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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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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 | July 29, 2024 |
| Disease ID | Disease Name | Alliance of Genome Resources ID | Species | Gene ID | Gene Symbol ▲ | FlyGlycoDB | Evidence Code Names | References |
|---|---|---|---|---|---|---|---|---|
| DOID:0070264 | congenital disorder of glycosylation type IIl | HGNC:18621 | Homo sapiens (human) | 57511 | COG6 |
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| DOID:0070264 | congenital disorder of glycosylation type IIl | SGD:S000004986 | Saccharomyces cerevisiae S288C | 855687 | COG6 |
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| DOID:630 | genetic disease | HGNC:18622 | Homo sapiens (human) | 91949 | COG7 |
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| DOID:0070257 | congenital disorder of glycosylation type IIe | HGNC:18622 | Homo sapiens (human) | 91949 | COG7 |
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| DOID:0070260 | congenital disorder of glycosylation type IIh | SGD:S000004536 | Saccharomyces cerevisiae S288C | 854904 | COG8 |
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| DOID:0070260 | congenital disorder of glycosylation type IIh | HGNC:18623 | Homo sapiens (human) | 84342 | COG8 |
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| DOID:0050558 | Ullrich congenital muscular dystrophy | HGNC:2211 | Homo sapiens (human) | 1291 | COL6A1 |
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| DOID:0050663 | Bethlem myopathy | HGNC:2211 | Homo sapiens (human) | 1291 | COL6A1 |
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| DOID:9884 | muscular dystrophy | HGNC:2211 | Homo sapiens (human) | 1291 | COL6A1 |
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| DOID:0050557 | congenital muscular dystrophy | HGNC:2211 | Homo sapiens (human) | 1291 | COL6A1 |
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| DOID:2256 | osteochondrodysplasia | HGNC:2218 | Homo sapiens (human) | 1298 | COL9A2 |
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| DOID:0080046 | Stickler syndrome | HGNC:2218 | Homo sapiens (human) | 1298 | COL9A2 |
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| DOID:0070298 | multiple epiphyseal dysplasia 2 | HGNC:2218 | Homo sapiens (human) | 1298 | COL9A2 |
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| DOID:0060577 | 3MC syndrome 3 | HGNC:2220 | Homo sapiens (human) | 10584 | COLEC10 |
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| DOID:0060576 | 3MC syndrome 2 | HGNC:17213 | Homo sapiens (human) | 78989 | COLEC11 |
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| DOID:674 | cleft palate | HGNC:17213 | Homo sapiens (human) | 78989 | COLEC11 |
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| DOID:0112315 | brain small vessel disease 3 | HGNC:26182 | Homo sapiens (human) | 79709 | COLGALT1 |
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| DOID:10763 | hypertension | HGNC:2228 | Homo sapiens (human) | 1312 | COMT |
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| DOID:1574 | alcohol use disorder | HGNC:2228 | Homo sapiens (human) | 1312 | COMT |
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| DOID:12306 | vitiligo | HGNC:2228 | Homo sapiens (human) | 1312 | COMT |
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| DOID:1612 | breast cancer | HGNC:2228 | Homo sapiens (human) | 1312 | COMT |
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| DOID:11612 | polycystic ovary syndrome | HGNC:2228 | Homo sapiens (human) | 1312 | COMT |
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| DOID:0060041 | autism spectrum disorder | HGNC:2228 | Homo sapiens (human) | 1312 | COMT |
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| DOID:4450 | renal cell carcinoma | HGNC:2228 | Homo sapiens (human) | 1312 | COMT |
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| DOID:2559 | opiate dependence | HGNC:2228 | Homo sapiens (human) | 1312 | COMT |
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