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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
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:0050902 | medulloblastoma | HGNC:12363 | Homo sapiens (human) | 7249 | TSC2 |
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| DOID:2030 | anxiety disorder | HGNC:12363 | Homo sapiens (human) | 7249 | TSC2 |
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| DOID:13515 | tuberous sclerosis | HGNC:12362 | Homo sapiens (human) | 7248 | TSC1 |
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| DOID:1612 | breast cancer | HGNC:12362 | Homo sapiens (human) | 7248 | TSC1 |
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| DOID:3319 | lymphangioleiomyomatosis | HGNC:12362 | Homo sapiens (human) | 7248 | TSC1 |
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| DOID:0060648 | anterior segment dysgenesis | HGNC:12362 | Homo sapiens (human) | 7248 | TSC1 |
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| DOID:0080324 | tuberous sclerosis 1 | HGNC:12362 | Homo sapiens (human) | 7248 | TSC1 |
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| DOID:9970 | obesity | HGNC:12362 | Homo sapiens (human) | 7248 | TSC1 |
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| DOID:4852 | pleomorphic xanthoastrocytoma | HGNC:12362 | Homo sapiens (human) | 7248 | TSC1 |
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| DOID:0060564 | spinal disease | HGNC:12362 | Homo sapiens (human) | 7248 | TSC1 |
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| DOID:0060041 | autism spectrum disorder | HGNC:12362 | Homo sapiens (human) | 7248 | TSC1 |
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| DOID:1059 | intellectual disability | HGNC:12362 | Homo sapiens (human) | 7248 | TSC1 |
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| DOID:0110861 | autosomal recessive polycystic kidney disease | HGNC:12362 | Homo sapiens (human) | 7248 | TSC1 |
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| DOID:0050564 | autosomal dominant nonsyndromic deafness | HGNC:12347 | Homo sapiens (human) | 8295 | TRRAP |
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| DOID:0112166 | autosomal dominant nonsyndromic deafness 75 | HGNC:12347 | Homo sapiens (human) | 8295 | TRRAP |
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| DOID:0080376 | trichorhinophalangeal syndrome type III | HGNC:12340 | Homo sapiens (human) | 7227 | TRPS1 |
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| DOID:2256 | osteochondrodysplasia | HGNC:12340 | Homo sapiens (human) | 7227 | TRPS1 |
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| DOID:14743 | trichorhinophalangeal syndrome type I | HGNC:12340 | Homo sapiens (human) | 7227 | TRPS1 |
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| DOID:224 | transient cerebral ischemia | HGNC:12338 | Homo sapiens (human) | 7225 | TRPC6 |
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| DOID:6432 | pulmonary hypertension | HGNC:12338 | Homo sapiens (human) | 7225 | TRPC6 |
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| DOID:0111129 | focal segmental glomerulosclerosis 2 | HGNC:12338 | Homo sapiens (human) | 7225 | TRPC6 |
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| DOID:8544 | chronic fatigue syndrome | HGNC:12338 | Homo sapiens (human) | 7225 | TRPC6 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:12338 | Homo sapiens (human) | 7225 | TRPC6 |
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| DOID:557 | kidney disease | HGNC:12338 | Homo sapiens (human) | 7225 | TRPC6 |
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| DOID:0080379 | nephrotic syndrome type 2 | HGNC:12338 | Homo sapiens (human) | 7225 | TRPC6 |
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