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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:2513 | basal cell carcinoma | HGNC:8125 | Homo sapiens (human) | 4968 | OGG1 |
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| DOID:4450 | renal cell carcinoma | HGNC:8125 | Homo sapiens (human) | 4968 | OGG1 |
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| DOID:10591 | pre-eclampsia | HGNC:8125 | Homo sapiens (human) | 4968 | OGG1 |
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| DOID:0070468 | Yoon-Bellen neurodevelopmental syndrome | HGNC:8124 | Homo sapiens (human) | 4967 | OGDH |
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| DOID:0081326 | oxoglutarate dehydrogenase deficiency | HGNC:8124 | Homo sapiens (human) | 4967 | OGDH |
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| DOID:1056 | oculocerebrorenal syndrome | HGNC:8108 | Homo sapiens (human) | 4952 | OCRL |
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| DOID:0050699 | Dent disease | HGNC:8108 | Homo sapiens (human) | 4952 | OCRL |
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| DOID:612 | primary immunodeficiency disease | HGNC:8086 | Homo sapiens (human) | 4938 | OAS1 |
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| DOID:0110870 | congenital stationary night blindness 1A | HGNC:8082 | Homo sapiens (human) | 60506 | NYX |
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| DOID:8499 | night blindness | HGNC:8082 | Homo sapiens (human) | 60506 | NYX |
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| DOID:0050534 | congenital stationary night blindness | HGNC:8082 | Homo sapiens (human) | 60506 | NYX |
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| DOID:0080411 | familial adenomatous polyposis 3 | HGNC:8028 | Homo sapiens (human) | 4913 | NTHL1 |
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| DOID:1824 | status epilepticus | HGNC:8021 | Homo sapiens (human) | 4907 | NT5E |
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| DOID:0111582 | hereditary arterial and articular multiple calcification syndrome | HGNC:8021 | Homo sapiens (human) | 4907 | NT5E |
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| DOID:863 | nervous system disease | HGNC:800 | Homo sapiens (human) | 477 | ATP1A2 |
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| DOID:1574 | alcohol use disorder | HGNC:800 | Homo sapiens (human) | 477 | ATP1A2 |
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| DOID:0050635 | alternating hemiplegia of childhood | HGNC:800 | Homo sapiens (human) | 477 | ATP1A2 |
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| DOID:0111182 | familial hemiplegic migraine 2 | HGNC:800 | Homo sapiens (human) | 477 | ATP1A2 |
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| DOID:10024 | migraine with aura | HGNC:800 | Homo sapiens (human) | 477 | ATP1A2 |
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| DOID:0070384 | developmental and epileptic encephalopathy 98 | HGNC:800 | Homo sapiens (human) | 477 | ATP1A2 |
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| DOID:14264 | benign neonatal seizures | HGNC:800 | Homo sapiens (human) | 477 | ATP1A2 |
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| DOID:0060178 | familial hemiplegic migraine | HGNC:800 | Homo sapiens (human) | 477 | ATP1A2 |
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| DOID:1826 | epilepsy | HGNC:800 | Homo sapiens (human) | 477 | ATP1A2 |
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| DOID:10763 | hypertension | HGNC:800 | Homo sapiens (human) | 477 | ATP1A2 |
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| DOID:9279 | hyperhomocysteinemia | HGNC:800 | Homo sapiens (human) | 477 | ATP1A2 |
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