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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:5419 | schizophrenia | HGNC:1396 | Homo sapiens (human) | 8911 | CACNA1I |
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| DOID:1825 | childhood absence epilepsy | HGNC:1395 | Homo sapiens (human) | 8912 | CACNA1H |
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| DOID:11446 | sciatic neuropathy | HGNC:1395 | Homo sapiens (human) | 8912 | CACNA1H |
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| DOID:446 | primary hyperaldosteronism | HGNC:1395 | Homo sapiens (human) | 8912 | CACNA1H |
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| DOID:0111742 | cerebellar ataxia type 42 | HGNC:1394 | Homo sapiens (human) | 8913 | CACNA1G |
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| DOID:0060173 | Timothy syndrome | HGNC:1393 | Homo sapiens (human) | 778 | CACNA1F |
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| DOID:0110871 | congenital stationary night blindness 2A | HGNC:1393 | Homo sapiens (human) | 778 | CACNA1F |
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| DOID:0111007 | X-linked cone-rod dystrophy 3 | HGNC:1393 | Homo sapiens (human) | 778 | CACNA1F |
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| DOID:0050534 | congenital stationary night blindness | HGNC:1393 | Homo sapiens (human) | 778 | CACNA1F |
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| DOID:11723 | Duchenne muscular dystrophy | HGNC:1393 | Homo sapiens (human) | 778 | CACNA1F |
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| DOID:0050630 | Aland Island eye disease | HGNC:1393 | Homo sapiens (human) | 778 | CACNA1F |
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| DOID:0111181 | familial hemiplegic migraine 1 | HGNC:1392 | Homo sapiens (human) | 777 | CACNA1E |
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| DOID:0050951 | hereditary ataxia | HGNC:1392 | Homo sapiens (human) | 777 | CACNA1E |
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| DOID:0112205 | developmental and epileptic encephalopathy 69 | HGNC:1392 | Homo sapiens (human) | 777 | CACNA1E |
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| DOID:6364 | migraine | HGNC:1392 | Homo sapiens (human) | 777 | CACNA1E |
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| DOID:1826 | epilepsy | HGNC:1392 | Homo sapiens (human) | 777 | CACNA1E |
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| DOID:11446 | sciatic neuropathy | HGNC:1391 | Homo sapiens (human) | 776 | CACNA1D |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:1391 | Homo sapiens (human) | 776 | CACNA1D |
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| DOID:11723 | Duchenne muscular dystrophy | HGNC:1391 | Homo sapiens (human) | 776 | CACNA1D |
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| DOID:0060173 | Timothy syndrome | HGNC:1391 | Homo sapiens (human) | 776 | CACNA1D |
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| DOID:5419 | schizophrenia | HGNC:1391 | Homo sapiens (human) | 776 | CACNA1D |
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| DOID:0110649 | long QT syndrome 8 | HGNC:1390 | Homo sapiens (human) | 775 | CACNA1C |
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| DOID:0070536 | neurodevelopmental disorder with hypotonia, language delay, and skeletal defects with or without seizures | HGNC:1390 | Homo sapiens (human) | 775 | CACNA1C |
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| DOID:0050741 | alcohol dependence | HGNC:1390 | Homo sapiens (human) | 775 | CACNA1C |
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| DOID:0060173 | Timothy syndrome | HGNC:1390 | Homo sapiens (human) | 775 | CACNA1C |
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