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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:0110928 | nemaline myopathy 2 | HGNC:7720 | Homo sapiens (human) | 4703 | NEB |
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| DOID:0110350 | osteogenesis imperfecta type 6 | HGNC:8824 | Homo sapiens (human) | 5176 | SERPINF1 |
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| DOID:0111442 | optic atrophy 9 | HGNC:118 | Homo sapiens (human) | 50 | ACO2 |
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| DOID:0050649 | atransferrinemia | HGNC:11740 | Homo sapiens (human) | 7018 | TF |
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| DOID:12930 | dilated cardiomyopathy | HGNC:20039 | Homo sapiens (human) | 10486 | CAP2 |
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| DOID:0110615 | primary ciliary dyskinesia 25 | HGNC:21493 | Homo sapiens (human) | 161582 | DNAAF4 |
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| DOID:0081266 | pachygyria, microcephaly, developmental delay, and dysmorphic facies, with or without seizures | HGNC:18599 | Homo sapiens (human) | 10844 | TUBGCP2 |
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| DOID:11830 | myopia | HGNC:6701 | Homo sapiens (human) | 4043 | LRPAP1 |
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| DOID:0060801 | MEHMO syndrome | HGNC:3267 | Homo sapiens (human) | 1968 | EIF2S3 |
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| DOID:0060248 | Simpson-Golabi-Behmel syndrome type 1 | HGNC:4451 | Homo sapiens (human) | 2719 | GPC3 |
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| DOID:0110639 | congenital muscular dystrophy due to integrin alpha-7 deficiency | HGNC:6143 | Homo sapiens (human) | 3679 | ITGA7 |
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| DOID:0110764 | hereditary spastic paraplegia 11 | HGNC:11226 | Homo sapiens (human) | 80208 | SPG11 |
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| DOID:0080486 | peroxisome biogenesis disorder 12A | HGNC:9713 | Homo sapiens (human) | 5824 | PEX19 |
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| DOID:0110076 | arrhythmogenic right ventricular dysplasia 8 | HGNC:3052 | Homo sapiens (human) | 1832 | DSP |
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| DOID:0070442 | paroxysmal nonkinesigenic dyskinesia 3 | HGNC:6284 | Homo sapiens (human) | 3778 | KCNMA1 |
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| DOID:0050540 | Charcot-Marie-Tooth disease type 3 | HGNC:9118 | Homo sapiens (human) | 5376 | PMP22 |
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| DOID:0080095 | myofibrillar myopathy 4 | HGNC:15710 | Homo sapiens (human) | 11155 | LDB3 |
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| DOID:10016 | multiple endocrine neoplasia type 2B | HGNC:9967 | Homo sapiens (human) | 5979 | RET |
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| DOID:0081276 | cerebellar atrophy, visual impairment, and psychomotor retardation | HGNC:28957 | Homo sapiens (human) | 23065 | EMC1 |
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| DOID:0110243 | cataract 46 juvenile-onset | HGNC:21244 | Homo sapiens (human) | 221496 | LEMD2 |
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| DOID:0110598 | primary ciliary dyskinesia 14 | HGNC:25244 | Homo sapiens (human) | 339829 | CCDC39 |
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| DOID:0110060 | amelogenesis imperfecta hypomaturation type 2A2 | HGNC:7167 | Homo sapiens (human) | 9313 | MMP20 |
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| DOID:0110424 | dilated cardiomyopathy 1CC | HGNC:29557 | Homo sapiens (human) | 91624 | NEXN |
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| DOID:0110858 | polycystic kidney disease 1 | HGNC:9008 | Homo sapiens (human) | 5310 | PKD1 |
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| DOID:0070238 | primary coenzyme Q10 deficiency 1 | HGNC:25223 | Homo sapiens (human) | 27235 | COQ2 |
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