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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:0050579 | glycogen storage disease XV | HGNC:4699 | Homo sapiens (human) | 2992 | GYG1 |
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| DOID:12241 | beta thalassemia | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:1793 | pancreatic cancer | HGNC:9235 | Homo sapiens (human) | 5467 | PPARD |
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| DOID:9252 | amino acid metabolic disorder | HGNC:8653 | Homo sapiens (human) | 5095 | PCCA |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:391 | Homo sapiens (human) | 207 | AKT1 |
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| DOID:10923 | sickle cell anemia | HGNC:4553 | Homo sapiens (human) | 2876 | GPX1 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:11007 | Homo sapiens (human) | 6515 | SLC2A3 |
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| DOID:0080546 | non-alcoholic fatty liver | HGNC:4250 | Homo sapiens (human) | 2678 | GGT1 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:5208 | Homo sapiens (human) | 3290 | HSD11B1 |
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| DOID:10754 | otitis media | HGNC:11850 | Homo sapiens (human) | 7099 | TLR4 |
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| DOID:0111313 | idiopathic generalized epilepsy 12 | HGNC:11005 | Homo sapiens (human) | 6513 | SLC2A1 |
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| DOID:9970 | obesity | HGNC:2228 | Homo sapiens (human) | 1312 | COMT |
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| DOID:3083 | chronic obstructive pulmonary disease | HGNC:10721 | Homo sapiens (human) | 6403 | SELP |
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| DOID:687 | hepatoblastoma | HGNC:3002 | Homo sapiens (human) | 1800 | DPEP1 |
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| DOID:1825 | childhood absence epilepsy | HGNC:7956 | Homo sapiens (human) | 4886 | NPY1R |
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| DOID:1380 | endometrial cancer | HGNC:587 | Homo sapiens (human) | 328 | APEX1 |
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| DOID:0060892 | late onset Parkinson's disease | HGNC:9498 | Homo sapiens (human) | 5660 | PSAP |
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| DOID:1742 | drug psychosis | HGNC:4092 | Homo sapiens (human) | 2571 | GAD1 |
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| DOID:289 | endometriosis | HGNC:10720 | Homo sapiens (human) | 6402 | SELL |
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| DOID:3742 | bladder squamous cell carcinoma | HGNC:9588 | Homo sapiens (human) | 5728 | PTEN |
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| DOID:3770 | pulmonary fibrosis | HGNC:1516 | Homo sapiens (human) | 847 | CAT |
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| DOID:10763 | hypertension | HGNC:6553 | Homo sapiens (human) | 3952 | LEP |
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| DOID:397 | restrictive cardiomyopathy | HGNC:21088 | Homo sapiens (human) | 79966 | SCD5 |
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| DOID:11612 | polycystic ovary syndrome | HGNC:13633 | Homo sapiens (human) | 9370 | ADIPOQ |
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| DOID:3068 | glioblastoma | HGNC:5382 | Homo sapiens (human) | 3417 | IDH1 |
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