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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:12930 | dilated cardiomyopathy | HGNC:11180 | Homo sapiens (human) | 6648 | SOD2 |
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| DOID:0112175 | spermatogenic failure 47 | HGNC:20908 | Homo sapiens (human) | 22873 | DZIP1 |
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| DOID:0060870 | isolated growth hormone deficiency | HGNC:4266 | Homo sapiens (human) | 2692 | GHRHR |
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| DOID:14499 | Fabry disease | HGNC:4296 | Homo sapiens (human) | 2717 | GLA |
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| DOID:0111029 | hemochromatosis type 1 | HGNC:4886 | Homo sapiens (human) | 3077 | HFE |
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| DOID:4989 | pancreatitis | HGNC:10632 | Homo sapiens (human) | 6352 | CCL5 |
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| DOID:0060599 | Nance-Horan syndrome | HGNC:7820 | Homo sapiens (human) | 4810 | NHS |
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| DOID:0110007 | achromatopsia 2 | HGNC:2150 | Homo sapiens (human) | 1261 | CNGA3 |
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| DOID:0110486 | autosomal recessive nonsyndromic deafness 28 | HGNC:17009 | Homo sapiens (human) | 11078 | TRIOBP |
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| DOID:0070055 | Xia-Gibbs Syndrome | HGNC:25230 | Homo sapiens (human) | 27245 | AHDC1 |
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| DOID:12930 | dilated cardiomyopathy | HGNC:11947 | Homo sapiens (human) | 7137 | TNNI3 |
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| DOID:0110800 | hereditary spastic paraplegia 48 | HGNC:22197 | Homo sapiens (human) | 9907 | AP5Z1 |
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| DOID:0110957 | Gaucher's disease type I | HGNC:4177 | Homo sapiens (human) | 2629 | GBA1 |
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| DOID:14737 | craniofrontonasal syndrome | HGNC:3226 | Homo sapiens (human) | 1947 | EFNB1 |
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| DOID:0110280 | autosomal recessive limb-girdle muscular dystrophy type 2F | HGNC:10807 | Homo sapiens (human) | 6444 | SGCD |
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| DOID:0110170 | Charcot-Marie-Tooth disease axonal type 2Q | HGNC:23537 | Homo sapiens (human) | 55526 | DHTKD1 |
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| DOID:0070346 | neurodevelopmental disorder with cataracts, poor growth, and dysmorphic facies | HGNC:24555 | Homo sapiens (human) | 26173 | INTS1 |
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| DOID:0050793 | short QT syndrome | HGNC:6251 | Homo sapiens (human) | 3757 | KCNH2 |
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| DOID:9976 | heroin dependence | HGNC:2345 | Homo sapiens (human) | 1385 | CREB1 |
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| DOID:5419 | schizophrenia | HGNC:5293 | Homo sapiens (human) | 3356 | HTR2A |
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| DOID:9970 | obesity | HGNC:7957 | Homo sapiens (human) | 4887 | NPY2R |
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| DOID:0060692 | platelet-type bleeding disorder 8 | HGNC:18124 | Homo sapiens (human) | 64805 | P2RY12 |
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| DOID:0111807 | syndromic microphthalmia 9 | HGNC:30650 | Homo sapiens (human) | 64220 | STRA6 |
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| DOID:0070356 | visual impairment and progressive phthisis bulbi | HGNC:6897 | Homo sapiens (human) | 4140 | MARK3 |
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| DOID:0110248 | cataract 30 | HGNC:12692 | Homo sapiens (human) | 7431 | VIM |
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