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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:4195 | hyperglycemia | HGNC:9237 | Homo sapiens (human) | 10891 | PPARGC1A |
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| DOID:1380 | endometrial cancer | HGNC:11377 | Homo sapiens (human) | 6783 | SULT1E1 |
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| DOID:0111263 | combined malonic and methylmalonic acidemia | HGNC:27288 | Homo sapiens (human) | 197322 | ACSF3 |
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| DOID:8549 | chronic ulcer of skin | HGNC:5344 | Homo sapiens (human) | 3383 | ICAM1 |
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| DOID:0050773 | paraganglioma | HGNC:10981 | Homo sapiens (human) | 8402 | SLC25A11 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:2631 | Homo sapiens (human) | 1571 | CYP2E1 |
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| DOID:936 | brain disease | HGNC:9588 | Homo sapiens (human) | 5728 | PTEN |
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| DOID:10128 | venous insufficiency | HGNC:5344 | Homo sapiens (human) | 3383 | ICAM1 |
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| DOID:1936 | atherosclerosis | HGNC:26876 | Homo sapiens (human) | 165631 | PARP15 |
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| DOID:874 | bacterial pneumonia | HGNC:10798 | Homo sapiens (human) | 653509 | SFTPA1 |
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| DOID:3908 | lung non-small cell carcinoma | HGNC:5383 | Homo sapiens (human) | 3418 | IDH2 |
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| DOID:1574 | alcohol use disorder | HGNC:5466 | Homo sapiens (human) | 3481 | IGF2 |
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| DOID:2671 | transitional cell carcinoma | HGNC:8125 | Homo sapiens (human) | 4968 | OGG1 |
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| DOID:1849 | cannabis dependence | HGNC:2228 | Homo sapiens (human) | 1312 | COMT |
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| DOID:3083 | chronic obstructive pulmonary disease | HGNC:2596 | Homo sapiens (human) | 1544 | CYP1A2 |
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| DOID:5844 | myocardial infarction | HGNC:9056 | Homo sapiens (human) | 5331 | PLCB3 |
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| DOID:4362 | cervical cancer | HGNC:2665 | Homo sapiens (human) | 1604 | CD55 |
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| DOID:422 | congenital structural myopathy | HGNC:7448 | Homo sapiens (human) | 4534 | MTM1 |
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| DOID:1432 | blindness | HGNC:24768 | Homo sapiens (human) | 375775 | PNPLA7 |
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| DOID:0050571 | congenital disorder of glycosylation type II | HGNC:4124 | Homo sapiens (human) | 2590 | GALNT2 |
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| DOID:1214 | tympanosclerosis | HGNC:1516 | Homo sapiens (human) | 847 | CAT |
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| DOID:5199 | ureteral obstruction | HGNC:391 | Homo sapiens (human) | 207 | AKT1 |
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| DOID:8466 | retinal degeneration | HGNC:9059 | Homo sapiens (human) | 5332 | PLCB4 |
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| DOID:9470 | bacterial meningitis | HGNC:1932 | Homo sapiens (human) | 1116 | CHI3L1 |
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| DOID:0070330 | multiple mitochondrial dysfunctions syndrome | HGNC:4208 | Homo sapiens (human) | 2653 | GCSH |
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