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GlyTouCan
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
LM-GlycoRepo
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:10609 | rickets | MGI:2136853 | Mus musculus (house mouse) | 80752 | Fam20c |
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| DOID:0050445 | X-linked dominant hypophosphatemic rickets | MGI:2136853 | Mus musculus (house mouse) | 80752 | Fam20c |
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| DOID:14004 | thoracic aortic aneurysm | HGNC:29673 | Homo sapiens (human) | 8076 | MFAP5 |
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| DOID:10808 | gastric ulcer | HGNC:2195 | Homo sapiens (human) | 80781 | COL18A1 |
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| DOID:0050700 | cardiomyopathy | HGNC:2195 | Homo sapiens (human) | 80781 | COL18A1 |
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| DOID:0060680 | pigment dispersion syndrome | HGNC:2195 | Homo sapiens (human) | 80781 | COL18A1 |
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| DOID:1405 | primary angle-closure glaucoma | HGNC:2195 | Homo sapiens (human) | 80781 | COL18A1 |
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| DOID:423 | myopathy | HGNC:2195 | Homo sapiens (human) | 80781 | COL18A1 |
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| DOID:12930 | dilated cardiomyopathy | HGNC:2195 | Homo sapiens (human) | 80781 | COL18A1 |
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| DOID:684 | hepatocellular carcinoma | HGNC:2195 | Homo sapiens (human) | 80781 | COL18A1 |
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| DOID:699 | mitochondrial myopathy | HGNC:2195 | Homo sapiens (human) | 80781 | COL18A1 |
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| DOID:8577 | ulcerative colitis | HGNC:2195 | Homo sapiens (human) | 80781 | COL18A1 |
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| DOID:0080893 | Bainbridge-Ropers syndrome | HGNC:29357 | Homo sapiens (human) | 80816 | ASXL3 |
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| DOID:0110779 | hereditary spastic paraplegia 28 | HGNC:19714 | Homo sapiens (human) | 80821 | DDHD1 |
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| DOID:0110806 | hereditary spastic paraplegia 54 | HGNC:19714 | Homo sapiens (human) | 80821 | DDHD1 |
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| DOID:224 | transient cerebral ischemia | HGNC:17909 | Homo sapiens (human) | 80824 | DUSP16 |
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| DOID:557 | kidney disease | HGNC:14868 | Homo sapiens (human) | 80833 | APOL3 |
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| DOID:9970 | obesity | RGD:68333 | Rattus norvegicus (Norway rat) | 80840 | Gpr12 |
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| DOID:3393 | coronary artery disease | RGD:68355 | Rattus norvegicus (Norway rat) | 80848 | Cubn |
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| DOID:557 | kidney disease | RGD:68355 | Rattus norvegicus (Norway rat) | 80848 | Cubn |
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| DOID:10591 | pre-eclampsia | RGD:68355 | Rattus norvegicus (Norway rat) | 80848 | Cubn |
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| DOID:3717 | gastric adenocarcinoma | HGNC:7133 | Homo sapiens (human) | 8085 | KMT2D |
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| DOID:3748 | esophagus squamous cell carcinoma | HGNC:7133 | Homo sapiens (human) | 8085 | KMT2D |
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| DOID:903 | gastrointestinal lymphoma | HGNC:7133 | Homo sapiens (human) | 8085 | KMT2D |
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| DOID:3565 | meningioma | HGNC:7133 | Homo sapiens (human) | 8085 | KMT2D |
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