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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:4795 | GM2 gangliosidosis, AB variant | HGNC:4367 | Homo sapiens (human) | 2760 | GM2A |
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| DOID:1067 | open-angle glaucoma | HGNC:4369 | Homo sapiens (human) | 2762 | GMDS |
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| DOID:0070255 | congenital disorder of glycosylation type IIc | HGNC:4369 | Homo sapiens (human) | 2762 | GMDS |
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| DOID:8778 | Crohn's disease | HGNC:437 | Homo sapiens (human) | 248 | ALPI |
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| DOID:0050589 | inflammatory bowel disease | HGNC:437 | Homo sapiens (human) | 248 | ALPI |
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| DOID:8577 | ulcerative colitis | HGNC:437 | Homo sapiens (human) | 248 | ALPI |
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| DOID:0110914 | infantile hypophosphatasia | HGNC:438 | Homo sapiens (human) | 249 | ALPL |
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| DOID:4676 | uremia | HGNC:438 | Homo sapiens (human) | 249 | ALPL |
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| DOID:8719 | in situ carcinoma | HGNC:438 | Homo sapiens (human) | 249 | ALPL |
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| DOID:0110915 | childhood hypophosphatasia | HGNC:438 | Homo sapiens (human) | 249 | ALPL |
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| DOID:13809 | familial combined hyperlipidemia | HGNC:438 | Homo sapiens (human) | 249 | ALPL |
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| DOID:2349 | arteriosclerosis | HGNC:438 | Homo sapiens (human) | 249 | ALPL |
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| DOID:0110913 | adult hypophosphatasia | HGNC:438 | Homo sapiens (human) | 249 | ALPL |
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| DOID:9452 | steatotic liver disease | HGNC:438 | Homo sapiens (human) | 249 | ALPL |
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| DOID:14213 | hypophosphatasia | HGNC:438 | Homo sapiens (human) | 249 | ALPL |
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| DOID:684 | hepatocellular carcinoma | HGNC:4415 | Homo sapiens (human) | 27232 | GNMT |
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| DOID:0111037 | glycine N-methyltransferase deficiency | HGNC:4415 | Homo sapiens (human) | 27232 | GNMT |
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| DOID:150 | disease of mental health | HGNC:4416 | Homo sapiens (human) | 8443 | GNPAT |
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| DOID:0110852 | rhizomelic chondrodysplasia punctata type 2 | HGNC:4416 | Homo sapiens (human) | 8443 | GNPAT |
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| DOID:0111402 | mucopolysaccharidosis type IIID | HGNC:4422 | Homo sapiens (human) | 2799 | GNS |
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| DOID:12801 | mucopolysaccharidosis III | HGNC:4422 | Homo sapiens (human) | 2799 | GNS |
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| DOID:3498 | pancreatic ductal adenocarcinoma | HGNC:4432 | Homo sapiens (human) | 2805 | GOT1 |
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| DOID:9120 | amyloidosis | HGNC:4432 | Homo sapiens (human) | 2805 | GOT1 |
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| DOID:332 | amyotrophic lateral sclerosis | HGNC:4432 | Homo sapiens (human) | 2805 | GOT1 |
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| DOID:0050700 | cardiomyopathy | HGNC:4432 | Homo sapiens (human) | 2805 | GOT1 |
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