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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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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 | July 29, 2024 |
| Disease ID | Disease Name | Alliance of Genome Resources ID ▼ | Species | Gene ID | Gene Symbol | FlyGlycoDB | Evidence Code Names | References |
|---|---|---|---|---|---|---|---|---|
| DOID:9884 | muscular dystrophy | HGNC:2211 | Homo sapiens (human) | 1291 | COL6A1 |
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| DOID:0050557 | congenital muscular dystrophy | HGNC:2211 | Homo sapiens (human) | 1291 | COL6A1 |
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| DOID:0110245 | cataract 38 | HGNC:21869 | Homo sapiens (human) | 55750 | AGK |
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| DOID:0080132 | Sengers syndrome | HGNC:21869 | Homo sapiens (human) | 55750 | AGK |
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| DOID:3070 | high grade glioma | HGNC:2172 | Homo sapiens (human) | 6900 | CNTN2 |
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| DOID:850 | lung disease | HGNC:2172 | Homo sapiens (human) | 6900 | CNTN2 |
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| DOID:0111691 | familial adult myoclonic epilepsy 5 | HGNC:2172 | Homo sapiens (human) | 6900 | CNTN2 |
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| DOID:0080101 | Compton-North congenital myopathy | HGNC:2171 | Homo sapiens (human) | 1272 | CNTN1 |
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| DOID:3534 | Lafora disease | HGNC:21576 | Homo sapiens (human) | 378884 | NHLRC1 |
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| DOID:0014667 | disease of metabolism | HGNC:21481 | Homo sapiens (human) | 92483 | LDHAL6B |
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| DOID:0050777 | Joubert syndrome | HGNC:21474 | Homo sapiens (human) | 56623 | INPP5E |
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| DOID:0110980 | Joubert syndrome 1 | HGNC:21474 | Homo sapiens (human) | 56623 | INPP5E |
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| DOID:9970 | obesity | HGNC:21474 | Homo sapiens (human) | 56623 | INPP5E |
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| DOID:1115 | sarcoma | HGNC:21350 | Homo sapiens (human) | 8050 | PDHX |
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| DOID:3649 | pyruvate decarboxylase deficiency | HGNC:21350 | Homo sapiens (human) | 8050 | PDHX |
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| DOID:0050985 | spinocerebellar ataxia type 38 | HGNC:21308 | Homo sapiens (human) | 60481 | ELOVL5 |
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| DOID:0070352 | stress-induced childhood-onset neurodegeneration with variable ataxia and seizures | HGNC:21304 | Homo sapiens (human) | 54936 | ADPRS |
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| DOID:9970 | obesity | HGNC:21298 | Homo sapiens (human) | 65985 | AACS |
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| DOID:0080737 | Ehlers-Danlos syndrome musculocontractural type 2 | HGNC:21144 | Homo sapiens (human) | 29940 | DSE |
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| DOID:0112160 | autosomal dominant nonsyndromic deafness 79 | HGNC:21088 | Homo sapiens (human) | 79966 | SCD5 |
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| DOID:397 | restrictive cardiomyopathy | HGNC:21088 | Homo sapiens (human) | 79966 | SCD5 |
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| DOID:594 | panic disorder | HGNC:21072 | Homo sapiens (human) | 79694 | MANEA |
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| DOID:9975 | cocaine dependence | HGNC:21072 | Homo sapiens (human) | 79694 | MANEA |
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| DOID:2030 | anxiety disorder | HGNC:21072 | Homo sapiens (human) | 79694 | MANEA |
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| DOID:0060480 | left ventricular noncompaction | HGNC:20862 | Homo sapiens (human) | 64116 | SLC39A8 |
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