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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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MIRAGE
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:1070 | primary open angle glaucoma | HGNC:30696 | Homo sapiens (human) | 134430 | WDR36 |
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| DOID:1686 | glaucoma | HGNC:30696 | Homo sapiens (human) | 134430 | WDR36 |
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| DOID:0111675 | neurooculocardiogenitourinary syndrome | HGNC:31406 | Homo sapiens (human) | 22884 | WDR37 |
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| DOID:0110739 | neurodegeneration with brain iron accumulation 5 | HGNC:28912 | Homo sapiens (human) | 11152 | WDR45 |
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| DOID:1682 | congenital heart disease | HGNC:12757 | Homo sapiens (human) | 11091 | WDR5 |
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| DOID:3070 | high grade glioma | HGNC:24502 | Homo sapiens (human) | 284403 | WDR62 |
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| DOID:0070296 | primary autosomal recessive microcephaly | HGNC:24502 | Homo sapiens (human) | 284403 | WDR62 |
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| DOID:0080918 | polymicrogyria | HGNC:24502 | Homo sapiens (human) | 284403 | WDR62 |
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| DOID:1059 | intellectual disability | HGNC:24502 | Homo sapiens (human) | 284403 | WDR62 |
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| DOID:0070293 | primary autosomal recessive microcephaly 2 with or without cortical malformations | HGNC:24502 | Homo sapiens (human) | 284403 | WDR62 |
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| DOID:10907 | microcephaly | HGNC:24502 | Homo sapiens (human) | 284403 | WDR62 |
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| DOID:0110061 | amelogenesis imperfecta hypomaturation type 2A3 | HGNC:26790 | Homo sapiens (human) | 256764 | WDR72 |
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| DOID:0060041 | autism spectrum disorder | HGNC:25725 | Homo sapiens (human) | 84128 | WDR75 |
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| DOID:0111169 | subcortical band heterotopia | HGNC:25725 | Homo sapiens (human) | 84128 | WDR75 |
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| DOID:0050453 | lissencephaly | HGNC:25725 | Homo sapiens (human) | 84128 | WDR75 |
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| DOID:9970 | obesity | HGNC:29175 | Homo sapiens (human) | 23038 | WDTC1 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:12762 | Homo sapiens (human) | 7466 | WFS1 |
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| DOID:11832 | visual epilepsy | HGNC:12762 | Homo sapiens (human) | 7466 | WFS1 |
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| DOID:9744 | type 1 diabetes mellitus | HGNC:12762 | Homo sapiens (human) | 7466 | WFS1 |
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| DOID:10603 | glucose intolerance | HGNC:12762 | Homo sapiens (human) | 7466 | WFS1 |
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| DOID:0050563 | nonsyndromic deafness | HGNC:12762 | Homo sapiens (human) | 7466 | WFS1 |
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| DOID:5723 | optic atrophy | HGNC:12762 | Homo sapiens (human) | 7466 | WFS1 |
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| DOID:0110584 | autosomal dominant nonsyndromic deafness 6 | HGNC:12762 | Homo sapiens (human) | 7466 | WFS1 |
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| DOID:83 | cataract | HGNC:12762 | Homo sapiens (human) | 7466 | WFS1 |
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| DOID:0110241 | cataract 41 | HGNC:12762 | Homo sapiens (human) | 7466 | WFS1 |
|
