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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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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
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:0050700 | cardiomyopathy | HGNC:17075 | Homo sapiens (human) | 23118 | TAB2 |
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| DOID:1380 | endometrial cancer | HGNC:8905 | Homo sapiens (human) | 5236 | PGM1 |
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| DOID:0112361 | spondylocostal dysostosis 3 | HGNC:6560 | Homo sapiens (human) | 3955 | LFNG |
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| DOID:10123 | pigmentation disease | HGNC:6343 | Homo sapiens (human) | 4254 | KITLG |
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| DOID:0050563 | nonsyndromic deafness | HGNC:12601 | Homo sapiens (human) | 7399 | USH2A |
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| DOID:12732 | intermediate uveitis | HGNC:1603 | Homo sapiens (human) | 729230 | CCR2 |
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| DOID:4483 | rhinitis | HGNC:8583 | Homo sapiens (human) | 5054 | SERPINE1 |
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| DOID:0070370 | restrictive dermopathy 2 | HGNC:6636 | Homo sapiens (human) | 4000 | LMNA |
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| DOID:0081339 | congenital myopathy 2B | HGNC:129 | Homo sapiens (human) | 58 | ACTA1 |
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| DOID:1612 | breast cancer | HGNC:3542 | Homo sapiens (human) | 2153 | F5 |
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| DOID:10003 | sensorineural hearing loss | HGNC:7594 | Homo sapiens (human) | 51168 | MYO15A |
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| DOID:10652 | Alzheimer's disease | HGNC:288 | Homo sapiens (human) | 155 | ADRB3 |
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| DOID:9970 | obesity | HGNC:6080 | Homo sapiens (human) | 3636 | INPPL1 |
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| DOID:0050741 | alcohol dependence | HGNC:1957 | Homo sapiens (human) | 1136 | CHRNA3 |
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| DOID:988 | mitral valve prolapse | HGNC:12373 | Homo sapiens (human) | 7253 | TSHR |
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| DOID:2152 | ovary epithelial cancer | HGNC:17075 | Homo sapiens (human) | 23118 | TAB2 |
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| DOID:3748 | esophagus squamous cell carcinoma | HGNC:6848 | Homo sapiens (human) | 4214 | MAP3K1 |
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| DOID:0050440 | familial partial lipodystrophy | HGNC:6636 | Homo sapiens (human) | 4000 | LMNA |
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| DOID:0060731 | congenital central hypoventilation syndrome | HGNC:1033 | Homo sapiens (human) | 627 | BDNF |
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| DOID:12297 | Vogt-Koyanagi-Harada disease | HGNC:4942 | Homo sapiens (human) | 3117 | HLA-DQA1 |
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| DOID:0112218 | developmental and epileptic encephalopathy 83 | HGNC:12527 | Homo sapiens (human) | 7360 | UGP2 |
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| DOID:8924 | autoimmune thrombocytopenic purpura | HGNC:5991 | Homo sapiens (human) | 3552 | IL1A |
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| DOID:0070221 | progressive familial intrahepatic cholestasis | HGNC:20758 | Homo sapiens (human) | 84936 | ZFYVE19 |
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| DOID:0080348 | Alzheimer's disease 1 | HGNC:9052 | Homo sapiens (human) | 5328 | PLAU |
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| DOID:3070 | high grade glioma | HGNC:18798 | Homo sapiens (human) | 23446 | SLC44A1 |
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