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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:1324 | lung cancer | HGNC:7325 | Homo sapiens (human) | 4436 | MSH2 |
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| DOID:0050545 | visceral heterotaxy | HGNC:4214 | Homo sapiens (human) | 2657 | GDF1 |
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| DOID:10941 | intracranial aneurysm | HGNC:2464 | Homo sapiens (human) | 1462 | VCAN |
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| DOID:9952 | acute lymphoblastic leukemia | HGNC:12441 | Homo sapiens (human) | 7298 | TYMS |
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| DOID:0081216 | autosomal recessive intellectual developmental disorder 54 | HGNC:30765 | Homo sapiens (human) | 23043 | TNIK |
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| DOID:0060558 | lethal congenital contracture syndrome | HGNC:13841 | Homo sapiens (human) | 57211 | ADGRG6 |
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| DOID:8577 | ulcerative colitis | HGNC:11364 | Homo sapiens (human) | 6774 | STAT3 |
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| DOID:12306 | vitiligo | HGNC:5438 | Homo sapiens (human) | 3458 | IFNG |
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| DOID:0111780 | TARP syndrome | HGNC:9896 | Homo sapiens (human) | 8241 | RBM10 |
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| DOID:13810 | familial hypercholesterolemia | HGNC:600 | Homo sapiens (human) | 335 | APOA1 |
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| DOID:0080527 | bronchiectasis 2 | HGNC:10599 | Homo sapiens (human) | 6337 | SCNN1A |
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| DOID:0080288 | spinocerebellar ataxia 46 | HGNC:17158 | Homo sapiens (human) | 23646 | PLD3 |
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| DOID:4914 | esophagus adenocarcinoma | HGNC:2594 | Homo sapiens (human) | 1588 | CYP19A1 |
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| DOID:0111530 | linear nevus sebaceous syndrome | HGNC:5173 | Homo sapiens (human) | 3265 | HRAS |
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| DOID:0110661 | congenital myasthenic syndrome 20 | HGNC:14025 | Homo sapiens (human) | 60482 | SLC5A7 |
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| DOID:2236 | congenital afibrinogenemia | HGNC:3662 | Homo sapiens (human) | 2244 | FGB |
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| DOID:2355 | anemia | HGNC:492 | Homo sapiens (human) | 286 | ANK1 |
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| DOID:9296 | cleft lip | HGNC:4221 | Homo sapiens (human) | 392255 | GDF6 |
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| DOID:1024 | leprosy | HGNC:11848 | Homo sapiens (human) | 7097 | TLR2 |
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| DOID:1612 | breast cancer | HGNC:10050 | Homo sapiens (human) | 6041 | RNASEL |
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| DOID:10325 | silicosis | HGNC:1318 | Homo sapiens (human) | 718 | C3 |
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| DOID:0060805 | Prieto syndrome | HGNC:14543 | Homo sapiens (human) | 65267 | WNK3 |
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| DOID:1324 | lung cancer | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
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| DOID:3393 | coronary artery disease | HGNC:1142 | Homo sapiens (human) | 56244 | BTNL2 |
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| DOID:0050902 | medulloblastoma | HGNC:583 | Homo sapiens (human) | 324 | APC |
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