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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
LM-GlycoRepo
Repository for lectin-assisted multimodality data
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MIRAGE
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:936 | brain disease | HGNC:15594 | Homo sapiens (human) | 51163 | DBR1 |
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| DOID:557 | kidney disease | HGNC:15583 | Homo sapiens (human) | 197021 | LCTL |
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| DOID:1793 | pancreatic cancer | HGNC:15582 | Homo sapiens (human) | 94025 | MUC16 |
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| DOID:4947 | cholangiocarcinoma | HGNC:15582 | Homo sapiens (human) | 94025 | MUC16 |
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| DOID:10140 | dry eye syndrome | HGNC:15582 | Homo sapiens (human) | 94025 | MUC16 |
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| DOID:2394 | ovarian cancer | HGNC:15582 | Homo sapiens (human) | 94025 | MUC16 |
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| DOID:12894 | Sjogren's syndrome | HGNC:15582 | Homo sapiens (human) | 94025 | MUC16 |
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| DOID:9368 | keratoconjunctivitis | HGNC:15582 | Homo sapiens (human) | 94025 | MUC16 |
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| DOID:4001 | ovarian carcinoma | HGNC:15582 | Homo sapiens (human) | 94025 | MUC16 |
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| DOID:0110734 | neurodegeneration with brain iron accumulation | HGNC:15578 | Homo sapiens (human) | 85021 | REPS1 |
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| DOID:1612 | breast cancer | HGNC:15574 | Homo sapiens (human) | 9821 | RB1CC1 |
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| DOID:0070509 | Schinzel Giedion syndrome | HGNC:15573 | Homo sapiens (human) | 26040 | SETBP1 |
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| DOID:0070059 | autosomal dominant intellectual developmental disorder 29 | HGNC:15573 | Homo sapiens (human) | 26040 | SETBP1 |
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| DOID:12336 | male infertility | HGNC:15569 | Homo sapiens (human) | 26256 | CABYR |
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| DOID:0080010 | bone structure disease | HGNC:15565 | Homo sapiens (human) | 84109 | QRFPR |
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| DOID:3910 | lung adenocarcinoma | HGNC:1555 | Homo sapiens (human) | 23468 | CBX5 |
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| DOID:10283 | prostate cancer | HGNC:1555 | Homo sapiens (human) | 23468 | CBX5 |
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| DOID:162 | cancer | HGNC:1554 | Homo sapiens (human) | 8535 | CBX4 |
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| DOID:684 | hepatocellular carcinoma | HGNC:1554 | Homo sapiens (human) | 8535 | CBX4 |
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| DOID:0060340 | ciliopathy | HGNC:15534 | Homo sapiens (human) | 83659 | TEKT1 |
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| DOID:11446 | sciatic neuropathy | HGNC:15532 | Homo sapiens (human) | 83700 | JAM3 |
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| DOID:418 | systemic scleroderma | HGNC:15532 | Homo sapiens (human) | 83700 | JAM3 |
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| DOID:0060041 | autism spectrum disorder | HGNC:15529 | Homo sapiens (human) | 22829 | NLGN4Y |
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| DOID:557 | kidney disease | HGNC:15527 | Homo sapiens (human) | 152831 | KLB |
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| DOID:0110705 | hypotrichosis 8 | HGNC:15520 | Homo sapiens (human) | 10161 | LPAR6 |
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