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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:0110429 | dilated cardiomyopathy 1H | HGNC:2592 | Homo sapiens (human) | 1585 | CYP11B2 |
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| DOID:0070146 | hereditary sensory neuropathy type 4 | HGNC:8031 | Homo sapiens (human) | 4914 | NTRK1 |
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| DOID:2377 | multiple sclerosis | HGNC:5438 | Homo sapiens (human) | 3458 | IFNG |
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| DOID:1307 | dementia | HGNC:6700 | Homo sapiens (human) | 7804 | LRP8 |
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| DOID:0110446 | dilated cardiomyopathy 1W | HGNC:12665 | Homo sapiens (human) | 7414 | VCL |
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| DOID:0060875 | isolated growth hormone deficiency type III | HGNC:1133 | Homo sapiens (human) | 695 | BTK |
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| DOID:5082 | liver cirrhosis | HGNC:5962 | Homo sapiens (human) | 3586 | IL10 |
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| DOID:4780 | anti-basement membrane glomerulonephritis | HGNC:4948 | Homo sapiens (human) | 3123 | HLA-DRB1 |
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| DOID:936 | brain disease | HGNC:2330 | Homo sapiens (human) | 1376 | CPT2 |
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| DOID:5082 | liver cirrhosis | HGNC:3691 | Homo sapiens (human) | 2264 | FGFR4 |
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| DOID:0110274 | autosomal recessive limb-girdle muscular dystrophy | HGNC:17649 | Homo sapiens (human) | 64208 | POPDC3 |
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| DOID:0111551 | neurogenic scapuloperoneal syndrome Kaeser type | HGNC:2770 | Homo sapiens (human) | 1674 | DES |
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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:0070529 | Sifrim-Hitz-Weiss syndrome | HGNC:1919 | Homo sapiens (human) | 1108 | CHD4 |
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| DOID:0070210 | hereditary lymphedema IA | HGNC:3767 | Homo sapiens (human) | 2324 | FLT4 |
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| DOID:1574 | alcohol use disorder | HGNC:90 | Homo sapiens (human) | 35 | ACADS |
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| DOID:5844 | myocardial infarction | HGNC:2505 | Homo sapiens (human) | 1493 | CTLA4 |
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| DOID:7147 | ankylosing spondylitis | HGNC:4932 | Homo sapiens (human) | 3106 | HLA-B |
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| DOID:10283 | prostate cancer | HGNC:393 | Homo sapiens (human) | 10000 | AKT3 |
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| DOID:0080289 | orofaciodigital syndrome XVII | HGNC:29239 | Homo sapiens (human) | 27152 | INTU |
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| DOID:0060706 | X-linked lymphoproliferative syndrome 2 | HGNC:592 | Homo sapiens (human) | 331 | XIAP |
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| DOID:0050741 | alcohol dependence | HGNC:8781 | Homo sapiens (human) | 5142 | PDE4B |
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| DOID:2377 | multiple sclerosis | HGNC:7158 | Homo sapiens (human) | 4321 | MMP12 |
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| DOID:4948 | gallbladder carcinoma | HGNC:11730 | Homo sapiens (human) | 7015 | TERT |
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| DOID:653 | purine-pyrimidine metabolic disorder | HGNC:7892 | Homo sapiens (human) | 4860 | PNP |
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