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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:5844 | myocardial infarction | HGNC:2422 | Homo sapiens (human) | 1431 | CS |
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| DOID:3312 | bipolar disorder | HGNC:2422 | Homo sapiens (human) | 1431 | CS |
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| DOID:11984 | hypertrophic cardiomyopathy | HGNC:2422 | Homo sapiens (human) | 1431 | CS |
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| DOID:0050852 | limb ischemia | HGNC:2422 | Homo sapiens (human) | 1431 | CS |
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| DOID:6000 | congestive heart failure | HGNC:2422 | Homo sapiens (human) | 1431 | CS |
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| DOID:0110566 | autosomal dominant nonsyndromic deafness 40 | HGNC:2418 | Homo sapiens (human) | 1428 | CRYM |
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| DOID:0080309 | fatal infantile hypertonic myofibrillar myopathy | HGNC:2389 | Homo sapiens (human) | 1410 | CRYAB |
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| DOID:0080093 | myofibrillar myopathy 2 | HGNC:2389 | Homo sapiens (human) | 1410 | CRYAB |
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| DOID:0110450 | dilated cardiomyopathy 1II | HGNC:2389 | Homo sapiens (human) | 1410 | CRYAB |
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| DOID:0110250 | cataract 16 multiple types | HGNC:2389 | Homo sapiens (human) | 1410 | CRYAB |
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| DOID:4448 | macular degeneration | HGNC:2389 | Homo sapiens (human) | 1410 | CRYAB |
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| DOID:83 | cataract | HGNC:2389 | Homo sapiens (human) | 1410 | CRYAB |
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| DOID:9870 | galactosemia | HGNC:2388 | Homo sapiens (human) | 1409 | CRYAA |
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| DOID:83 | cataract | HGNC:2388 | Homo sapiens (human) | 1409 | CRYAA |
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| DOID:0110266 | cataract 9 multiple types | HGNC:2388 | Homo sapiens (human) | 1409 | CRYAA |
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| DOID:0111206 | autosomal dominant distal hereditary motor neuronopathy 2 | HGNC:2388 | Homo sapiens (human) | 1409 | CRYAA |
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| DOID:0110174 | Charcot-Marie-Tooth disease axonal type 2L | HGNC:2388 | Homo sapiens (human) | 1409 | CRYAA |
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| DOID:9282 | ocular hypertension | HGNC:2388 | Homo sapiens (human) | 1409 | CRYAA |
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| DOID:0080093 | myofibrillar myopathy 2 | HGNC:2388 | Homo sapiens (human) | 1409 | CRYAA |
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| DOID:0111141 | delayed sleep phase syndrome | HGNC:2384 | Homo sapiens (human) | 1407 | CRY1 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:27301 | Homo sapiens (human) | 200186 | CRTC2 |
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| DOID:3525 | middle cerebral artery infarction | HGNC:16062 | Homo sapiens (human) | 23373 | CRTC1 |
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| DOID:1470 | major depressive disorder | HGNC:16062 | Homo sapiens (human) | 23373 | CRTC1 |
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| DOID:0110337 | osteogenesis imperfecta type 7 | HGNC:2379 | Homo sapiens (human) | 10491 | CRTAP |
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| DOID:0110295 | autosomal recessive limb-girdle muscular dystrophy type 2U | HGNC:37276 | Homo sapiens (human) | 729920 | CRPPA |
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