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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:0112148 | Uruguay faciocardiomusculoskeletal syndrome | HGNC:3702 | Homo sapiens (human) | 2273 | FHL1 |
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| DOID:1596 | depressive disorder | HGNC:7809 | Homo sapiens (human) | 4804 | NGFR |
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| DOID:1686 | glaucoma | HGNC:3800 | Homo sapiens (human) | 2296 | FOXC1 |
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| DOID:9074 | systemic lupus erythematosus | HGNC:11919 | Homo sapiens (human) | 958 | CD40 |
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| DOID:0112295 | spondylometaphyseal dysplasia | HGNC:124 | Homo sapiens (human) | 54 | ACP5 |
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| DOID:8552 | chronic myeloid leukemia | HGNC:4944 | Homo sapiens (human) | 3119 | HLA-DQB1 |
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| DOID:3905 | lung carcinoma | HGNC:1957 | Homo sapiens (human) | 1136 | CHRNA3 |
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| DOID:0050968 | autosomal dominant cerebellar ataxia, deafness and narcolepsy | HGNC:2976 | Homo sapiens (human) | 1786 | DNMT1 |
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| DOID:3525 | middle cerebral artery infarction | RGD:2283 | Rattus norvegicus (Norway rat) | 50662 | Runx1 |
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| DOID:5082 | liver cirrhosis | HGNC:11050 | Homo sapiens (human) | 6532 | SLC6A4 |
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| DOID:0060175 | succinic semialdehyde dehydrogenase deficiency | HGNC:408 | Homo sapiens (human) | 7915 | ALDH5A1 |
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| DOID:0111480 | combined oxidative phosphorylation deficiency 10 | HGNC:19261 | Homo sapiens (human) | 25821 | MTO1 |
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| DOID:0111758 | Y-linked deafness 2 | HGNC:18502 | Homo sapiens (human) | 90665 | TBL1Y |
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| DOID:9663 | aphthous stomatitis | HGNC:4886 | Homo sapiens (human) | 3077 | HFE |
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| DOID:0081154 | common variable immunodeficiency 12 | HGNC:7794 | Homo sapiens (human) | 4790 | NFKB1 |
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| DOID:1793 | pancreatic cancer | HGNC:703 | Homo sapiens (human) | 10552 | ARPC1A |
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| DOID:1123 | spondyloarthropathy | HGNC:2200 | Homo sapiens (human) | 1280 | COL2A1 |
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| DOID:0050168 | autoimmune polyendocrine syndrome type 2 | HGNC:4948 | Homo sapiens (human) | 3123 | HLA-DRB1 |
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| DOID:0080393 | nephrotic syndrome type 18 | HGNC:18016 | Homo sapiens (human) | 55746 | NUP133 |
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| DOID:399 | tuberculosis | HGNC:11917 | Homo sapiens (human) | 7133 | TNFRSF1B |
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| DOID:2841 | asthma | HGNC:79 | Homo sapiens (human) | 28 | ABO |
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| DOID:6846 | familial melanoma | HGNC:6929 | Homo sapiens (human) | 4157 | MC1R |
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| DOID:0050908 | myelodysplastic syndrome | HGNC:4886 | Homo sapiens (human) | 3077 | HFE |
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| DOID:12849 | autistic disorder | HGNC:7468 | Homo sapiens (human) | 4548 | MTR |
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| DOID:0111277 | mitochondrial trifunctional protein deficiency | HGNC:4801 | Homo sapiens (human) | 3030 | HADHA |
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