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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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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 | July 29, 2024 |
| Disease ID | Disease Name | Alliance of Genome Resources ID | Species | Gene ID | Gene Symbol | FlyGlycoDB | Evidence Code Names | References ▼ |
|---|---|---|---|---|---|---|---|---|
| DOID:0111773 | 46,XY sex reversal 8 | HGNC:387 | Homo sapiens (human) | 1109 | AKR1C4 |
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| DOID:9269 | maple syrup urine disease | HGNC:2898 | Homo sapiens (human) | 1738 | DLD |
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| DOID:0111843 | Paganini-Miozzo syndrome | HGNC:19133 | Homo sapiens (human) | 90161 | HS6ST2 |
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| DOID:0110736 | neurodegeneration with brain iron accumulation 2b | HGNC:9039 | Homo sapiens (human) | 8398 | PLA2G6 |
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| DOID:1700 | X-linked ichthyosis | HGNC:11425 | Homo sapiens (human) | 412 | STS |
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| DOID:0110409 | retinitis pigmentosa 46 | HGNC:5385 | Homo sapiens (human) | 3420 | IDH3B |
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| DOID:0111070 | congenital bile acid synthesis defect 3 | HGNC:2652 | Homo sapiens (human) | 9420 | CYP7B1 |
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| DOID:0112218 | developmental and epileptic encephalopathy 83 | HGNC:12527 | Homo sapiens (human) | 7360 | UGP2 |
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| DOID:0111451 | progressive myoclonus epilepsy 8 | HGNC:14253 | Homo sapiens (human) | 10715 | CERS1 |
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| DOID:3659 | sialuria | HGNC:23657 | Homo sapiens (human) | 10020 | GNE |
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| DOID:0111390 | mucopolysaccharidosis Ih | HGNC:5391 | Homo sapiens (human) | 3425 | IDUA |
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| DOID:3635 | congenital myasthenic syndrome | HGNC:10979 | Homo sapiens (human) | 6576 | SLC25A1 |
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| DOID:0080564 | congenital disorder of glycosylation Il | HGNC:15672 | Homo sapiens (human) | 79796 | ALG9 |
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| DOID:0070434 | hyperphosphatasia with impaired intellectual development syndrome 2 | HGNC:23215 | Homo sapiens (human) | 84720 | PIGO |
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| DOID:0111236 | congenital muscular dystrophy-dystroglycanopathy type A3 | HGNC:19139 | Homo sapiens (human) | 55624 | POMGNT1 |
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| DOID:0110676 | congenital myasthenic syndrome 13 | HGNC:2995 | Homo sapiens (human) | 1798 | DPAGT1 |
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| DOID:0080140 | multiple congenital anomalies-hypotonia-seizures syndrome 3 | HGNC:14938 | Homo sapiens (human) | 51604 | PIGT |
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| DOID:0112105 | X-linked parkinsonism-spasticity syndrome | HGNC:18305 | Homo sapiens (human) | 10159 | ATP6AP2 |
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| DOID:0111231 | congenital muscular dystrophy-dystroglycanopathy type A8 | HGNC:25902 | Homo sapiens (human) | 84892 | POMGNT2 |
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| DOID:5723 | optic atrophy | HGNC:29622 | Homo sapiens (human) | 27349 | MCAT |
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| DOID:0111527 | spinal muscular atrophy with progressive myoclonic epilepsy | HGNC:735 | Homo sapiens (human) | 427 | ASAH1 |
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| DOID:0080576 | spondyloepimetaphyseal dysplasia, Genevieve-type | HGNC:19237 | Homo sapiens (human) | 54187 | NANS |
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| DOID:0080575 | Larsen-like syndrome B3GAT3 type | HGNC:923 | Homo sapiens (human) | 26229 | B3GAT3 |
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| DOID:0050636 | familial visceral amyloidosis | HGNC:6740 | Homo sapiens (human) | 4069 | LYZ |
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| DOID:10825 | essential hypertension | HGNC:2638 | Homo sapiens (human) | 1577 | CYP3A5 |
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