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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:1826 | epilepsy | RGD:1306716 | Rattus norvegicus (Norway rat) | 298566 | C1qa |
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| DOID:1826 | epilepsy | MGI:88223 | Mus musculus (house mouse) | 12259 | C1qa |
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| DOID:3393 | coronary artery disease | HGNC:25262 | Homo sapiens (human) | 284498 | C1orf167 |
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| DOID:0080520 | Tn polyagglutination syndrome | RGD:1311230 | Rattus norvegicus (Norway rat) | 302499 | C1galt1c1 |
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| DOID:0080520 | Tn polyagglutination syndrome | MGI:1913493 | Mus musculus (house mouse) | 59048 | C1galt1c1 |
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| DOID:12554 | hemolytic-uremic syndrome | MGI:1913493 | Mus musculus (house mouse) | 59048 | C1galt1c1 |
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| DOID:12554 | hemolytic-uremic syndrome | RGD:1311230 | Rattus norvegicus (Norway rat) | 302499 | C1galt1c1 |
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| DOID:0060050 | autoimmune disease of blood | RGD:621105 | Rattus norvegicus (Norway rat) | 65044 | C1galt1 |
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| DOID:0060050 | autoimmune disease of blood | MGI:2151071 | Mus musculus (house mouse) | 94192 | C1galt1 |
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| DOID:0080987 | Ehlers-Danlos syndrome periodontal type 2 | HGNC:1247 | Homo sapiens (human) | 716 | C1S |
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| DOID:0080986 | Ehlers-Danlos syndrome periodontal type 1 | HGNC:1246 | Homo sapiens (human) | 715 | C1R |
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| DOID:37 | skin disease | HGNC:28732 | Homo sapiens (human) | 338872 | C1QTNF9 |
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| DOID:3525 | middle cerebral artery infarction | HGNC:14343 | Homo sapiens (human) | 114904 | C1QTNF6 |
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| DOID:0111495 | combined oxidative phosphorylation deficiency 33 | HGNC:1243 | Homo sapiens (human) | 708 | C1QBP |
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| DOID:11758 | iron deficiency anemia | HGNC:1241 | Homo sapiens (human) | 712 | C1QA |
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| DOID:1826 | epilepsy | HGNC:1241 | Homo sapiens (human) | 712 | C1QA |
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| DOID:2921 | glomerulonephritis | HGNC:1241 | Homo sapiens (human) | 712 | C1QA |
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| DOID:9074 | systemic lupus erythematosus | HGNC:1241 | Homo sapiens (human) | 712 | C1QA |
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| DOID:0060050 | autoimmune disease of blood | FB:FBgn0032078 | Drosophila melanogaster (fruit fly) | 34215 | C1GalTA | CG9520 |
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| DOID:0080520 | Tn polyagglutination syndrome | HGNC:24338 | Homo sapiens (human) | 29071 | C1GALT1C1 |
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| DOID:12554 | hemolytic-uremic syndrome | HGNC:24338 | Homo sapiens (human) | 29071 | C1GALT1C1 |
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| DOID:0060050 | autoimmune disease of blood | HGNC:24337 | Homo sapiens (human) | 56913 | C1GALT1 |
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| DOID:0112209 | developmental and epileptic encephalopathy 73 | WB:WBGene00007666 | Caenorhabditis elegans | 181600 | C18B12.4 |
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| DOID:0110593 | autosomal dominant nonsyndromic deafness 9 | WB:WBGene00015865 | Caenorhabditis elegans | 182693 | C16E9.1 |
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| DOID:12554 | hemolytic-uremic syndrome | WB:WBGene00015861 | Caenorhabditis elegans | 182687 | C16D9.6 |
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