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GlyTouCan
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:0080585 | Van Maldergem syndrome 1 | RGD:1309878 | Rattus norvegicus (Norway rat) | 308912 | Dchs1 |
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| DOID:5204 | fructose-1,6-bisphosphatase deficiency | MGI:95492 | Mus musculus (house mouse) | 14121 | Fbp1 |
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| DOID:3910 | lung adenocarcinoma | HGNC:12028 | Homo sapiens (human) | 7184 | HSP90B1 |
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| DOID:3393 | coronary artery disease | RGD:2794 | Rattus norvegicus (Norway rat) | 24446 | Hgf |
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| DOID:0050625 | biliary tract benign neoplasm | MGI:99255 | Mus musculus (house mouse) | 14103 | Fasl |
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| DOID:3393 | coronary artery disease | MGI:95804 | Mus musculus (house mouse) | 14782 | Gsr |
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| DOID:7147 | ankylosing spondylitis | MGI:96438 | Mus musculus (house mouse) | 16009 | Igfbp3 |
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| DOID:6432 | pulmonary hypertension | HGNC:3177 | Homo sapiens (human) | 1907 | EDN2 |
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| DOID:0070261 | congenital disorder of glycosylation type IIi | SGD:S000004996 | Saccharomyces cerevisiae S288C | 855676 | COG5 |
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| DOID:3635 | congenital myasthenic syndrome | HGNC:1961 | Homo sapiens (human) | 1140 | CHRNB1 |
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| DOID:5199 | ureteral obstruction | HGNC:10610 | Homo sapiens (human) | 6356 | CCL11 |
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| DOID:12215 | oligohydramnios | HGNC:29602 | Homo sapiens (human) | 10630 | PDPN |
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| DOID:1470 | major depressive disorder | MGI:88145 | Mus musculus (house mouse) | 12064 | Bdnf |
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| DOID:83 | cataract | HGNC:24555 | Homo sapiens (human) | 26173 | INTS1 |
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| DOID:0080559 | congenital disorder of glycosylation Ig | Xenbase:XB-GENE-6486398 | Xenopus laevis (African clawed frog) | 108711164 | alg12.L |
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| DOID:0081155 | common variable immunodeficiency 13 | HGNC:13176 | Homo sapiens (human) | 10320 | IKZF1 |
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| DOID:8536 | herpes zoster | MGI:96556 | Mus musculus (house mouse) | 16189 | Il4 |
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| DOID:0080119 | mitochondrial DNA depletion syndrome 1 | MGI:1920212 | Mus musculus (house mouse) | 72962 | Tymp |
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| DOID:2741 | bilirubin metabolic disorder | WB:WBGene00003407 | Caenorhabditis elegans | 180409 | mrp-1 |
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| DOID:0080333 | aortic valve disease 1 | HGNC:3356 | Homo sapiens (human) | 5167 | ENPP1 |
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| DOID:557 | kidney disease | HGNC:4057 | Homo sapiens (human) | 2539 | G6PD |
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| DOID:0060604 | ankyloglossia | HGNC:4504 | Homo sapiens (human) | 8549 | LGR5 |
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| DOID:3021 | acute kidney failure | WB:WBGene00003842 | Caenorhabditis elegans | 172841 | 45566 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:700 | Homo sapiens (human) | 405 | ARNT |
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| DOID:0060193 | amyotrophic lateral sclerosis type 1 | MGI:107745 | Mus musculus (house mouse) | 13191 | Dctn1 |
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