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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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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 | October 9, 2024 |
| Disease ID | Disease Name | Alliance of Genome Resources ID | Species | Gene ID | Gene Symbol | FlyGlycoDB | Evidence Code Names ▲ | References |
|---|---|---|---|---|---|---|---|---|
| DOID:8618 | oral cavity cancer | HGNC:11181 | Homo sapiens (human) | 6649 | SOD3 |
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| DOID:2841 | asthma | HGNC:4938 | Homo sapiens (human) | 3113 | HLA-DPA1 |
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| DOID:9675 | pulmonary emphysema | HGNC:11766 | Homo sapiens (human) | 7040 | TGFB1 |
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| DOID:13641 | exfoliation syndrome | HGNC:7155 | Homo sapiens (human) | 4312 | MMP1 |
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| DOID:1596 | depressive disorder | HGNC:8599 | Homo sapiens (human) | 24145 | PANX1 |
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| DOID:0110315 | hypertrophic cardiomyopathy 9 | HGNC:12403 | Homo sapiens (human) | 7273 | TTN |
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| DOID:1287 | cardiovascular system disease | HGNC:4706 | Homo sapiens (human) | 2997 | GYS1 |
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| DOID:2862 | glucosephosphate dehydrogenase deficiency | HGNC:6018 | Homo sapiens (human) | 3569 | IL6 |
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| DOID:14067 | Plasmodium falciparum malaria | HGNC:3616 | Homo sapiens (human) | 2212 | FCGR2A |
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| DOID:0080261 | autosomal recessive nonsyndromic deafness 106 | HGNC:21296 | Homo sapiens (human) | 64787 | EPS8L2 |
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| DOID:8577 | ulcerative colitis | HGNC:3616 | Homo sapiens (human) | 2212 | FCGR2A |
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| DOID:9408 | acute myocardial infarction | HGNC:14388 | Homo sapiens (human) | 51206 | GP6 |
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| DOID:2152 | ovary epithelial cancer | HGNC:1604 | Homo sapiens (human) | 1232 | CCR3 |
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| DOID:11963 | esophagitis | HGNC:6015 | Homo sapiens (human) | 3566 | IL4R |
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| DOID:0111958 | immunodeficiency 11B | HGNC:16393 | Homo sapiens (human) | 84433 | CARD11 |
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| DOID:0070145 | hereditary sensory and autonomic neuropathy type 5 | HGNC:7808 | Homo sapiens (human) | 4803 | NGF |
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| DOID:0070462 | mitochondrial complex V (ATP synthase) deficiency nuclear type 4B | HGNC:823 | Homo sapiens (human) | 498 | ATP5F1A |
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| DOID:3083 | chronic obstructive pulmonary disease | HGNC:2357 | Homo sapiens (human) | 1394 | CRHR1 |
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| DOID:9970 | obesity | HGNC:30022 | Homo sapiens (human) | 133522 | PPARGC1B |
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| DOID:0070004 | myeloid neoplasm | HGNC:4553 | Homo sapiens (human) | 2876 | GPX1 |
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| DOID:11105 | fundus albipunctatus | HGNC:9940 | Homo sapiens (human) | 5959 | RDH5 |
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| DOID:422 | congenital structural myopathy | HGNC:7448 | Homo sapiens (human) | 4534 | MTM1 |
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| DOID:0070138 | autosomal recessive cutis laxa type IIIB | HGNC:9721 | Homo sapiens (human) | 5831 | PYCR1 |
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| DOID:1587 | thrombocytopenia due to platelet alloimmunization | HGNC:3619 | Homo sapiens (human) | 2214 | FCGR3A |
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| DOID:0081212 | autosomal recessive intellectual developmental disorder 48 | HGNC:31399 | Homo sapiens (human) | 388662 | SLC6A17 |
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