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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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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:8398 | osteoarthritis | MGI:95688 | Mus musculus (house mouse) | 14563 | Gdf5 |
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| DOID:0080052 | acromesomelic dysplasia, Grebe type | MGI:95688 | Mus musculus (house mouse) | 14563 | Gdf5 |
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| DOID:0050794 | multiple synostoses syndrome | MGI:95688 | Mus musculus (house mouse) | 14563 | Gdf5 |
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| DOID:0080788 | proximal symphalangism 2 | MGI:95688 | Mus musculus (house mouse) | 14563 | Gdf5 |
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| DOID:0080051 | acromesomelic dysplasia, Hunter-Thompson type | MGI:95688 | Mus musculus (house mouse) | 14563 | Gdf5 |
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| DOID:0081317 | multiple synostoses syndrome 1 | MGI:95688 | Mus musculus (house mouse) | 14563 | Gdf5 |
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| DOID:14330 | Parkinson's disease | MGI:95688 | Mus musculus (house mouse) | 14563 | Gdf5 |
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| DOID:0110977 | brachydactyly type A1C | MGI:95688 | Mus musculus (house mouse) | 14563 | Gdf5 |
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| DOID:0110964 | brachydactyly type A1 | MGI:95688 | Mus musculus (house mouse) | 14563 | Gdf5 |
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| DOID:0081318 | multiple synostoses syndrome 2 | MGI:95688 | Mus musculus (house mouse) | 14563 | Gdf5 |
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| DOID:0110965 | brachydactyly type A2 | MGI:95688 | Mus musculus (house mouse) | 14563 | Gdf5 |
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| DOID:0080591 | Klippel-Feil syndrome 3 | MGI:95686 | Mus musculus (house mouse) | 14562 | Gdf3 |
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| DOID:0060838 | isolated microphthalmia 7 | MGI:95686 | Mus musculus (house mouse) | 14562 | Gdf3 |
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| DOID:0070418 | vertebral hypersegmentation and orofacial anomalies | MGI:1338027 | Mus musculus (house mouse) | 14561 | Gdf11 |
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| DOID:12930 | dilated cardiomyopathy | MGI:95683 | Mus musculus (house mouse) | 14559 | Gdf1 |
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| DOID:0060850 | annular pancreas | MGI:95683 | Mus musculus (house mouse) | 14559 | Gdf1 |
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| DOID:5082 | liver cirrhosis | MGI:95683 | Mus musculus (house mouse) | 14559 | Gdf1 |
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| DOID:0050545 | visceral heterotaxy | MGI:95683 | Mus musculus (house mouse) | 14559 | Gdf1 |
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| DOID:1682 | congenital heart disease | MGI:95683 | Mus musculus (house mouse) | 14559 | Gdf1 |
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| DOID:0060772 | multiple types of congenital heart defects 6 | MGI:95683 | Mus musculus (house mouse) | 14559 | Gdf1 |
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| DOID:10534 | stomach cancer | MGI:95678 | Mus musculus (house mouse) | 14544 | Gda |
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| DOID:0050679 | blue cone monochromacy | MGI:1097692 | Mus musculus (house mouse) | 14539 | Opn1mw |
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| DOID:13909 | red-green color blindness | MGI:1097692 | Mus musculus (house mouse) | 14539 | Opn1mw |
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| DOID:13910 | red color blindness | MGI:1097692 | Mus musculus (house mouse) | 14539 | Opn1mw |
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| DOID:0110242 | cataract 13 with adult i phenotype | MGI:1100870 | Mus musculus (house mouse) | 14538 | Gcnt2 |
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