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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:2957 | pulmonary tuberculosis | HGNC:391 | Homo sapiens (human) | 207 | AKT1 |
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| DOID:0050840 | cervical dystonia | HGNC:4944 | Homo sapiens (human) | 3119 | HLA-DQB1 |
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| DOID:8725 | vascular dementia | HGNC:29168 | Homo sapiens (human) | 23322 | RPGRIP1L |
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| DOID:12185 | otosclerosis | HGNC:2197 | Homo sapiens (human) | 1277 | COL1A1 |
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| DOID:11563 | retinal vasculitis | HGNC:4932 | Homo sapiens (human) | 3106 | HLA-B |
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| DOID:0111432 | essential tremor 5 | HGNC:29945 | Homo sapiens (human) | 26011 | TENM4 |
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| DOID:0111352 | D-2-hydroxyglutaric aciduria 2 | HGNC:5383 | Homo sapiens (human) | 3418 | IDH2 |
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| DOID:1307 | dementia | HGNC:4601 | Homo sapiens (human) | 2896 | GRN |
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| DOID:0111837 | congenital nongoitrous hypothyroidism 8 | HGNC:11585 | Homo sapiens (human) | 6907 | TBL1X |
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| DOID:10591 | pre-eclampsia | HGNC:19012 | Homo sapiens (human) | 10699 | CORIN |
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| DOID:0081381 | juvenile amyotrophic lateral sclerosis type 27 | HGNC:11277 | Homo sapiens (human) | 10558 | SPTLC1 |
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| DOID:1561 | cognitive disorder | HGNC:9236 | Homo sapiens (human) | 5468 | PPARG |
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| DOID:9976 | heroin dependence | HGNC:40 | Homo sapiens (human) | 5243 | ABCB1 |
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| DOID:2841 | asthma | HGNC:5977 | Homo sapiens (human) | 3600 | IL15 |
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| DOID:10123 | pigmentation disease | HGNC:8101 | Homo sapiens (human) | 4948 | OCA2 |
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| DOID:0050741 | alcohol dependence | HGNC:7656 | Homo sapiens (human) | 4684 | NCAM1 |
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| DOID:0050431 | arrhythmogenic right ventricular cardiomyopathy | HGNC:1759 | Homo sapiens (human) | 1000 | CDH2 |
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| DOID:0080176 | meningococcal meningitis | HGNC:11848 | Homo sapiens (human) | 7097 | TLR2 |
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| DOID:4780 | anti-basement membrane glomerulonephritis | HGNC:4948 | Homo sapiens (human) | 3123 | HLA-DRB1 |
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| DOID:0111508 | Torrance type platyspondylic dysplasia | HGNC:2200 | Homo sapiens (human) | 1280 | COL2A1 |
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| DOID:5082 | liver cirrhosis | HGNC:225 | Homo sapiens (human) | 103 | ADAR |
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| DOID:0050569 | Seckel syndrome | HGNC:18672 | Homo sapiens (human) | 55755 | CDK5RAP2 |
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| DOID:12306 | vitiligo | HGNC:11180 | Homo sapiens (human) | 6648 | SOD2 |
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| DOID:2366 | West Nile fever | HGNC:1606 | Homo sapiens (human) | 1234 | CCR5 |
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| DOID:14330 | Parkinson's disease | HGNC:20956 | Homo sapiens (human) | 9749 | PHACTR2 |
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