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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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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:7148 | rheumatoid arthritis | HGNC:6919 | Homo sapiens (human) | 8930 | MBD4 |
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| DOID:9970 | obesity | HGNC:5293 | Homo sapiens (human) | 3356 | HTR2A |
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| DOID:10611 | protein-losing enteropathy | HGNC:2665 | Homo sapiens (human) | 1604 | CD55 |
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| DOID:77 | gastrointestinal system disease | HGNC:12663 | Homo sapiens (human) | 7412 | VCAM1 |
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| DOID:0050861 | colorectal adenocarcinoma | HGNC:2648 | Homo sapiens (human) | 11283 | CYP4F8 |
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| DOID:2841 | asthma | HGNC:5988 | Homo sapiens (human) | 8809 | IL18R1 |
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| DOID:0111507 | Lenz-Majewski hyperostotic dwarfism | HGNC:9587 | Homo sapiens (human) | 9791 | PTDSS1 |
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| DOID:13922 | eosinophilic esophagitis | HGNC:2621 | Homo sapiens (human) | 1557 | CYP2C19 |
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| DOID:11476 | osteoporosis | HGNC:2594 | Homo sapiens (human) | 1588 | CYP19A1 |
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| DOID:0110274 | autosomal recessive limb-girdle muscular dystrophy | HGNC:19743 | Homo sapiens (human) | 29954 | POMT2 |
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| DOID:0111677 | familial benign fleck retina | HGNC:9038 | Homo sapiens (human) | 5322 | PLA2G5 |
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| DOID:9828 | neonatal abstinence syndrome | HGNC:2228 | Homo sapiens (human) | 1312 | COMT |
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| DOID:2154 | nephroblastoma | HGNC:5467 | Homo sapiens (human) | 3482 | IGF2R |
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| DOID:0050453 | lissencephaly | HGNC:19743 | Homo sapiens (human) | 29954 | POMT2 |
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| DOID:853 | polymyalgia rheumatica | HGNC:6922 | Homo sapiens (human) | 4153 | MBL2 |
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| DOID:0110669 | congenital myasthenic syndrome 14 | HGNC:23159 | Homo sapiens (human) | 85365 | ALG2 |
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| DOID:0111110 | maturity-onset diabetes of the young type 13 | HGNC:6257 | Homo sapiens (human) | 3767 | KCNJ11 |
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| DOID:2280 | hidradenitis suppurativa | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:417 | autoimmune disease | HGNC:5382 | Homo sapiens (human) | 3417 | IDH1 |
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| DOID:0060075 | estrogen-receptor positive breast cancer | HGNC:8975 | Homo sapiens (human) | 5290 | PIK3CA |
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| DOID:0090139 | cortisone reductase deficiency | HGNC:4795 | Homo sapiens (human) | 9563 | H6PD |
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| DOID:7148 | rheumatoid arthritis | HGNC:29013 | Homo sapiens (human) | 23274 | CLEC16A |
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| DOID:10283 | prostate cancer | HGNC:1929 | Homo sapiens (human) | 1113 | CHGA |
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| DOID:12140 | Chagas disease | HGNC:11177 | Homo sapiens (human) | 6646 | SOAT1 |
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| DOID:1612 | breast cancer | HGNC:2596 | Homo sapiens (human) | 1544 | CYP1A2 |
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