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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:0060589 | Yunis-Varon syndrome | SGD:S000005269 | Saccharomyces cerevisiae S288C | 855392 | FIG4 |
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| DOID:10652 | Alzheimer's disease | SGD:S000006125 | Saccharomyces cerevisiae S288C | 855897 | HRR25 |
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| DOID:0080923 | bilateral parasagittal parieto-occipital polymicrogyria | SGD:S000005269 | Saccharomyces cerevisiae S288C | 855392 | FIG4 |
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| DOID:0060558 | lethal congenital contracture syndrome | SGD:S000001709 | Saccharomyces cerevisiae S288C | 853870 | VPS1 |
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| DOID:0060202 | amyotrophic lateral sclerosis type 11 | SGD:S000005269 | Saccharomyces cerevisiae S288C | 855392 | FIG4 |
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| DOID:0090117 | thiamine-responsive megaloblastic anemia syndrome | WB:WBGene00018138 | Caenorhabditis elegans | 178745 | folt-2 |
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| DOID:5844 | myocardial infarction | RGD:619850 | Rattus norvegicus (Norway rat) | 94203 | Pgf |
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| DOID:5844 | myocardial infarction | RGD:3249 | Rattus norvegicus (Norway rat) | 24617 | Serpine1 |
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| DOID:0080208 | metabolic dysfunction-associated steatotic liver disease | HGNC:16940 | Homo sapiens (human) | 84649 | DGAT2 |
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| DOID:9452 | steatotic liver disease | RGD:2998 | Rattus norvegicus (Norway rat) | 300438 | Ldlr |
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| DOID:12308 | Dubin-Johnson syndrome | RGD:2366 | Rattus norvegicus (Norway rat) | 25303 | Abcc2 |
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| DOID:3021 | acute kidney failure | HGNC:286 | Homo sapiens (human) | 154 | ADRB2 |
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| DOID:9352 | type 2 diabetes mellitus | RGD:2803 | Rattus norvegicus (Norway rat) | 25675 | Hmgcr |
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| DOID:2738 | pseudoxanthoma elasticum | RGD:620268 | Rattus norvegicus (Norway rat) | 81642 | Abcc6 |
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| DOID:9352 | type 2 diabetes mellitus | RGD:3876 | Rattus norvegicus (Norway rat) | 24835 | Tnf |
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| DOID:1596 | depressive disorder | HGNC:1963 | Homo sapiens (human) | 1142 | CHRNB3 |
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| DOID:594 | panic disorder | RGD:2845 | Rattus norvegicus (Norway rat) | 24473 | Htr1a |
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| DOID:1824 | status epilepticus | RGD:2202 | Rattus norvegicus (Norway rat) | 24225 | Bdnf |
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| DOID:9975 | cocaine dependence | RGD:2520 | Rattus norvegicus (Norway rat) | 24318 | Drd2 |
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| DOID:0111862 | congenital bilateral absence of vas deferens | RGD:2332 | Rattus norvegicus (Norway rat) | 24255 | Cftr |
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| DOID:0050328 | congenital hypothyroidism | RGD:3911 | Rattus norvegicus (Norway rat) | 25360 | Tshr |
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| DOID:3070 | high grade glioma | HGNC:3416 | Homo sapiens (human) | 2057 | EPOR |
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| DOID:0060041 | autism spectrum disorder | RGD:628659 | Rattus norvegicus (Norway rat) | 60391 | Nrxn1 |
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| DOID:10652 | Alzheimer's disease | RGD:620596 | Rattus norvegicus (Norway rat) | 117029 | Ccr5 |
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| DOID:0050852 | limb ischemia | HGNC:7876 | Homo sapiens (human) | 4846 | NOS3 |
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