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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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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:2841 | asthma | HGNC:9591 | Homo sapiens (human) | 5729 | PTGDR |
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| DOID:0060041 | autism spectrum disorder | HGNC:896 | Homo sapiens (human) | 553 | AVPR1B |
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| DOID:0070396 | progressive leukoencephalopathy with ovarian failure | HGNC:21022 | Homo sapiens (human) | 57505 | AARS2 |
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| DOID:0070269 | congenital disorder of glycosylation type IIq | HGNC:6546 | Homo sapiens (human) | 22796 | COG2 |
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| DOID:0060224 | atrial fibrillation | HGNC:333 | Homo sapiens (human) | 183 | AGT |
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| DOID:12241 | beta thalassemia | HGNC:4886 | Homo sapiens (human) | 3077 | HFE |
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| DOID:0112122 | X-linked epilepsy with variable learning disabilities and behavior disorders | HGNC:11494 | Homo sapiens (human) | 6853 | SYN1 |
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| DOID:1485 | cystic fibrosis | HGNC:7097 | Homo sapiens (human) | 4282 | MIF |
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| DOID:12217 | Lewy body dementia | HGNC:6367 | Homo sapiens (human) | 5653 | KLK6 |
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| DOID:0060308 | autosomal recessive intellectual developmental disorder | HGNC:18697 | Homo sapiens (human) | 10973 | ASCC3 |
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| DOID:5844 | myocardial infarction | HGNC:5962 | Homo sapiens (human) | 3586 | IL10 |
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| DOID:0050454 | periventricular nodular heterotopia | HGNC:6836 | Homo sapiens (human) | 4131 | MAP1B |
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| DOID:0060307 | autosomal dominant intellectual developmental disorder | HGNC:22474 | Homo sapiens (human) | 9969 | MED13 |
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| DOID:0110976 | brachydactyly type E2 | HGNC:9607 | Homo sapiens (human) | 5744 | PTHLH |
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| DOID:0080990 | King Denborough syndrome | HGNC:10483 | Homo sapiens (human) | 6261 | RYR1 |
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| DOID:3526 | cerebral infarction | HGNC:3535 | Homo sapiens (human) | 2147 | F2 |
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| DOID:2921 | glomerulonephritis | HGNC:20675 | Homo sapiens (human) | 84735 | CNDP1 |
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| DOID:1094 | attention deficit hyperactivity disorder | HGNC:12008 | Homo sapiens (human) | 7166 | TPH1 |
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| DOID:13359 | Ehlers-Danlos syndrome | HGNC:2201 | Homo sapiens (human) | 1281 | COL3A1 |
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| DOID:4483 | rhinitis | HGNC:10803 | Homo sapiens (human) | 6441 | SFTPD |
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| DOID:1697 | ichthyosis | HGNC:6439 | Homo sapiens (human) | 3849 | KRT2 |
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| DOID:9352 | type 2 diabetes mellitus | RGD:2289 | Rattus norvegicus (Norway rat) | 24889 | Cckar |
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| DOID:7148 | rheumatoid arthritis | HGNC:8156 | Homo sapiens (human) | 4988 | OPRM1 |
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| DOID:9970 | obesity | HGNC:10660 | Homo sapiens (human) | 9672 | SDC3 |
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| DOID:0050628 | advanced sleep phase syndrome | HGNC:8847 | Homo sapiens (human) | 8863 | PER3 |
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