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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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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:9296 | cleft lip | HGNC:3688 | Homo sapiens (human) | 2260 | FGFR1 |
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| DOID:1380 | endometrial cancer | HGNC:7329 | Homo sapiens (human) | 2956 | MSH6 |
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| DOID:2377 | multiple sclerosis | HGNC:4947 | Homo sapiens (human) | 3122 | HLA-DRA |
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| DOID:10763 | hypertension | HGNC:7468 | Homo sapiens (human) | 4548 | MTR |
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| DOID:10652 | Alzheimer's disease | HGNC:3146 | Homo sapiens (human) | 1889 | ECE1 |
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| DOID:0110032 | autosomal dominant Alport syndrome | HGNC:2204 | Homo sapiens (human) | 1285 | COL4A3 |
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| DOID:1485 | cystic fibrosis | HGNC:9692 | Homo sapiens (human) | 5806 | PTX3 |
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| DOID:0112202 | developmental and epileptic encephalopathy | HGNC:20566 | Homo sapiens (human) | 9900 | SV2A |
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| DOID:0081217 | autosomal recessive intellectual developmental disorder 56 | HGNC:20509 | Homo sapiens (human) | 79882 | ZC3H14 |
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| DOID:4247 | coronary restenosis | HGNC:6922 | Homo sapiens (human) | 4153 | MBL2 |
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| DOID:2978 | carbohydrate metabolic disorder | HGNC:93 | Homo sapiens (human) | 38 | ACAT1 |
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| DOID:10908 | hydrocephalus | HGNC:19967 | Homo sapiens (human) | 440193 | CCDC88C |
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| DOID:0070070 | autosomal dominant intellectual developmental disorder 40 | HGNC:20311 | Homo sapiens (human) | 283489 | CHAMP1 |
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| DOID:3910 | lung adenocarcinoma | HGNC:6693 | Homo sapiens (human) | 53353 | LRP1B |
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| DOID:0080071 | mucolipidosis III alpha/beta | HGNC:29670 | Homo sapiens (human) | 79158 | GNPTAB |
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| DOID:0080584 | autosomal dominant Wolfram syndrome | HGNC:12762 | Homo sapiens (human) | 7466 | WFS1 |
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| DOID:0111783 | otopalatodigital syndrome type 1 | HGNC:3754 | Homo sapiens (human) | 2316 | FLNA |
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| DOID:0050873 | follicular lymphoma | HGNC:4021 | Homo sapiens (human) | 2531 | KDSR |
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| DOID:9119 | acute myeloid leukemia | HGNC:16496 | Homo sapiens (human) | 23305 | ACSL6 |
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| DOID:437 | myasthenia gravis | HGNC:4944 | Homo sapiens (human) | 3119 | HLA-DQB1 |
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| DOID:7148 | rheumatoid arthritis | HGNC:10907 | Homo sapiens (human) | 6556 | SLC11A1 |
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| DOID:0080822 | aspirin-induced respiratory disease | HGNC:4951 | Homo sapiens (human) | 3125 | HLA-DRB3 |
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| DOID:0060174 | GABA aminotransferase deficiency | HGNC:23 | Homo sapiens (human) | 18 | ABAT |
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| DOID:0112250 | Gaucher's disease type IIIC | HGNC:4177 | Homo sapiens (human) | 2629 | GBA1 |
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| DOID:1612 | breast cancer | HGNC:587 | Homo sapiens (human) | 328 | APEX1 |
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