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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
LM-GlycoRepo
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:0060690 | autosomal dominant auditory neuropathy 1 | HGNC:15480 | Homo sapiens (human) | 81624 | DIAPH3 |
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| DOID:1338 | congenital dyserythropoietic anemia | HGNC:15480 | Homo sapiens (human) | 81624 | DIAPH3 |
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| DOID:3526 | cerebral infarction | HGNC:1550 | Homo sapiens (human) | 875 | CBS |
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| DOID:2394 | ovarian cancer | HGNC:1550 | Homo sapiens (human) | 875 | CBS |
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| DOID:0050731 | vitamin B12 deficiency | HGNC:1550 | Homo sapiens (human) | 875 | CBS |
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| DOID:14250 | Down syndrome | HGNC:1550 | Homo sapiens (human) | 875 | CBS |
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| DOID:9279 | hyperhomocysteinemia | HGNC:1550 | Homo sapiens (human) | 875 | CBS |
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| DOID:0080074 | neural tube defect | HGNC:1550 | Homo sapiens (human) | 875 | CBS |
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| DOID:219 | colon cancer | HGNC:1550 | Homo sapiens (human) | 875 | CBS |
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| DOID:12365 | malaria | HGNC:1550 | Homo sapiens (human) | 875 | CBS |
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| DOID:9263 | homocystinuria | HGNC:1550 | Homo sapiens (human) | 875 | CBS |
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| DOID:3393 | coronary artery disease | HGNC:1550 | Homo sapiens (human) | 875 | CBS |
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| DOID:1612 | breast cancer | HGNC:1550 | Homo sapiens (human) | 875 | CBS |
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| DOID:10908 | hydrocephalus | HGNC:15505 | Homo sapiens (human) | 79143 | MBOAT7 |
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| DOID:0081219 | autosomal recessive intellectual developmental disorder 57 | HGNC:15505 | Homo sapiens (human) | 79143 | MBOAT7 |
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| DOID:9119 | acute myeloid leukemia | HGNC:15514 | Homo sapiens (human) | 8301 | PICALM |
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| DOID:557 | kidney disease | HGNC:15516 | Homo sapiens (human) | 64131 | XYLT1 |
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| DOID:0060462 | Desbuquois dysplasia | HGNC:15516 | Homo sapiens (human) | 64131 | XYLT1 |
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| DOID:9744 | type 1 diabetes mellitus | HGNC:15516 | Homo sapiens (human) | 64131 | XYLT1 |
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| DOID:2738 | pseudoxanthoma elasticum | HGNC:15516 | Homo sapiens (human) | 64131 | XYLT1 |
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| DOID:2738 | pseudoxanthoma elasticum | HGNC:15517 | Homo sapiens (human) | 64132 | XYLT2 |
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| DOID:0080322 | polycystic kidney disease | HGNC:15517 | Homo sapiens (human) | 64132 | XYLT2 |
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| DOID:14447 | gonadal dysgenesis | HGNC:1552 | Homo sapiens (human) | 84733 | CBX2 |
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| DOID:162 | cancer | HGNC:1552 | Homo sapiens (human) | 84733 | CBX2 |
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| DOID:0050866 | oral squamous cell carcinoma | HGNC:1552 | Homo sapiens (human) | 84733 | CBX2 |
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