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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:1574 | alcohol use disorder | HGNC:253 | Homo sapiens (human) | 128 | ADH5 |
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| DOID:13580 | cholestasis | HGNC:253 | Homo sapiens (human) | 128 | ADH5 |
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| DOID:987 | alopecia | HGNC:25531 | Homo sapiens (human) | 55711 | FAR2 |
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| DOID:10140 | dry eye syndrome | HGNC:25531 | Homo sapiens (human) | 55711 | FAR2 |
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| DOID:10907 | microcephaly | HGNC:25575 | Homo sapiens (human) | 55224 | ETNK2 |
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| DOID:10273 | heart conduction disease | HGNC:25575 | Homo sapiens (human) | 55224 | ETNK2 |
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| DOID:1826 | epilepsy | HGNC:25575 | Homo sapiens (human) | 55224 | ETNK2 |
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| DOID:0070468 | Yoon-Bellen neurodevelopmental syndrome | HGNC:25590 | Homo sapiens (human) | 55753 | OGDHL |
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| DOID:0081326 | oxoglutarate dehydrogenase deficiency | HGNC:25590 | Homo sapiens (human) | 55753 | OGDHL |
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| DOID:14330 | Parkinson's disease | HGNC:256 | Homo sapiens (human) | 131 | ADH7 |
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| DOID:4621 | holoprosencephaly | HGNC:25712 | Homo sapiens (human) | 80055 | PGAP1 |
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| DOID:0080568 | congenital disorder of glycosylation Iq | HGNC:25812 | Homo sapiens (human) | 79644 | SRD5A3 |
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| DOID:0050570 | congenital disorder of glycosylation type I | HGNC:25812 | Homo sapiens (human) | 79644 | SRD5A3 |
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| DOID:0050807 | Kahrizi syndrome | HGNC:25812 | Homo sapiens (human) | 79644 | SRD5A3 |
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| DOID:1824 | status epilepticus | HGNC:2590 | Homo sapiens (human) | 1583 | CYP11A1 |
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| DOID:1924 | hypogonadism | HGNC:2590 | Homo sapiens (human) | 1583 | CYP11A1 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:2590 | Homo sapiens (human) | 1583 | CYP11A1 |
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| DOID:10763 | hypertension | HGNC:2590 | Homo sapiens (human) | 1583 | CYP11A1 |
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| DOID:0050546 | congenital adrenal insufficiency | HGNC:2590 | Homo sapiens (human) | 1583 | CYP11A1 |
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| DOID:4195 | hyperglycemia | HGNC:2590 | Homo sapiens (human) | 1583 | CYP11A1 |
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| DOID:2527 | nephrosis | HGNC:2590 | Homo sapiens (human) | 1583 | CYP11A1 |
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| DOID:11446 | sciatic neuropathy | HGNC:2590 | Homo sapiens (human) | 1583 | CYP11A1 |
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| DOID:0050811 | congenital adrenal hyperplasia | HGNC:2590 | Homo sapiens (human) | 1583 | CYP11A1 |
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| DOID:0112382 | muscular dystrophy-dystroglycanopathy type C8 | HGNC:25902 | Homo sapiens (human) | 84892 | POMGNT2 |
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| DOID:0111231 | congenital muscular dystrophy-dystroglycanopathy type A8 | HGNC:25902 | Homo sapiens (human) | 84892 | POMGNT2 |
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