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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:0110361 | retinitis pigmentosa 75 | HGNC:26147 | Homo sapiens (human) | 60509 | AGBL5 |
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| DOID:2671 | transitional cell carcinoma | HGNC:9816 | Homo sapiens (human) | 10111 | RAD50 |
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| DOID:8437 | intestinal obstruction | HGNC:4886 | Homo sapiens (human) | 3077 | HFE |
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| DOID:0060081 | triple-receptor negative breast cancer | HGNC:12637 | Homo sapiens (human) | 7403 | KDM6A |
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| DOID:9119 | acute myeloid leukemia | HGNC:1541 | Homo sapiens (human) | 867 | CBL |
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| DOID:4248 | coronary stenosis | HGNC:8823 | Homo sapiens (human) | 5175 | PECAM1 |
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| DOID:1270 | hereditary hemorrhagic telangiectasia | HGNC:4217 | Homo sapiens (human) | 2658 | GDF2 |
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| DOID:0080037 | Worth syndrome | HGNC:6697 | Homo sapiens (human) | 4041 | LRP5 |
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| DOID:0111913 | spermatogenic failure 30 | HGNC:20122 | Homo sapiens (human) | 122402 | TDRD9 |
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| DOID:5844 | myocardial infarction | HGNC:7966 | Homo sapiens (human) | 10062 | NR1H3 |
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| DOID:0081188 | autosomal recessive intellectual developmental disorder 14 | HGNC:4551 | Homo sapiens (human) | 9524 | TECR |
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| DOID:0112363 | spondylocostal dysostosis 5 | HGNC:11605 | Homo sapiens (human) | 6911 | TBX6 |
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| DOID:0112182 | mismatch repair cancer syndrome | HGNC:16261 | Homo sapiens (human) | 114571 | SLC22A9 |
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| DOID:5517 | stomach carcinoma | HGNC:20893 | Homo sapiens (human) | 54880 | BCOR |
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| DOID:0050650 | familial atrial fibrillation | HGNC:10593 | Homo sapiens (human) | 6331 | SCN5A |
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| DOID:0050773 | paraganglioma | HGNC:10981 | Homo sapiens (human) | 8402 | SLC25A11 |
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| DOID:13636 | Fanconi anemia | HGNC:3588 | Homo sapiens (human) | 2189 | FANCG |
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| DOID:0110734 | neurodegeneration with brain iron accumulation | HGNC:15578 | Homo sapiens (human) | 85021 | REPS1 |
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| DOID:1350 | paranasal sinus benign neoplasm | HGNC:11998 | Homo sapiens (human) | 7157 | TP53 |
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| DOID:9074 | systemic lupus erythematosus | HGNC:6922 | Homo sapiens (human) | 4153 | MBL2 |
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| DOID:0081074 | Teebi hypertelorism syndrome 2 | HGNC:1750 | Homo sapiens (human) | 1009 | CDH11 |
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| DOID:10123 | pigmentation disease | HGNC:6119 | Homo sapiens (human) | 3662 | IRF4 |
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| DOID:9669 | senile cataract | HGNC:8125 | Homo sapiens (human) | 4968 | OGG1 |
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| DOID:8398 | osteoarthritis | HGNC:2197 | Homo sapiens (human) | 1277 | COL1A1 |
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| DOID:4914 | esophagus adenocarcinoma | HGNC:18129 | Homo sapiens (human) | 51738 | GHRL |
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