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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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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:10286 | prostate carcinoma | HGNC:10901 | Homo sapiens (human) | 6502 | SKP2 |
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| DOID:10283 | prostate cancer | HGNC:10901 | Homo sapiens (human) | 6502 | SKP2 |
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| DOID:0080365 | endometrial hyperplasia | HGNC:10901 | Homo sapiens (human) | 6502 | SKP2 |
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| DOID:4450 | renal cell carcinoma | HGNC:10901 | Homo sapiens (human) | 6502 | SKP2 |
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| DOID:5409 | lung small cell carcinoma | HGNC:10901 | Homo sapiens (human) | 6502 | SKP2 |
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| DOID:684 | hepatocellular carcinoma | HGNC:10901 | Homo sapiens (human) | 6502 | SKP2 |
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| DOID:2671 | transitional cell carcinoma | HGNC:10901 | Homo sapiens (human) | 6502 | SKP2 |
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| DOID:4644 | epidermolysis bullosa simplex | HGNC:1090 | Homo sapiens (human) | 667 | DST |
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| DOID:162 | cancer | HGNC:1090 | Homo sapiens (human) | 667 | DST |
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| DOID:0070151 | hereditary sensory and autonomic neuropathy type 6 | HGNC:1090 | Homo sapiens (human) | 667 | DST |
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| DOID:0050548 | hereditary sensory neuropathy | HGNC:1090 | Homo sapiens (human) | 667 | DST |
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| DOID:0111416 | trichohepatoenteric syndrome 2 | HGNC:10898 | Homo sapiens (human) | 6499 | SKIC2 |
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| DOID:5199 | ureteral obstruction | HGNC:10897 | Homo sapiens (human) | 6498 | SKIL |
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| DOID:2340 | craniosynostosis | HGNC:10896 | Homo sapiens (human) | 6497 | SKI |
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| DOID:4440 | seminoma | HGNC:10894 | Homo sapiens (human) | 10419 | PRMT5 |
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| DOID:2696 | Leydig cell tumor | HGNC:10894 | Homo sapiens (human) | 10419 | PRMT5 |
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| DOID:2841 | asthma | HGNC:10894 | Homo sapiens (human) | 10419 | PRMT5 |
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| DOID:0060250 | idiopathic scoliosis | HGNC:10894 | Homo sapiens (human) | 10419 | PRMT5 |
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| DOID:0111424 | branchiootorenal syndrome 2 | HGNC:10891 | Homo sapiens (human) | 147912 | SIX5 |
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| DOID:14702 | branchiootorenal syndrome | HGNC:10891 | Homo sapiens (human) | 147912 | SIX5 |
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| DOID:11722 | myotonic dystrophy type 1 | HGNC:10891 | Homo sapiens (human) | 147912 | SIX5 |
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| DOID:11722 | myotonic dystrophy type 1 | HGNC:10890 | Homo sapiens (human) | 51804 | SIX4 |
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| DOID:14702 | branchiootorenal syndrome | HGNC:10890 | Homo sapiens (human) | 51804 | SIX4 |
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| DOID:0110553 | autosomal dominant nonsyndromic deafness 23 | HGNC:10887 | Homo sapiens (human) | 6495 | SIX1 |
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| DOID:2154 | nephroblastoma | HGNC:10887 | Homo sapiens (human) | 6495 | SIX1 |
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