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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:0110831 | Usher syndrome type 1D | HGNC:14674 | Homo sapiens (human) | 65217 | PCDH15 |
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| DOID:10273 | heart conduction disease | HGNC:14668 | Homo sapiens (human) | 79258 | MMEL1 |
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||
| DOID:0060041 | autism spectrum disorder | HGNC:14656 | Homo sapiens (human) | 57453 | DSCAML1 |
|
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| DOID:14250 | Down syndrome | HGNC:14656 | Homo sapiens (human) | 57453 | DSCAML1 |
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| DOID:700 | mitochondrial metabolism disease | HGNC:14648 | Homo sapiens (human) | 137994 | LETM2 |
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| DOID:0050460 | Wolf-Hirschhorn syndrome | HGNC:14648 | Homo sapiens (human) | 137994 | LETM2 |
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| DOID:1485 | cystic fibrosis | HGNC:14640 | Homo sapiens (human) | 94160 | ABCC12 |
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| DOID:1574 | alcohol use disorder | HGNC:1464 | Homo sapiens (human) | 814 | CAMK4 |
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| DOID:0060001 | withdrawal disorder | HGNC:1464 | Homo sapiens (human) | 814 | CAMK4 |
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| DOID:9975 | cocaine dependence | HGNC:1464 | Homo sapiens (human) | 814 | CAMK4 |
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| DOID:3717 | gastric adenocarcinoma | HGNC:14638 | Homo sapiens (human) | 154664 | ABCA13 |
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| DOID:0060712 | autosomal recessive congenital ichthyosis 4A | HGNC:14637 | Homo sapiens (human) | 26154 | ABCA12 |
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| DOID:0060713 | autosomal recessive congenital ichthyosis 4B | HGNC:14637 | Homo sapiens (human) | 26154 | ABCA12 |
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| DOID:0060656 | autosomal recessive congenital ichthyosis 1 | HGNC:14637 | Homo sapiens (human) | 26154 | ABCA12 |
|
||
| DOID:1875 | impotence | HGNC:14631 | Homo sapiens (human) | 9719 | ADAMTSL2 |
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| DOID:0111725 | geleophysic dysplasia 1 | HGNC:14631 | Homo sapiens (human) | 9719 | ADAMTSL2 |
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| DOID:0050651 | atrioventricular septal defect | HGNC:14630 | Homo sapiens (human) | 78987 | CRELD1 |
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| DOID:1681 | heart septal defect | HGNC:14630 | Homo sapiens (human) | 78987 | CRELD1 |
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| DOID:3069 | malignant astrocytoma | HGNC:1463 | Homo sapiens (human) | 818 | CAMK2G |
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| DOID:10273 | heart conduction disease | HGNC:1463 | Homo sapiens (human) | 818 | CAMK2G |
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| DOID:0060307 | autosomal dominant intellectual developmental disorder | HGNC:1463 | Homo sapiens (human) | 818 | CAMK2G |
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| DOID:10534 | stomach cancer | HGNC:14621 | Homo sapiens (human) | 83540 | NUF2 |
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| DOID:0050610 | oral cavity carcinoma in situ | HGNC:14621 | Homo sapiens (human) | 83540 | NUF2 |
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| DOID:1793 | pancreatic cancer | HGNC:14621 | Homo sapiens (human) | 83540 | NUF2 |
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| DOID:1909 | melanoma | HGNC:14621 | Homo sapiens (human) | 83540 | NUF2 |
|
