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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
LM-GlycoRepo
Repository for lectin-assisted multimodality data
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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
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:13100 | intracranial vasospasm | HGNC:10483 | Homo sapiens (human) | 6261 | RYR1 |
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| DOID:9976 | heroin dependence | HGNC:8153 | Homo sapiens (human) | 4985 | OPRD1 |
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| DOID:13223 | uterine fibroid | HGNC:29190 | Homo sapiens (human) | 23112 | TNRC6B |
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| DOID:0080679 | neuronal intestinal dysplasia type A | HGNC:3431 | Homo sapiens (human) | 2065 | ERBB3 |
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| DOID:10584 | retinitis pigmentosa | HGNC:4922 | Homo sapiens (human) | 3098 | HK1 |
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| DOID:0111665 | ectodermal dysplasia 10B | HGNC:2895 | Homo sapiens (human) | 10913 | EDAR |
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| DOID:5409 | lung small cell carcinoma | HGNC:14079 | Homo sapiens (human) | 55584 | CHRNA9 |
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| DOID:0090088 | hypogonadotropic hypogonadism 24 without anosmia | HGNC:3964 | Homo sapiens (human) | 2488 | FSHB |
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| DOID:13809 | familial combined hyperlipidemia | HGNC:6677 | Homo sapiens (human) | 4023 | LPL |
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| DOID:12030 | panuveitis | HGNC:5962 | Homo sapiens (human) | 3586 | IL10 |
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| DOID:11695 | portal vein thrombosis | HGNC:8583 | Homo sapiens (human) | 5054 | SERPINE1 |
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| DOID:1287 | cardiovascular system disease | HGNC:333 | Homo sapiens (human) | 183 | AGT |
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| DOID:3312 | bipolar disorder | HGNC:17582 | Homo sapiens (human) | 23522 | KAT6B |
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| DOID:12894 | Sjogren's syndrome | HGNC:5962 | Homo sapiens (human) | 3586 | IL10 |
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| DOID:0050630 | Aland Island eye disease | HGNC:1393 | Homo sapiens (human) | 778 | CACNA1F |
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| DOID:0110777 | hereditary spastic paraplegia 26 | HGNC:4117 | Homo sapiens (human) | 2583 | B4GALNT1 |
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| DOID:1788 | peritoneal mesothelioma | HGNC:20456 | Homo sapiens (human) | 84231 | TRAF7 |
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| DOID:5419 | schizophrenia | HGNC:1932 | Homo sapiens (human) | 1116 | CHI3L1 |
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| DOID:3748 | esophagus squamous cell carcinoma | HGNC:6919 | Homo sapiens (human) | 8930 | MBD4 |
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| DOID:0070409 | autosomal recessive spinocerebellar ataxia 28 | HGNC:26053 | Homo sapiens (human) | 54974 | THG1L |
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| DOID:9415 | allergic asthma | HGNC:4932 | Homo sapiens (human) | 3106 | HLA-B |
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| DOID:936 | brain disease | HGNC:13481 | Homo sapiens (human) | 81622 | UNC93B1 |
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| DOID:0080326 | familial hypertrophic cardiomyopathy | HGNC:26178 | Homo sapiens (human) | 80206 | FHOD3 |
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| DOID:987 | alopecia | RGD:619973 | Rattus norvegicus (Norway rat) | 192107 | Prss8 |
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| DOID:12361 | Graves' disease | HGNC:11998 | Homo sapiens (human) | 7157 | TP53 |
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