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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:3146 | lipid metabolism disorder | HGNC:3575 | Homo sapiens (human) | 9415 | FADS2 |
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| DOID:9744 | type 1 diabetes mellitus | HGNC:3575 | Homo sapiens (human) | 9415 | FADS2 |
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| DOID:12930 | dilated cardiomyopathy | HGNC:3575 | Homo sapiens (human) | 9415 | FADS2 |
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| DOID:1574 | alcohol use disorder | HGNC:3575 | Homo sapiens (human) | 9415 | FADS2 |
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| DOID:6000 | congestive heart failure | HGNC:3575 | Homo sapiens (human) | 9415 | FADS2 |
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| DOID:5804 | discrete subaortic stenosis | HGNC:3575 | Homo sapiens (human) | 9415 | FADS2 |
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| DOID:1485 | cystic fibrosis | HGNC:14640 | Homo sapiens (human) | 94160 | ABCC12 |
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| DOID:0050709 | early infantile epileptic encephalopathy | RGD:621881 | Rattus norvegicus (Norway rat) | 94173 | Idh3b |
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| DOID:0110409 | retinitis pigmentosa 46 | RGD:621881 | Rattus norvegicus (Norway rat) | 94173 | Idh3b |
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| DOID:0111903 | thrombophilia due to HRG deficiency | MGI:2146636 | Mus musculus (house mouse) | 94175 | Hrg |
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| DOID:4074 | pancreatic adenocarcinoma | MGI:2146636 | Mus musculus (house mouse) | 94175 | Hrg |
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| DOID:0060903 | thrombosis | MGI:2146636 | Mus musculus (house mouse) | 94175 | Hrg |
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| DOID:0111951 | immunodeficiency 40 | MGI:2149010 | Mus musculus (house mouse) | 94176 | Dock2 |
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| DOID:0080490 | mucolipidosis type IV | MGI:1890498 | Mus musculus (house mouse) | 94178 | Mcoln1 |
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| DOID:0060450 | Lisch epithelial corneal dystrophy | MGI:1890498 | Mus musculus (house mouse) | 94178 | Mcoln1 |
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| DOID:3343 | glycoproteinosis | MGI:1890498 | Mus musculus (house mouse) | 94178 | Mcoln1 |
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| DOID:0080576 | spondyloepimetaphyseal dysplasia, Genevieve-type | MGI:2149820 | Mus musculus (house mouse) | 94181 | Nans |
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| DOID:0060050 | autoimmune disease of blood | MGI:2151071 | Mus musculus (house mouse) | 94192 | C1galt1 |
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| DOID:1059 | intellectual disability | RGD:621092 | Rattus norvegicus (Norway rat) | 94198 | Psmb1 |
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| DOID:10907 | microcephaly | RGD:621092 | Rattus norvegicus (Norway rat) | 94198 | Psmb1 |
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| DOID:1289 | neurodegenerative disease | RGD:621092 | Rattus norvegicus (Norway rat) | 94198 | Psmb1 |
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| DOID:687 | hepatoblastoma | RGD:620324 | Rattus norvegicus (Norway rat) | 94199 | Dpep1 |
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| DOID:3083 | chronic obstructive pulmonary disease | HGNC:1705 | Homo sapiens (human) | 942 | CD86 |
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| DOID:9744 | type 1 diabetes mellitus | HGNC:1705 | Homo sapiens (human) | 942 | CD86 |
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| DOID:2377 | multiple sclerosis | HGNC:1705 | Homo sapiens (human) | 942 | CD86 |
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