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GlyTouCan
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
LM-GlycoRepo
Repository for lectin-assisted multimodality data
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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 | October 9, 2024 |
| Disease ID | Disease Name | Alliance of Genome Resources ID | Species | Gene ID | Gene Symbol | FlyGlycoDB | Evidence Code Names ▲ | References |
|---|---|---|---|---|---|---|---|---|
| DOID:1394 | urinary schistosomiasis | HGNC:2505 | Homo sapiens (human) | 1493 | CTLA4 |
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| DOID:1210 | optic neuritis | HGNC:4944 | Homo sapiens (human) | 3119 | HLA-DQB1 |
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| DOID:409 | liver disease | HGNC:6922 | Homo sapiens (human) | 4153 | MBL2 |
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| DOID:0111369 | hyperalphalipoproteinemia 1 | HGNC:1869 | Homo sapiens (human) | 1071 | CETP |
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| DOID:12132 | granulomatosis with polyangiitis | HGNC:5962 | Homo sapiens (human) | 3586 | IL10 |
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| DOID:0110015 | age related macular degeneration 2 | HGNC:34 | Homo sapiens (human) | 24 | ABCA4 |
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| DOID:0080108 | myoglobinuria | HGNC:8889 | Homo sapiens (human) | 5224 | PGAM2 |
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| DOID:0081003 | Cowden syndrome 7 | HGNC:10702 | Homo sapiens (human) | 10483 | SEC23B |
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| DOID:2841 | asthma | HGNC:5974 | Homo sapiens (human) | 3597 | IL13RA1 |
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| DOID:0080634 | nanophthalmos | HGNC:1181 | Homo sapiens (human) | 745 | MYRF |
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| DOID:12835 | quadriplegia | HGNC:6018 | Homo sapiens (human) | 3569 | IL6 |
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| DOID:12716 | newborn respiratory distress syndrome | HGNC:1516 | Homo sapiens (human) | 847 | CAT |
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| DOID:1612 | breast cancer | HGNC:4942 | Homo sapiens (human) | 3117 | HLA-DQA1 |
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| DOID:3459 | breast carcinoma | HGNC:1052 | Homo sapiens (human) | 274 | BIN1 |
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| DOID:332 | amyotrophic lateral sclerosis | HGNC:24537 | Homo sapiens (human) | 25978 | CHMP2B |
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| DOID:9952 | acute lymphoblastic leukemia | HGNC:6407 | Homo sapiens (human) | 3845 | KRAS |
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| DOID:10485 | esophageal atresia | HGNC:30858 | Homo sapiens (human) | 9343 | EFTUD2 |
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| DOID:0081210 | autosomal recessive intellectual developmental disorder 46 | HGNC:7680 | Homo sapiens (human) | 3340 | NDST1 |
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| DOID:11265 | trachoma | HGNC:4932 | Homo sapiens (human) | 3106 | HLA-B |
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| DOID:0050749 | peripheral T-cell lymphoma | HGNC:6119 | Homo sapiens (human) | 3662 | IRF4 |
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| DOID:12306 | vitiligo | HGNC:5438 | Homo sapiens (human) | 3458 | IFNG |
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| DOID:9256 | colorectal cancer | HGNC:16627 | Homo sapiens (human) | 11200 | CHEK2 |
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| DOID:1681 | heart septal defect | HGNC:14630 | Homo sapiens (human) | 78987 | CRELD1 |
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| DOID:11720 | distal myopathy | HGNC:15710 | Homo sapiens (human) | 11155 | LDB3 |
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| DOID:684 | hepatocellular carcinoma | HGNC:11119 | Homo sapiens (human) | 6608 | SMO |
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