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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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Repository for lectin-assisted multimodality data
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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 | October 9, 2024 |
| Disease ID | Disease Name | Alliance of Genome Resources ID | Species | Gene ID | Gene Symbol | FlyGlycoDB | Evidence Code Names ▲ | References |
|---|---|---|---|---|---|---|---|---|
| DOID:0111461 | cardiofaciocutaneous syndrome 2 | HGNC:6407 | Homo sapiens (human) | 3845 | KRAS |
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| DOID:0060307 | autosomal dominant intellectual developmental disorder | HGNC:4571 | Homo sapiens (human) | 2890 | GRIA1 |
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| DOID:0070221 | progressive familial intrahepatic cholestasis | HGNC:10741 | Homo sapiens (human) | 8482 | SEMA7A |
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| DOID:0070220 | familial hyperinsulinemic hypoglycemia 5 | HGNC:6091 | Homo sapiens (human) | 3643 | INSR |
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| DOID:3969 | thyroid gland papillary carcinoma | HGNC:795 | Homo sapiens (human) | 472 | ATM |
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| DOID:399 | tuberculosis | HGNC:11847 | Homo sapiens (human) | 7096 | TLR1 |
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| DOID:3393 | coronary artery disease | HGNC:1603 | Homo sapiens (human) | 729230 | CCR2 |
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| DOID:437 | myasthenia gravis | HGNC:6009 | Homo sapiens (human) | 3560 | IL2RB |
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| DOID:2340 | craniosynostosis | HGNC:3690 | Homo sapiens (human) | 2261 | FGFR3 |
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| DOID:0090085 | hypogonadotropic hypogonadism 9 with or without anosmia | HGNC:29843 | Homo sapiens (human) | 26012 | NSMF |
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| DOID:0111186 | myopathy, lactic acidosis, and sideroblastic anemia 2 | HGNC:24249 | Homo sapiens (human) | 51067 | YARS2 |
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| DOID:0080820 | occupational asthma | HGNC:4932 | Homo sapiens (human) | 3106 | HLA-B |
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| DOID:0080388 | nephrotic syndrome type 7 | HGNC:2852 | Homo sapiens (human) | 8526 | DGKE |
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| DOID:1380 | endometrial cancer | HGNC:392 | Homo sapiens (human) | 208 | AKT2 |
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| DOID:3748 | esophagus squamous cell carcinoma | HGNC:2602 | Homo sapiens (human) | 1591 | CYP24A1 |
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| DOID:9119 | acute myeloid leukemia | HGNC:4888 | Homo sapiens (human) | 3078 | CFHR1 |
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| DOID:1115 | sarcoma | HGNC:24054 | Homo sapiens (human) | 57082 | KNL1 |
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| DOID:1555 | urticaria | HGNC:4948 | Homo sapiens (human) | 3123 | HLA-DRB1 |
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| DOID:0070096 | oculocutaneous albinism type II | HGNC:8101 | Homo sapiens (human) | 4948 | OCA2 |
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| DOID:5409 | lung small cell carcinoma | HGNC:6493 | Homo sapiens (human) | 3918 | LAMC2 |
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| DOID:1059 | intellectual disability | HGNC:3025 | Homo sapiens (human) | 1815 | DRD4 |
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| DOID:0080428 | developmental and epileptic encephalopathy 45 | HGNC:4081 | Homo sapiens (human) | 2560 | GABRB1 |
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| DOID:0070388 | developmental and epileptic encephalopathy 102 | HGNC:18044 | Homo sapiens (human) | 10991 | SLC38A3 |
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| DOID:0050450 | Gitelman syndrome | HGNC:2027 | Homo sapiens (human) | 1188 | CLCNKB |
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| DOID:14004 | thoracic aortic aneurysm | HGNC:7569 | Homo sapiens (human) | 4629 | MYH11 |
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