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GlyTouCan
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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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:0090019 | sitosterolemia | HGNC:13886 | Homo sapiens (human) | 64240 | ABCG5 |
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| DOID:0080208 | metabolic dysfunction-associated steatotic liver disease | HGNC:13886 | Homo sapiens (human) | 64240 | ABCG5 |
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| DOID:2349 | arteriosclerosis | HGNC:13886 | Homo sapiens (human) | 64240 | ABCG5 |
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| DOID:9970 | obesity | HGNC:13886 | Homo sapiens (human) | 64240 | ABCG5 |
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| DOID:13580 | cholestasis | HGNC:13886 | Homo sapiens (human) | 64240 | ABCG5 |
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| DOID:0111181 | familial hemiplegic migraine 1 | HGNC:1388 | Homo sapiens (human) | 773 | CACNA1A |
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| DOID:10024 | migraine with aura | HGNC:1388 | Homo sapiens (human) | 773 | CACNA1A |
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| DOID:0060178 | familial hemiplegic migraine | HGNC:1388 | Homo sapiens (human) | 773 | CACNA1A |
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| DOID:6364 | migraine | HGNC:1388 | Homo sapiens (human) | 773 | CACNA1A |
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| DOID:1825 | childhood absence epilepsy | HGNC:1388 | Homo sapiens (human) | 773 | CACNA1A |
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| DOID:0070309 | absence epilepsy | HGNC:1388 | Homo sapiens (human) | 773 | CACNA1A |
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| DOID:0050951 | hereditary ataxia | HGNC:1388 | Homo sapiens (human) | 773 | CACNA1A |
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| DOID:0050753 | cerebellar ataxia | HGNC:1388 | Homo sapiens (human) | 773 | CACNA1A |
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| DOID:0050214 | Lambert-Eaton myasthenic syndrome | HGNC:1388 | Homo sapiens (human) | 773 | CACNA1A |
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| DOID:1826 | epilepsy | HGNC:1388 | Homo sapiens (human) | 773 | CACNA1A |
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| DOID:0050956 | spinocerebellar ataxia type 6 | HGNC:1388 | Homo sapiens (human) | 773 | CACNA1A |
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| DOID:3328 | temporal lobe epilepsy | HGNC:1388 | Homo sapiens (human) | 773 | CACNA1A |
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| DOID:0050990 | episodic ataxia type 2 | HGNC:1388 | Homo sapiens (human) | 773 | CACNA1A |
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| DOID:0050835 | generalized dystonia | HGNC:1388 | Homo sapiens (human) | 773 | CACNA1A |
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| DOID:0080454 | developmental and epileptic encephalopathy 42 | HGNC:1388 | Homo sapiens (human) | 773 | CACNA1A |
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| DOID:0050704 | childhood electroclinical syndrome | HGNC:1388 | Homo sapiens (human) | 773 | CACNA1A |
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| DOID:4186 | articulation disorder | HGNC:13875 | Homo sapiens (human) | 93986 | FOXP2 |
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| DOID:1094 | attention deficit hyperactivity disorder | HGNC:13875 | Homo sapiens (human) | 93986 | FOXP2 |
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| DOID:0060038 | specific developmental disorder | HGNC:13875 | Homo sapiens (human) | 93986 | FOXP2 |
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| DOID:1470 | major depressive disorder | HGNC:13875 | Homo sapiens (human) | 93986 | FOXP2 |
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