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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:0111958 | immunodeficiency 11B | HGNC:16393 | Homo sapiens (human) | 84433 | CARD11 |
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| DOID:612 | primary immunodeficiency disease | HGNC:16422 | Homo sapiens (human) | 29775 | CARD10 |
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| DOID:674 | cleft palate | HGNC:1491 | Homo sapiens (human) | 832 | CAPZB |
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| DOID:1307 | dementia | HGNC:1491 | Homo sapiens (human) | 832 | CAPZB |
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| DOID:12336 | male infertility | HGNC:24205 | Homo sapiens (human) | 93661 | CAPZA3 |
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| DOID:11723 | Duchenne muscular dystrophy | HGNC:1480 | Homo sapiens (human) | 825 | CAPN3 |
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| DOID:0110275 | autosomal recessive limb-girdle muscular dystrophy type 2A | HGNC:1480 | Homo sapiens (human) | 825 | CAPN3 |
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| DOID:9884 | muscular dystrophy | HGNC:1480 | Homo sapiens (human) | 825 | CAPN3 |
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| DOID:1059 | intellectual disability | HGNC:1480 | Homo sapiens (human) | 825 | CAPN3 |
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| DOID:0110821 | hereditary spastic paraplegia 76 | HGNC:1480 | Homo sapiens (human) | 825 | CAPN3 |
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| DOID:2476 | hereditary spastic paraplegia | HGNC:1480 | Homo sapiens (human) | 825 | CAPN3 |
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| DOID:0110273 | autosomal dominant limb-girdle muscular dystrophy | HGNC:1480 | Homo sapiens (human) | 825 | CAPN3 |
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| DOID:684 | hepatocellular carcinoma | HGNC:1480 | Homo sapiens (human) | 825 | CAPN3 |
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| DOID:9970 | obesity | HGNC:1480 | Homo sapiens (human) | 825 | CAPN3 |
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| DOID:11612 | polycystic ovary syndrome | HGNC:1477 | Homo sapiens (human) | 11132 | CAPN10 |
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| DOID:1793 | pancreatic cancer | HGNC:1477 | Homo sapiens (human) | 11132 | CAPN10 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:1477 | Homo sapiens (human) | 11132 | CAPN10 |
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| DOID:9970 | obesity | HGNC:1477 | Homo sapiens (human) | 11132 | CAPN10 |
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| DOID:10230 | aortic atherosclerosis | HGNC:1476 | Homo sapiens (human) | 823 | CAPN1 |
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| DOID:11723 | Duchenne muscular dystrophy | HGNC:1476 | Homo sapiens (human) | 823 | CAPN1 |
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| DOID:10652 | Alzheimer's disease | HGNC:1476 | Homo sapiens (human) | 823 | CAPN1 |
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| DOID:1826 | epilepsy | HGNC:1476 | Homo sapiens (human) | 823 | CAPN1 |
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| DOID:11446 | sciatic neuropathy | HGNC:1476 | Homo sapiens (human) | 823 | CAPN1 |
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| DOID:2476 | hereditary spastic paraplegia | HGNC:1476 | Homo sapiens (human) | 823 | CAPN1 |
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| DOID:3021 | acute kidney failure | HGNC:1476 | Homo sapiens (human) | 823 | CAPN1 |
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