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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
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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:3393 | coronary artery disease | HGNC:6709 | Homo sapiens (human) | 4049 | LTA |
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| DOID:11476 | osteoporosis | HGNC:2593 | Homo sapiens (human) | 1586 | CYP17A1 |
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| DOID:3310 | atopic dermatitis | HGNC:11766 | Homo sapiens (human) | 7040 | TGFB1 |
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| DOID:1024 | leprosy | HGNC:4948 | Homo sapiens (human) | 3123 | HLA-DRB1 |
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| DOID:12449 | aplastic anemia | HGNC:11795 | Homo sapiens (human) | 7066 | THPO |
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| DOID:7147 | ankylosing spondylitis | HGNC:9596 | Homo sapiens (human) | 5734 | PTGER4 |
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| DOID:0112377 | muscular dystrophy-dystroglycanopathy type B14 | HGNC:22932 | Homo sapiens (human) | 29925 | GMPPB |
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| DOID:10763 | hypertension | HGNC:6145 | Homo sapiens (human) | 3680 | ITGA9 |
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| DOID:0050477 | Liddle syndrome | HGNC:10602 | Homo sapiens (human) | 6340 | SCNN1G |
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| DOID:4914 | esophagus adenocarcinoma | HGNC:7876 | Homo sapiens (human) | 4846 | NOS3 |
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| DOID:5844 | myocardial infarction | HGNC:7943 | Homo sapiens (human) | 4881 | NPR1 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:11936 | Homo sapiens (human) | 356 | FASLG |
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| DOID:526 | human immunodeficiency virus infectious disease | HGNC:6338 | Homo sapiens (human) | 3811 | KIR3DL1 |
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| DOID:9975 | cocaine dependence | HGNC:29349 | Homo sapiens (human) | 401145 | CCSER1 |
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| DOID:0080055 | achondrogenesis type IB | HGNC:10994 | Homo sapiens (human) | 1836 | SLC26A2 |
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| DOID:1094 | attention deficit hyperactivity disorder | HGNC:4600 | Homo sapiens (human) | 2918 | GRM8 |
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| DOID:0111683 | neurofibromatosis-Noonan syndrome | HGNC:7765 | Homo sapiens (human) | 4763 | NF1 |
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| DOID:341 | peripheral vascular disease | HGNC:4886 | Homo sapiens (human) | 3077 | HFE |
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| DOID:870 | neuropathy | HGNC:2545 | Homo sapiens (human) | 1520 | CTSS |
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| DOID:0110557 | autosomal dominant nonsyndromic deafness 28 | HGNC:2799 | Homo sapiens (human) | 79977 | GRHL2 |
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| DOID:0080448 | developmental and epileptic encephalopathy 48 | HGNC:567 | Homo sapiens (human) | 8120 | AP3B2 |
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| DOID:9952 | acute lymphoblastic leukemia | HGNC:13176 | Homo sapiens (human) | 10320 | IKZF1 |
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| DOID:1059 | intellectual disability | HGNC:24502 | Homo sapiens (human) | 284403 | WDR62 |
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| DOID:10763 | hypertension | HGNC:14540 | Homo sapiens (human) | 65125 | WNK1 |
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| DOID:8691 | mycosis fungoides | HGNC:4944 | Homo sapiens (human) | 3119 | HLA-DQB1 |
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