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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:0111979 | immunodeficiency 49 | HGNC:13222 | Homo sapiens (human) | 64919 | BCL11B |
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| DOID:1289 | neurodegenerative disease | HGNC:13222 | Homo sapiens (human) | 64919 | BCL11B |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:13221 | Homo sapiens (human) | 53335 | BCL11A |
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| DOID:5419 | schizophrenia | HGNC:13221 | Homo sapiens (human) | 53335 | BCL11A |
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| DOID:3908 | lung non-small cell carcinoma | HGNC:13221 | Homo sapiens (human) | 53335 | BCL11A |
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| DOID:0060038 | specific developmental disorder | HGNC:13221 | Homo sapiens (human) | 53335 | BCL11A |
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| DOID:1289 | neurodegenerative disease | HGNC:13221 | Homo sapiens (human) | 53335 | BCL11A |
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| DOID:10923 | sickle cell anemia | HGNC:13221 | Homo sapiens (human) | 53335 | BCL11A |
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| DOID:12241 | beta thalassemia | HGNC:13221 | Homo sapiens (human) | 53335 | BCL11A |
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| DOID:0060041 | autism spectrum disorder | HGNC:13221 | Homo sapiens (human) | 53335 | BCL11A |
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| DOID:1289 | neurodegenerative disease | HGNC:13206 | Homo sapiens (human) | 66008 | TRAK2 |
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| DOID:0060249 | scoliosis | HGNC:13202 | Homo sapiens (human) | 56999 | ADAMTS9 |
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| DOID:9970 | obesity | HGNC:13202 | Homo sapiens (human) | 56999 | ADAMTS9 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:13202 | Homo sapiens (human) | 56999 | ADAMTS9 |
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| DOID:0050475 | Weill-Marchesani syndrome | HGNC:13201 | Homo sapiens (human) | 81794 | ADAMTS10 |
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| DOID:11984 | hypertrophic cardiomyopathy | HGNC:132 | Homo sapiens (human) | 60 | ACTB |
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| DOID:10881 | hand, foot and mouth disease | HGNC:132 | Homo sapiens (human) | 60 | ACTB |
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| DOID:1588 | thrombocytopenia | HGNC:132 | Homo sapiens (human) | 60 | ACTB |
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| DOID:14004 | thoracic aortic aneurysm | HGNC:132 | Homo sapiens (human) | 60 | ACTB |
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| DOID:0110317 | hypertrophic cardiomyopathy 11 | HGNC:132 | Homo sapiens (human) | 60 | ACTB |
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| DOID:0110550 | autosomal dominant nonsyndromic deafness 20 | HGNC:132 | Homo sapiens (human) | 60 | ACTB |
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| DOID:0080208 | metabolic dysfunction-associated steatotic liver disease | HGNC:132 | Homo sapiens (human) | 60 | ACTB |
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| DOID:3328 | temporal lobe epilepsy | HGNC:132 | Homo sapiens (human) | 60 | ACTB |
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| DOID:423 | myopathy | HGNC:132 | Homo sapiens (human) | 60 | ACTB |
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| DOID:13832 | patent ductus arteriosus | HGNC:132 | Homo sapiens (human) | 60 | ACTB |
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