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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:0080386 | nephrotic syndrome type 10 | MGI:1098726 | Mus musculus (house mouse) | 13731 | Emp2 |
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| DOID:9970 | obesity | HGNC:2323 | Homo sapiens (human) | 1373 | CPS1 |
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| DOID:9452 | steatotic liver disease | HGNC:2323 | Homo sapiens (human) | 1373 | CPS1 |
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| DOID:10763 | hypertension | HGNC:2323 | Homo sapiens (human) | 1373 | CPS1 |
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| DOID:684 | hepatocellular carcinoma | HGNC:2323 | Homo sapiens (human) | 1373 | CPS1 |
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| DOID:178 | vascular disease | HGNC:2323 | Homo sapiens (human) | 1373 | CPS1 |
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| DOID:9280 | carbamoyl phosphate synthetase I deficiency disease | HGNC:2323 | Homo sapiens (human) | 1373 | CPS1 |
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| DOID:13042 | persistent fetal circulation syndrome | HGNC:2323 | Homo sapiens (human) | 1373 | CPS1 |
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| DOID:1289 | neurodegenerative disease | MGI:99638 | Mus musculus (house mouse) | 13728 | Mark2 |
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| DOID:0070356 | visual impairment and progressive phthisis bulbi | MGI:99638 | Mus musculus (house mouse) | 13728 | Mark2 |
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| DOID:0070246 | X-linked Emery-Dreifuss muscular dystrophy 1 | MGI:108117 | Mus musculus (house mouse) | 13726 | Emd |
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| DOID:11726 | Emery-Dreifuss muscular dystrophy | MGI:108117 | Mus musculus (house mouse) | 13726 | Emd |
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| DOID:12930 | dilated cardiomyopathy | MGI:108117 | Mus musculus (house mouse) | 13726 | Emd |
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| DOID:224 | transient cerebral ischemia | MGI:101833 | Mus musculus (house mouse) | 13712 | Elk1 |
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| DOID:10652 | Alzheimer's disease | MGI:101833 | Mus musculus (house mouse) | 13712 | Elk1 |
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| DOID:2030 | anxiety disorder | MGI:101833 | Mus musculus (house mouse) | 13712 | Elk1 |
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| DOID:12858 | Huntington's disease | MGI:101833 | Mus musculus (house mouse) | 13712 | Elk1 |
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| DOID:5419 | schizophrenia | MGI:101833 | Mus musculus (house mouse) | 13712 | Elk1 |
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| DOID:12217 | Lewy body dementia | MGI:101833 | Mus musculus (house mouse) | 13712 | Elk1 |
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| DOID:409 | liver disease | HGNC:2321 | Homo sapiens (human) | 1371 | CPOX |
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| DOID:13269 | hereditary coproporphyria | HGNC:2321 | Homo sapiens (human) | 1371 | CPOX |
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| DOID:14330 | Parkinson's disease | MGI:109207 | Mus musculus (house mouse) | 13690 | Eif4g2 |
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| DOID:10763 | hypertension | MGI:109207 | Mus musculus (house mouse) | 13690 | Eif4g2 |
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| DOID:1591 | renovascular hypertension | MGI:109207 | Mus musculus (house mouse) | 13690 | Eif4g2 |
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| DOID:0111583 | carboxypeptidase N deficiency | HGNC:2312 | Homo sapiens (human) | 1369 | CPN1 |
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