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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:0050700 | cardiomyopathy | HGNC:12373 | Homo sapiens (human) | 7253 | TSHR |
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| DOID:988 | mitral valve prolapse | HGNC:12373 | Homo sapiens (human) | 7253 | TSHR |
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| DOID:0081120 | Graves ophthalmopathy | HGNC:12373 | Homo sapiens (human) | 7253 | TSHR |
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| DOID:2945 | severe acute respiratory syndrome | HGNC:12372 | Homo sapiens (human) | 7252 | TSHB |
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| DOID:4195 | hyperglycemia | HGNC:12372 | Homo sapiens (human) | 7252 | TSHB |
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| DOID:1459 | hypothyroidism | HGNC:12372 | Homo sapiens (human) | 7252 | TSHB |
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| DOID:0070123 | congenital nongoitrous hypothyroidism 4 | HGNC:12372 | Homo sapiens (human) | 7252 | TSHB |
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| DOID:0110984 | Joubert syndrome 15 | HGNC:12370 | Homo sapiens (human) | 95681 | CEP41 |
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| DOID:9255 | frontotemporal dementia | HGNC:1237 | Homo sapiens (human) | 56893 | UBQLN4 |
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| DOID:1289 | neurodegenerative disease | HGNC:1237 | Homo sapiens (human) | 56893 | UBQLN4 |
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| DOID:332 | amyotrophic lateral sclerosis | HGNC:1237 | Homo sapiens (human) | 56893 | UBQLN4 |
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| DOID:0060206 | amyotrophic lateral sclerosis type 15 | HGNC:1237 | Homo sapiens (human) | 56893 | UBQLN4 |
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| DOID:4450 | renal cell carcinoma | HGNC:12363 | Homo sapiens (human) | 7249 | TSC2 |
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| DOID:0060041 | autism spectrum disorder | HGNC:12363 | Homo sapiens (human) | 7249 | TSC2 |
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| DOID:3319 | lymphangioleiomyomatosis | HGNC:12363 | Homo sapiens (human) | 7249 | TSC2 |
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| DOID:3587 | pancreatic ductal carcinoma | HGNC:12363 | Homo sapiens (human) | 7249 | TSC2 |
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| DOID:10652 | Alzheimer's disease | HGNC:12363 | Homo sapiens (human) | 7249 | TSC2 |
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| DOID:3314 | angiomyolipoma | HGNC:12363 | Homo sapiens (human) | 7249 | TSC2 |
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| DOID:13223 | uterine fibroid | HGNC:12363 | Homo sapiens (human) | 7249 | TSC2 |
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| DOID:684 | hepatocellular carcinoma | HGNC:12363 | Homo sapiens (human) | 7249 | TSC2 |
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| DOID:3317 | hepatic angiomyolipoma | HGNC:12363 | Homo sapiens (human) | 7249 | TSC2 |
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| DOID:0080325 | tuberous sclerosis 2 | HGNC:12363 | Homo sapiens (human) | 7249 | TSC2 |
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| DOID:1612 | breast cancer | HGNC:12363 | Homo sapiens (human) | 7249 | TSC2 |
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| DOID:13515 | tuberous sclerosis | HGNC:12363 | Homo sapiens (human) | 7249 | TSC2 |
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| DOID:127 | leiomyoma | HGNC:12363 | Homo sapiens (human) | 7249 | TSC2 |
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