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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:11054 | urinary bladder cancer | HGNC:16627 | Homo sapiens (human) | 11200 | CHEK2 |
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| DOID:4440 | seminoma | HGNC:16627 | Homo sapiens (human) | 11200 | CHEK2 |
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| DOID:0050671 | female breast cancer | HGNC:16627 | Homo sapiens (human) | 11200 | CHEK2 |
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| DOID:0111504 | Li-Fraumeni syndrome 2 | HGNC:16627 | Homo sapiens (human) | 11200 | CHEK2 |
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| DOID:1614 | male breast cancer | HGNC:16627 | Homo sapiens (human) | 11200 | CHEK2 |
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| DOID:1612 | breast cancer | HGNC:16627 | Homo sapiens (human) | 11200 | CHEK2 |
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| DOID:10283 | prostate cancer | HGNC:16627 | Homo sapiens (human) | 11200 | CHEK2 |
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| DOID:3308 | embryonal carcinoma | HGNC:16627 | Homo sapiens (human) | 11200 | CHEK2 |
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| DOID:1793 | pancreatic cancer | HGNC:1925 | Homo sapiens (human) | 1111 | CHEK1 |
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| DOID:1682 | congenital heart disease | HGNC:25701 | Homo sapiens (human) | 80205 | CHD9 |
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| DOID:0050834 | CHARGE syndrome | HGNC:25701 | Homo sapiens (human) | 80205 | CHD9 |
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| DOID:0060041 | autism spectrum disorder | HGNC:25701 | Homo sapiens (human) | 80205 | CHD9 |
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| DOID:1682 | congenital heart disease | HGNC:20153 | Homo sapiens (human) | 57680 | CHD8 |
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| DOID:0060041 | autism spectrum disorder | HGNC:20153 | Homo sapiens (human) | 57680 | CHD8 |
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| DOID:0050834 | CHARGE syndrome | HGNC:20153 | Homo sapiens (human) | 57680 | CHD8 |
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| DOID:0060041 | autism spectrum disorder | HGNC:20626 | Homo sapiens (human) | 55636 | CHD7 |
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| DOID:1682 | congenital heart disease | HGNC:20626 | Homo sapiens (human) | 55636 | CHD7 |
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| DOID:0050834 | CHARGE syndrome | HGNC:20626 | Homo sapiens (human) | 55636 | CHD7 |
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| DOID:0090084 | hypogonadotropic hypogonadism 5 with or without anosmia | HGNC:20626 | Homo sapiens (human) | 55636 | CHD7 |
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| DOID:1682 | congenital heart disease | HGNC:19057 | Homo sapiens (human) | 84181 | CHD6 |
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| DOID:0060041 | autism spectrum disorder | HGNC:19057 | Homo sapiens (human) | 84181 | CHD6 |
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| DOID:0050834 | CHARGE syndrome | HGNC:19057 | Homo sapiens (human) | 84181 | CHD6 |
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| DOID:684 | hepatocellular carcinoma | HGNC:16816 | Homo sapiens (human) | 26038 | CHD5 |
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| DOID:234 | colon adenocarcinoma | HGNC:1919 | Homo sapiens (human) | 1108 | CHD4 |
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| DOID:1993 | rectum cancer | HGNC:1919 | Homo sapiens (human) | 1108 | CHD4 |
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