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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:11984 | hypertrophic cardiomyopathy | HGNC:2597 | Homo sapiens (human) | 1545 | CYP1B1 |
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| DOID:0050570 | congenital disorder of glycosylation type I | HGNC:23161 | Homo sapiens (human) | 79053 | ALG8 |
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| DOID:13276 | Mycoplasma pneumoniae pneumonia | HGNC:4115 | Homo sapiens (human) | 2581 | GALC |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:10659 | Homo sapiens (human) | 6383 | SDC2 |
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| DOID:10908 | hydrocephalus | HGNC:15505 | Homo sapiens (human) | 79143 | MBOAT7 |
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| DOID:12800 | mucopolysaccharidosis VI | HGNC:714 | Homo sapiens (human) | 411 | ARSB |
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| DOID:0080208 | metabolic dysfunction-associated steatotic liver disease | HGNC:2653 | Homo sapiens (human) | 1582 | CYP8B1 |
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| DOID:8778 | Crohn's disease | HGNC:4553 | Homo sapiens (human) | 2876 | GPX1 |
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| DOID:0050776 | non-syndromic X-linked intellectual disability | HGNC:3571 | Homo sapiens (human) | 2182 | ACSL4 |
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| DOID:0060178 | familial hemiplegic migraine | HGNC:800 | Homo sapiens (human) | 477 | ATP1A2 |
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| DOID:1470 | major depressive disorder | HGNC:9588 | Homo sapiens (human) | 5728 | PTEN |
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| DOID:10595 | Charcot-Marie-Tooth disease | HGNC:7449 | Homo sapiens (human) | 8776 | MTMR1 |
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| DOID:0050575 | D-2-hydroxyglutaric aciduria | HGNC:5382 | Homo sapiens (human) | 3417 | IDH1 |
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| DOID:10652 | Alzheimer's disease | HGNC:2594 | Homo sapiens (human) | 1588 | CYP19A1 |
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| DOID:0050753 | cerebellar ataxia | HGNC:20499 | Homo sapiens (human) | 79944 | L2HGDH |
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| DOID:4677 | keratitis | HGNC:11850 | Homo sapiens (human) | 7099 | TLR4 |
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| DOID:3652 | Leigh disease | HGNC:10680 | Homo sapiens (human) | 6389 | SDHA |
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| DOID:1612 | breast cancer | HGNC:16049 | Homo sapiens (human) | 10728 | PTGES3 |
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| DOID:3385 | bacterial vaginosis | HGNC:6922 | Homo sapiens (human) | 4153 | MBL2 |
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| DOID:4195 | hyperglycemia | HGNC:9449 | Homo sapiens (human) | 5621 | PRNP |
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| DOID:0050581 | brachydactyly | HGNC:10994 | Homo sapiens (human) | 1836 | SLC26A2 |
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| DOID:10763 | hypertension | HGNC:5217 | Homo sapiens (human) | 3283 | HSD3B1 |
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| DOID:9538 | multiple myeloma | HGNC:2621 | Homo sapiens (human) | 1557 | CYP2C19 |
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| DOID:12177 | common variable immunodeficiency | HGNC:6922 | Homo sapiens (human) | 4153 | MBL2 |
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| DOID:1059 | intellectual disability | HGNC:5996 | Homo sapiens (human) | 11141 | IL1RAPL1 |
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