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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:4948 | gallbladder carcinoma | HGNC:11730 | Homo sapiens (human) | 7015 | TERT |
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| DOID:12236 | primary biliary cholangitis | HGNC:2505 | Homo sapiens (human) | 1493 | CTLA4 |
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| DOID:11151 | cholecystolithiasis | HGNC:12530 | Homo sapiens (human) | 54658 | UGT1A1 |
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| DOID:0050675 | Birk-Barel syndrome | HGNC:6283 | Homo sapiens (human) | 51305 | KCNK9 |
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| DOID:2256 | osteochondrodysplasia | HGNC:11766 | Homo sapiens (human) | 7040 | TGFB1 |
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| DOID:0070281 | primary autosomal recessive microcephaly 19 | HGNC:2232 | Homo sapiens (human) | 9276 | COPB2 |
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| DOID:0081268 | pulmonary venoocclusive disease 1 | HGNC:1078 | Homo sapiens (human) | 659 | BMPR2 |
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| DOID:4450 | renal cell carcinoma | HGNC:7173 | Homo sapiens (human) | 4314 | MMP3 |
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| DOID:11198 | DiGeorge syndrome | HGNC:12520 | Homo sapiens (human) | 7353 | UFD1 |
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| DOID:0112349 | hereditary spastic paraplegia 81 | HGNC:29361 | Homo sapiens (human) | 85465 | SELENOI |
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| DOID:7235 | pancreatic mucinous cystadenoma | HGNC:6407 | Homo sapiens (human) | 3845 | KRAS |
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| DOID:0050741 | alcohol dependence | HGNC:1569 | Homo sapiens (human) | 885 | CCK |
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| DOID:1596 | depressive disorder | HGNC:5298 | Homo sapiens (human) | 9177 | HTR3B |
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| DOID:14004 | thoracic aortic aneurysm | HGNC:25835 | Homo sapiens (human) | 79875 | THSD4 |
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| DOID:0111167 | Dyggve-Melchior-Clausen disease | HGNC:21317 | Homo sapiens (human) | 54808 | DYM |
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| DOID:2211 | factor XIII deficiency | HGNC:6631 | Homo sapiens (human) | 3998 | LMAN1 |
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| DOID:0111386 | inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 3 | HGNC:5031 | Homo sapiens (human) | 3178 | HNRNPA1 |
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| DOID:6364 | migraine | HGNC:19439 | Homo sapiens (human) | 338567 | KCNK18 |
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| DOID:2394 | ovarian cancer | HGNC:1748 | Homo sapiens (human) | 999 | CDH1 |
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| DOID:1657 | ventricular septal defect | HGNC:15924 | Homo sapiens (human) | 57167 | SALL4 |
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| DOID:2316 | brain ischemia | HGNC:7939 | Homo sapiens (human) | 4878 | NPPA |
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| DOID:1579 | respiratory system disease | HGNC:3616 | Homo sapiens (human) | 2212 | FCGR2A |
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| DOID:3526 | cerebral infarction | HGNC:18001 | Homo sapiens (human) | 10452 | TOMM40 |
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| DOID:1742 | drug psychosis | HGNC:8156 | Homo sapiens (human) | 4988 | OPRM1 |
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| DOID:3388 | periodontal disease | HGNC:6018 | Homo sapiens (human) | 3569 | IL6 |
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