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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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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:12377 | spinal muscular atrophy | MGI:94921 | Mus musculus (house mouse) | 13483 | Dpp6 |
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| DOID:0070063 | autosomal dominant intellectual developmental disorder 33 | MGI:94921 | Mus musculus (house mouse) | 13483 | Dpp6 |
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| DOID:332 | amyotrophic lateral sclerosis | MGI:94921 | Mus musculus (house mouse) | 13483 | Dpp6 |
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| DOID:9352 | type 2 diabetes mellitus | MGI:94919 | Mus musculus (house mouse) | 13482 | Dpp4 |
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| DOID:3748 | esophagus squamous cell carcinoma | MGI:94919 | Mus musculus (house mouse) | 13482 | Dpp4 |
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| DOID:0080642 | Middle East respiratory syndrome | MGI:94919 | Mus musculus (house mouse) | 13482 | Dpp4 |
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| DOID:0080571 | congenital disorder of glycosylation Iu | MGI:1330238 | Mus musculus (house mouse) | 13481 | Dpm2 |
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| DOID:0050570 | congenital disorder of glycosylation type I | MGI:1330238 | Mus musculus (house mouse) | 13481 | Dpm2 |
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| DOID:0050570 | congenital disorder of glycosylation type I | MGI:1330239 | Mus musculus (house mouse) | 13480 | Dpm1 |
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| DOID:0080557 | congenital disorder of glycosylation Ie | MGI:1330239 | Mus musculus (house mouse) | 13480 | Dpm1 |
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| DOID:687 | hepatoblastoma | MGI:94917 | Mus musculus (house mouse) | 13479 | Dpep1 |
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| DOID:0110676 | congenital myasthenic syndrome 13 | MGI:1196396 | Mus musculus (house mouse) | 13478 | Dpagt1 |
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| DOID:0080562 | congenital disorder of glycosylation Ij | MGI:1196396 | Mus musculus (house mouse) | 13478 | Dpagt1 |
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| DOID:3571 | liver cancer | HGNC:24436 | Homo sapiens (human) | 134526 | ACOT12 |
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| 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:10584 | retinitis pigmentosa | HGNC:26658 | Homo sapiens (human) | 134359 | POC5 |
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| DOID:11054 | urinary bladder cancer | MGI:94912 | Mus musculus (house mouse) | 13433 | Dnmt1 |
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| DOID:3905 | lung carcinoma | MGI:94912 | Mus musculus (house mouse) | 13433 | Dnmt1 |
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| DOID:11984 | hypertrophic cardiomyopathy | MGI:94912 | Mus musculus (house mouse) | 13433 | Dnmt1 |
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| DOID:684 | hepatocellular carcinoma | MGI:94912 | Mus musculus (house mouse) | 13433 | Dnmt1 |
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| DOID:9352 | type 2 diabetes mellitus | MGI:94912 | Mus musculus (house mouse) | 13433 | Dnmt1 |
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| DOID:5082 | liver cirrhosis | MGI:94912 | Mus musculus (house mouse) | 13433 | Dnmt1 |
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| DOID:0050968 | autosomal dominant cerebellar ataxia, deafness and narcolepsy | MGI:94912 | Mus musculus (house mouse) | 13433 | Dnmt1 |
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| DOID:0070158 | hereditary sensory neuropathy type 1E | MGI:94912 | Mus musculus (house mouse) | 13433 | Dnmt1 |
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