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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:93 | language disorder | HGNC:13875 | Homo sapiens (human) | 93986 | FOXP2 |
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| DOID:0110265 | cataract 31 multiple types | HGNC:16171 | Homo sapiens (human) | 128866 | CHMP4B |
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| DOID:6364 | migraine | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:104 | bacterial infectious disease | HGNC:4948 | Homo sapiens (human) | 3123 | HLA-DRB1 |
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| DOID:0111994 | immunodeficiency 45 | HGNC:5433 | Homo sapiens (human) | 3455 | IFNAR2 |
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| DOID:0081124 | craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development syndrome 1 | HGNC:18188 | Homo sapiens (human) | 54499 | TMCO1 |
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| DOID:2237 | hepatitis | HGNC:79 | Homo sapiens (human) | 28 | ABO |
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| DOID:9182 | pemphigus | HGNC:4944 | Homo sapiens (human) | 3119 | HLA-DQB1 |
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| DOID:12361 | Graves' disease | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:0060574 | von Willebrand's disease 2 | HGNC:6138 | Homo sapiens (human) | 3674 | ITGA2B |
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| DOID:5295 | intestinal disease | HGNC:5331 | Homo sapiens (human) | 64127 | NOD2 |
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| DOID:1171 | hyperlipoproteinemia type V | HGNC:17288 | Homo sapiens (human) | 116519 | APOA5 |
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| DOID:0050741 | alcohol dependence | HGNC:701 | Homo sapiens (human) | 406 | BMAL1 |
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| DOID:0060108 | brain glioma | HGNC:12828 | Homo sapiens (human) | 7515 | XRCC1 |
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| DOID:10584 | retinitis pigmentosa | HGNC:23302 | Homo sapiens (human) | 80201 | HKDC1 |
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| DOID:2366 | West Nile fever | HGNC:9969 | Homo sapiens (human) | 5981 | RFC1 |
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| DOID:1273 | respiratory syncytial virus infectious disease | HGNC:10802 | Homo sapiens (human) | 6440 | SFTPC |
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| DOID:0070028 | APP-related cerebral amyloid angiopathy | HGNC:620 | Homo sapiens (human) | 351 | APP |
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| DOID:0070461 | mitochondrial complex V (ATP synthase) deficiency nuclear type 4A | HGNC:823 | Homo sapiens (human) | 498 | ATP5F1A |
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| DOID:14018 | alcoholic liver cirrhosis | HGNC:404 | Homo sapiens (human) | 217 | ALDH2 |
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| DOID:0080872 | primary ovarian insufficiency 15 | HGNC:23168 | Homo sapiens (human) | 57697 | FANCM |
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| DOID:289 | endometriosis | HGNC:4948 | Homo sapiens (human) | 3123 | HLA-DRB1 |
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| DOID:1793 | pancreatic cancer | HGNC:10473 | Homo sapiens (human) | 864 | RUNX3 |
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| DOID:2957 | pulmonary tuberculosis | HGNC:435 | Homo sapiens (human) | 240 | ALOX5 |
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| DOID:0112381 | muscular dystrophy-dystroglycanopathy type C12 | HGNC:26267 | Homo sapiens (human) | 84197 | POMK |
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