 | exudative vitreoretinopathy 7 | HGNC:2514 | Homo sapiens (human) | 1499 | CTNNB1 |
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