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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: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: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: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: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: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:0080208 | metabolic dysfunction-associated steatotic liver disease | HGNC:14932 | Homo sapiens (human) | 23409 | SIRT4 |
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| DOID:0080208 | metabolic dysfunction-associated steatotic liver disease | HGNC:7150 | Homo sapiens (human) | 23417 | MLYCD |
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| DOID:0050700 | cardiomyopathy | HGNC:7150 | Homo sapiens (human) | 23417 | MLYCD |
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| DOID:684 | hepatocellular carcinoma | MGI:2384588 | Mus musculus (house mouse) | 234258 | Neil3 |
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| DOID:0112315 | brain small vessel disease 3 | MGI:1924348 | Mus musculus (house mouse) | 234407 | Colgalt1 |
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| DOID:12858 | Huntington's disease | HGNC:9755 | Homo sapiens (human) | 23475 | QPRT |
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| DOID:0050719 | cerebral folate receptor alpha deficiency | HGNC:3791 | Homo sapiens (human) | 2348 | FOLR1 |
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| DOID:0081122 | Catel Manzke syndrome | HGNC:20324 | Homo sapiens (human) | 23483 | TGDS |
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| DOID:0060256 | Dowling-Degos disease | HGNC:14988 | Homo sapiens (human) | 23509 | POFUT1 |
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| DOID:0080537 | hypermanganesemia with dystonia 2 | HGNC:20858 | Homo sapiens (human) | 23516 | SLC39A14 |
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