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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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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:8466 | retinal degeneration | HGNC:8806 | Homo sapiens (human) | 5160 | PDHA1 |
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| DOID:0111043 | glycogen storage disease IXc | HGNC:8931 | Homo sapiens (human) | 5261 | PHKG2 |
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| DOID:10283 | prostate cancer | HGNC:386 | Homo sapiens (human) | 8644 | AKR1C3 |
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| DOID:3892 | insulinoma | HGNC:11006 | Homo sapiens (human) | 6514 | SLC2A2 |
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| DOID:9452 | steatotic liver disease | HGNC:6553 | Homo sapiens (human) | 3952 | LEP |
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| DOID:0050571 | congenital disorder of glycosylation type II | HGNC:18305 | Homo sapiens (human) | 10159 | ATP6AP2 |
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| DOID:614 | lymphopenia | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:0080208 | metabolic dysfunction-associated steatotic liver disease | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:5844 | myocardial infarction | HGNC:9232 | Homo sapiens (human) | 5465 | PPARA |
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| DOID:0112347 | hereditary spastic paraplegia 84 | HGNC:8983 | Homo sapiens (human) | 5297 | PI4KA |
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| DOID:0080000 | muscular disease | HGNC:84 | Homo sapiens (human) | 31 | ACACA |
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| DOID:11612 | polycystic ovary syndrome | HGNC:392 | Homo sapiens (human) | 208 | AKT2 |
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| DOID:874 | bacterial pneumonia | HGNC:6922 | Homo sapiens (human) | 4153 | MBL2 |
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| DOID:9743 | diabetic neuropathy | HGNC:381 | Homo sapiens (human) | 231 | AKR1B1 |
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| DOID:1923 | disorder of sexual development | HGNC:2594 | Homo sapiens (human) | 1588 | CYP19A1 |
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| DOID:0110312 | hypertrophic cardiomyopathy 6 | HGNC:9386 | Homo sapiens (human) | 51422 | PRKAG2 |
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| DOID:9744 | type 1 diabetes mellitus | HGNC:1932 | Homo sapiens (human) | 1116 | CHI3L1 |
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| DOID:9970 | obesity | HGNC:29175 | Homo sapiens (human) | 23038 | WDTC1 |
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| DOID:3407 | carotid artery disease | HGNC:9592 | Homo sapiens (human) | 5730 | PTGDS |
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| DOID:162 | cancer | HGNC:9281 | Homo sapiens (human) | 5499 | PPP1CA |
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| DOID:0060158 | acquired metabolic disease | HGNC:18590 | Homo sapiens (human) | 80339 | PNPLA3 |
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| DOID:2749 | glycogen storage disease Ia | HGNC:4061 | Homo sapiens (human) | 2542 | SLC37A4 |
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| DOID:13949 | interstitial cystitis | HGNC:12663 | Homo sapiens (human) | 7412 | VCAM1 |
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| DOID:399 | tuberculosis | HGNC:11848 | Homo sapiens (human) | 7097 | TLR2 |
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| DOID:10534 | stomach cancer | HGNC:4555 | Homo sapiens (human) | 2878 | GPX3 |
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