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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:1612 | breast cancer | HGNC:18541 | Homo sapiens (human) | 55904 | KMT2E |
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| DOID:526 | human immunodeficiency virus infectious disease | HGNC:18541 | Homo sapiens (human) | 55904 | KMT2E |
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| DOID:4362 | cervical cancer | HGNC:18541 | Homo sapiens (human) | 55904 | KMT2E |
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| DOID:12849 | autistic disorder | HGNC:18541 | Homo sapiens (human) | 55904 | KMT2E |
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| DOID:0060318 | acute promyelocytic leukemia | HGNC:18541 | Homo sapiens (human) | 55904 | KMT2E |
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| DOID:10283 | prostate cancer | HGNC:18541 | Homo sapiens (human) | 55904 | KMT2E |
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| DOID:0070283 | primary autosomal recessive microcephaly 13 | HGNC:1856 | Homo sapiens (human) | 1062 | CENPE |
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| DOID:0110595 | Stromme syndrome | HGNC:1857 | Homo sapiens (human) | 1063 | CENPF |
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| DOID:12930 | dilated cardiomyopathy | HGNC:1857 | Homo sapiens (human) | 1063 | CENPF |
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| DOID:1094 | attention deficit hyperactivity disorder | HGNC:18582 | Homo sapiens (human) | 23266 | ADGRL2 |
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| DOID:5082 | liver cirrhosis | HGNC:18590 | Homo sapiens (human) | 80339 | PNPLA3 |
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| DOID:0050729 | Chanarin-Dorfman syndrome | HGNC:18590 | Homo sapiens (human) | 80339 | PNPLA3 |
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| DOID:1459 | hypothyroidism | HGNC:18590 | Homo sapiens (human) | 80339 | PNPLA3 |
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| DOID:0080208 | metabolic dysfunction-associated steatotic liver disease | HGNC:18590 | Homo sapiens (human) | 80339 | PNPLA3 |
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| DOID:3393 | coronary artery disease | HGNC:18590 | Homo sapiens (human) | 80339 | PNPLA3 |
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| DOID:0060158 | acquired metabolic disease | HGNC:18590 | Homo sapiens (human) | 80339 | PNPLA3 |
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| DOID:9452 | steatotic liver disease | HGNC:18590 | Homo sapiens (human) | 80339 | PNPLA3 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:18590 | Homo sapiens (human) | 80339 | PNPLA3 |
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| DOID:9970 | obesity | HGNC:18590 | Homo sapiens (human) | 80339 | PNPLA3 |
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| DOID:684 | hepatocellular carcinoma | HGNC:18590 | Homo sapiens (human) | 80339 | PNPLA3 |
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| DOID:0060558 | lethal congenital contracture syndrome | HGNC:18591 | Homo sapiens (human) | 91754 | NEK9 |
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| DOID:0081378 | amyotrophic lateral sclerosis type 24 | HGNC:18591 | Homo sapiens (human) | 91754 | NEK9 |
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| DOID:0050741 | alcohol dependence | HGNC:18596 | Homo sapiens (human) | 91227 | GGTLC2 |
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| DOID:5022 | aflatoxins-related hepatocellular carcinoma | HGNC:18596 | Homo sapiens (human) | 91227 | GGTLC2 |
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| DOID:0081266 | pachygyria, microcephaly, developmental delay, and dysmorphic facies, with or without seizures | HGNC:18599 | Homo sapiens (human) | 10844 | TUBGCP2 |
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