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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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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:13359 | Ehlers-Danlos syndrome | RGD:1309214 | Rattus norvegicus (Norway rat) | 364675 | B4galt7 |
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| DOID:0080738 | Ehlers-Danlos syndrome spondylodysplastic type 1 | MGI:2384987 | Mus musculus (house mouse) | 218271 | B4galt7 |
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| DOID:13359 | Ehlers-Danlos syndrome | MGI:2384987 | Mus musculus (house mouse) | 218271 | B4galt7 |
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| DOID:0080738 | Ehlers-Danlos syndrome spondylodysplastic type 1 | RGD:1309214 | Rattus norvegicus (Norway rat) | 364675 | B4galt7 |
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| DOID:0050588 | muscular dystrophy-dystroglycanopathy type B1 | MGI:1919680 | Mus musculus (house mouse) | 108902 | B4gat1 |
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| DOID:0111238 | congenital muscular dystrophy-dystroglycanopathy type A13 | MGI:1919680 | Mus musculus (house mouse) | 108902 | B4gat1 |
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| DOID:0050588 | muscular dystrophy-dystroglycanopathy type B1 | RGD:1309541 | Rattus norvegicus (Norway rat) | 293667 | B4gat1 |
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| DOID:0111238 | congenital muscular dystrophy-dystroglycanopathy type A13 | RGD:1309541 | Rattus norvegicus (Norway rat) | 293667 | B4gat1 |
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| DOID:0050560 | Walker-Warburg syndrome | MGI:1919680 | Mus musculus (house mouse) | 108902 | B4gat1 |
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| DOID:0050560 | Walker-Warburg syndrome | RGD:1309541 | Rattus norvegicus (Norway rat) | 293667 | B4gat1 |
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| DOID:0014667 | disease of metabolism | HGNC:932 | Homo sapiens (human) | 570 | BAAT |
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| DOID:1380 | endometrial cancer | HGNC:936 | Homo sapiens (human) | 572 | BAD |
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| DOID:11832 | visual epilepsy | HGNC:936 | Homo sapiens (human) | 572 | BAD |
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| DOID:4450 | renal cell carcinoma | HGNC:936 | Homo sapiens (human) | 572 | BAD |
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| DOID:3669 | intermittent claudication | HGNC:936 | Homo sapiens (human) | 572 | BAD |
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| DOID:3908 | lung non-small cell carcinoma | HGNC:936 | Homo sapiens (human) | 572 | BAD |
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| DOID:0081292 | traumatic brain injury | HGNC:936 | Homo sapiens (human) | 572 | BAD |
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| DOID:9970 | obesity | HGNC:936 | Homo sapiens (human) | 572 | BAD |
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| DOID:10763 | hypertension | HGNC:936 | Homo sapiens (human) | 572 | BAD |
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| DOID:1686 | glaucoma | HGNC:936 | Homo sapiens (human) | 572 | BAD |
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| DOID:1793 | pancreatic cancer | HGNC:936 | Homo sapiens (human) | 572 | BAD |
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| DOID:3021 | acute kidney failure | HGNC:936 | Homo sapiens (human) | 572 | BAD |
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| DOID:11132 | prostatic hypertrophy | HGNC:936 | Homo sapiens (human) | 572 | BAD |
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| DOID:4448 | macular degeneration | HGNC:936 | Homo sapiens (human) | 572 | BAD |
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| DOID:3525 | middle cerebral artery infarction | HGNC:936 | Homo sapiens (human) | 572 | BAD |
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