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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:0050873 | follicular lymphoma | HGNC:11919 | Homo sapiens (human) | 958 | CD40 |
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| DOID:3070 | high grade glioma | HGNC:12828 | Homo sapiens (human) | 7515 | XRCC1 |
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| DOID:11476 | osteoporosis | HGNC:1437 | Homo sapiens (human) | 796 | CALCA |
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| DOID:4914 | esophagus adenocarcinoma | HGNC:7173 | Homo sapiens (human) | 4314 | MMP3 |
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| DOID:0110661 | congenital myasthenic syndrome 20 | HGNC:14025 | Homo sapiens (human) | 60482 | SLC5A7 |
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| DOID:2841 | asthma | HGNC:18124 | Homo sapiens (human) | 64805 | P2RY12 |
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| DOID:0110814 | hereditary spastic paraplegia 63 | HGNC:469 | Homo sapiens (human) | 271 | AMPD2 |
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| DOID:0050650 | familial atrial fibrillation | HGNC:10586 | Homo sapiens (human) | 6324 | SCN1B |
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| DOID:0081373 | disabling pansclerotic morphea | HGNC:11365 | Homo sapiens (human) | 6775 | STAT4 |
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| DOID:9952 | acute lymphoblastic leukemia | HGNC:4944 | Homo sapiens (human) | 3119 | HLA-DQB1 |
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| DOID:0081138 | agammaglobulinemia 6 | HGNC:1699 | Homo sapiens (human) | 974 | CD79B |
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| DOID:0050866 | oral squamous cell carcinoma | HGNC:2631 | Homo sapiens (human) | 1571 | CYP2E1 |
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| DOID:10611 | protein-losing enteropathy | HGNC:2665 | Homo sapiens (human) | 1604 | CD55 |
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| DOID:0050811 | congenital adrenal hyperplasia | HGNC:2600 | Homo sapiens (human) | 1589 | CYP21A2 |
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| DOID:9970 | obesity | HGNC:4132 | Homo sapiens (human) | 2587 | GALR1 |
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| DOID:0110645 | long QT syndrome 2 | HGNC:6251 | Homo sapiens (human) | 3757 | KCNH2 |
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| DOID:0060455 | Thiel-Behnke corneal dystrophy | HGNC:11771 | Homo sapiens (human) | 7045 | TGFBI |
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| DOID:332 | amyotrophic lateral sclerosis | HGNC:9206 | Homo sapiens (human) | 5446 | PON3 |
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| DOID:4483 | rhinitis | HGNC:6922 | Homo sapiens (human) | 4153 | MBL2 |
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| DOID:0111481 | combined oxidative phosphorylation deficiency 11 | HGNC:21176 | Homo sapiens (human) | 55005 | RMND1 |
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| DOID:1273 | respiratory syncytial virus infectious disease | HGNC:6029 | Homo sapiens (human) | 3578 | IL9 |
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| DOID:11984 | hypertrophic cardiomyopathy | HGNC:12665 | Homo sapiens (human) | 7414 | VCL |
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| DOID:0060230 | basal ganglia calcification | HGNC:14686 | Homo sapiens (human) | 58494 | JAM2 |
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| DOID:0050741 | alcohol dependence | HGNC:8010 | Homo sapiens (human) | 9369 | NRXN3 |
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| DOID:5409 | lung small cell carcinoma | HGNC:30064 | Homo sapiens (human) | 55193 | PBRM1 |
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