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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
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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 | July 29, 2024 |
| Disease ID | Disease Name | Alliance of Genome Resources ID | Species ▼ | Gene ID | Gene Symbol | FlyGlycoDB | Evidence Code Names | References |
|---|---|---|---|---|---|---|---|---|
| DOID:2723 | dermatitis | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:11054 | urinary bladder cancer | HGNC:2595 | Homo sapiens (human) | 1543 | CYP1A1 |
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| DOID:0110721 | neuronal ceroid lipofuscinosis 1 | HGNC:9325 | Homo sapiens (human) | 5538 | PPT1 |
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| DOID:11612 | polycystic ovary syndrome | HGNC:5218 | Homo sapiens (human) | 3284 | HSD3B2 |
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| DOID:0080565 | congenital disorder of glycosylation Im | HGNC:23406 | Homo sapiens (human) | 22845 | DOLK |
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| DOID:206 | hereditary multiple exostoses | HGNC:3518 | Homo sapiens (human) | 2137 | EXTL3 |
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| DOID:2799 | bronchiolitis obliterans | HGNC:10803 | Homo sapiens (human) | 6441 | SFTPD |
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| DOID:1793 | pancreatic cancer | HGNC:920 | Homo sapiens (human) | 10317 | B3GALT5 |
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| DOID:9452 | steatotic liver disease | HGNC:6563 | Homo sapiens (human) | 3958 | LGALS3 |
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| DOID:4948 | gallbladder carcinoma | HGNC:4555 | Homo sapiens (human) | 2878 | GPX3 |
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| DOID:0060643 | primary sclerosing cholangitis | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:1391 | Norum disease | HGNC:6522 | Homo sapiens (human) | 3931 | LCAT |
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| DOID:9253 | gastrointestinal stromal tumor | HGNC:10682 | Homo sapiens (human) | 6391 | SDHC |
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| DOID:10652 | Alzheimer's disease | HGNC:4341 | Homo sapiens (human) | 2752 | GLUL |
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| DOID:11054 | urinary bladder cancer | HGNC:2597 | Homo sapiens (human) | 1545 | CYP1B1 |
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| DOID:1574 | alcohol use disorder | HGNC:8977 | Homo sapiens (human) | 5293 | PIK3CD |
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| DOID:0070269 | congenital disorder of glycosylation type IIq | HGNC:6546 | Homo sapiens (human) | 22796 | COG2 |
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| DOID:0080208 | metabolic dysfunction-associated steatotic liver disease | HGNC:13633 | Homo sapiens (human) | 9370 | ADIPOQ |
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| DOID:7575 | pancreatic intraductal papillary-mucinous neoplasm | HGNC:11998 | Homo sapiens (human) | 7157 | TP53 |
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| DOID:83 | cataract | HGNC:1516 | Homo sapiens (human) | 847 | CAT |
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| DOID:11446 | sciatic neuropathy | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:0050570 | congenital disorder of glycosylation type I | HGNC:9115 | Homo sapiens (human) | 5373 | PMM2 |
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| DOID:0080568 | congenital disorder of glycosylation Iq | HGNC:25812 | Homo sapiens (human) | 79644 | SRD5A3 |
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| DOID:409 | liver disease | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:2671 | transitional cell carcinoma | HGNC:11026 | Homo sapiens (human) | 6520 | SLC3A2 |
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