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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:12306 | vitiligo | HGNC:11850 | Homo sapiens (human) | 7099 | TLR4 |
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| DOID:0080328 | Culler-Jones syndrome | HGNC:4318 | Homo sapiens (human) | 2736 | GLI2 |
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| DOID:0050741 | alcohol dependence | HGNC:11050 | Homo sapiens (human) | 6532 | SLC6A4 |
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| DOID:13241 | Behcet's disease | HGNC:4932 | Homo sapiens (human) | 3106 | HLA-B |
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| DOID:684 | hepatocellular carcinoma | HGNC:3229 | Homo sapiens (human) | 1950 | EGF |
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| DOID:0080946 | retinal dystrophy with leukodystrophy | HGNC:23338 | Homo sapiens (human) | 91452 | ACBD5 |
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| DOID:0060366 | Hennekam syndrome | HGNC:219 | Homo sapiens (human) | 9508 | ADAMTS3 |
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| DOID:705 | Leber hereditary optic neuropathy | HGNC:11998 | Homo sapiens (human) | 7157 | TP53 |
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| DOID:3119 | gastrointestinal system cancer | HGNC:1863 | Homo sapiens (human) | 1066 | CES1 |
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| DOID:0060901 | lymphoplasmacytic lymphoma | HGNC:7562 | Homo sapiens (human) | 4615 | MYD88 |
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| DOID:1596 | depressive disorder | HGNC:14303 | Homo sapiens (human) | 129446 | XIRP2 |
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| DOID:0050628 | advanced sleep phase syndrome | HGNC:11813 | Homo sapiens (human) | 8914 | TIMELESS |
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| DOID:0111648 | ectopia lentis with ectopia of pupil | HGNC:19706 | Homo sapiens (human) | 54507 | ADAMTSL4 |
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| DOID:437 | myasthenia gravis | HGNC:286 | Homo sapiens (human) | 154 | ADRB2 |
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| DOID:0110925 | familial hemophagocytic lymphohistiocytosis 5 | HGNC:11445 | Homo sapiens (human) | 6813 | STXBP2 |
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| DOID:0110818 | hereditary spastic paraplegia 73 | HGNC:18540 | Homo sapiens (human) | 126129 | CPT1C |
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| DOID:4927 | Klatskin's tumor | HGNC:13726 | Homo sapiens (human) | 58508 | KMT2C |
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| DOID:0060770 | dextro-looped transposition of the great arteries | HGNC:22962 | Homo sapiens (human) | 23389 | MED13L |
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| DOID:0080337 | mitochondrial DNA depletion syndrome 15 | HGNC:11741 | Homo sapiens (human) | 7019 | TFAM |
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| DOID:13909 | red-green color blindness | HGNC:4206 | Homo sapiens (human) | 2652 | OPN1MW |
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| DOID:783 | end stage renal disease | HGNC:6144 | Homo sapiens (human) | 8516 | ITGA8 |
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| DOID:14791 | Leber congenital amaurosis | HGNC:7606 | Homo sapiens (human) | 4647 | MYO7A |
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| DOID:0111333 | early-onset myopathy-areflexia-respiratory distress-dysphagia syndrome | HGNC:29634 | Homo sapiens (human) | 84466 | MEGF10 |
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| DOID:0060720 | autosomal recessive congenital ichthyosis 11 | HGNC:11344 | Homo sapiens (human) | 6768 | ST14 |
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| DOID:0080224 | autosomal dominant dystrophic epidermolysis bullosa | HGNC:2214 | Homo sapiens (human) | 1294 | COL7A1 |
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