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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:5419 | schizophrenia | HGNC:1951 | Homo sapiens (human) | 1129 | CHRM2 |
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| DOID:9976 | heroin dependence | HGNC:1951 | Homo sapiens (human) | 1129 | CHRM2 |
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| DOID:1470 | major depressive disorder | HGNC:1951 | Homo sapiens (human) | 1129 | CHRM2 |
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| DOID:8947 | diabetic retinopathy | HGNC:25156 | Homo sapiens (human) | 112869 | SGF29 |
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| DOID:0080738 | Ehlers-Danlos syndrome spondylodysplastic type 1 | HGNC:930 | Homo sapiens (human) | 11285 | B4GALT7 |
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| DOID:13359 | Ehlers-Danlos syndrome | HGNC:930 | Homo sapiens (human) | 11285 | B4GALT7 |
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| DOID:10763 | hypertension | HGNC:2648 | Homo sapiens (human) | 11283 | CYP4F8 |
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| DOID:0050861 | colorectal adenocarcinoma | HGNC:2648 | Homo sapiens (human) | 11283 | CYP4F8 |
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| DOID:0111672 | primary hyperoxaluria type 3 | HGNC:25155 | Homo sapiens (human) | 112817 | HOGA1 |
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| DOID:2977 | primary hyperoxaluria | HGNC:25155 | Homo sapiens (human) | 112817 | HOGA1 |
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| DOID:0110710 | hypotrichosis 13 | HGNC:28927 | Homo sapiens (human) | 112802 | KRT71 |
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| DOID:987 | alopecia | HGNC:28927 | Homo sapiens (human) | 112802 | KRT71 |
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| DOID:0050548 | hereditary sensory neuropathy | HGNC:10583 | Homo sapiens (human) | 11280 | SCN11A |
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| DOID:0080422 | Dravet syndrome | HGNC:10583 | Homo sapiens (human) | 11280 | SCN11A |
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| DOID:1826 | epilepsy | HGNC:10583 | Homo sapiens (human) | 11280 | SCN11A |
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| DOID:0060170 | generalized epilepsy with febrile seizures plus | HGNC:10583 | Homo sapiens (human) | 11280 | SCN11A |
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| DOID:0111731 | familial episodic pain syndrome 3 | HGNC:10583 | Homo sapiens (human) | 11280 | SCN11A |
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| DOID:0070149 | hereditary sensory and autonomic neuropathy type 7 | HGNC:10583 | Homo sapiens (human) | 11280 | SCN11A |
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| DOID:0111294 | generalized epilepsy with febrile seizures plus 2 | HGNC:10583 | Homo sapiens (human) | 11280 | SCN11A |
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| DOID:2841 | asthma | HGNC:1950 | Homo sapiens (human) | 1128 | CHRM1 |
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| DOID:437 | myasthenia gravis | HGNC:1950 | Homo sapiens (human) | 1128 | CHRM1 |
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| DOID:0050214 | Lambert-Eaton myasthenic syndrome | HGNC:1950 | Homo sapiens (human) | 1128 | CHRM1 |
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| DOID:2058 | chronic mucocutaneous candidiasis | HGNC:16404 | Homo sapiens (human) | 112744 | IL17F |
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| DOID:0050955 | spinocerebellar ataxia type 2 | HGNC:31326 | Homo sapiens (human) | 11273 | ATXN2L |
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| DOID:0070515 | chromosome 16p11.2 deletion syndrome, 593-kb | HGNC:31326 | Homo sapiens (human) | 11273 | ATXN2L |
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