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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:9256 | colorectal cancer | HGNC:2701 | Homo sapiens (human) | 1630 | DCC |
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| DOID:0111797 | autosomal recessive congenital nystagmus | HGNC:10249 | Homo sapiens (human) | 6091 | ROBO1 |
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| DOID:9351 | diabetes mellitus | HGNC:2592 | Homo sapiens (human) | 1585 | CYP11B2 |
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| DOID:0111651 | ectodermal dysplasia 15 | HGNC:2478 | Homo sapiens (human) | 1474 | CST6 |
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| DOID:612 | primary immunodeficiency disease | HGNC:6598 | Homo sapiens (human) | 3978 | LIG1 |
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| DOID:0080386 | nephrotic syndrome type 10 | HGNC:3334 | Homo sapiens (human) | 2013 | EMP2 |
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| DOID:0111581 | C syndrome | HGNC:16892 | Homo sapiens (human) | 10225 | CD96 |
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| DOID:0080109 | infantile myofibromatosis | HGNC:7883 | Homo sapiens (human) | 4854 | NOTCH3 |
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| DOID:0060001 | withdrawal disorder | HGNC:8153 | Homo sapiens (human) | 4985 | OPRD1 |
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| DOID:7693 | abdominal aortic aneurysm | HGNC:3788 | Homo sapiens (human) | 2346 | FOLH1 |
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| DOID:0111698 | proprotein convertase 1/3 deficiency | HGNC:8743 | Homo sapiens (human) | 5122 | PCSK1 |
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| DOID:0080630 | B-lymphoblastic leukemia/lymphoma | HGNC:13176 | Homo sapiens (human) | 10320 | IKZF1 |
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| DOID:12549 | hepatitis A | HGNC:12828 | Homo sapiens (human) | 7515 | XRCC1 |
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| DOID:12678 | hypercalcemia | HGNC:2602 | Homo sapiens (human) | 1591 | CYP24A1 |
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| DOID:2841 | asthma | HGNC:4942 | Homo sapiens (human) | 3117 | HLA-DQA1 |
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| DOID:0060224 | atrial fibrillation | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
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| DOID:1148 | polydactyly | HGNC:4319 | Homo sapiens (human) | 2737 | GLI3 |
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| DOID:50 | thyroid gland disease | HGNC:30972 | Homo sapiens (human) | 79048 | SECISBP2 |
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| DOID:12365 | malaria | HGNC:4703 | Homo sapiens (human) | 2994 | GYPB |
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| DOID:219 | colon cancer | HGNC:6876 | Homo sapiens (human) | 1432 | MAPK14 |
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| DOID:0080820 | occupational asthma | HGNC:4940 | Homo sapiens (human) | 3115 | HLA-DPB1 |
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| DOID:7693 | abdominal aortic aneurysm | HGNC:10937 | Homo sapiens (human) | 6573 | SLC19A1 |
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| DOID:4440 | seminoma | HGNC:6342 | Homo sapiens (human) | 3815 | KIT |
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| DOID:526 | human immunodeficiency virus infectious disease | HGNC:4944 | Homo sapiens (human) | 3119 | HLA-DQB1 |
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| DOID:0050571 | congenital disorder of glycosylation type II | HGNC:18305 | Homo sapiens (human) | 10159 | ATP6AP2 |
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