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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:0070268 | congenital disorder of glycosylation type IIp | HGNC:18085 | Homo sapiens (human) | 147007 | TMEM199 |
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| DOID:114 | heart disease | HGNC:4341 | Homo sapiens (human) | 2752 | GLUL |
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| DOID:10652 | Alzheimer's disease | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
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| DOID:10487 | Hirschsprung's disease | HGNC:11005 | Homo sapiens (human) | 6513 | SLC2A1 |
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| DOID:8805 | intermediate coronary syndrome | HGNC:10721 | Homo sapiens (human) | 6403 | SELP |
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| DOID:10763 | hypertension | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:1273 | respiratory syncytial virus infectious disease | HGNC:5344 | Homo sapiens (human) | 3383 | ICAM1 |
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| DOID:3343 | glycoproteinosis | HGNC:23026 | Homo sapiens (human) | 84572 | GNPTG |
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| DOID:1682 | congenital heart disease | HGNC:9055 | Homo sapiens (human) | 5330 | PLCB2 |
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| DOID:684 | hepatocellular carcinoma | HGNC:9588 | Homo sapiens (human) | 5728 | PTEN |
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| DOID:2957 | pulmonary tuberculosis | HGNC:1637 | Homo sapiens (human) | 912 | CD1D |
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| DOID:0050981 | spinocerebellar ataxia type 34 | HGNC:14415 | Homo sapiens (human) | 6785 | ELOVL4 |
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| DOID:409 | liver disease | HGNC:2631 | Homo sapiens (human) | 1571 | CYP2E1 |
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| DOID:1588 | thrombocytopenia | HGNC:4116 | Homo sapiens (human) | 2582 | GALE |
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| DOID:13241 | Behcet's disease | HGNC:5344 | Homo sapiens (human) | 3383 | ICAM1 |
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| DOID:0110660 | congenital myasthenic syndrome 12 | HGNC:4241 | Homo sapiens (human) | 2673 | GFPT1 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:2592 | Homo sapiens (human) | 1585 | CYP11B2 |
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| DOID:11729 | Lyme disease | HGNC:9053 | Homo sapiens (human) | 5329 | PLAUR |
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| DOID:0050809 | mucopolysaccharidosis IX | HGNC:5320 | Homo sapiens (human) | 3373 | HYAL1 |
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| DOID:3121 | gallbladder cancer | HGNC:9922 | Homo sapiens (human) | 5950 | RBP4 |
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| DOID:9427 | hypertensive encephalopathy | HGNC:9232 | Homo sapiens (human) | 5465 | PPARA |
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| DOID:9119 | acute myeloid leukemia | HGNC:5382 | Homo sapiens (human) | 3417 | IDH1 |
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| DOID:418 | systemic scleroderma | HGNC:543 | Homo sapiens (human) | 308 | ANXA5 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:4250 | Homo sapiens (human) | 2678 | GGT1 |
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| DOID:14264 | benign neonatal seizures | HGNC:800 | Homo sapiens (human) | 477 | ATP1A2 |
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