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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:1909 | melanoma | HGNC:1097 | Homo sapiens (human) | 673 | BRAF |
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| DOID:5844 | myocardial infarction | HGNC:20580 | Homo sapiens (human) | 120227 | CYP2R1 |
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| DOID:3068 | glioblastoma | HGNC:6470 | Homo sapiens (human) | 3897 | L1CAM |
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| DOID:3649 | pyruvate decarboxylase deficiency | HGNC:8807 | Homo sapiens (human) | 5161 | PDHA2 |
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| DOID:0110435 | dilated cardiomyopathy 1GG | HGNC:10680 | Homo sapiens (human) | 6389 | SDHA |
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| DOID:10003 | sensorineural hearing loss | HGNC:6922 | Homo sapiens (human) | 4153 | MBL2 |
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| DOID:0050685 | small cell carcinoma | HGNC:1932 | Homo sapiens (human) | 1116 | CHI3L1 |
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| DOID:5419 | schizophrenia | HGNC:9605 | Homo sapiens (human) | 5743 | PTGS2 |
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| DOID:10652 | Alzheimer's disease | HGNC:10720 | Homo sapiens (human) | 6402 | SELL |
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| DOID:13564 | aspergillosis | HGNC:14558 | Homo sapiens (human) | 64581 | CLEC7A |
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| DOID:9119 | acute myeloid leukemia | HGNC:5383 | Homo sapiens (human) | 3418 | IDH2 |
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| DOID:3312 | bipolar disorder | HGNC:2228 | Homo sapiens (human) | 1312 | COMT |
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| DOID:11400 | pyelonephritis | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
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| DOID:0070264 | congenital disorder of glycosylation type IIl | HGNC:18621 | Homo sapiens (human) | 57511 | COG6 |
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| DOID:0060470 | salt and pepper syndrome | HGNC:10872 | Homo sapiens (human) | 8869 | ST3GAL5 |
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| DOID:4159 | skin cancer | HGNC:545 | Homo sapiens (human) | 310 | ANXA7 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:2622 | Homo sapiens (human) | 1558 | CYP2C8 |
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| DOID:13276 | Mycoplasma pneumoniae pneumonia | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:5463 | cochlear disease | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:9970 | obesity | HGNC:936 | Homo sapiens (human) | 572 | BAD |
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| DOID:0080855 | Parkinsonism | HGNC:23 | Homo sapiens (human) | 18 | ABAT |
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| DOID:12858 | Huntington's disease | HGNC:4558 | Homo sapiens (human) | 257202 | GPX6 |
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| DOID:0060189 | ileitis | HGNC:11848 | Homo sapiens (human) | 7097 | TLR2 |
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| DOID:409 | liver disease | HGNC:404 | Homo sapiens (human) | 217 | ALDH2 |
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| DOID:219 | colon cancer | HGNC:391 | Homo sapiens (human) | 207 | AKT1 |
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