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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:0050864 | non-arteritic anterior ischemic optic neuropathy | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
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| DOID:0080119 | mitochondrial DNA depletion syndrome 1 | HGNC:3148 | Homo sapiens (human) | 1890 | TYMP |
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| DOID:3748 | esophagus squamous cell carcinoma | HGNC:2602 | Homo sapiens (human) | 1591 | CYP24A1 |
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| DOID:11204 | allergic conjunctivitis | HGNC:5344 | Homo sapiens (human) | 3383 | ICAM1 |
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| DOID:1184 | nephrotic syndrome | HGNC:4553 | Homo sapiens (human) | 2876 | GPX1 |
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| DOID:1574 | alcohol use disorder | HGNC:2228 | Homo sapiens (human) | 1312 | COMT |
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| DOID:3393 | coronary artery disease | HGNC:11850 | Homo sapiens (human) | 7099 | TLR4 |
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| DOID:11832 | visual epilepsy | HGNC:936 | Homo sapiens (human) | 572 | BAD |
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| DOID:0111225 | centronuclear myopathy X-linked | HGNC:7452 | Homo sapiens (human) | 9110 | MTMR4 |
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| DOID:299 | adenocarcinoma | HGNC:11240 | Homo sapiens (human) | 8877 | SPHK1 |
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| DOID:1793 | pancreatic cancer | HGNC:1097 | Homo sapiens (human) | 673 | BRAF |
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| DOID:11446 | sciatic neuropathy | HGNC:4617 | Homo sapiens (human) | 2932 | GSK3B |
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| DOID:162 | cancer | HGNC:20603 | Homo sapiens (human) | 79947 | DHDDS |
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| DOID:1924 | hypogonadism | HGNC:2590 | Homo sapiens (human) | 1583 | CYP11A1 |
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| DOID:4914 | esophagus adenocarcinoma | HGNC:18129 | Homo sapiens (human) | 51738 | GHRL |
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| DOID:3393 | coronary artery disease | HGNC:30092 | Homo sapiens (human) | 10135 | NAMPT |
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| DOID:0081219 | autosomal recessive intellectual developmental disorder 57 | HGNC:15505 | Homo sapiens (human) | 79143 | MBOAT7 |
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| DOID:0050731 | vitamin B12 deficiency | HGNC:4555 | Homo sapiens (human) | 2878 | GPX3 |
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| DOID:0060363 | glycerol kinase deficiency | HGNC:4289 | Homo sapiens (human) | 2710 | GK |
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| DOID:10964 | cholesteatoma of middle ear | HGNC:11848 | Homo sapiens (human) | 7097 | TLR2 |
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| DOID:0111442 | optic atrophy 9 | HGNC:118 | Homo sapiens (human) | 50 | ACO2 |
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| DOID:1380 | endometrial cancer | HGNC:2596 | Homo sapiens (human) | 1544 | CYP1A2 |
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| DOID:0060180 | colitis | HGNC:1516 | Homo sapiens (human) | 847 | CAT |
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| DOID:12306 | vitiligo | HGNC:2228 | Homo sapiens (human) | 1312 | COMT |
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| DOID:3213 | demyelinating disease | HGNC:9605 | Homo sapiens (human) | 5743 | PTGS2 |
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