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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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Repository for lectin-assisted multimodality data
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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 | October 9, 2024 |
| Disease ID | Disease Name | Alliance of Genome Resources ID ▲ | Species | Gene ID | Gene Symbol | FlyGlycoDB | Evidence Code Names | References |
|---|---|---|---|---|---|---|---|---|
| DOID:0060307 | autosomal dominant intellectual developmental disorder | HGNC:18420 | Homo sapiens (human) | 29072 | SETD2 |
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| DOID:0050156 | idiopathic pulmonary fibrosis | HGNC:18420 | Homo sapiens (human) | 29072 | SETD2 |
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| DOID:9253 | gastrointestinal stromal tumor | HGNC:18420 | Homo sapiens (human) | 29072 | SETD2 |
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| DOID:1826 | epilepsy | HGNC:18423 | Homo sapiens (human) | 9681 | DEPDC5 |
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| DOID:0081423 | familial focal epilepsy with variable foci 3 | HGNC:18423 | Homo sapiens (human) | 9681 | DEPDC5 |
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| DOID:162 | cancer | HGNC:18423 | Homo sapiens (human) | 9681 | DEPDC5 |
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| DOID:2234 | focal epilepsy | HGNC:18423 | Homo sapiens (human) | 9681 | DEPDC5 |
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| DOID:0112202 | developmental and epileptic encephalopathy | HGNC:18423 | Homo sapiens (human) | 9681 | DEPDC5 |
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| DOID:0081421 | familial focal epilepsy with variable foci 1 | HGNC:18423 | Homo sapiens (human) | 9681 | DEPDC5 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:18431 | Homo sapiens (human) | 10965 | ACOT2 |
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| DOID:684 | hepatocellular carcinoma | HGNC:18437 | Homo sapiens (human) | 84868 | HAVCR2 |
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| DOID:2957 | pulmonary tuberculosis | HGNC:18437 | Homo sapiens (human) | 84868 | HAVCR2 |
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| DOID:224 | transient cerebral ischemia | HGNC:18437 | Homo sapiens (human) | 84868 | HAVCR2 |
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| DOID:1485 | cystic fibrosis | HGNC:18437 | Homo sapiens (human) | 84868 | HAVCR2 |
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| DOID:4450 | renal cell carcinoma | HGNC:18437 | Homo sapiens (human) | 84868 | HAVCR2 |
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| DOID:9970 | obesity | HGNC:18448 | Homo sapiens (human) | 79661 | NEIL1 |
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| DOID:0060611 | abdominal obesity-metabolic syndrome | HGNC:18448 | Homo sapiens (human) | 79661 | NEIL1 |
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| DOID:224 | transient cerebral ischemia | HGNC:18451 | Homo sapiens (human) | 90411 | MCFD2 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:1848 | Homo sapiens (human) | 1056 | CEL |
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| DOID:3153 | lipomatosis | HGNC:1848 | Homo sapiens (human) | 1056 | CEL |
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| DOID:0111105 | maturity-onset diabetes of the young type 8 | HGNC:1848 | Homo sapiens (human) | 1056 | CEL |
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| DOID:9744 | type 1 diabetes mellitus | HGNC:1848 | Homo sapiens (human) | 1056 | CEL |
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| DOID:0070134 | autosomal recessive cutis laxa type IIA | HGNC:18481 | Homo sapiens (human) | 23545 | ATP6V0A2 |
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| DOID:0112171 | wrinkly skin syndrome | HGNC:18481 | Homo sapiens (human) | 23545 | ATP6V0A2 |
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| DOID:0110942 | autosomal recessive osteopetrosis 1 | HGNC:18481 | Homo sapiens (human) | 23545 | ATP6V0A2 |
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