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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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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:0050742 | nicotine dependence | HGNC:12338 | Homo sapiens (human) | 7225 | TRPC6 |
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| DOID:1312 | focal segmental glomerulosclerosis | HGNC:12338 | Homo sapiens (human) | 7225 | TRPC6 |
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| DOID:576 | proteinuria | HGNC:12338 | Homo sapiens (human) | 7225 | TRPC6 |
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| DOID:0060041 | autism spectrum disorder | HGNC:12337 | Homo sapiens (human) | 7224 | TRPC5 |
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| DOID:0110429 | dilated cardiomyopathy 1H | HGNC:12337 | Homo sapiens (human) | 7224 | TRPC5 |
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| DOID:1289 | neurodegenerative disease | HGNC:12337 | Homo sapiens (human) | 7224 | TRPC5 |
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| DOID:0050742 | nicotine dependence | HGNC:12337 | Homo sapiens (human) | 7224 | TRPC5 |
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| DOID:0060041 | autism spectrum disorder | HGNC:12336 | Homo sapiens (human) | 7223 | TRPC4 |
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| DOID:1324 | lung cancer | HGNC:12336 | Homo sapiens (human) | 7223 | TRPC4 |
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| DOID:0050742 | nicotine dependence | HGNC:12336 | Homo sapiens (human) | 7223 | TRPC4 |
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| DOID:1289 | neurodegenerative disease | HGNC:12336 | Homo sapiens (human) | 7223 | TRPC4 |
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| DOID:6432 | pulmonary hypertension | HGNC:12335 | Homo sapiens (human) | 7222 | TRPC3 |
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| DOID:0050742 | nicotine dependence | HGNC:12335 | Homo sapiens (human) | 7222 | TRPC3 |
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| DOID:0111744 | cerebellar ataxia type 41 | HGNC:12335 | Homo sapiens (human) | 7222 | TRPC3 |
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| DOID:1574 | alcohol use disorder | HGNC:12313 | Homo sapiens (human) | 221037 | JMJD1C |
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| DOID:0080689 | mosaic variegated aneuploidy syndrome 3 | HGNC:12307 | Homo sapiens (human) | 9319 | TRIP13 |
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| DOID:162 | cancer | HGNC:12306 | Homo sapiens (human) | 9320 | TRIP12 |
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| DOID:0080234 | Clark-Baraitser syndrome | HGNC:12306 | Homo sapiens (human) | 9320 | TRIP12 |
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| DOID:0080054 | achondrogenesis type IA | HGNC:12305 | Homo sapiens (human) | 9321 | TRIP11 |
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| DOID:12858 | Huntington's disease | HGNC:12304 | Homo sapiens (human) | 9322 | TRIP10 |
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| DOID:0060307 | autosomal dominant intellectual developmental disorder | HGNC:12303 | Homo sapiens (human) | 7204 | TRIO |
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| DOID:0070074 | autosomal dominant intellectual developmental disorder 44 | HGNC:12303 | Homo sapiens (human) | 7204 | TRIO |
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| DOID:1826 | epilepsy | HGNC:12303 | Homo sapiens (human) | 7204 | TRIO |
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| DOID:0050328 | congenital hypothyroidism | HGNC:12299 | Homo sapiens (human) | 7201 | TRHR |
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| DOID:10763 | hypertension | HGNC:12299 | Homo sapiens (human) | 7201 | TRHR |
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