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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:9976 | heroin dependence | HGNC:277 | Homo sapiens (human) | 148 | ADRA1A |
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| DOID:3393 | coronary artery disease | HGNC:25262 | Homo sapiens (human) | 284498 | C1orf167 |
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| DOID:3393 | coronary artery disease | HGNC:6554 | Homo sapiens (human) | 3953 | LEPR |
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| DOID:2841 | asthma | HGNC:4943 | Homo sapiens (human) | 3118 | HLA-DQA2 |
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| DOID:13365 | reading disorder | HGNC:13830 | Homo sapiens (human) | 26047 | CNTNAP2 |
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| DOID:0111110 | maturity-onset diabetes of the young type 13 | HGNC:6257 | Homo sapiens (human) | 3767 | KCNJ11 |
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| DOID:289 | endometriosis | HGNC:644 | Homo sapiens (human) | 367 | AR |
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| DOID:0060558 | lethal congenital contracture syndrome | HGNC:29514 | Homo sapiens (human) | 342035 | GLDN |
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| DOID:0111784 | otopalatodigital syndrome type 2 | HGNC:3754 | Homo sapiens (human) | 2316 | FLNA |
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| DOID:0080282 | developmental and epileptic encephalopathy 56 | HGNC:12852 | Homo sapiens (human) | 7532 | YWHAG |
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| DOID:0111777 | 46,XY sex reversal 2 | HGNC:7960 | Homo sapiens (human) | 190 | NR0B1 |
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| DOID:10283 | prostate cancer | HGNC:7534 | Homo sapiens (human) | 4601 | MXI1 |
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| DOID:1936 | atherosclerosis | HGNC:3616 | Homo sapiens (human) | 2212 | FCGR2A |
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| DOID:0060902 | Norman-Roberts syndrome | HGNC:9957 | Homo sapiens (human) | 5649 | RELN |
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| DOID:0060286 | combined oxidative phosphorylation deficiency | HGNC:26223 | Homo sapiens (human) | 79736 | TEFM |
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| DOID:1555 | urticaria | HGNC:286 | Homo sapiens (human) | 154 | ADRB2 |
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| DOID:0080773 | delta beta-thalassemia | HGNC:4827 | Homo sapiens (human) | 3043 | HBB |
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| DOID:4362 | cervical cancer | HGNC:4940 | Homo sapiens (human) | 3115 | HLA-DPB1 |
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| DOID:10126 | keratoconus | HGNC:4893 | Homo sapiens (human) | 3082 | HGF |
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| DOID:2986 | IgA glomerulonephritis | HGNC:15633 | Homo sapiens (human) | 54106 | TLR9 |
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| DOID:2862 | glucosephosphate dehydrogenase deficiency | HGNC:5438 | Homo sapiens (human) | 3458 | IFNG |
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| DOID:0080673 | fibrochondrogenesis 2 | HGNC:2187 | Homo sapiens (human) | 1302 | COL11A2 |
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| DOID:2921 | glomerulonephritis | HGNC:3618 | Homo sapiens (human) | 2213 | FCGR2B |
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| DOID:12849 | autistic disorder | HGNC:4082 | Homo sapiens (human) | 2561 | GABRB2 |
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| DOID:1883 | hepatitis C | HGNC:6018 | Homo sapiens (human) | 3569 | IL6 |
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