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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:11198 | DiGeorge syndrome | HGNC:16817 | Homo sapiens (human) | 8220 | ESS2 |
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| DOID:0060041 | autism spectrum disorder | HGNC:11496 | Homo sapiens (human) | 8224 | SYN3 |
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| DOID:10230 | aortic atherosclerosis | HGNC:1476 | Homo sapiens (human) | 823 | CAPN1 |
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| DOID:11723 | Duchenne muscular dystrophy | HGNC:1476 | Homo sapiens (human) | 823 | CAPN1 |
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| DOID:10652 | Alzheimer's disease | HGNC:1476 | Homo sapiens (human) | 823 | CAPN1 |
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| DOID:1826 | epilepsy | HGNC:1476 | Homo sapiens (human) | 823 | CAPN1 |
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| DOID:11446 | sciatic neuropathy | HGNC:1476 | Homo sapiens (human) | 823 | CAPN1 |
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| DOID:2476 | hereditary spastic paraplegia | HGNC:1476 | Homo sapiens (human) | 823 | CAPN1 |
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| DOID:3021 | acute kidney failure | HGNC:1476 | Homo sapiens (human) | 823 | CAPN1 |
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| DOID:0110821 | hereditary spastic paraplegia 76 | HGNC:1476 | Homo sapiens (human) | 823 | CAPN1 |
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| DOID:0081292 | traumatic brain injury | HGNC:1476 | Homo sapiens (human) | 823 | CAPN1 |
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| DOID:0050908 | myelodysplastic syndrome | HGNC:23019 | Homo sapiens (human) | 8233 | ZRSR2 |
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| DOID:9119 | acute myeloid leukemia | HGNC:23019 | Homo sapiens (human) | 8233 | ZRSR2 |
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| DOID:0112025 | female-restricted syndromic X-linked intellectual disability 99 | HGNC:12632 | Homo sapiens (human) | 8239 | USP9X |
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| DOID:0112026 | non-syndromic X-linked intellectual disability 99 | HGNC:12632 | Homo sapiens (human) | 8239 | USP9X |
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| DOID:1324 | lung cancer | HGNC:9896 | Homo sapiens (human) | 8241 | RBM10 |
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| DOID:0111780 | TARP syndrome | HGNC:9896 | Homo sapiens (human) | 8241 | RBM10 |
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| DOID:9256 | colorectal cancer | HGNC:9896 | Homo sapiens (human) | 8241 | RBM10 |
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| DOID:3910 | lung adenocarcinoma | HGNC:9896 | Homo sapiens (human) | 8241 | RBM10 |
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| DOID:684 | hepatocellular carcinoma | HGNC:9896 | Homo sapiens (human) | 8241 | RBM10 |
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| DOID:6000 | congestive heart failure | HGNC:9896 | Homo sapiens (human) | 8241 | RBM10 |
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| DOID:0070380 | developmental and epileptic encephalopathy 85 | HGNC:11111 | Homo sapiens (human) | 8243 | SMC1A |
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| DOID:11725 | Cornelia de Lange syndrome | HGNC:11111 | Homo sapiens (human) | 8243 | SMC1A |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:11111 | Homo sapiens (human) | 8243 | SMC1A |
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| DOID:0080506 | Cornelia de Lange syndrome 2 | HGNC:11111 | Homo sapiens (human) | 8243 | SMC1A |
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