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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:8689 | anorexia nervosa | HGNC:376 | Homo sapiens (human) | 9472 | AKAP6 |
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| DOID:2152 | ovary epithelial cancer | HGNC:376 | Homo sapiens (human) | 9472 | AKAP6 |
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| DOID:0080199 | colorectal carcinoma | HGNC:370 | Homo sapiens (human) | 9590 | AKAP12 |
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| DOID:0050458 | juvenile myelomonocytic leukemia | HGNC:370 | Homo sapiens (human) | 9590 | AKAP12 |
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| DOID:11446 | sciatic neuropathy | HGNC:370 | Homo sapiens (human) | 9590 | AKAP12 |
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| DOID:3347 | osteosarcoma | HGNC:370 | Homo sapiens (human) | 9590 | AKAP12 |
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| DOID:784 | chronic kidney disease | HGNC:370 | Homo sapiens (human) | 9590 | AKAP12 |
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| DOID:5082 | liver cirrhosis | HGNC:370 | Homo sapiens (human) | 9590 | AKAP12 |
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| DOID:2316 | brain ischemia | HGNC:370 | Homo sapiens (human) | 9590 | AKAP12 |
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| DOID:2316 | brain ischemia | HGNC:367 | Homo sapiens (human) | 8165 | AKAP1 |
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| DOID:1572 | normal pressure hydrocephalus | HGNC:33814 | Homo sapiens (human) | 221264 | AK9 |
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| DOID:684 | hepatocellular carcinoma | HGNC:17376 | Homo sapiens (human) | 50808 | AK3 |
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| DOID:1040 | chronic lymphocytic leukemia | HGNC:17376 | Homo sapiens (human) | 50808 | AK3 |
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| DOID:3328 | temporal lobe epilepsy | HGNC:362 | Homo sapiens (human) | 204 | AK2 |
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| DOID:0060020 | reticular dysgenesis | HGNC:362 | Homo sapiens (human) | 204 | AK2 |
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| DOID:0060790 | hypomyelinating leukodystrophy 3 | HGNC:10648 | Homo sapiens (human) | 9255 | AIMP1 |
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| DOID:1289 | neurodegenerative disease | HGNC:10648 | Homo sapiens (human) | 9255 | AIMP1 |
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| DOID:5844 | myocardial infarction | HGNC:10648 | Homo sapiens (human) | 9255 | AIMP1 |
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| DOID:10584 | retinitis pigmentosa | HGNC:8768 | Homo sapiens (human) | 9131 | AIFM1 |
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| DOID:0110429 | dilated cardiomyopathy 1H | HGNC:8768 | Homo sapiens (human) | 9131 | AIFM1 |
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| DOID:0110212 | Charcot-Marie-Tooth disease X-linked recessive 4 | HGNC:8768 | Homo sapiens (human) | 9131 | AIFM1 |
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| DOID:0111502 | combined oxidative phosphorylation deficiency 6 | HGNC:8768 | Homo sapiens (human) | 9131 | AIFM1 |
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| DOID:5327 | retinal detachment | HGNC:8768 | Homo sapiens (human) | 9131 | AIFM1 |
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| DOID:0111741 | X-linked deafness 5 | HGNC:8768 | Homo sapiens (human) | 9131 | AIFM1 |
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| DOID:0060536 | mitochondrial complex I deficiency | HGNC:8768 | Homo sapiens (human) | 9131 | AIFM1 |
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