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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:0080403 | orofacial cleft 10 | HGNC:12502 | Homo sapiens (human) | 7341 | SUMO1 |
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| DOID:4450 | renal cell carcinoma | HGNC:16628 | Homo sapiens (human) | 84925 | SLC49A4 |
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| DOID:3407 | carotid artery disease | HGNC:9445 | Homo sapiens (human) | 5617 | PRL |
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| DOID:10534 | stomach cancer | HGNC:583 | Homo sapiens (human) | 324 | APC |
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| DOID:0110677 | congenital myasthenic syndrome 4B | HGNC:1966 | Homo sapiens (human) | 1145 | CHRNE |
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| DOID:1825 | childhood absence epilepsy | HGNC:11005 | Homo sapiens (human) | 6513 | SLC2A1 |
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| DOID:5419 | schizophrenia | HGNC:4600 | Homo sapiens (human) | 2918 | GRM8 |
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| DOID:0050580 | hereditary lymphedema | HGNC:11809 | Homo sapiens (human) | 7075 | TIE1 |
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| DOID:5419 | schizophrenia | HGNC:5962 | Homo sapiens (human) | 3586 | IL10 |
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| DOID:9976 | heroin dependence | HGNC:2621 | Homo sapiens (human) | 1557 | CYP2C19 |
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| DOID:3307 | teratoma | HGNC:8905 | Homo sapiens (human) | 5236 | PGM1 |
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| DOID:9074 | systemic lupus erythematosus | HGNC:6006 | Homo sapiens (human) | 50615 | IL21R |
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| DOID:1485 | cystic fibrosis | HGNC:2595 | Homo sapiens (human) | 1543 | CYP1A1 |
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| DOID:0080557 | congenital disorder of glycosylation Ie | HGNC:3005 | Homo sapiens (human) | 8813 | DPM1 |
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| DOID:0070495 | mitochondrial complex IV deficiency nuclear type 8 | HGNC:24316 | Homo sapiens (human) | 51204 | TACO1 |
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| DOID:1324 | lung cancer | HGNC:6922 | Homo sapiens (human) | 4153 | MBL2 |
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| DOID:9351 | diabetes mellitus | HGNC:21050 | Homo sapiens (human) | 54901 | CDKAL1 |
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| DOID:783 | end stage renal disease | HGNC:3356 | Homo sapiens (human) | 5167 | ENPP1 |
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| DOID:0111053 | platelet-type bleeding disorder 15 | HGNC:163 | Homo sapiens (human) | 87 | ACTN1 |
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| DOID:9976 | heroin dependence | HGNC:404 | Homo sapiens (human) | 217 | ALDH2 |
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| DOID:12365 | malaria | HGNC:2334 | Homo sapiens (human) | 1378 | CR1 |
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| DOID:8499 | night blindness | HGNC:10012 | Homo sapiens (human) | 6010 | RHO |
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| DOID:9074 | systemic lupus erythematosus | HGNC:15633 | Homo sapiens (human) | 54106 | TLR9 |
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| DOID:1909 | melanoma | HGNC:11936 | Homo sapiens (human) | 356 | FASLG |
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| DOID:0080958 | primary hypoalphalipoproteinemia 2 | HGNC:600 | Homo sapiens (human) | 335 | APOA1 |
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