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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:1612 | breast cancer | HGNC:5012 | Homo sapiens (human) | 3161 | HMMR |
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| DOID:11132 | prostatic hypertrophy | HGNC:9605 | Homo sapiens (human) | 5743 | PTGS2 |
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| DOID:1205 | allergic disease | HGNC:1628 | Homo sapiens (human) | 929 | CD14 |
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| DOID:0060894 | early-onset Parkinson's disease | HGNC:11504 | Homo sapiens (human) | 8871 | SYNJ2 |
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| DOID:2921 | glomerulonephritis | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
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| DOID:8677 | perinatal necrotizing enterocolitis | HGNC:9053 | Homo sapiens (human) | 5329 | PLAUR |
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| DOID:0081312 | T-cell non-Hodgkin lymphoma | HGNC:20185 | Homo sapiens (human) | 54916 | TMEM260 |
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| DOID:1070 | primary open angle glaucoma | HGNC:11998 | Homo sapiens (human) | 7157 | TP53 |
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| DOID:3393 | coronary artery disease | HGNC:9040 | Homo sapiens (human) | 7941 | PLA2G7 |
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| DOID:3211 | lysosomal storage disease | HGNC:4296 | Homo sapiens (human) | 2717 | GLA |
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| DOID:399 | tuberculosis | HGNC:2621 | Homo sapiens (human) | 1557 | CYP2C19 |
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| DOID:3312 | bipolar disorder | HGNC:4617 | Homo sapiens (human) | 2932 | GSK3B |
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| DOID:1826 | epilepsy | HGNC:408 | Homo sapiens (human) | 7915 | ALDH5A1 |
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| DOID:9538 | multiple myeloma | HGNC:4922 | Homo sapiens (human) | 3098 | HK1 |
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| DOID:10933 | obsessive-compulsive disorder | HGNC:2228 | Homo sapiens (human) | 1312 | COMT |
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| DOID:12449 | aplastic anemia | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:4483 | rhinitis | HGNC:5998 | Homo sapiens (human) | 9173 | IL1RL1 |
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| DOID:0060669 | cerebral cavernous malformation | HGNC:8975 | Homo sapiens (human) | 5290 | PIK3CA |
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| DOID:11832 | visual epilepsy | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:9743 | diabetic neuropathy | HGNC:4250 | Homo sapiens (human) | 2678 | GGT1 |
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| DOID:3526 | cerebral infarction | HGNC:4555 | Homo sapiens (human) | 2878 | GPX3 |
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| DOID:4231 | histiocytoma | HGNC:18788 | Homo sapiens (human) | 22914 | KLRK1 |
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| DOID:5199 | ureteral obstruction | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
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| DOID:12306 | vitiligo | HGNC:1516 | Homo sapiens (human) | 847 | CAT |
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| DOID:0060050 | autoimmune disease of blood | HGNC:24337 | Homo sapiens (human) | 56913 | C1GALT1 |
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