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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:10763 | hypertension | HGNC:20580 | Homo sapiens (human) | 120227 | CYP2R1 |
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| DOID:3526 | cerebral infarction | HGNC:11609 | Homo sapiens (human) | 6916 | TBXAS1 |
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| DOID:12849 | autistic disorder | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:0070432 | hyperphosphatasia with impaired intellectual development syndrome 5 | HGNC:23213 | Homo sapiens (human) | 284098 | PIGW |
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| DOID:285 | hairy cell leukemia | HGNC:4553 | Homo sapiens (human) | 2876 | GPX1 |
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| DOID:0111673 | Saul-Wilson syndrome | HGNC:18620 | Homo sapiens (human) | 25839 | COG4 |
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| DOID:684 | hepatocellular carcinoma | HGNC:6922 | Homo sapiens (human) | 4153 | MBL2 |
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| DOID:5679 | retinal disease | HGNC:8999 | Homo sapiens (human) | 23761 | PISD |
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| DOID:0080139 | multiple congenital anomalies-hypotonia-seizures syndrome 2 | HGNC:8957 | Homo sapiens (human) | 5277 | PIGA |
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| DOID:0080533 | Carney-Stratakis syndrome | HGNC:10683 | Homo sapiens (human) | 6392 | SDHD |
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| DOID:0112171 | wrinkly skin syndrome | HGNC:18481 | Homo sapiens (human) | 23545 | ATP6V0A2 |
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| DOID:0080599 | Coronavirus infectious disease | HGNC:6922 | Homo sapiens (human) | 4153 | MBL2 |
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| DOID:12466 | secondary hyperparathyroidism | HGNC:6344 | Homo sapiens (human) | 9365 | KL |
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| DOID:874 | bacterial pneumonia | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:5041 | esophageal cancer | HGNC:9588 | Homo sapiens (human) | 5728 | PTEN |
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| DOID:11714 | gestational diabetes | HGNC:4195 | Homo sapiens (human) | 2645 | GCK |
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| DOID:9970 | obesity | HGNC:13709 | Homo sapiens (human) | 8560 | DEGS1 |
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| DOID:0080571 | congenital disorder of glycosylation Iu | HGNC:3006 | Homo sapiens (human) | 8818 | DPM2 |
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| 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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