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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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MIRAGE
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: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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| 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:9970 | obesity | HGNC:1473 | Homo sapiens (human) | 821 | CANX |
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| DOID:3070 | high grade glioma | HGNC:1470 | Homo sapiens (human) | 10645 | CAMKK2 |
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| DOID:0060230 | basal ganglia calcification | HGNC:14686 | Homo sapiens (human) | 58494 | JAM2 |
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| DOID:10763 | hypertension | HGNC:14685 | Homo sapiens (human) | 50848 | F11R |
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| DOID:418 | systemic scleroderma | HGNC:14685 | Homo sapiens (human) | 50848 | F11R |
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| DOID:1612 | breast cancer | HGNC:14685 | Homo sapiens (human) | 50848 | F11R |
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| DOID:224 | transient cerebral ischemia | HGNC:14685 | Homo sapiens (human) | 50848 | F11R |
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| DOID:13976 | peptic esophagitis | HGNC:14685 | Homo sapiens (human) | 50848 | F11R |
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| DOID:14250 | Down syndrome | HGNC:14683 | Homo sapiens (human) | 23275 | POFUT2 |
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| DOID:0070054 | Vulto-van Silfout-de Vries syndrome | HGNC:14677 | Homo sapiens (human) | 10522 | DEAF1 |
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| DOID:0110481 | autosomal recessive nonsyndromic deafness 23 | HGNC:14674 | Homo sapiens (human) | 65217 | PCDH15 |
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| DOID:0110832 | Usher syndrome type 1F | HGNC:14674 | Homo sapiens (human) | 65217 | PCDH15 |
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