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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:0060363 | glycerol kinase deficiency | HGNC:4289 | Homo sapiens (human) | 2710 | GK |
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| DOID:0050868 | hepatocellular adenoma | HGNC:11621 | Homo sapiens (human) | 6927 | HNF1A |
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| DOID:0111029 | hemochromatosis type 1 | HGNC:4886 | Homo sapiens (human) | 3077 | HFE |
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| DOID:0111815 | low molecular weight proteinuria with hypercalciuric nephrocalcinosis | HGNC:2023 | Homo sapiens (human) | 1184 | CLCN5 |
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| DOID:0110679 | congenital myasthenic syndrome 4C | HGNC:1966 | Homo sapiens (human) | 1145 | CHRNE |
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| DOID:2861 | congenital nonspherocytic hemolytic anemia | HGNC:4458 | Homo sapiens (human) | 2821 | GPI |
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| DOID:684 | hepatocellular carcinoma | HGNC:5962 | Homo sapiens (human) | 3586 | IL10 |
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| DOID:0060697 | hyperekplexia 2 | HGNC:4329 | Homo sapiens (human) | 2743 | GLRB |
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| DOID:4989 | pancreatitis | HGNC:9475 | Homo sapiens (human) | 5644 | PRSS1 |
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| DOID:10763 | hypertension | HGNC:11068 | Homo sapiens (human) | 6546 | SLC8A1 |
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| DOID:0090113 | RIDDLE syndrome | HGNC:26661 | Homo sapiens (human) | 165918 | RNF168 |
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| DOID:9252 | amino acid metabolic disorder | HGNC:5005 | Homo sapiens (human) | 3155 | HMGCL |
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| DOID:10652 | Alzheimer's disease | HGNC:6692 | Homo sapiens (human) | 4035 | LRP1 |
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| DOID:0050797 | peroxisomal acyl-CoA oxidase deficiency | HGNC:119 | Homo sapiens (human) | 51 | ACOX1 |
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| DOID:0110970 | brachydactyly type C | HGNC:4220 | Homo sapiens (human) | 8200 | GDF5 |
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| DOID:0070339 | cerebellar hyplasia/atrophy, epilepsy, and global developmental delay | HGNC:15822 | Homo sapiens (human) | 55074 | OXR1 |
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| DOID:0060479 | Shwachman-Diamond syndrome | HGNC:25789 | Homo sapiens (human) | 79631 | EFL1 |
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| DOID:0050475 | Weill-Marchesani syndrome | HGNC:13201 | Homo sapiens (human) | 81794 | ADAMTS10 |
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| DOID:3649 | pyruvate decarboxylase deficiency | HGNC:8806 | Homo sapiens (human) | 5160 | PDHA1 |
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| DOID:0112051 | non-syndromic X-linked intellectual disability 30 | HGNC:8592 | Homo sapiens (human) | 5063 | PAK3 |
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| DOID:12930 | dilated cardiomyopathy | HGNC:11947 | Homo sapiens (human) | 7137 | TNNI3 |
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| DOID:0060369 | Parkinson's disease 6 | HGNC:14581 | Homo sapiens (human) | 65018 | PINK1 |
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| DOID:0110526 | autosomal recessive nonsyndromic deafness 79 | HGNC:26894 | Homo sapiens (human) | 286262 | TPRN |
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| DOID:0060601 | alpha-2-plasmin inhibitor deficiency | HGNC:9075 | Homo sapiens (human) | 5345 | SERPINF2 |
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| DOID:0090071 | hypogonadotropic hypogonadism 11 with or without anosmia | HGNC:11528 | Homo sapiens (human) | 6870 | TACR3 |
|
