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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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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 | July 29, 2024 |
| Disease ID | Disease Name | Alliance of Genome Resources ID | Species ▼ | Gene ID | Gene Symbol | FlyGlycoDB | Evidence Code Names | References |
|---|---|---|---|---|---|---|---|---|
| DOID:3908 | lung non-small cell carcinoma | HGNC:11998 | Homo sapiens (human) | 7157 | TP53 |
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| DOID:0111411 | exudative vitreoretinopathy 4 | HGNC:6697 | Homo sapiens (human) | 4041 | LRP5 |
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| DOID:10273 | heart conduction disease | HGNC:15460 | Homo sapiens (human) | 55799 | CACNA2D3 |
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| DOID:0080721 | calvarial doughnut lesions with bone fragility | HGNC:28395 | Homo sapiens (human) | 166929 | SGMS2 |
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| DOID:0080208 | metabolic dysfunction-associated steatotic liver disease | HGNC:89 | Homo sapiens (human) | 34 | ACADM |
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| DOID:3146 | lipid metabolism disorder | HGNC:9232 | Homo sapiens (human) | 5465 | PPARA |
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| DOID:9970 | obesity | HGNC:18859 | Homo sapiens (human) | 56848 | SPHK2 |
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| DOID:1679 | cystitis | HGNC:1516 | Homo sapiens (human) | 847 | CAT |
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| DOID:3905 | lung carcinoma | HGNC:2602 | Homo sapiens (human) | 1591 | CYP24A1 |
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| DOID:6543 | acne | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:1596 | depressive disorder | HGNC:2638 | Homo sapiens (human) | 1577 | CYP3A5 |
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| DOID:3805 | porokeratosis | HGNC:3631 | Homo sapiens (human) | 2224 | FDPS |
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| DOID:224 | transient cerebral ischemia | HGNC:4092 | Homo sapiens (human) | 2571 | GAD1 |
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| DOID:61 | mitral valve disease | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
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| DOID:10892 | hypospadias | HGNC:2595 | Homo sapiens (human) | 1543 | CYP1A1 |
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| DOID:0110794 | hereditary spastic paraplegia 42 | HGNC:95 | Homo sapiens (human) | 9197 | SLC33A1 |
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| DOID:7614 | meninges sarcoma | HGNC:11998 | Homo sapiens (human) | 7157 | TP53 |
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| DOID:2986 | IgA glomerulonephritis | HGNC:9040 | Homo sapiens (human) | 7941 | PLA2G7 |
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| DOID:0050535 | exudative vitreoretinopathy | HGNC:6697 | Homo sapiens (human) | 4041 | LRP5 |
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| DOID:3525 | middle cerebral artery infarction | HGNC:936 | Homo sapiens (human) | 572 | BAD |
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| DOID:2921 | glomerulonephritis | HGNC:9040 | Homo sapiens (human) | 7941 | PLA2G7 |
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| DOID:13241 | Behcet's disease | HGNC:6922 | Homo sapiens (human) | 4153 | MBL2 |
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| DOID:0090140 | cortisone reductase deficiency 2 | HGNC:5208 | Homo sapiens (human) | 3290 | HSD11B1 |
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| DOID:2394 | ovarian cancer | HGNC:391 | Homo sapiens (human) | 207 | AKT1 |
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| DOID:0111037 | glycine N-methyltransferase deficiency | HGNC:4415 | Homo sapiens (human) | 27232 | GNMT |
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