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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:104 | bacterial infectious disease | HGNC:11022 | Homo sapiens (human) | 7355 | SLC35A2 |
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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:1793 | pancreatic cancer | Xenbase:XB-GENE-5796042 | Xenopus laevis (African clawed frog) | 734685 | a4gnt.L |
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| DOID:0112216 | developmental and epileptic encephalopathy 80 | Xenbase:XB-GENE-996683 | Xenopus laevis (African clawed frog) | 734564 | pigb.S |
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| DOID:0080557 | congenital disorder of glycosylation Ie | Xenbase:XB-GENE-976628 | Xenopus laevis (African clawed frog) | 734516 | dpm1.S |
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| DOID:1459 | hypothyroidism | Xenbase:XB-GENE-5916631 | Xenopus tropicalis (tropical clawed frog) | 734090 | plod3 |
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| DOID:684 | hepatocellular carcinoma | Xenbase:XB-GENE-5916631 | Xenopus tropicalis (tropical clawed frog) | 734090 | plod3 |
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| DOID:0080567 | congenital disorder of glycosylation Ip | Xenbase:XB-GENE-5934162 | Xenopus laevis (African clawed frog) | 733388 | alg11.L |
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| DOID:5419 | schizophrenia | Xenbase:XB-GENE-921709 | Xenopus laevis (African clawed frog) | 733177 | b3gat2.S |
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| DOID:9206 | Barrett's esophagus | Xenbase:XB-GENE-921709 | Xenopus laevis (African clawed frog) | 733177 | b3gat2.S |
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| DOID:10534 | stomach cancer | MGI:1920318 | Mus musculus (house mouse) | 73068 | Fut11 |
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| DOID:0110295 | autosomal recessive limb-girdle muscular dystrophy type 2U | HGNC:37276 | Homo sapiens (human) | 729920 | CRPPA |
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