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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:0090044 | dystonia 9 | HGNC:11005 | Homo sapiens (human) | 6513 | SLC2A1 |
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| DOID:0112204 | developmental and epileptic encephalopathy 68 | HGNC:29947 | Homo sapiens (human) | 22906 | TRAK1 |
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| DOID:0050117 | disease by infectious agent | HGNC:4838 | Homo sapiens (human) | 3053 | SERPIND1 |
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| DOID:0080162 | lupus nephritis | HGNC:4948 | Homo sapiens (human) | 3123 | HLA-DRB1 |
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| DOID:3526 | cerebral infarction | HGNC:4814 | Homo sapiens (human) | 8997 | KALRN |
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| DOID:0111343 | lateral meningocele syndrome | HGNC:7883 | Homo sapiens (human) | 4854 | NOTCH3 |
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| DOID:0050869 | villous adenoma | HGNC:18505 | Homo sapiens (human) | 54894 | RNF43 |
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| DOID:0111349 | hereditary desmoid disease | HGNC:583 | Homo sapiens (human) | 324 | APC |
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| DOID:13809 | familial combined hyperlipidemia | HGNC:613 | Homo sapiens (human) | 348 | APOE |
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| DOID:0110307 | hypertrophic cardiomyopathy 1 | HGNC:7577 | Homo sapiens (human) | 4625 | MYH7 |
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| DOID:5419 | schizophrenia | HGNC:12008 | Homo sapiens (human) | 7166 | TPH1 |
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| DOID:809 | cocaine abuse | HGNC:1959 | Homo sapiens (human) | 1138 | CHRNA5 |
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| DOID:13001 | carotid stenosis | HGNC:7173 | Homo sapiens (human) | 4314 | MMP3 |
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| DOID:5517 | stomach carcinoma | HGNC:270 | Homo sapiens (human) | 142 | PARP1 |
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| DOID:0110084 | arrhythmogenic right ventricular dysplasia 13 | HGNC:2511 | Homo sapiens (human) | 29119 | CTNNA3 |
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| DOID:13258 | typhoid fever | HGNC:6709 | Homo sapiens (human) | 4049 | LTA |
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| DOID:0080202 | adenoid cystic carcinoma | HGNC:12836 | Homo sapiens (human) | 22803 | XRN2 |
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| DOID:1702 | ichthyosis vulgaris | HGNC:3748 | Homo sapiens (human) | 2312 | FLG |
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| DOID:0050127 | sinusitis | HGNC:5973 | Homo sapiens (human) | 3596 | IL13 |
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| DOID:0060892 | late onset Parkinson's disease | HGNC:3296 | Homo sapiens (human) | 1981 | EIF4G1 |
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| DOID:3310 | atopic dermatitis | HGNC:6015 | Homo sapiens (human) | 3566 | IL4R |
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| DOID:2841 | asthma | HGNC:11848 | Homo sapiens (human) | 7097 | TLR2 |
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| DOID:12377 | spinal muscular atrophy | HGNC:644 | Homo sapiens (human) | 367 | AR |
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| DOID:2590 | familial nephrotic syndrome | HGNC:18143 | Homo sapiens (human) | 23500 | DAAM2 |
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| DOID:0110050 | Alzheimer's disease 18 | HGNC:188 | Homo sapiens (human) | 102 | ADAM10 |
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