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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:1612 | breast cancer | HGNC:206 | Homo sapiens (human) | 10863 | ADAM28 |
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| DOID:3910 | lung adenocarcinoma | HGNC:206 | Homo sapiens (human) | 10863 | ADAM28 |
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| DOID:3459 | breast carcinoma | HGNC:206 | Homo sapiens (human) | 10863 | ADAM28 |
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| DOID:9256 | colorectal cancer | HGNC:206 | Homo sapiens (human) | 10863 | ADAM28 |
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| DOID:0080652 | calcium oxalate nephrolithiasis | HGNC:10993 | Homo sapiens (human) | 10861 | SLC26A1 |
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| DOID:10652 | Alzheimer's disease | HGNC:2641 | Homo sapiens (human) | 10858 | CYP46A1 |
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| DOID:0050431 | arrhythmogenic right ventricular cardiomyopathy | HGNC:18838 | Homo sapiens (human) | 10848 | PPP1R13L |
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| DOID:0050737 | autosomal recessive disease | HGNC:18838 | Homo sapiens (human) | 10848 | PPP1R13L |
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| DOID:0060037 | developmental disorder of mental health | HGNC:16974 | Homo sapiens (human) | 10847 | SRCAP |
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| DOID:0111358 | Floating-Harbor syndrome | HGNC:16974 | Homo sapiens (human) | 10847 | SRCAP |
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| DOID:0081292 | traumatic brain injury | HGNC:8772 | Homo sapiens (human) | 10846 | PDE10A |
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| DOID:13270 | erythropoietic protoporphyria | HGNC:2088 | Homo sapiens (human) | 10845 | CLPX |
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| DOID:0081266 | pachygyria, microcephaly, developmental delay, and dysmorphic facies, with or without seizures | HGNC:18599 | Homo sapiens (human) | 10844 | TUBGCP2 |
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| DOID:4450 | renal cell carcinoma | HGNC:16971 | Homo sapiens (human) | 10818 | FRS2 |
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| DOID:7693 | abdominal aortic aneurysm | MGI:1342005 | Mus musculus (house mouse) | 108156 | Mthfd1 |
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| DOID:9296 | cleft lip | MGI:1342005 | Mus musculus (house mouse) | 108156 | Mthfd1 |
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| DOID:6419 | tetralogy of Fallot | MGI:1342005 | Mus musculus (house mouse) | 108156 | Mthfd1 |
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| DOID:674 | cleft palate | MGI:1342005 | Mus musculus (house mouse) | 108156 | Mthfd1 |
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| DOID:0080633 | developmental cardiac valvular defect | MGI:1342005 | Mus musculus (house mouse) | 108156 | Mthfd1 |
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| DOID:0080074 | neural tube defect | MGI:1342005 | Mus musculus (house mouse) | 108156 | Mthfd1 |
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| DOID:0080016 | spina bifida | MGI:1342005 | Mus musculus (house mouse) | 108156 | Mthfd1 |
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| DOID:14250 | Down syndrome | MGI:1342005 | Mus musculus (house mouse) | 108156 | Mthfd1 |
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| DOID:1712 | aortic valve stenosis | MGI:1339639 | Mus musculus (house mouse) | 108155 | Ogt |
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| DOID:9351 | diabetes mellitus | MGI:1339639 | Mus musculus (house mouse) | 108155 | Ogt |
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| DOID:9352 | type 2 diabetes mellitus | MGI:1339639 | Mus musculus (house mouse) | 108155 | Ogt |
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