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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:9120 | amyloidosis | HGNC:12405 | Homo sapiens (human) | 7276 | TTR |
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| DOID:9256 | colorectal cancer | HGNC:12405 | Homo sapiens (human) | 7276 | TTR |
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| DOID:684 | hepatocellular carcinoma | HGNC:12405 | Homo sapiens (human) | 7276 | TTR |
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| DOID:0050860 | colorectal adenoma | HGNC:12405 | Homo sapiens (human) | 7276 | TTR |
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| DOID:10534 | stomach cancer | HGNC:12405 | Homo sapiens (human) | 7276 | TTR |
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| DOID:0050866 | oral squamous cell carcinoma | HGNC:12405 | Homo sapiens (human) | 7276 | TTR |
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| DOID:0110430 | dilated cardiomyopathy 1G | HGNC:12403 | Homo sapiens (human) | 7273 | TTN |
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| DOID:3393 | coronary artery disease | HGNC:12403 | Homo sapiens (human) | 7273 | TTN |
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| DOID:5844 | myocardial infarction | HGNC:12403 | Homo sapiens (human) | 7273 | TTN |
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| DOID:0111078 | tibial muscular dystrophy | HGNC:12403 | Homo sapiens (human) | 7273 | TTN |
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| DOID:0060224 | atrial fibrillation | HGNC:12403 | Homo sapiens (human) | 7273 | TTN |
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| DOID:0111188 | myofibrillar myopathy 9 | HGNC:12403 | Homo sapiens (human) | 7273 | TTN |
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| DOID:0081341 | congenital myopathy 5 | HGNC:12403 | Homo sapiens (human) | 7273 | TTN |
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| DOID:12930 | dilated cardiomyopathy | HGNC:12403 | Homo sapiens (human) | 7273 | TTN |
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| DOID:0110315 | hypertrophic cardiomyopathy 9 | HGNC:12403 | Homo sapiens (human) | 7273 | TTN |
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| DOID:0110283 | autosomal recessive limb-girdle muscular dystrophy type 2J | HGNC:12403 | Homo sapiens (human) | 7273 | TTN |
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| DOID:3312 | bipolar disorder | HGNC:12401 | Homo sapiens (human) | 7272 | TTK |
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| DOID:684 | hepatocellular carcinoma | HGNC:12401 | Homo sapiens (human) | 7272 | TTK |
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| DOID:0110344 | osteogenesis imperfecta type 5 | HGNC:1240 | Homo sapiens (human) | 51430 | SUCO |
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| DOID:0112295 | spondylometaphyseal dysplasia | HGNC:124 | Homo sapiens (human) | 54 | ACP5 |
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| DOID:0081101 | nonautoimmune hyperthyroidism | HGNC:12373 | Homo sapiens (human) | 7253 | TSHR |
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| DOID:0081102 | familial gestational hyperthyroidism | HGNC:12373 | Homo sapiens (human) | 7253 | TSHR |
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| DOID:12361 | Graves' disease | HGNC:12373 | Homo sapiens (human) | 7253 | TSHR |
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| DOID:7998 | hyperthyroidism | HGNC:12373 | Homo sapiens (human) | 7253 | TSHR |
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| DOID:0050328 | congenital hypothyroidism | HGNC:12373 | Homo sapiens (human) | 7253 | TSHR |
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