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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
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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:0111389 | mucopolysaccharidosis Ih/s | HGNC:5391 | Homo sapiens (human) | 3425 | IDUA |
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| DOID:0080652 | calcium oxalate nephrolithiasis | HGNC:4531 | Homo sapiens (human) | 27199 | OXGR1 |
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| DOID:11612 | polycystic ovary syndrome | HGNC:1477 | Homo sapiens (human) | 11132 | CAPN10 |
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| DOID:2843 | long QT syndrome | HGNC:10593 | Homo sapiens (human) | 6331 | SCN5A |
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| DOID:10763 | hypertension | HGNC:263 | Homo sapiens (human) | 135 | ADORA2A |
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| DOID:0080179 | haemophilus meningitis | HGNC:3616 | Homo sapiens (human) | 2212 | FCGR2A |
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| DOID:0060788 | hypomyelinating leukodystrophy 10 | HGNC:30262 | Homo sapiens (human) | 29920 | PYCR2 |
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| DOID:0081213 | autosomal recessive intellectual developmental disorder 50 | HGNC:26114 | Homo sapiens (human) | 80153 | EDC3 |
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| DOID:0070296 | primary autosomal recessive microcephaly | HGNC:25604 | Homo sapiens (human) | 55262 | TRAPPC14 |
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| DOID:0090084 | hypogonadotropic hypogonadism 5 with or without anosmia | HGNC:20626 | Homo sapiens (human) | 55636 | CHD7 |
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| DOID:0110895 | inflammatory bowel disease 14 | HGNC:6120 | Homo sapiens (human) | 3663 | IRF5 |
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| DOID:0110026 | age related macular degeneration 14 | HGNC:1037 | Homo sapiens (human) | 629 | CFB |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:286 | Homo sapiens (human) | 154 | ADRB2 |
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| DOID:2394 | ovarian cancer | HGNC:7876 | Homo sapiens (human) | 4846 | NOS3 |
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| DOID:3672 | rhabdoid cancer | HGNC:11100 | Homo sapiens (human) | 6597 | SMARCA4 |
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| DOID:7693 | abdominal aortic aneurysm | HGNC:7468 | Homo sapiens (human) | 4548 | MTR |
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| DOID:14735 | hereditary angioedema | HGNC:9071 | Homo sapiens (human) | 5340 | PLG |
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| DOID:707 | B-cell lymphoma | HGNC:6006 | Homo sapiens (human) | 50615 | IL21R |
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| DOID:1926 | Gaucher's disease | HGNC:9020 | Homo sapiens (human) | 5313 | PKLR |
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| DOID:8398 | osteoarthritis | HGNC:1663 | Homo sapiens (human) | 948 | CD36 |
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| DOID:3393 | coronary artery disease | HGNC:7876 | Homo sapiens (human) | 4846 | NOS3 |
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| DOID:6713 | cerebrovascular disease | HGNC:336 | Homo sapiens (human) | 185 | AGTR1 |
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| DOID:0111257 | gamma-glutamyl transpeptidase deficiency | HGNC:4250 | Homo sapiens (human) | 2678 | GGT1 |
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| DOID:0060335 | autosomal dominant sideroblastic anemia 4 | HGNC:5244 | Homo sapiens (human) | 3313 | HSPA9 |
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| DOID:2216 | factor V deficiency | HGNC:3542 | Homo sapiens (human) | 2153 | F5 |
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