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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:0080445 | developmental and epileptic encephalopathy 13 | HGNC:10596 | Homo sapiens (human) | 6334 | SCN8A |
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| DOID:0060170 | generalized epilepsy with febrile seizures plus | HGNC:10596 | Homo sapiens (human) | 6334 | SCN8A |
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| DOID:0050709 | early infantile epileptic encephalopathy | HGNC:10596 | Homo sapiens (human) | 6334 | SCN8A |
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| DOID:0080422 | Dravet syndrome | HGNC:10594 | Homo sapiens (human) | 6332 | SCN7A |
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| DOID:1826 | epilepsy | HGNC:10594 | Homo sapiens (human) | 6332 | SCN7A |
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| DOID:0111294 | generalized epilepsy with febrile seizures plus 2 | HGNC:10594 | Homo sapiens (human) | 6332 | SCN7A |
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| DOID:3454 | brain infarction | HGNC:10594 | Homo sapiens (human) | 6332 | SCN7A |
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| DOID:0060170 | generalized epilepsy with febrile seizures plus | HGNC:10594 | Homo sapiens (human) | 6332 | SCN7A |
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| DOID:0111074 | progressive familial heart block type IA | HGNC:10593 | Homo sapiens (human) | 6331 | SCN5A |
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| DOID:9007 | sudden infant death syndrome | HGNC:10593 | Homo sapiens (human) | 6331 | SCN5A |
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| DOID:6000 | congestive heart failure | HGNC:10593 | Homo sapiens (human) | 6331 | SCN5A |
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| DOID:0050650 | familial atrial fibrillation | HGNC:10593 | Homo sapiens (human) | 6331 | SCN5A |
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| DOID:1826 | epilepsy | HGNC:10593 | Homo sapiens (human) | 6331 | SCN5A |
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| DOID:0111294 | generalized epilepsy with febrile seizures plus 2 | HGNC:10593 | Homo sapiens (human) | 6331 | SCN5A |
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| DOID:0110218 | Brugada syndrome 1 | HGNC:10593 | Homo sapiens (human) | 6331 | SCN5A |
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| DOID:13884 | sick sinus syndrome | HGNC:10593 | Homo sapiens (human) | 6331 | SCN5A |
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| DOID:0110646 | long QT syndrome 3 | HGNC:10593 | Homo sapiens (human) | 6331 | SCN5A |
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| DOID:0110433 | dilated cardiomyopathy 1E | HGNC:10593 | Homo sapiens (human) | 6331 | SCN5A |
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| DOID:0060170 | generalized epilepsy with febrile seizures plus | HGNC:10593 | Homo sapiens (human) | 6331 | SCN5A |
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| DOID:2843 | long QT syndrome | HGNC:10593 | Homo sapiens (human) | 6331 | SCN5A |
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| DOID:0080422 | Dravet syndrome | HGNC:10593 | Homo sapiens (human) | 6331 | SCN5A |
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| DOID:0050431 | arrhythmogenic right ventricular cardiomyopathy | HGNC:10593 | Homo sapiens (human) | 6331 | SCN5A |
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| DOID:2316 | brain ischemia | HGNC:10593 | Homo sapiens (human) | 6331 | SCN5A |
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| DOID:0110651 | long QT syndrome 10 | HGNC:10592 | Homo sapiens (human) | 6330 | SCN4B |
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| DOID:0080422 | Dravet syndrome | HGNC:10591 | Homo sapiens (human) | 6329 | SCN4A |
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