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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:0060038 | specific developmental disorder | HGNC:13221 | Homo sapiens (human) | 53335 | BCL11A |
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| DOID:1289 | neurodegenerative disease | HGNC:13221 | Homo sapiens (human) | 53335 | BCL11A |
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| DOID:10923 | sickle cell anemia | HGNC:13221 | Homo sapiens (human) | 53335 | BCL11A |
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| DOID:12241 | beta thalassemia | HGNC:13221 | Homo sapiens (human) | 53335 | BCL11A |
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| DOID:0060041 | autism spectrum disorder | HGNC:13221 | Homo sapiens (human) | 53335 | BCL11A |
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| DOID:9269 | maple syrup urine disease | HGNC:987 | Homo sapiens (human) | 594 | BCKDHB |
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| DOID:9269 | maple syrup urine disease | HGNC:986 | Homo sapiens (human) | 593 | BCKDHA |
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| DOID:9279 | hyperhomocysteinemia | HGNC:983 | Homo sapiens (human) | 590 | BCHE |
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| DOID:10113 | trypanosomiasis | HGNC:983 | Homo sapiens (human) | 590 | BCHE |
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| DOID:9505 | cannabis abuse | HGNC:983 | Homo sapiens (human) | 590 | BCHE |
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| DOID:10652 | Alzheimer's disease | HGNC:983 | Homo sapiens (human) | 590 | BCHE |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:983 | Homo sapiens (human) | 590 | BCHE |
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| DOID:1307 | dementia | HGNC:983 | Homo sapiens (human) | 590 | BCHE |
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| DOID:4247 | coronary restenosis | HGNC:983 | Homo sapiens (human) | 590 | BCHE |
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| DOID:543 | dystonia | HGNC:983 | Homo sapiens (human) | 590 | BCHE |
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| DOID:1826 | epilepsy | HGNC:983 | Homo sapiens (human) | 590 | BCHE |
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| DOID:9470 | bacterial meningitis | HGNC:983 | Homo sapiens (human) | 590 | BCHE |
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| DOID:2297 | leptospirosis | HGNC:983 | Homo sapiens (human) | 590 | BCHE |
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| DOID:1168 | familial hyperlipidemia | HGNC:983 | Homo sapiens (human) | 590 | BCHE |
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| DOID:3393 | coronary artery disease | HGNC:983 | Homo sapiens (human) | 590 | BCHE |
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| DOID:10763 | hypertension | HGNC:983 | Homo sapiens (human) | 590 | BCHE |
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| DOID:12858 | Huntington's disease | HGNC:983 | Homo sapiens (human) | 590 | BCHE |
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| DOID:10914 | amnestic disorder | HGNC:983 | Homo sapiens (human) | 590 | BCHE |
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| DOID:655 | inherited metabolic disorder | HGNC:983 | Homo sapiens (human) | 590 | BCHE |
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| DOID:0050784 | primary progressive multiple sclerosis | HGNC:983 | Homo sapiens (human) | 590 | BCHE |
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