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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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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:0060688 | arteriovenous malformations of the brain | HGNC:6018 | Homo sapiens (human) | 3569 | IL6 |
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| DOID:1909 | melanoma | HGNC:11850 | Homo sapiens (human) | 7099 | TLR4 |
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| DOID:8893 | psoriasis | HGNC:1248 | Homo sapiens (human) | 717 | C2 |
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| DOID:670 | amphetamine abuse | HGNC:4070 | Homo sapiens (human) | 2550 | GABBR1 |
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| DOID:9975 | cocaine dependence | HGNC:29944 | Homo sapiens (human) | 55714 | TENM3 |
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| DOID:12849 | autistic disorder | HGNC:4323 | Homo sapiens (human) | 2739 | GLO1 |
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| DOID:0050961 | spinocerebellar ataxia type 11 | HGNC:19141 | Homo sapiens (human) | 146057 | TTBK2 |
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| DOID:0080266 | primary ciliary dyskinesia 37 | HGNC:2940 | Homo sapiens (human) | 25981 | DNAH1 |
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| DOID:0110026 | age related macular degeneration 14 | HGNC:1248 | Homo sapiens (human) | 717 | C2 |
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| DOID:10887 | lepromatous leprosy | HGNC:4942 | Homo sapiens (human) | 3117 | HLA-DQA1 |
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| DOID:783 | end stage renal disease | HGNC:7173 | Homo sapiens (human) | 4314 | MMP3 |
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| DOID:0060826 | syndromic X-linked intellectual disability Shashi type | HGNC:9910 | Homo sapiens (human) | 27316 | RBMX |
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| DOID:12236 | primary biliary cholangitis | HGNC:4942 | Homo sapiens (human) | 3117 | HLA-DQA1 |
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| DOID:0111007 | X-linked cone-rod dystrophy 3 | HGNC:1393 | Homo sapiens (human) | 778 | CACNA1F |
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| DOID:0050741 | alcohol dependence | HGNC:250 | Homo sapiens (human) | 125 | ADH1B |
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| DOID:0070036 | autosomal dominant intellectual developmental disorder 6 | HGNC:4586 | Homo sapiens (human) | 2904 | GRIN2B |
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| DOID:5419 | schizophrenia | HGNC:320 | Homo sapiens (human) | 177 | AGER |
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| DOID:10534 | stomach cancer | HGNC:3437 | Homo sapiens (human) | 2073 | ERCC5 |
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| DOID:12849 | autistic disorder | HGNC:6486 | Homo sapiens (human) | 3912 | LAMB1 |
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| DOID:684 | hepatocellular carcinoma | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
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| DOID:9744 | type 1 diabetes mellitus | HGNC:10632 | Homo sapiens (human) | 6352 | CCL5 |
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| DOID:11204 | allergic conjunctivitis | HGNC:5318 | Homo sapiens (human) | 3371 | TNC |
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| DOID:2921 | glomerulonephritis | HGNC:3619 | Homo sapiens (human) | 2214 | FCGR3A |
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| DOID:9206 | Barrett's esophagus | HGNC:18831 | Homo sapiens (human) | 115908 | CTHRC1 |
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| DOID:0070395 | developmental and epileptic encephalopathy 110 | HGNC:1399 | Homo sapiens (human) | 781 | CACNA2D1 |
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