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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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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 | July 29, 2024 |
| Disease ID | Disease Name | Alliance of Genome Resources ID | Species | Gene ID ▼ | Gene Symbol | FlyGlycoDB | Evidence Code Names | References |
|---|---|---|---|---|---|---|---|---|
| DOID:0080208 | metabolic dysfunction-associated steatotic liver disease | HGNC:14932 | Homo sapiens (human) | 23409 | SIRT4 |
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| DOID:0060653 | lethal congenital contracture syndrome 3 | HGNC:8996 | Homo sapiens (human) | 23396 | PIP5K1C |
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| DOID:162 | cancer | HGNC:8996 | Homo sapiens (human) | 23396 | PIP5K1C |
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| DOID:9744 | type 1 diabetes mellitus | MGI:2451073 | Mus musculus (house mouse) | 233781 | Xylt1 |
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| DOID:2738 | pseudoxanthoma elasticum | MGI:2451073 | Mus musculus (house mouse) | 233781 | Xylt1 |
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| DOID:557 | kidney disease | MGI:2451073 | Mus musculus (house mouse) | 233781 | Xylt1 |
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| DOID:0060462 | Desbuquois dysplasia | MGI:2451073 | Mus musculus (house mouse) | 233781 | Xylt1 |
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| DOID:824 | periodontitis | HGNC:3774 | Homo sapiens (human) | 2331 | FMOD |
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| DOID:3087 | gingivitis | HGNC:3774 | Homo sapiens (human) | 2331 | FMOD |
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| DOID:971 | tendinitis | HGNC:3774 | Homo sapiens (human) | 2331 | FMOD |
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| DOID:1240 | leukemia | HGNC:16496 | Homo sapiens (human) | 23305 | ACSL6 |
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| DOID:9119 | acute myeloid leukemia | HGNC:16496 | Homo sapiens (human) | 23305 | ACSL6 |
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| DOID:1826 | epilepsy | MGI:88107 | Mus musculus (house mouse) | 232975 | Atp1a3 |
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| DOID:0090056 | dystonia 12 | MGI:88107 | Mus musculus (house mouse) | 232975 | Atp1a3 |
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| DOID:3312 | bipolar disorder | MGI:88107 | Mus musculus (house mouse) | 232975 | Atp1a3 |
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| DOID:0050635 | alternating hemiplegia of childhood | MGI:88107 | Mus musculus (house mouse) | 232975 | Atp1a3 |
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| DOID:0070385 | developmental and epileptic encephalopathy 99 | MGI:88107 | Mus musculus (house mouse) | 232975 | Atp1a3 |
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| DOID:863 | nervous system disease | MGI:88107 | Mus musculus (house mouse) | 232975 | Atp1a3 |
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| DOID:1574 | alcohol use disorder | MGI:88107 | Mus musculus (house mouse) | 232975 | Atp1a3 |
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| DOID:0060178 | familial hemiplegic migraine | MGI:88107 | Mus musculus (house mouse) | 232975 | Atp1a3 |
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| DOID:14250 | Down syndrome | HGNC:14683 | Homo sapiens (human) | 23275 | POFUT2 |
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| DOID:2377 | multiple sclerosis | HGNC:29013 | Homo sapiens (human) | 23274 | CLEC16A |
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| DOID:9744 | type 1 diabetes mellitus | HGNC:29013 | Homo sapiens (human) | 23274 | CLEC16A |
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| DOID:13774 | Addison's disease | HGNC:29013 | Homo sapiens (human) | 23274 | CLEC16A |
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| DOID:7148 | rheumatoid arthritis | HGNC:29013 | Homo sapiens (human) | 23274 | CLEC16A |
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