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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:0050694 | Brown-Vialetto-Van Laere syndrome | HGNC:30225 | Homo sapiens (human) | 55065 | SLC52A1 |
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| DOID:6000 | congestive heart failure | WB:WBGene00000903 | Caenorhabditis elegans | 175237 | daf-7 |
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| DOID:0111140 | IGSF1 deficiency syndrome | MGI:2147913 | Mus musculus (house mouse) | 209268 | Igsf1 |
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| DOID:0110539 | autosomal recessive nonsyndromic deafness 97 | MGI:96969 | Mus musculus (house mouse) | 17295 | Met |
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| DOID:8778 | Crohn's disease | HGNC:6018 | Homo sapiens (human) | 3569 | IL6 |
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| DOID:893 | Wilson disease | HGNC:11120 | Homo sapiens (human) | 6609 | SMPD1 |
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| DOID:5082 | liver cirrhosis | HGNC:6371 | Homo sapiens (human) | 3818 | KLKB1 |
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| DOID:589 | congenital hemolytic anemia | SGD:S000006012 | Saccharomyces cerevisiae S288C | 856014 | GLR1 |
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| DOID:0050891 | adrenal cortical adenoma | HGNC:2592 | Homo sapiens (human) | 1585 | CYP11B2 |
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| DOID:2876 | laryngeal squamous cell carcinoma | MGI:97009 | Mus musculus (house mouse) | 17390 | Mmp2 |
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| DOID:769 | neuroblastoma | MGI:103305 | Mus musculus (house mouse) | 11682 | Alk |
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| DOID:12205 | dengue disease | HGNC:4187 | Homo sapiens (human) | 2638 | GC |
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| DOID:3393 | coronary artery disease | MGI:103181 | Mus musculus (house mouse) | 20657 | Sod3 |
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| DOID:1574 | alcohol use disorder | MGI:95819 | Mus musculus (house mouse) | 14810 | Grin1 |
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| DOID:11199 | hypoparathyroidism | HGNC:11582 | Homo sapiens (human) | 6905 | TBCE |
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| DOID:6000 | congestive heart failure | MGI:96673 | Mus musculus (house mouse) | 16509 | Kcne1 |
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| DOID:10763 | hypertension | Xenbase:XB-GENE-6251686 | Xenopus laevis (African clawed frog) | 734211 | epor.L |
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| DOID:557 | kidney disease | HGNC:11290 | Homo sapiens (human) | 6721 | SREBF2 |
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| DOID:1289 | neurodegenerative disease | HGNC:7795 | Homo sapiens (human) | 4791 | NFKB2 |
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| DOID:9744 | type 1 diabetes mellitus | HGNC:600 | Homo sapiens (human) | 335 | APOA1 |
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| DOID:0050073 | invasive aspergillosis | HGNC:11850 | Homo sapiens (human) | 7099 | TLR4 |
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| DOID:10933 | obsessive-compulsive disorder | MGI:88470 | Mus musculus (house mouse) | 12846 | Comt |
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| DOID:8552 | chronic myeloid leukemia | HGNC:10885 | Homo sapiens (human) | 6494 | SIPA1 |
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| DOID:5520 | head and neck squamous cell carcinoma | WB:WBGene00017381 | Caenorhabditis elegans | 180622 | ddr-2 |
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| DOID:4441 | dysgerminoma | RGD:70964 | Rattus norvegicus (Norway rat) | 29530 | Amhr2 |
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