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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:3526 | cerebral infarction | HGNC:12441 | Homo sapiens (human) | 7298 | TYMS |
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| DOID:0112338 | spermatogenic failure 57 | HGNC:21185 | Homo sapiens (human) | 154197 | PNLDC1 |
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| DOID:12849 | autistic disorder | HGNC:26392 | Homo sapiens (human) | 139411 | PTCHD1 |
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| DOID:289 | endometriosis | HGNC:3467 | Homo sapiens (human) | 2099 | ESR1 |
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| DOID:0112108 | myofibrillar myopathy 10 | HGNC:11480 | Homo sapiens (human) | 6840 | SVIL |
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| DOID:4988 | alcoholic pancreatitis | HGNC:1884 | Homo sapiens (human) | 1080 | CFTR |
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| DOID:2058 | chronic mucocutaneous candidiasis | HGNC:16404 | Homo sapiens (human) | 112744 | IL17F |
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| DOID:0080281 | schizophrenia 19 | HGNC:9898 | Homo sapiens (human) | 10137 | RBM12 |
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| DOID:0111236 | congenital muscular dystrophy-dystroglycanopathy type A3 | HGNC:19139 | Homo sapiens (human) | 55624 | POMGNT1 |
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| DOID:768 | retinoblastoma | HGNC:9884 | Homo sapiens (human) | 5925 | RB1 |
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| DOID:0080142 | mosaic variegated aneuploidy syndrome 2 | HGNC:30794 | Homo sapiens (human) | 9702 | CEP57 |
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| DOID:10825 | essential hypertension | HGNC:5208 | Homo sapiens (human) | 3290 | HSD11B1 |
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| DOID:0060041 | autism spectrum disorder | HGNC:20445 | Homo sapiens (human) | 114785 | MBD6 |
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| DOID:0080694 | Galloway-Mowat syndrome | HGNC:18016 | Homo sapiens (human) | 55746 | NUP133 |
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| DOID:0060903 | thrombosis | HGNC:3542 | Homo sapiens (human) | 2153 | F5 |
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| DOID:0080287 | spinocerebellar ataxia 45 | HGNC:3596 | Homo sapiens (human) | 2196 | FAT2 |
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| DOID:14018 | alcoholic liver cirrhosis | HGNC:4087 | Homo sapiens (human) | 2566 | GABRG2 |
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| DOID:2841 | asthma | HGNC:1941 | Homo sapiens (human) | 1122 | CHML |
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| DOID:5409 | lung small cell carcinoma | HGNC:12637 | Homo sapiens (human) | 7403 | KDM6A |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:5467 | Homo sapiens (human) | 3482 | IGF2R |
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| DOID:8552 | chronic myeloid leukemia | HGNC:4942 | Homo sapiens (human) | 3117 | HLA-DQA1 |
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| DOID:3910 | lung adenocarcinoma | HGNC:777 | Homo sapiens (human) | 463 | ZFHX3 |
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| DOID:0060342 | acromelic frontonasal dysostosis | HGNC:29316 | Homo sapiens (human) | 57688 | ZSWIM6 |
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| DOID:0090136 | complex cortical dysplasia with other brain malformations 6 | HGNC:20778 | Homo sapiens (human) | 203068 | TUBB |
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| DOID:0070391 | developmental and epileptic encephalopathy 105 | HGNC:15736 | Homo sapiens (human) | 283987 | HID1 |
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