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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:0110284 | autosomal recessive limb-girdle muscular dystrophy type 2L | HGNC:3622 | Homo sapiens (human) | 2218 | FKTN |
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| DOID:12930 | dilated cardiomyopathy | HGNC:5344 | Homo sapiens (human) | 3383 | ICAM1 |
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| DOID:0080208 | metabolic dysfunction-associated steatotic liver disease | HGNC:6677 | Homo sapiens (human) | 4023 | LPL |
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| DOID:2679 | dysembryoplastic neuroepithelial tumor | HGNC:1097 | Homo sapiens (human) | 673 | BRAF |
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| DOID:3572 | intracranial sinus thrombosis | HGNC:4555 | Homo sapiens (human) | 2878 | GPX3 |
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| DOID:6406 | double outlet right ventricle | HGNC:18292 | Homo sapiens (human) | 55997 | CFC1 |
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| DOID:4483 | rhinitis | HGNC:16711 | Homo sapiens (human) | 10333 | TLR6 |
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| DOID:8577 | ulcerative colitis | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:332 | amyotrophic lateral sclerosis | HGNC:4616 | Homo sapiens (human) | 2931 | GSK3A |
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| DOID:10608 | celiac disease | HGNC:1628 | Homo sapiens (human) | 929 | CD14 |
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| DOID:1909 | melanoma | HGNC:1516 | Homo sapiens (human) | 847 | CAT |
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| DOID:7998 | hyperthyroidism | HGNC:543 | Homo sapiens (human) | 308 | ANXA5 |
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| DOID:0050797 | peroxisomal acyl-CoA oxidase deficiency | HGNC:119 | Homo sapiens (human) | 51 | ACOX1 |
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| DOID:8893 | psoriasis | HGNC:429 | Homo sapiens (human) | 239 | ALOX12 |
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| DOID:8947 | diabetic retinopathy | HGNC:4250 | Homo sapiens (human) | 2678 | GGT1 |
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| DOID:10003 | sensorineural hearing loss | HGNC:9592 | Homo sapiens (human) | 5730 | PTGDS |
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| DOID:0050709 | early infantile epileptic encephalopathy | HGNC:5385 | Homo sapiens (human) | 3420 | IDH3B |
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| DOID:13580 | cholestasis | HGNC:2638 | Homo sapiens (human) | 1577 | CYP3A5 |
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| DOID:1588 | thrombocytopenia | HGNC:4021 | Homo sapiens (human) | 2531 | KDSR |
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| DOID:893 | Wilson disease | HGNC:2606 | Homo sapiens (human) | 1594 | CYP27B1 |
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| DOID:11212 | hydrophthalmos | HGNC:2597 | Homo sapiens (human) | 1545 | CYP1B1 |
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| DOID:11714 | gestational diabetes | HGNC:6081 | Homo sapiens (human) | 3630 | INS |
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| DOID:12858 | Huntington's disease | HGNC:6553 | Homo sapiens (human) | 3952 | LEP |
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| DOID:14330 | Parkinson's disease | HGNC:392 | Homo sapiens (human) | 208 | AKT2 |
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| DOID:5022 | aflatoxins-related hepatocellular carcinoma | HGNC:4250 | Homo sapiens (human) | 2678 | GGT1 |
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