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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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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:1470 | major depressive disorder | HGNC:1951 | Homo sapiens (human) | 1129 | CHRM2 |
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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:5419 | schizophrenia | HGNC:15781 | Homo sapiens (human) | 89832 | CHRFAM7A |
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| DOID:1561 | cognitive disorder | HGNC:15781 | Homo sapiens (human) | 89832 | CHRFAM7A |
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| DOID:0050742 | nicotine dependence | HGNC:15781 | Homo sapiens (human) | 89832 | CHRFAM7A |
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| DOID:7148 | rheumatoid arthritis | HGNC:15781 | Homo sapiens (human) | 89832 | CHRFAM7A |
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| DOID:12583 | velocardiofacial syndrome | HGNC:1949 | Homo sapiens (human) | 8646 | CHRD |
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| DOID:11198 | DiGeorge syndrome | HGNC:1949 | Homo sapiens (human) | 8646 | CHRD |
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| DOID:5679 | retinal disease | HGNC:17852 | Homo sapiens (human) | 56994 | CHPT1 |
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| DOID:0110265 | cataract 31 multiple types | HGNC:16171 | Homo sapiens (human) | 128866 | CHMP4B |
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| DOID:9255 | frontotemporal dementia | HGNC:24537 | Homo sapiens (human) | 25978 | CHMP2B |
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| DOID:0111227 | frontotemporal dementia and/or amyotrophic lateral sclerosis 7 | HGNC:24537 | Homo sapiens (human) | 25978 | CHMP2B |
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| DOID:332 | amyotrophic lateral sclerosis | HGNC:24537 | Homo sapiens (human) | 25978 | CHMP2B |
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| DOID:2841 | asthma | HGNC:1941 | Homo sapiens (human) | 1122 | CHML |
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| DOID:9821 | choroideremia | HGNC:1941 | Homo sapiens (human) | 1122 | CHML |
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| DOID:9821 | choroideremia | HGNC:1940 | Homo sapiens (human) | 1121 | CHM |
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| DOID:1826 | epilepsy | HGNC:1939 | Homo sapiens (human) | 10752 | CHL1 |
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| DOID:5419 | schizophrenia | HGNC:1939 | Homo sapiens (human) | 10752 | CHL1 |
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| DOID:0060246 | MASA syndrome | HGNC:1939 | Homo sapiens (human) | 10752 | CHL1 |
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| DOID:0110632 | megaconial type congenital muscular dystrophy | HGNC:1938 | Homo sapiens (human) | 1120 | CHKB |
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| DOID:10907 | microcephaly | HGNC:1938 | Homo sapiens (human) | 1120 | CHKB |
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| DOID:9884 | muscular dystrophy | HGNC:1938 | Homo sapiens (human) | 1120 | CHKB |
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| DOID:8986 | narcolepsy | HGNC:1938 | Homo sapiens (human) | 1120 | CHKB |
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