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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:14219 | renal tubular acidosis | RGD:68936 | Rattus norvegicus (Norway rat) | 84484 | Slc4a4 |
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| DOID:10763 | hypertension | RGD:68936 | Rattus norvegicus (Norway rat) | 84484 | Slc4a4 |
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| DOID:4947 | cholangiocarcinoma | RGD:68936 | Rattus norvegicus (Norway rat) | 84484 | Slc4a4 |
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| DOID:2355 | anemia | RGD:68936 | Rattus norvegicus (Norway rat) | 84484 | Slc4a4 |
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| DOID:12387 | nephrogenic diabetes insipidus | RGD:68936 | Rattus norvegicus (Norway rat) | 84484 | Slc4a4 |
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| DOID:1289 | neurodegenerative disease | RGD:620531 | Rattus norvegicus (Norway rat) | 84487 | Slc17a6 |
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| DOID:14330 | Parkinson's disease | RGD:620531 | Rattus norvegicus (Norway rat) | 84487 | Slc17a6 |
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| DOID:224 | transient cerebral ischemia | RGD:620531 | Rattus norvegicus (Norway rat) | 84487 | Slc17a6 |
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| DOID:14679 | VACTERL association | RGD:68957 | Rattus norvegicus (Norway rat) | 84491 | Qsox1 |
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| DOID:6000 | congestive heart failure | HGNC:1513 | Homo sapiens (human) | 845 | CASQ2 |
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| DOID:0060676 | catecholaminergic polymorphic ventricular tachycardia 2 | HGNC:1513 | Homo sapiens (human) | 845 | CASQ2 |
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| DOID:1929 | supravalvular aortic stenosis | HGNC:1513 | Homo sapiens (human) | 845 | CASQ2 |
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| DOID:0060822 | syndromic X-linked intellectual disability Cabezas type | HGNC:2555 | Homo sapiens (human) | 8450 | CUL4B |
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| DOID:1059 | intellectual disability | HGNC:2555 | Homo sapiens (human) | 8450 | CUL4B |
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| DOID:0050700 | cardiomyopathy | HGNC:20156 | Homo sapiens (human) | 84502 | JPH4 |
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| DOID:12236 | primary biliary cholangitis | RGD:628660 | Rattus norvegicus (Norway rat) | 84511 | Slco1c1 |
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| DOID:4479 | pseudohypoaldosteronism | HGNC:2553 | Homo sapiens (human) | 8452 | CUL3 |
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| DOID:0060041 | autism spectrum disorder | HGNC:2553 | Homo sapiens (human) | 8452 | CUL3 |
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| DOID:0111581 | C syndrome | MGI:1934368 | Mus musculus (house mouse) | 84544 | Cd96 |
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| DOID:5419 | schizophrenia | RGD:620000 | Rattus norvegicus (Norway rat) | 84556 | Rims1 |
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| DOID:0060041 | autism spectrum disorder | RGD:620000 | Rattus norvegicus (Norway rat) | 84556 | Rims1 |
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| DOID:0081020 | congenital fibrosis of the extraocular muscles 5 | HGNC:18603 | Homo sapiens (human) | 84570 | COL25A1 |
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| DOID:0080678 | mucolipidosis III gamma | HGNC:23026 | Homo sapiens (human) | 84572 | GNPTG |
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| DOID:3343 | glycoproteinosis | HGNC:23026 | Homo sapiens (human) | 84572 | GNPTG |
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| DOID:1508 | candidiasis | RGD:619955 | Rattus norvegicus (Norway rat) | 84597 | Fut9 |
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