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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:2349 | arteriosclerosis | HGNC:6137 | Homo sapiens (human) | 3673 | ITGA2 |
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| DOID:5419 | schizophrenia | HGNC:1951 | Homo sapiens (human) | 1129 | CHRM2 |
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| DOID:1192 | peripheral nervous system neoplasm | HGNC:9588 | Homo sapiens (human) | 5728 | PTEN |
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| DOID:2986 | IgA glomerulonephritis | HGNC:4944 | Homo sapiens (human) | 3119 | HLA-DQB1 |
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| DOID:3393 | coronary artery disease | HGNC:11178 | Homo sapiens (human) | 8435 | SOAT2 |
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| DOID:0111122 | nephronophthisis 14 | HGNC:16762 | Homo sapiens (human) | 23090 | ZNF423 |
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| DOID:0110019 | age related macular degeneration 7 | HGNC:1318 | Homo sapiens (human) | 718 | C3 |
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| DOID:13241 | Behcet's disease | HGNC:4944 | Homo sapiens (human) | 3119 | HLA-DQB1 |
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| DOID:0110465 | autosomal recessive nonsyndromic deafness 104 | HGNC:13872 | Homo sapiens (human) | 9750 | RIPOR2 |
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| DOID:0050580 | hereditary lymphedema | HGNC:485 | Homo sapiens (human) | 285 | ANGPT2 |
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| DOID:0080615 | nephroma | HGNC:17098 | Homo sapiens (human) | 23405 | DICER1 |
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| DOID:11934 | head and neck cancer | HGNC:17071 | Homo sapiens (human) | 23081 | KDM4C |
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| DOID:0112198 | spondyloepimetaphyseal dysplasia with joint laxity type 1 | HGNC:17978 | Homo sapiens (human) | 126792 | B3GALT6 |
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| DOID:583 | hemolytic anemia | HGNC:4311 | Homo sapiens (human) | 2729 | GCLC |
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| DOID:0111865 | MEND syndrome | HGNC:3133 | Homo sapiens (human) | 10682 | EBP |
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| DOID:0081151 | common variable immunodeficiency 8 | HGNC:1742 | Homo sapiens (human) | 987 | LRBA |
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| DOID:0080455 | developmental and epileptic encephalopathy 52 | HGNC:10586 | Homo sapiens (human) | 6324 | SCN1B |
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| DOID:14069 | cerebral malaria | HGNC:13557 | Homo sapiens (human) | 59272 | ACE2 |
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| DOID:783 | end stage renal disease | HGNC:3023 | Homo sapiens (human) | 1813 | DRD2 |
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| DOID:10652 | Alzheimer's disease | HGNC:6619 | Homo sapiens (human) | 3990 | LIPC |
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| DOID:2978 | carbohydrate metabolic disorder | HGNC:11559 | Homo sapiens (human) | 6888 | TALDO1 |
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| DOID:182 | calcinosis | HGNC:4553 | Homo sapiens (human) | 2876 | GPX1 |
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| DOID:612 | primary immunodeficiency disease | HGNC:12016 | Homo sapiens (human) | 7174 | TPP2 |
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| DOID:4677 | keratitis | HGNC:6018 | Homo sapiens (human) | 3569 | IL6 |
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| DOID:0060019 | coronin-1A deficiency | HGNC:2252 | Homo sapiens (human) | 11151 | CORO1A |
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