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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
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:0060733 | junctional epidermolysis bullosa with pyloric atresia | HGNC:6158 | Homo sapiens (human) | 3691 | ITGB4 |
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| DOID:0110339 | osteogenesis imperfecta type 3 | HGNC:2198 | Homo sapiens (human) | 1278 | COL1A2 |
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| DOID:0070307 | craniolenticulosutural dysplasia | HGNC:10701 | Homo sapiens (human) | 10484 | SEC23A |
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| DOID:83 | cataract | HGNC:17992 | Homo sapiens (human) | 80036 | TRPM3 |
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| DOID:0070491 | mitochondrial complex IV deficiency nuclear type 1 | HGNC:11474 | Homo sapiens (human) | 6834 | SURF1 |
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| DOID:0060676 | catecholaminergic polymorphic ventricular tachycardia 2 | HGNC:1513 | Homo sapiens (human) | 845 | CASQ2 |
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| DOID:9256 | colorectal cancer | HGNC:11283 | Homo sapiens (human) | 6714 | SRC |
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| DOID:0070516 | Mitchell syndrome | HGNC:119 | Homo sapiens (human) | 51 | ACOX1 |
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| DOID:0110195 | Charcot-Marie-Tooth disease type 4E | HGNC:3239 | Homo sapiens (human) | 1959 | EGR2 |
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| DOID:0050437 | Danon disease | HGNC:6501 | Homo sapiens (human) | 3920 | LAMP2 |
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| DOID:0060349 | microcephaly with or without chorioretinopathy, lymphedema, or mental retardation | HGNC:6388 | Homo sapiens (human) | 3832 | KIF11 |
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| DOID:0110074 | arrhythmogenic right ventricular dysplasia 5 | HGNC:28472 | Homo sapiens (human) | 79188 | TMEM43 |
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| DOID:0080394 | nephrotic syndrome type 19 | HGNC:18017 | Homo sapiens (human) | 23279 | NUP160 |
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| DOID:0110354 | retinitis pigmentosa 19 | HGNC:34 | Homo sapiens (human) | 24 | ABCA4 |
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| DOID:0070216 | familial hyperinsulinemic hypoglycemia 3 | HGNC:4195 | Homo sapiens (human) | 2645 | GCK |
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| DOID:0090120 | hereditary neutrophilia | HGNC:2439 | Homo sapiens (human) | 1441 | CSF3R |
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| DOID:0110792 | hereditary spastic paraplegia 4 | HGNC:11233 | Homo sapiens (human) | 6683 | SPAST |
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| DOID:0080155 | very long chain acyl-CoA dehydrogenase deficiency | HGNC:92 | Homo sapiens (human) | 37 | ACADVL |
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| DOID:0050477 | Liddle syndrome | HGNC:10600 | Homo sapiens (human) | 6338 | SCNN1B |
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| DOID:0110169 | Charcot-Marie-Tooth disease axonal type 2P | HGNC:25135 | Homo sapiens (human) | 90678 | LRSAM1 |
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| DOID:0090034 | myoclonic dystonia 11 | HGNC:10808 | Homo sapiens (human) | 8910 | SGCE |
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| DOID:0090107 | autosomal dominant hypocalcemia 1 | HGNC:1514 | Homo sapiens (human) | 846 | CASR |
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| DOID:0111555 | Alkuraya-Kucinskas syndrome | HGNC:26953 | Homo sapiens (human) | 84162 | BLTP1 |
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| DOID:0050475 | Weill-Marchesani syndrome | HGNC:13201 | Homo sapiens (human) | 81794 | ADAMTS10 |
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| DOID:0060581 | Noonan syndrome 3 | HGNC:6407 | Homo sapiens (human) | 3845 | KRAS |
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