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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:0111035 | CADASIL 1 | HGNC:7883 | Homo sapiens (human) | 4854 | NOTCH3 |
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| DOID:0110205 | Charcot-Marie-Tooth disease dominant intermediate E | HGNC:23791 | Homo sapiens (human) | 64423 | INF2 |
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| DOID:0110255 | cataract 5 multiple types | HGNC:5227 | Homo sapiens (human) | 3299 | HSF4 |
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| DOID:0060365 | mandibulofacial dysostosis with alopecia | HGNC:3179 | Homo sapiens (human) | 1909 | EDNRA |
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| DOID:0110779 | hereditary spastic paraplegia 28 | HGNC:19714 | Homo sapiens (human) | 80821 | DDHD1 |
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| DOID:0070341 | neonatal-onset type II citrullinemia | HGNC:10983 | Homo sapiens (human) | 10165 | SLC25A13 |
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| DOID:12365 | malaria | HGNC:5344 | Homo sapiens (human) | 3383 | ICAM1 |
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| DOID:0110310 | hypertrophic cardiomyopathy 4 | HGNC:7551 | Homo sapiens (human) | 4607 | MYBPC3 |
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| DOID:0070137 | autosomal recessive cutis laxa type IIB | HGNC:9721 | Homo sapiens (human) | 5831 | PYCR1 |
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| DOID:0070056 | autosomal dominant intellectual developmental disorder 26 | HGNC:14262 | Homo sapiens (human) | 26053 | AUTS2 |
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| DOID:0090117 | thiamine-responsive megaloblastic anemia syndrome | HGNC:10938 | Homo sapiens (human) | 10560 | SLC19A2 |
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| DOID:0111237 | congenital muscular dystrophy-dystroglycanopathy type A1 | HGNC:9202 | Homo sapiens (human) | 10585 | POMT1 |
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| DOID:0110250 | cataract 16 multiple types | HGNC:2389 | Homo sapiens (human) | 1410 | CRYAB |
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| DOID:0112306 | Mahvash Disease | HGNC:4192 | Homo sapiens (human) | 2642 | GCGR |
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| DOID:0050644 | arterial calcification of infancy | HGNC:57 | Homo sapiens (human) | 368 | ABCC6 |
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| DOID:0112103 | Sotos syndrome 1 | HGNC:14234 | Homo sapiens (human) | 64324 | NSD1 |
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| DOID:0050800 | cerebral creatine deficiency syndrome 1 | HGNC:11055 | Homo sapiens (human) | 6535 | SLC6A8 |
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| DOID:0111670 | primary hyperoxaluria type 1 | HGNC:341 | Homo sapiens (human) | 189 | AGXT |
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| DOID:0050629 | Aicardi-Goutieres syndrome | HGNC:15925 | Homo sapiens (human) | 25939 | SAMHD1 |
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| DOID:0050809 | mucopolysaccharidosis IX | HGNC:5320 | Homo sapiens (human) | 3373 | HYAL1 |
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| DOID:0110148 | Charcot-Marie-Tooth disease type 1A | HGNC:9118 | Homo sapiens (human) | 5376 | PMP22 |
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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:0080552 | congenital disorder of glycosylation Ia | HGNC:9115 | Homo sapiens (human) | 5373 | PMM2 |
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| DOID:0080348 | Alzheimer's disease 1 | HGNC:620 | Homo sapiens (human) | 351 | APP |
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