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GlyTouCan
Glycan Structure Repository
GlyComb
Glycoconjugate Repository
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Glycomics MS raw data Repository
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Glycomics MS Repository for glycan annotations from GlycoWorkbench
LM-GlycoRepo
Repository for lectin-assisted multimodality data
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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
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:0080526 | bronchiectasis 1 | HGNC:10600 | Homo sapiens (human) | 6338 | SCNN1B |
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| DOID:1485 | cystic fibrosis | HGNC:10600 | Homo sapiens (human) | 6338 | SCNN1B |
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| DOID:1184 | nephrotic syndrome | HGNC:10600 | Homo sapiens (human) | 6338 | SCNN1B |
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| DOID:14452 | hypokalemic periodic paralysis | HGNC:10600 | Homo sapiens (human) | 6338 | SCNN1B |
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| DOID:1289 | neurodegenerative disease | HGNC:10600 | Homo sapiens (human) | 6338 | SCNN1B |
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| DOID:4479 | pseudohypoaldosteronism | HGNC:10600 | Homo sapiens (human) | 6338 | SCNN1B |
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| DOID:0050477 | Liddle syndrome | HGNC:10599 | Homo sapiens (human) | 6337 | SCNN1A |
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| DOID:326 | ischemia | HGNC:10599 | Homo sapiens (human) | 6337 | SCNN1A |
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| DOID:0080527 | bronchiectasis 2 | HGNC:10599 | Homo sapiens (human) | 6337 | SCNN1A |
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| DOID:4479 | pseudohypoaldosteronism | HGNC:10599 | Homo sapiens (human) | 6337 | SCNN1A |
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| DOID:1289 | neurodegenerative disease | HGNC:10599 | Homo sapiens (human) | 6337 | SCNN1A |
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| DOID:769 | neuroblastoma | HGNC:10599 | Homo sapiens (human) | 6337 | SCNN1A |
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| DOID:1184 | nephrotic syndrome | HGNC:10599 | Homo sapiens (human) | 6337 | SCNN1A |
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| DOID:0111537 | paroxysmal extreme pain disorder | HGNC:10597 | Homo sapiens (human) | 6335 | SCN9A |
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| DOID:2030 | anxiety disorder | HGNC:10597 | Homo sapiens (human) | 6335 | SCN9A |
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| DOID:0111294 | generalized epilepsy with febrile seizures plus 2 | HGNC:10597 | Homo sapiens (human) | 6335 | SCN9A |
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| DOID:9240 | erythromelalgia | HGNC:10597 | Homo sapiens (human) | 6335 | SCN9A |
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| DOID:1826 | epilepsy | HGNC:10597 | Homo sapiens (human) | 6335 | SCN9A |
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| DOID:0080422 | Dravet syndrome | HGNC:10597 | Homo sapiens (human) | 6335 | SCN9A |
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| DOID:0060170 | generalized epilepsy with febrile seizures plus | HGNC:10597 | Homo sapiens (human) | 6335 | SCN9A |
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| DOID:1826 | epilepsy | HGNC:10596 | Homo sapiens (human) | 6334 | SCN8A |
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| DOID:0081118 | benign familial infantile seizures 5 | HGNC:10596 | Homo sapiens (human) | 6334 | SCN8A |
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| DOID:0080422 | Dravet syndrome | HGNC:10596 | Homo sapiens (human) | 6334 | SCN8A |
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| DOID:6000 | congestive heart failure | HGNC:10596 | Homo sapiens (human) | 6334 | SCN8A |
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| DOID:0111294 | generalized epilepsy with febrile seizures plus 2 | HGNC:10596 | Homo sapiens (human) | 6334 | SCN8A |
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