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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:4450 | renal cell carcinoma | MGI:1920212 | Mus musculus (house mouse) | 72962 | Tymp |
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| DOID:3744 | cervical squamous cell carcinoma | RGD:1305756 | Rattus norvegicus (Norway rat) | 315219 | Tymp |
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| DOID:0050770 | polycystic liver disease | HGNC:12518 | Homo sapiens (human) | 7351 | UCP2 |
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| DOID:9970 | obesity | HGNC:12518 | Homo sapiens (human) | 7351 | UCP2 |
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| DOID:783 | end stage renal disease | HGNC:12518 | Homo sapiens (human) | 7351 | UCP2 |
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| DOID:9452 | steatotic liver disease | HGNC:12518 | Homo sapiens (human) | 7351 | UCP2 |
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| DOID:12858 | Huntington's disease | HGNC:12518 | Homo sapiens (human) | 7351 | UCP2 |
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| DOID:3407 | carotid artery disease | HGNC:12518 | Homo sapiens (human) | 7351 | UCP2 |
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| DOID:6000 | congestive heart failure | HGNC:12518 | Homo sapiens (human) | 7351 | UCP2 |
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| DOID:224 | transient cerebral ischemia | HGNC:12518 | Homo sapiens (human) | 7351 | UCP2 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:12518 | Homo sapiens (human) | 7351 | UCP2 |
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| DOID:13603 | obstructive jaundice | HGNC:12518 | Homo sapiens (human) | 7351 | UCP2 |
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| DOID:9743 | diabetic neuropathy | HGNC:12518 | Homo sapiens (human) | 7351 | UCP2 |
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| DOID:10763 | hypertension | HGNC:12518 | Homo sapiens (human) | 7351 | UCP2 |
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| DOID:1459 | hypothyroidism | HGNC:12518 | Homo sapiens (human) | 7351 | UCP2 |
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| DOID:0080208 | metabolic dysfunction-associated steatotic liver disease | HGNC:12518 | Homo sapiens (human) | 7351 | UCP2 |
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| DOID:10763 | hypertension | HGNC:12524 | Homo sapiens (human) | 7357 | UGCG |
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| DOID:0112219 | developmental and epileptic encephalopathy 84 | HGNC:12525 | Homo sapiens (human) | 7358 | UGDH |
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| DOID:162 | cancer | SGD:S000001518 | Saccharomyces cerevisiae S288C | 853830 | UGP1 |
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| DOID:0112218 | developmental and epileptic encephalopathy 83 | SGD:S000001518 | Saccharomyces cerevisiae S288C | 853830 | UGP1 |
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| DOID:0112218 | developmental and epileptic encephalopathy 83 | HGNC:12527 | Homo sapiens (human) | 7360 | UGP2 |
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| DOID:162 | cancer | HGNC:12527 | Homo sapiens (human) | 7360 | UGP2 |
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| DOID:11151 | cholecystolithiasis | HGNC:12530 | Homo sapiens (human) | 54658 | UGT1A1 |
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| DOID:2043 | hepatitis B | HGNC:12530 | Homo sapiens (human) | 54658 | UGT1A1 |
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| DOID:74 | hematopoietic system disease | HGNC:12530 | Homo sapiens (human) | 54658 | UGT1A1 |
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