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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:0014667 | disease of metabolism | HGNC:932 | Homo sapiens (human) | 570 | BAAT |
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| DOID:9452 | steatotic liver disease | HGNC:2631 | Homo sapiens (human) | 1571 | CYP2E1 |
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| DOID:3070 | high grade glioma | HGNC:6563 | Homo sapiens (human) | 3958 | LGALS3 |
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| DOID:9256 | colorectal cancer | HGNC:4554 | Homo sapiens (human) | 2877 | GPX2 |
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| DOID:0050570 | congenital disorder of glycosylation type I | HGNC:18294 | Homo sapiens (human) | 56052 | ALG1 |
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| DOID:1580 | diffuse scleroderma | HGNC:13633 | Homo sapiens (human) | 9370 | ADIPOQ |
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| DOID:13141 | uveitis | HGNC:5344 | Homo sapiens (human) | 3383 | ICAM1 |
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| DOID:2957 | pulmonary tuberculosis | HGNC:11847 | Homo sapiens (human) | 7096 | TLR1 |
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| DOID:3314 | angiomyolipoma | HGNC:8125 | Homo sapiens (human) | 4968 | OGG1 |
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| DOID:0080664 | diaphyseal medullary stenosis with malignant fibrous histiocytoma | HGNC:7413 | Homo sapiens (human) | 4507 | MTAP |
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| DOID:2377 | multiple sclerosis | HGNC:319 | Homo sapiens (human) | 176 | ACAN |
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| DOID:1307 | dementia | HGNC:9040 | Homo sapiens (human) | 7941 | PLA2G7 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:2590 | Homo sapiens (human) | 1583 | CYP11A1 |
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| DOID:2526 | prostate adenocarcinoma | HGNC:391 | Homo sapiens (human) | 207 | AKT1 |
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| DOID:890 | mitochondrial encephalomyopathy | HGNC:10681 | Homo sapiens (human) | 6390 | SDHB |
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| DOID:3969 | thyroid gland papillary carcinoma | HGNC:1516 | Homo sapiens (human) | 847 | CAT |
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| DOID:8619 | recurrent hypersomnia | HGNC:1938 | Homo sapiens (human) | 1120 | CHKB |
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| DOID:3459 | breast carcinoma | HGNC:3353 | Homo sapiens (human) | 2026 | ENO2 |
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| DOID:11506 | suppurative otitis media | HGNC:11850 | Homo sapiens (human) | 7099 | TLR4 |
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| DOID:12236 | primary biliary cholangitis | HGNC:6554 | Homo sapiens (human) | 3953 | LEPR |
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| DOID:12732 | intermediate uveitis | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:10591 | pre-eclampsia | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
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| DOID:11832 | visual epilepsy | HGNC:20499 | Homo sapiens (human) | 79944 | L2HGDH |
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| DOID:0050559 | Fukuyama congenital muscular dystrophy | HGNC:2666 | Homo sapiens (human) | 1605 | DAG1 |
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| DOID:2870 | endometrial adenocarcinoma | HGNC:9599 | Homo sapiens (human) | 9536 | PTGES |
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