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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:7147 | ankylosing spondylitis | HGNC:14872 | Homo sapiens (human) | 54829 | ASPN |
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| DOID:3070 | high grade glioma | HGNC:19048 | Homo sapiens (human) | 259266 | ASPM |
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| DOID:3068 | glioblastoma | HGNC:19048 | Homo sapiens (human) | 259266 | ASPM |
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| DOID:10534 | stomach cancer | HGNC:19048 | Homo sapiens (human) | 259266 | ASPM |
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| DOID:0070296 | primary autosomal recessive microcephaly | HGNC:19048 | Homo sapiens (human) | 259266 | ASPM |
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| DOID:0070280 | primary autosomal recessive microcephaly 5 | HGNC:19048 | Homo sapiens (human) | 259266 | ASPM |
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| DOID:10907 | microcephaly | HGNC:19048 | Homo sapiens (human) | 259266 | ASPM |
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| DOID:11832 | visual epilepsy | HGNC:19048 | Homo sapiens (human) | 259266 | ASPM |
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| DOID:2152 | ovary epithelial cancer | HGNC:19048 | Homo sapiens (human) | 259266 | ASPM |
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| DOID:684 | hepatocellular carcinoma | HGNC:19048 | Homo sapiens (human) | 259266 | ASPM |
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| DOID:4947 | cholangiocarcinoma | HGNC:757 | Homo sapiens (human) | 444 | ASPH |
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| DOID:0070515 | chromosome 16p11.2 deletion syndrome, 593-kb | HGNC:757 | Homo sapiens (human) | 444 | ASPH |
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| DOID:9970 | obesity | HGNC:745 | Homo sapiens (human) | 434 | ASIP |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:745 | Homo sapiens (human) | 434 | ASIP |
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| DOID:10123 | pigmentation disease | HGNC:745 | Homo sapiens (human) | 434 | ASIP |
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| DOID:5419 | schizophrenia | HGNC:744 | Homo sapiens (human) | 9070 | ASH2L |
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| DOID:0060037 | developmental disorder of mental health | HGNC:19088 | Homo sapiens (human) | 55870 | ASH1L |
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| DOID:0080231 | autosomal dominant intellectual developmental disorder 52 | HGNC:19088 | Homo sapiens (human) | 55870 | ASH1L |
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| DOID:1240 | leukemia | HGNC:19088 | Homo sapiens (human) | 55870 | ASH1L |
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| DOID:0060041 | autism spectrum disorder | HGNC:19088 | Homo sapiens (human) | 55870 | ASH1L |
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| DOID:0060308 | autosomal recessive intellectual developmental disorder | HGNC:18697 | Homo sapiens (human) | 10973 | ASCC3 |
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| DOID:0050700 | cardiomyopathy | HGNC:18860 | Homo sapiens (human) | 56624 | ASAH2 |
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| DOID:0111527 | spinal muscular atrophy with progressive myoclonic epilepsy | HGNC:735 | Homo sapiens (human) | 427 | ASAH1 |
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| DOID:0050464 | Farber lipogranulomatosis | HGNC:735 | Homo sapiens (human) | 427 | ASAH1 |
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| DOID:1927 | sphingolipidosis | HGNC:735 | Homo sapiens (human) | 427 | ASAH1 |
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