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GlyTouCan
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
LM-GlycoRepo
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:11252 | microcytic anemia | SGD:S000001709 | Saccharomyces cerevisiae S288C | 853870 | VPS1 |
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| DOID:0110184 | Charcot-Marie-Tooth disease type 4J | SGD:S000005269 | Saccharomyces cerevisiae S288C | 855392 | FIG4 |
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| DOID:0080556 | congenital disorder of glycosylation Id | SGD:S000000178 | Saccharomyces cerevisiae S288C | 852196 | ALG3 |
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| DOID:0111442 | optic atrophy 9 | SGD:S000004295 | Saccharomyces cerevisiae S288C | 851013 | ACO1 |
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| DOID:0111223 | centronuclear myopathy 1 | SGD:S000001709 | Saccharomyces cerevisiae S288C | 853870 | VPS1 |
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| DOID:0110197 | Charcot-Marie-Tooth disease dominant intermediate B | SGD:S000001709 | Saccharomyces cerevisiae S288C | 853870 | VPS1 |
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| DOID:3070 | high grade glioma | SGD:S000002224 | Saccharomyces cerevisiae S288C | 851493 | IDP1 |
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| DOID:162 | cancer | SGD:S000005816 | Saccharomyces cerevisiae S288C | 854465 | SNF2 |
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| DOID:0050560 | Walker-Warburg syndrome | SGD:S000003904 | Saccharomyces cerevisiae S288C | 853608 | PMT4 |
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| DOID:0070113 | Niemann-Pick disease type C1 | SGD:S000005927 | Saccharomyces cerevisiae S288C | 856101 | NCR1 |
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| DOID:0080572 | congenital disorder of glycosylation Iw | SGD:S000002990 | Saccharomyces cerevisiae S288C | 852862 | STT3 |
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| DOID:0080195 | Marinesco-Sjogren syndrome | SGD:S000005391 | Saccharomyces cerevisiae S288C | 854126 | SIL1 |
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| DOID:0050659 | biotin-responsive basal ganglia disease | WB:WBGene00044738 | Caenorhabditis elegans | 4363081 | folt-3 |
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| DOID:2987 | familial mediterranean fever | HGNC:6998 | Homo sapiens (human) | 4210 | MEFV |
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| DOID:0110725 | neuronal ceroid lipofuscinosis 10 | HGNC:2529 | Homo sapiens (human) | 1509 | CTSD |
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| DOID:0050955 | spinocerebellar ataxia type 2 | HGNC:10555 | Homo sapiens (human) | 6311 | ATXN2 |
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| DOID:12365 | malaria | HGNC:3618 | Homo sapiens (human) | 2213 | FCGR2B |
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| DOID:0110933 | nemaline myopathy 11 | HGNC:23246 | Homo sapiens (human) | 84665 | MYPN |
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| DOID:10763 | hypertension | HGNC:11068 | Homo sapiens (human) | 6546 | SLC8A1 |
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| DOID:3827 | congenital diaphragmatic hernia | HGNC:9091 | Homo sapiens (human) | 5358 | PLS3 |
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| DOID:0070170 | spermatogenic failure 19 | HGNC:26684 | Homo sapiens (human) | 80217 | CFAP43 |
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| DOID:0110181 | Charcot-Marie-Tooth disease axonal type 2Z | HGNC:23573 | Homo sapiens (human) | 22880 | MORC2 |
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| DOID:0050638 | transthyretin amyloidosis | HGNC:12405 | Homo sapiens (human) | 7276 | TTR |
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| DOID:0070417 | neurodevelopmental disorder with speech impairment and dysmorphic facies | HGNC:29010 | Homo sapiens (human) | 9739 | SETD1A |
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| DOID:0110660 | congenital myasthenic syndrome 12 | HGNC:4241 | Homo sapiens (human) | 2673 | GFPT1 |
|
