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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:1612 | breast cancer | 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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| DOID:0111954 | immunodeficiency 60 | HGNC:14078 | Homo sapiens (human) | 60468 | BACH2 |
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| DOID:10652 | Alzheimer's disease | HGNC:934 | Homo sapiens (human) | 25825 | BACE2 |
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| DOID:9255 | frontotemporal dementia | HGNC:934 | Homo sapiens (human) | 25825 | BACE2 |
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| DOID:10652 | Alzheimer's disease | HGNC:933 | Homo sapiens (human) | 23621 | BACE1 |
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| DOID:224 | transient cerebral ischemia | HGNC:933 | Homo sapiens (human) | 23621 | BACE1 |
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| DOID:2491 | sensory peripheral neuropathy | HGNC:933 | Homo sapiens (human) | 23621 | BACE1 |
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| DOID:1307 | dementia | HGNC:933 | Homo sapiens (human) | 23621 | BACE1 |
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| DOID:5419 | schizophrenia | HGNC:933 | Homo sapiens (human) | 23621 | BACE1 |
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| DOID:0014667 | disease of metabolism | HGNC:932 | Homo sapiens (human) | 570 | BAAT |
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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:0111238 | congenital muscular dystrophy-dystroglycanopathy type A13 | RGD:1309541 | Rattus norvegicus (Norway rat) | 293667 | B4gat1 |
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| DOID:0050560 | Walker-Warburg syndrome | RGD:1309541 | Rattus norvegicus (Norway rat) | 293667 | B4gat1 |
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| DOID:0050588 | muscular dystrophy-dystroglycanopathy type B1 | MGI:1919680 | Mus musculus (house mouse) | 108902 | B4gat1 |
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| DOID:0050560 | Walker-Warburg syndrome | 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:13359 | Ehlers-Danlos syndrome | RGD:1309214 | Rattus norvegicus (Norway rat) | 364675 | 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:0080738 | Ehlers-Danlos syndrome spondylodysplastic type 1 | MGI:2384987 | Mus musculus (house mouse) | 218271 | B4galt7 |
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| DOID:2377 | multiple sclerosis | RGD:71046 | Rattus norvegicus (Norway rat) | 65196 | B4galt6 |
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| DOID:2377 | multiple sclerosis | MGI:1928380 | Mus musculus (house mouse) | 56386 | B4galt6 |
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| DOID:2377 | multiple sclerosis | RGD:1310062 | Rattus norvegicus (Norway rat) | 362275 | B4galt5 |
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| DOID:2377 | multiple sclerosis | MGI:1927169 | Mus musculus (house mouse) | 56336 | B4galt5 |
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