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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:10763 | hypertension | WB:WBGene00014035 | Caenorhabditis elegans | 191374 | dhrr-1 |
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| DOID:0111453 | 2-aminoadipic 2-oxoadipic aciduria | WB:WBGene00014098 | Caenorhabditis elegans | 179674 | ogdh-2 |
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| DOID:0110170 | Charcot-Marie-Tooth disease axonal type 2Q | WB:WBGene00014098 | Caenorhabditis elegans | 179674 | ogdh-2 |
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| DOID:0111459 | classic galactosemia | WB:WBGene00014203 | Caenorhabditis elegans | 175506 | ZK1058.3 |
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| DOID:9870 | galactosemia | WB:WBGene00014203 | Caenorhabditis elegans | 175506 | ZK1058.3 |
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| DOID:0080953 | amelogenesis imperfecta type 1J | WB:WBGene00015161 | Caenorhabditis elegans | 176030 | pho-5 |
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| DOID:10283 | prostate cancer | WB:WBGene00015161 | Caenorhabditis elegans | 176030 | pho-5 |
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| DOID:0080567 | congenital disorder of glycosylation Ip | WB:WBGene00015162 | Caenorhabditis elegans | 176032 | algn-11 |
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| DOID:0070311 | oligoasthenoteratozoospermia | WB:WBGene00015204 | Caenorhabditis elegans | 174243 | B0495.5 |
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| DOID:0070221 | progressive familial intrahepatic cholestasis | WB:WBGene00015287 | Caenorhabditis elegans | 182062 | osta-1 |
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| DOID:0060419 | chromosome 3q29 microdeletion syndrome | WB:WBGene00015287 | Caenorhabditis elegans | 182062 | osta-1 |
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| DOID:10123 | pigmentation disease | WB:WBGene00015332 | Caenorhabditis elegans | 176105 | tyr-1 |
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| DOID:0050633 | ocular albinism 1 | WB:WBGene00015332 | Caenorhabditis elegans | 176105 | tyr-1 |
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| DOID:8465 | retinoschisis | WB:WBGene00015332 | Caenorhabditis elegans | 176105 | tyr-1 |
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| DOID:0070097 | oculocutaneous albinism type III | WB:WBGene00015332 | Caenorhabditis elegans | 176105 | tyr-1 |
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| DOID:11211 | buphthalmos | WB:WBGene00015332 | Caenorhabditis elegans | 176105 | tyr-1 |
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| DOID:0050632 | oculocutaneous albinism | WB:WBGene00015332 | Caenorhabditis elegans | 176105 | tyr-1 |
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| DOID:0070094 | oculocutaneous albinism type IA | WB:WBGene00015332 | Caenorhabditis elegans | 176105 | tyr-1 |
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| DOID:13399 | color blindness | WB:WBGene00015332 | Caenorhabditis elegans | 176105 | tyr-1 |
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| DOID:1909 | melanoma | WB:WBGene00015332 | Caenorhabditis elegans | 176105 | tyr-1 |
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| DOID:12306 | vitiligo | WB:WBGene00015332 | Caenorhabditis elegans | 176105 | tyr-1 |
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| DOID:0070095 | oculocutaneous albinism type IB | WB:WBGene00015332 | Caenorhabditis elegans | 176105 | tyr-1 |
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| DOID:8923 | skin melanoma | WB:WBGene00015332 | Caenorhabditis elegans | 176105 | tyr-1 |
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| DOID:10652 | Alzheimer's disease | WB:WBGene00015353 | Caenorhabditis elegans | 3565859 | C02F5.13 |
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| DOID:5844 | myocardial infarction | WB:WBGene00015389 | Caenorhabditis elegans | 180812 | scav-1 |
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