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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:8577 | ulcerative colitis | HGNC:10721 | Homo sapiens (human) | 6403 | SELP |
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| DOID:2526 | prostate adenocarcinoma | HGNC:8976 | Homo sapiens (human) | 5291 | PIK3CB |
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| DOID:0070266 | congenital disorder of glycosylation type IIn | HGNC:20862 | Homo sapiens (human) | 64116 | SLC39A8 |
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| DOID:3910 | lung adenocarcinoma | HGNC:380 | Homo sapiens (human) | 10327 | AKR1A1 |
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| DOID:8398 | osteoarthritis | HGNC:5466 | Homo sapiens (human) | 3481 | IGF2 |
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| DOID:3649 | pyruvate decarboxylase deficiency | HGNC:8806 | Homo sapiens (human) | 5160 | PDHA1 |
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| DOID:2349 | arteriosclerosis | HGNC:1753 | Homo sapiens (human) | 1012 | CDH13 |
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| DOID:1596 | depressive disorder | HGNC:9031 | Homo sapiens (human) | 5320 | PLA2G2A |
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| DOID:0112248 | 17-beta hydroxysteroid dehydrogenase 3 deficiency | HGNC:5212 | Homo sapiens (human) | 3293 | HSD17B3 |
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| DOID:11054 | urinary bladder cancer | HGNC:3353 | Homo sapiens (human) | 2026 | ENO2 |
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| DOID:0110429 | dilated cardiomyopathy 1H | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:0050464 | Farber lipogranulomatosis | HGNC:735 | Homo sapiens (human) | 427 | ASAH1 |
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| DOID:13241 | Behcet's disease | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
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| DOID:2957 | pulmonary tuberculosis | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:5082 | liver cirrhosis | HGNC:6563 | Homo sapiens (human) | 3958 | LGALS3 |
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| DOID:10763 | hypertension | HGNC:2642 | Homo sapiens (human) | 1579 | CYP4A11 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:6344 | Homo sapiens (human) | 9365 | KL |
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| DOID:1612 | breast cancer | HGNC:380 | Homo sapiens (human) | 10327 | AKR1A1 |
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| DOID:4195 | hyperglycemia | HGNC:5344 | Homo sapiens (human) | 3383 | ICAM1 |
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| DOID:224 | transient cerebral ischemia | HGNC:5344 | Homo sapiens (human) | 3383 | ICAM1 |
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| DOID:2513 | basal cell carcinoma | HGNC:11998 | Homo sapiens (human) | 7157 | TP53 |
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| DOID:9452 | steatotic liver disease | HGNC:84 | Homo sapiens (human) | 31 | ACACA |
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| DOID:1596 | depressive disorder | HGNC:2596 | Homo sapiens (human) | 1544 | CYP1A2 |
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| DOID:12930 | dilated cardiomyopathy | HGNC:2422 | Homo sapiens (human) | 1431 | CS |
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| DOID:11832 | visual epilepsy | HGNC:4341 | Homo sapiens (human) | 2752 | GLUL |
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