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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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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:9976 | heroin dependence | HGNC:3023 | Homo sapiens (human) | 1813 | DRD2 |
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| DOID:0080418 | developmental and epileptic encephalopathy 54 | HGNC:5048 | Homo sapiens (human) | 3192 | HNRNPU |
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| DOID:0060583 | Noonan syndrome 5 | HGNC:9829 | Homo sapiens (human) | 5894 | RAF1 |
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| DOID:12308 | Dubin-Johnson syndrome | HGNC:53 | Homo sapiens (human) | 1244 | ABCC2 |
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| DOID:1826 | epilepsy | HGNC:40 | Homo sapiens (human) | 5243 | ABCB1 |
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| DOID:0080552 | congenital disorder of glycosylation Ia | HGNC:9115 | Homo sapiens (human) | 5373 | PMM2 |
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| DOID:12799 | mucopolysaccharidosis II | HGNC:5389 | Homo sapiens (human) | 3423 | IDS |
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| DOID:3265 | chronic granulomatous disease | HGNC:2578 | Homo sapiens (human) | 1536 | CYBB |
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| DOID:0080348 | Alzheimer's disease 1 | HGNC:620 | Homo sapiens (human) | 351 | APP |
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| DOID:2741 | bilirubin metabolic disorder | HGNC:10961 | Homo sapiens (human) | 28234 | SLCO1B3 |
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| DOID:0080250 | erythrokeratodermia variabilis et progressiva 4 | HGNC:4021 | Homo sapiens (human) | 2531 | KDSR |
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| DOID:0111407 | Fraser syndrome 2 | HGNC:25396 | Homo sapiens (human) | 341640 | FREM2 |
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| DOID:0112034 | non-syndromic X-linked intellectual disability 9 | HGNC:13254 | Homo sapiens (human) | 24140 | FTSJ1 |
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| DOID:4603 | epidermolytic hyperkeratosis | HGNC:6412 | Homo sapiens (human) | 3848 | KRT1 |
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| DOID:0060785 | adult-onset autosomal dominant demyelinating leukodystrophy | HGNC:6637 | Homo sapiens (human) | 4001 | LMNB1 |
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| DOID:9256 | colorectal cancer | HGNC:9177 | Homo sapiens (human) | 5426 | POLE |
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| DOID:0050882 | spinocerebellar ataxia type 5 | HGNC:11276 | Homo sapiens (human) | 6712 | SPTBN2 |
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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:5844 | myocardial infarction | HGNC:320 | Homo sapiens (human) | 177 | AGER |
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| DOID:0110293 | autosomal recessive limb-girdle muscular dystrophy type 2P | HGNC:2666 | Homo sapiens (human) | 1605 | DAG1 |
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| DOID:0081397 | Vissers-Bodmer syndrome | HGNC:7877 | Homo sapiens (human) | 23019 | CNOT1 |
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| DOID:0110545 | autosomal dominant nonsyndromic deafness 13 | HGNC:2187 | Homo sapiens (human) | 1302 | COL11A2 |
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| DOID:0050787 | juvenile polyposis syndrome | HGNC:6770 | Homo sapiens (human) | 4089 | SMAD4 |
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| DOID:0110515 | autosomal recessive nonsyndromic deafness 63 | HGNC:25033 | Homo sapiens (human) | 220074 | LRTOMT |
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| DOID:14500 | fucosidosis | HGNC:4006 | Homo sapiens (human) | 2517 | FUCA1 |
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