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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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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:13619 | extrahepatic cholestasis | HGNC:5008 | Homo sapiens (human) | 3158 | HMGCS2 |
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| DOID:12148 | alveolar echinococcosis | HGNC:11848 | Homo sapiens (human) | 7097 | TLR2 |
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| DOID:3908 | lung non-small cell carcinoma | HGNC:10803 | Homo sapiens (human) | 6441 | SFTPD |
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| DOID:9970 | obesity | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:11054 | urinary bladder cancer | HGNC:391 | Homo sapiens (human) | 207 | AKT1 |
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| DOID:2526 | prostate adenocarcinoma | HGNC:13633 | Homo sapiens (human) | 9370 | ADIPOQ |
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| DOID:418 | systemic scleroderma | HGNC:5344 | Homo sapiens (human) | 3383 | ICAM1 |
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| DOID:9452 | steatotic liver disease | HGNC:5293 | Homo sapiens (human) | 3356 | HTR2A |
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| DOID:11054 | urinary bladder cancer | HGNC:429 | Homo sapiens (human) | 239 | ALOX12 |
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| DOID:4194 | glucose metabolism disease | HGNC:2853 | Homo sapiens (human) | 1608 | DGKG |
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| DOID:0110960 | Gaucher's disease perinatal lethal | HGNC:4177 | Homo sapiens (human) | 2629 | GBA1 |
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| DOID:11206 | opioid abuse | HGNC:7656 | Homo sapiens (human) | 4684 | NCAM1 |
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| DOID:1338 | congenital dyserythropoietic anemia | HGNC:6824 | Homo sapiens (human) | 4124 | MAN2A1 |
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| DOID:127 | leiomyoma | HGNC:8729 | Homo sapiens (human) | 5111 | PCNA |
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| DOID:2841 | asthma | HGNC:253 | Homo sapiens (human) | 128 | ADH5 |
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| DOID:0060759 | immunodeficiency with hyper IgM type 5 | HGNC:12572 | Homo sapiens (human) | 7374 | UNG |
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| DOID:684 | hepatocellular carcinoma | HGNC:6554 | Homo sapiens (human) | 3953 | LEPR |
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| DOID:674 | cleft palate | HGNC:10659 | Homo sapiens (human) | 6383 | SDC2 |
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| DOID:0111671 | primary hyperoxaluria type 2 | HGNC:4570 | Homo sapiens (human) | 9380 | GRHPR |
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| DOID:341 | peripheral vascular disease | HGNC:6922 | Homo sapiens (human) | 4153 | MBL2 |
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| DOID:13550 | angle-closure glaucoma | HGNC:1516 | Homo sapiens (human) | 847 | CAT |
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| DOID:0080855 | Parkinsonism | HGNC:4177 | Homo sapiens (human) | 2629 | GBA1 |
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| DOID:10652 | Alzheimer's disease | HGNC:24864 | Homo sapiens (human) | 26330 | GAPDHS |
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| DOID:7998 | hyperthyroidism | HGNC:4553 | Homo sapiens (human) | 2876 | GPX1 |
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| DOID:5844 | myocardial infarction | HGNC:15917 | Homo sapiens (human) | 23236 | PLCB1 |
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