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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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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 | July 29, 2024 |
| Disease ID | Disease Name | Alliance of Genome Resources ID | Species | Gene ID ▼ | Gene Symbol | FlyGlycoDB | Evidence Code Names | References |
|---|---|---|---|---|---|---|---|---|
| DOID:2154 | nephroblastoma | HGNC:1681 | Homo sapiens (human) | 960 | CD44 |
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| DOID:3457 | invasive lobular carcinoma | HGNC:1681 | Homo sapiens (human) | 960 | CD44 |
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| DOID:2671 | transitional cell carcinoma | HGNC:1681 | Homo sapiens (human) | 960 | CD44 |
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| DOID:11054 | urinary bladder cancer | HGNC:1681 | Homo sapiens (human) | 960 | CD44 |
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| DOID:10762 | portal hypertension | HGNC:7962 | Homo sapiens (human) | 9572 | NR1D1 |
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| DOID:1459 | hypothyroidism | HGNC:7962 | Homo sapiens (human) | 9572 | NR1D1 |
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| DOID:0112313 | brain small vessel disease | HGNC:7962 | Homo sapiens (human) | 9572 | NR1D1 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:7962 | Homo sapiens (human) | 9572 | NR1D1 |
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| DOID:7998 | hyperthyroidism | HGNC:7962 | Homo sapiens (human) | 9572 | NR1D1 |
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| DOID:14018 | alcoholic liver cirrhosis | HGNC:7962 | Homo sapiens (human) | 9572 | NR1D1 |
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| DOID:0090141 | cortisone reductase deficiency 1 | HGNC:4795 | Homo sapiens (human) | 9563 | H6PD |
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| DOID:2377 | multiple sclerosis | HGNC:4795 | Homo sapiens (human) | 9563 | H6PD |
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| DOID:0090139 | cortisone reductase deficiency | HGNC:4795 | Homo sapiens (human) | 9563 | H6PD |
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| DOID:0112333 | pontocerebellar hypoplasia type 16 | HGNC:7102 | Homo sapiens (human) | 9562 | MINPP1 |
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| DOID:3969 | thyroid gland papillary carcinoma | HGNC:7102 | Homo sapiens (human) | 9562 | MINPP1 |
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| DOID:326 | ischemia | HGNC:9599 | Homo sapiens (human) | 9536 | PTGES |
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| DOID:11624 | penile benign neoplasm | HGNC:9599 | Homo sapiens (human) | 9536 | PTGES |
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| DOID:2671 | transitional cell carcinoma | HGNC:9599 | Homo sapiens (human) | 9536 | PTGES |
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| DOID:2615 | papilloma | HGNC:9599 | Homo sapiens (human) | 9536 | PTGES |
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| DOID:9206 | Barrett's esophagus | HGNC:9599 | Homo sapiens (human) | 9536 | PTGES |
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| DOID:13976 | peptic esophagitis | HGNC:9599 | Homo sapiens (human) | 9536 | PTGES |
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| DOID:2870 | endometrial adenocarcinoma | HGNC:9599 | Homo sapiens (human) | 9536 | PTGES |
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| DOID:2152 | ovary epithelial cancer | HGNC:9599 | Homo sapiens (human) | 9536 | PTGES |
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| DOID:3908 | lung non-small cell carcinoma | HGNC:9599 | Homo sapiens (human) | 9536 | PTGES |
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| DOID:0060074 | ductal carcinoma in situ | HGNC:9599 | Homo sapiens (human) | 9536 | PTGES |
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