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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:5041 | esophageal cancer | HGNC:2602 | Homo sapiens (human) | 1591 | CYP24A1 |
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| DOID:1612 | breast cancer | HGNC:4553 | Homo sapiens (human) | 2876 | GPX1 |
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| DOID:0050127 | sinusitis | HGNC:11848 | Homo sapiens (human) | 7097 | TLR2 |
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| DOID:0050127 | sinusitis | HGNC:11850 | Homo sapiens (human) | 7099 | TLR4 |
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| DOID:4247 | coronary restenosis | HGNC:11998 | Homo sapiens (human) | 7157 | TP53 |
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| DOID:1936 | atherosclerosis | HGNC:16049 | Homo sapiens (human) | 10728 | PTGES3 |
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| DOID:3393 | coronary artery disease | HGNC:3402 | Homo sapiens (human) | 2053 | EPHX2 |
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| DOID:12783 | migraine without aura | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:0002116 | pterygium | HGNC:8125 | Homo sapiens (human) | 4968 | OGG1 |
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| DOID:3132 | porphyria cutanea tarda | HGNC:2595 | Homo sapiens (human) | 1543 | CYP1A1 |
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| DOID:1214 | tympanosclerosis | HGNC:1516 | Homo sapiens (human) | 847 | CAT |
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| DOID:0050570 | congenital disorder of glycosylation type I | SGD:S000000314 | Saccharomyces cerevisiae S288C | 852407 | ALG1 |
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| DOID:4450 | renal cell carcinoma | HGNC:451 | Homo sapiens (human) | 23600 | AMACR |
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| DOID:13378 | Kawasaki disease | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:2349 | arteriosclerosis | HGNC:435 | Homo sapiens (human) | 240 | ALOX5 |
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| DOID:10534 | stomach cancer | MGI:96560 | Mus musculus (house mouse) | 16195 | Il6st |
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| DOID:3213 | demyelinating disease | HGNC:9605 | Homo sapiens (human) | 5743 | PTGS2 |
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| DOID:6196 | reactive arthritis | HGNC:2595 | Homo sapiens (human) | 1543 | CYP1A1 |
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| DOID:0110429 | dilated cardiomyopathy 1H | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:4450 | renal cell carcinoma | HGNC:429 | Homo sapiens (human) | 239 | ALOX12 |
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| DOID:2352 | hemochromatosis | HGNC:4887 | Homo sapiens (human) | 148738 | HJV |
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| DOID:13406 | pulmonary sarcoidosis | HGNC:5988 | Homo sapiens (human) | 8809 | IL18R1 |
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| DOID:2237 | hepatitis | RGD:621168 | Rattus norvegicus (Norway rat) | 81528 | Ogg1 |
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| DOID:0050848 | obstructive sleep apnea | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:12849 | autistic disorder | HGNC:8978 | Homo sapiens (human) | 5294 | PIK3CG |
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