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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:3407 | carotid artery disease | HGNC:1869 | Homo sapiens (human) | 1071 | CETP |
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| DOID:0111210 | autosomal dominant distal hereditary motor neuronopathy 6 | MGI:2444639 | Mus musculus (house mouse) | 107035 | Fbxo38 |
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| DOID:1574 | alcohol use disorder | HGNC:232 | Homo sapiens (human) | 107 | ADCY1 |
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| DOID:0110501 | autosomal recessive nonsyndromic deafness 44 | HGNC:232 | Homo sapiens (human) | 107 | ADCY1 |
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| DOID:10763 | hypertension | HGNC:19012 | Homo sapiens (human) | 10699 | CORIN |
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| DOID:10591 | pre-eclampsia | HGNC:19012 | Homo sapiens (human) | 10699 | CORIN |
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| DOID:6000 | congestive heart failure | HGNC:19012 | Homo sapiens (human) | 10699 | CORIN |
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| DOID:0080326 | familial hypertrophic cardiomyopathy | HGNC:19012 | Homo sapiens (human) | 10699 | CORIN |
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| DOID:0080432 | developmental and epileptic encephalopathy 60 | HGNC:11968 | Homo sapiens (human) | 10695 | CNPY3 |
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| DOID:1508 | candidiasis | HGNC:4020 | Homo sapiens (human) | 10690 | FUT9 |
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| DOID:0080352 | X-linked chondrodysplasia punctata 2 | HGNC:3133 | Homo sapiens (human) | 10682 | EBP |
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| DOID:2581 | chondrodysplasia punctata | HGNC:3133 | Homo sapiens (human) | 10682 | EBP |
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| DOID:0060292 | X-linked chondrodysplasia punctata 1 | HGNC:3133 | Homo sapiens (human) | 10682 | EBP |
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| DOID:0111865 | MEND syndrome | HGNC:3133 | Homo sapiens (human) | 10682 | EBP |
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| DOID:936 | brain disease | MGI:2147032 | Mus musculus (house mouse) | 106759 | Ticam1 |
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| DOID:2986 | IgA glomerulonephritis | HGNC:11929 | Homo sapiens (human) | 10673 | TNFSF13B |
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| DOID:12894 | Sjogren's syndrome | HGNC:11929 | Homo sapiens (human) | 10673 | TNFSF13B |
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| DOID:3459 | breast carcinoma | HGNC:13723 | Homo sapiens (human) | 10664 | CTCF |
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| DOID:0080144 | childhood acute lymphocytic leukemia | HGNC:13723 | Homo sapiens (human) | 10664 | CTCF |
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| DOID:8923 | skin melanoma | HGNC:13723 | Homo sapiens (human) | 10664 | CTCF |
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| DOID:0070051 | autosomal dominant intellectual developmental disorder 21 | HGNC:13723 | Homo sapiens (human) | 10664 | CTCF |
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| DOID:3151 | skin squamous cell carcinoma | HGNC:13723 | Homo sapiens (human) | 10664 | CTCF |
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| DOID:1612 | breast cancer | HGNC:13723 | Homo sapiens (human) | 10664 | CTCF |
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| DOID:2513 | basal cell carcinoma | HGNC:13723 | Homo sapiens (human) | 10664 | CTCF |
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| DOID:0050671 | female breast cancer | HGNC:13723 | Homo sapiens (human) | 10664 | CTCF |
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