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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: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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| 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:0080411 | familial adenomatous polyposis 3 | HGNC:8028 | Homo sapiens (human) | 4913 | NTHL1 |
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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:612 | primary immunodeficiency disease | HGNC:8086 | Homo sapiens (human) | 4938 | OAS1 |
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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: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:9669 | senile cataract | HGNC:8125 | Homo sapiens (human) | 4968 | OGG1 |
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| DOID:11714 | gestational diabetes | HGNC:8125 | Homo sapiens (human) | 4968 | OGG1 |
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| DOID:1793 | pancreatic cancer | HGNC:8125 | Homo sapiens (human) | 4968 | OGG1 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:8125 | Homo sapiens (human) | 4968 | OGG1 |
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| DOID:0002116 | pterygium | HGNC:8125 | Homo sapiens (human) | 4968 | OGG1 |
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| DOID:2237 | hepatitis | HGNC:8125 | Homo sapiens (human) | 4968 | OGG1 |
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| DOID:1070 | primary open angle glaucoma | HGNC:8125 | Homo sapiens (human) | 4968 | OGG1 |
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| DOID:2394 | ovarian cancer | HGNC:8125 | Homo sapiens (human) | 4968 | OGG1 |
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| DOID:4947 | cholangiocarcinoma | HGNC:8125 | Homo sapiens (human) | 4968 | OGG1 |
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| DOID:3314 | angiomyolipoma | HGNC:8125 | Homo sapiens (human) | 4968 | OGG1 |
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| DOID:2671 | transitional cell carcinoma | HGNC:8125 | Homo sapiens (human) | 4968 | OGG1 |
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| DOID:83 | cataract | HGNC:8125 | Homo sapiens (human) | 4968 | OGG1 |
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