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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:0080422 | Dravet syndrome | HGNC:10588 | Homo sapiens (human) | 6326 | SCN2A |
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| DOID:2030 | anxiety disorder | HGNC:10588 | Homo sapiens (human) | 6326 | SCN2A |
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| DOID:0111302 | generalized epilepsy with febrile seizures plus 1 | HGNC:10586 | Homo sapiens (human) | 6324 | SCN1B |
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| DOID:0050650 | familial atrial fibrillation | HGNC:10586 | Homo sapiens (human) | 6324 | SCN1B |
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| DOID:0060170 | generalized epilepsy with febrile seizures plus | HGNC:10586 | Homo sapiens (human) | 6324 | SCN1B |
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| DOID:0110222 | Brugada syndrome 5 | HGNC:10586 | Homo sapiens (human) | 6324 | SCN1B |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:10586 | Homo sapiens (human) | 6324 | SCN1B |
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| DOID:0080455 | developmental and epileptic encephalopathy 52 | HGNC:10586 | Homo sapiens (human) | 6324 | SCN1B |
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| DOID:0080422 | Dravet syndrome | HGNC:10585 | Homo sapiens (human) | 6323 | SCN1A |
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| DOID:1826 | epilepsy | HGNC:10585 | Homo sapiens (human) | 6323 | SCN1A |
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| DOID:2030 | anxiety disorder | HGNC:10585 | Homo sapiens (human) | 6323 | SCN1A |
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| DOID:0111294 | generalized epilepsy with febrile seizures plus 2 | HGNC:10585 | Homo sapiens (human) | 6323 | SCN1A |
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| DOID:0060041 | autism spectrum disorder | HGNC:10585 | Homo sapiens (human) | 6323 | SCN1A |
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| DOID:0111183 | familial hemiplegic migraine 3 | HGNC:10585 | Homo sapiens (human) | 6323 | SCN1A |
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| DOID:0070379 | developmental and epileptic encephalopathy 6B | HGNC:10585 | Homo sapiens (human) | 6323 | SCN1A |
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| DOID:0060170 | generalized epilepsy with febrile seizures plus | HGNC:10585 | Homo sapiens (human) | 6323 | SCN1A |
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| DOID:0050548 | hereditary sensory neuropathy | HGNC:10583 | Homo sapiens (human) | 11280 | SCN11A |
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| DOID:0080422 | Dravet syndrome | HGNC:10583 | Homo sapiens (human) | 11280 | SCN11A |
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| DOID:1826 | epilepsy | HGNC:10583 | Homo sapiens (human) | 11280 | SCN11A |
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| DOID:0060170 | generalized epilepsy with febrile seizures plus | HGNC:10583 | Homo sapiens (human) | 11280 | SCN11A |
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| DOID:0111731 | familial episodic pain syndrome 3 | HGNC:10583 | Homo sapiens (human) | 11280 | SCN11A |
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| DOID:0070149 | hereditary sensory and autonomic neuropathy type 7 | HGNC:10583 | Homo sapiens (human) | 11280 | SCN11A |
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| DOID:0111294 | generalized epilepsy with febrile seizures plus 2 | HGNC:10583 | Homo sapiens (human) | 11280 | SCN11A |
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| DOID:11446 | sciatic neuropathy | HGNC:10582 | Homo sapiens (human) | 6336 | SCN10A |
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| DOID:0111294 | generalized epilepsy with febrile seizures plus 2 | HGNC:10582 | Homo sapiens (human) | 6336 | SCN10A |
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