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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
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Repository for lectin-assisted multimodality data
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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:0110821 | hereditary spastic paraplegia 76 | HGNC:1476 | Homo sapiens (human) | 823 | CAPN1 |
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| DOID:0081292 | traumatic brain injury | HGNC:1476 | Homo sapiens (human) | 823 | CAPN1 |
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| DOID:12930 | dilated cardiomyopathy | HGNC:20039 | Homo sapiens (human) | 10486 | CAP2 |
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| DOID:1793 | pancreatic cancer | HGNC:20040 | Homo sapiens (human) | 10487 | CAP1 |
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| DOID:9970 | obesity | HGNC:1473 | Homo sapiens (human) | 821 | CANX |
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| DOID:0070302 | multiple epiphyseal dysplasia 7 | HGNC:19721 | Homo sapiens (human) | 124583 | CANT1 |
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| DOID:0060462 | Desbuquois dysplasia | HGNC:19721 | Homo sapiens (human) | 124583 | CANT1 |
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| DOID:162 | cancer | HGNC:30689 | Homo sapiens (human) | 23066 | CAND2 |
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| DOID:0060224 | atrial fibrillation | HGNC:30689 | Homo sapiens (human) | 23066 | CAND2 |
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| DOID:162 | cancer | HGNC:30688 | Homo sapiens (human) | 55832 | CAND1 |
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| DOID:0050998 | nonprogressive cerebellar ataxia with mental retardation | HGNC:18806 | Homo sapiens (human) | 23261 | CAMTA1 |
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| DOID:0090131 | complex cortical dysplasia with other brain malformations | HGNC:19946 | Homo sapiens (human) | 157922 | CAMSAP1 |
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| DOID:0060858 | hypotonia-cystinuria syndrome | HGNC:26276 | Homo sapiens (human) | 79823 | CAMKMT |
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| DOID:3070 | high grade glioma | HGNC:1470 | Homo sapiens (human) | 10645 | CAMKK2 |
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| DOID:1574 | alcohol use disorder | HGNC:1464 | Homo sapiens (human) | 814 | CAMK4 |
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| DOID:0060001 | withdrawal disorder | HGNC:1464 | Homo sapiens (human) | 814 | CAMK4 |
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| DOID:9975 | cocaine dependence | HGNC:1464 | Homo sapiens (human) | 814 | CAMK4 |
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| DOID:3069 | malignant astrocytoma | HGNC:1463 | Homo sapiens (human) | 818 | CAMK2G |
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| DOID:10273 | heart conduction disease | HGNC:1463 | Homo sapiens (human) | 818 | CAMK2G |
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| DOID:0060307 | autosomal dominant intellectual developmental disorder | HGNC:1463 | Homo sapiens (human) | 818 | CAMK2G |
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| DOID:10273 | heart conduction disease | HGNC:1462 | Homo sapiens (human) | 817 | CAMK2D |
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| DOID:1826 | epilepsy | HGNC:1462 | Homo sapiens (human) | 817 | CAMK2D |
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| DOID:1591 | renovascular hypertension | HGNC:1462 | Homo sapiens (human) | 817 | CAMK2D |
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| DOID:5844 | myocardial infarction | HGNC:1462 | Homo sapiens (human) | 817 | CAMK2D |
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| DOID:10273 | heart conduction disease | HGNC:1461 | Homo sapiens (human) | 816 | CAMK2B |
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