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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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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:1682 | congenital heart disease | HGNC:4173 | Homo sapiens (human) | 2626 | GATA4 |
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| DOID:0110087 | asphyxiating thoracic dystrophy 3 | HGNC:2962 | Homo sapiens (human) | 79659 | DYNC2H1 |
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| DOID:0110175 | Charcot-Marie-Tooth disease axonal type 2O | HGNC:2961 | Homo sapiens (human) | 1778 | DYNC1H1 |
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| DOID:1056 | oculocerebrorenal syndrome | HGNC:8108 | Homo sapiens (human) | 4952 | OCRL |
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| DOID:2129 | atypical teratoid rhabdoid tumor | HGNC:11103 | Homo sapiens (human) | 6598 | SMARCB1 |
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| DOID:10629 | microphthalmia | HGNC:4837 | Homo sapiens (human) | 3052 | HCCS |
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| DOID:10584 | retinitis pigmentosa | HGNC:17340 | Homo sapiens (human) | 10594 | PRPF8 |
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| DOID:0060569 | hypertrichotic osteochondrodysplasia Cantu type | HGNC:60 | Homo sapiens (human) | 10060 | ABCC9 |
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| DOID:4483 | rhinitis | HGNC:1033 | Homo sapiens (human) | 627 | BDNF |
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| DOID:0110867 | congenital stationary night blindness 1C | HGNC:7146 | Homo sapiens (human) | 4308 | TRPM1 |
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| DOID:0081126 | DeSanto-Shinawi syndrome | HGNC:17327 | Homo sapiens (human) | 51322 | WAC |
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| DOID:0110659 | congenital myasthenic syndrome 7 | HGNC:11510 | Homo sapiens (human) | 127833 | SYT2 |
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| DOID:1572 | normal pressure hydrocephalus | HGNC:26684 | Homo sapiens (human) | 80217 | CFAP43 |
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| DOID:0050773 | paraganglioma | HGNC:10681 | Homo sapiens (human) | 6390 | SDHB |
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| DOID:0070248 | autosomal recessive Emery-Dreifuss muscular dystrophy 3 | HGNC:6636 | Homo sapiens (human) | 4000 | LMNA |
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| DOID:10588 | adrenoleukodystrophy | HGNC:61 | Homo sapiens (human) | 215 | ABCD1 |
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| DOID:0060545 | Hermansky-Pudlak syndrome 7 | HGNC:17328 | Homo sapiens (human) | 84062 | DTNBP1 |
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| DOID:11476 | osteoporosis | HGNC:6697 | Homo sapiens (human) | 4041 | LRP5 |
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| DOID:9074 | systemic lupus erythematosus | HGNC:1324 | Homo sapiens (human) | 721 | C4B |
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| DOID:0090078 | hypogonadotropic hypogonadism 7 with or without anosmia | HGNC:4421 | Homo sapiens (human) | 2798 | GNRHR |
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| DOID:9452 | steatotic liver disease | HGNC:2631 | Homo sapiens (human) | 1571 | CYP2E1 |
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| DOID:1929 | supravalvular aortic stenosis | HGNC:3327 | Homo sapiens (human) | 2006 | ELN |
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| DOID:14264 | benign neonatal seizures | HGNC:6296 | Homo sapiens (human) | 3785 | KCNQ2 |
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| DOID:0090144 | Donnai-Barrow syndrome | HGNC:6694 | Homo sapiens (human) | 4036 | LRP2 |
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| DOID:5813 | purine nucleoside phosphorylase deficiency | HGNC:7892 | Homo sapiens (human) | 4860 | PNP |
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