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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:2841 | asthma | HGNC:270 | Homo sapiens (human) | 142 | PARP1 |
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| DOID:5409 | lung small cell carcinoma | HGNC:2602 | Homo sapiens (human) | 1591 | CYP24A1 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:5217 | Homo sapiens (human) | 3283 | HSD3B1 |
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| DOID:0111040 | glycogen storage disease IXd | HGNC:8925 | Homo sapiens (human) | 5255 | PHKA1 |
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| DOID:0080162 | lupus nephritis | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:10595 | Charcot-Marie-Tooth disease | HGNC:16825 | Homo sapiens (human) | 55613 | MTMR8 |
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| DOID:3393 | coronary artery disease | HGNC:6344 | Homo sapiens (human) | 9365 | KL |
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| DOID:3068 | glioblastoma | HGNC:8977 | Homo sapiens (human) | 5293 | PIK3CD |
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| DOID:10652 | Alzheimer's disease | HGNC:7656 | Homo sapiens (human) | 4684 | NCAM1 |
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| DOID:11054 | urinary bladder cancer | HGNC:1681 | Homo sapiens (human) | 960 | CD44 |
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| DOID:1930 | Laurence-Moon syndrome | HGNC:16268 | Homo sapiens (human) | 10908 | PNPLA6 |
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| DOID:9993 | hypoglycemia | HGNC:4195 | Homo sapiens (human) | 2645 | GCK |
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| DOID:0080349 | developmental and epileptic encephalopathy 39 | HGNC:10982 | Homo sapiens (human) | 8604 | SLC25A12 |
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| DOID:1074 | kidney failure | HGNC:6344 | Homo sapiens (human) | 9365 | KL |
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| DOID:9884 | muscular dystrophy | HGNC:17997 | Homo sapiens (human) | 79147 | FKRP |
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| DOID:0050834 | CHARGE syndrome | HGNC:11998 | Homo sapiens (human) | 7157 | TP53 |
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| DOID:7147 | ankylosing spondylitis | HGNC:11850 | Homo sapiens (human) | 7099 | TLR4 |
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| DOID:4677 | keratitis | HGNC:11848 | Homo sapiens (human) | 7097 | TLR2 |
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| DOID:10808 | gastric ulcer | HGNC:936 | Homo sapiens (human) | 572 | BAD |
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| DOID:264 | hemangiopericytoma | HGNC:9588 | Homo sapiens (human) | 5728 | PTEN |
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| DOID:3083 | chronic obstructive pulmonary disease | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:12700 | hyperprolactinemia | HGNC:11284 | Homo sapiens (human) | 6715 | SRD5A1 |
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| DOID:3393 | coronary artery disease | HGNC:288 | Homo sapiens (human) | 155 | ADRB3 |
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| DOID:14330 | Parkinson's disease | HGNC:3402 | Homo sapiens (human) | 2053 | EPHX2 |
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| DOID:687 | hepatoblastoma | HGNC:4451 | Homo sapiens (human) | 2719 | GPC3 |
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