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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:0060170 | generalized epilepsy with febrile seizures plus | HGNC:10591 | Homo sapiens (human) | 6329 | SCN4A |
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| DOID:1826 | epilepsy | HGNC:10591 | Homo sapiens (human) | 6329 | SCN4A |
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| DOID:0111538 | paramyotonia congenita of Von Eulenburg | HGNC:10591 | Homo sapiens (human) | 6329 | SCN4A |
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| DOID:0081354 | congenital myopathy 22A | HGNC:10591 | Homo sapiens (human) | 6329 | SCN4A |
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| DOID:0081355 | congenital myopathy 22B | HGNC:10591 | Homo sapiens (human) | 6329 | SCN4A |
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| DOID:0111294 | generalized epilepsy with febrile seizures plus 2 | HGNC:10591 | Homo sapiens (human) | 6329 | SCN4A |
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| DOID:14451 | hyperkalemic periodic paralysis | HGNC:10591 | Homo sapiens (human) | 6329 | SCN4A |
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| DOID:14452 | hypokalemic periodic paralysis | HGNC:10591 | Homo sapiens (human) | 6329 | SCN4A |
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| DOID:0110682 | congenital myasthenic syndrome 16 | HGNC:10591 | Homo sapiens (human) | 6329 | SCN4A |
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| DOID:2030 | anxiety disorder | HGNC:10590 | Homo sapiens (human) | 6328 | SCN3A |
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| DOID:0080420 | developmental and epileptic encephalopathy 62 | HGNC:10590 | Homo sapiens (human) | 6328 | SCN3A |
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| DOID:0081424 | familial focal epilepsy with variable foci 4 | HGNC:10590 | Homo sapiens (human) | 6328 | SCN3A |
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| DOID:0060170 | generalized epilepsy with febrile seizures plus | HGNC:10590 | Homo sapiens (human) | 6328 | SCN3A |
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| DOID:0080422 | Dravet syndrome | HGNC:10590 | Homo sapiens (human) | 6328 | SCN3A |
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| DOID:0111294 | generalized epilepsy with febrile seizures plus 2 | HGNC:10590 | Homo sapiens (human) | 6328 | SCN3A |
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| DOID:1826 | epilepsy | HGNC:10590 | Homo sapiens (human) | 6328 | SCN3A |
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| DOID:10754 | otitis media | HGNC:10589 | Homo sapiens (human) | 6327 | SCN2B |
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| DOID:11832 | visual epilepsy | HGNC:10589 | Homo sapiens (human) | 6327 | SCN2B |
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| DOID:0050650 | familial atrial fibrillation | HGNC:10589 | Homo sapiens (human) | 6327 | SCN2B |
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| DOID:0081116 | benign familial infantile seizures 3 | HGNC:10588 | Homo sapiens (human) | 6326 | SCN2A |
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| DOID:1826 | epilepsy | HGNC:10588 | Homo sapiens (human) | 6326 | SCN2A |
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| DOID:0080421 | developmental and epileptic encephalopathy 11 | HGNC:10588 | Homo sapiens (human) | 6326 | SCN2A |
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| DOID:0060170 | generalized epilepsy with febrile seizures plus | HGNC:10588 | Homo sapiens (human) | 6326 | SCN2A |
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| DOID:0060041 | autism spectrum disorder | HGNC:10588 | Homo sapiens (human) | 6326 | SCN2A |
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| DOID:0111294 | generalized epilepsy with febrile seizures plus 2 | HGNC:10588 | Homo sapiens (human) | 6326 | SCN2A |
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