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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:5082 | liver cirrhosis | HGNC:4341 | Homo sapiens (human) | 2752 | GLUL |
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| DOID:11832 | visual epilepsy | HGNC:4341 | Homo sapiens (human) | 2752 | GLUL |
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||
| DOID:4795 | GM2 gangliosidosis, AB variant | HGNC:4367 | Homo sapiens (human) | 2760 | GM2A |
|
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| DOID:3321 | GM2 gangliosidosis | HGNC:4367 | Homo sapiens (human) | 2760 | GM2A |
|
||
| DOID:0070255 | congenital disorder of glycosylation type IIc | HGNC:4369 | Homo sapiens (human) | 2762 | GMDS |
|
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| DOID:1067 | open-angle glaucoma | HGNC:4369 | Homo sapiens (human) | 2762 | GMDS |
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| DOID:1858 | McCune Albright syndrome | HGNC:4384 | Homo sapiens (human) | 2770 | GNAI1 |
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| DOID:0110887 | inflammatory bowel disease 12 | HGNC:4385 | Homo sapiens (human) | 2771 | GNAI2 |
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| DOID:1858 | McCune Albright syndrome | HGNC:4385 | Homo sapiens (human) | 2771 | GNAI2 |
|
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| DOID:10763 | hypertension | HGNC:4385 | Homo sapiens (human) | 2771 | GNAI2 |
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| DOID:10763 | hypertension | HGNC:4387 | Homo sapiens (human) | 2773 | GNAI3 |
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| DOID:1858 | McCune Albright syndrome | HGNC:4387 | Homo sapiens (human) | 2773 | GNAI3 |
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| DOID:0111623 | ACTH-independent macronodular adrenal hyperplasia 1 | HGNC:4392 | Homo sapiens (human) | 2778 | GNAS |
|
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| DOID:10763 | hypertension | HGNC:4392 | Homo sapiens (human) | 2778 | GNAS |
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| DOID:0111535 | progressive osseous heteroplasia | HGNC:4392 | Homo sapiens (human) | 2778 | GNAS |
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| DOID:0112010 | pituitary adenoma 3 | HGNC:4392 | Homo sapiens (human) | 2778 | GNAS |
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| DOID:0080322 | polycystic kidney disease | HGNC:4392 | Homo sapiens (human) | 2778 | GNAS |
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| DOID:0080222 | pseudohypoparathyroidism type IB | HGNC:4392 | Homo sapiens (human) | 2778 | GNAS |
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| DOID:10652 | Alzheimer's disease | HGNC:4392 | Homo sapiens (human) | 2778 | GNAS |
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| DOID:4947 | cholangiocarcinoma | HGNC:4392 | Homo sapiens (human) | 2778 | GNAS |
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| DOID:4184 | pseudohypoparathyroidism | HGNC:4392 | Homo sapiens (human) | 2778 | GNAS |
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| DOID:4183 | pseudopseudohypoparathyroidism | HGNC:4392 | Homo sapiens (human) | 2778 | GNAS |
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| DOID:1793 | pancreatic cancer | HGNC:4392 | Homo sapiens (human) | 2778 | GNAS |
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| DOID:0080053 | Albright's hereditary osteodystrophy | HGNC:4392 | Homo sapiens (human) | 2778 | GNAS |
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| DOID:9970 | obesity | HGNC:4392 | Homo sapiens (human) | 2778 | GNAS |
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