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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:0050866 | oral squamous cell carcinoma | HGNC:1603 | Homo sapiens (human) | 729230 | CCR2 |
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| DOID:9538 | multiple myeloma | HGNC:2595 | Homo sapiens (human) | 1543 | CYP1A1 |
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| DOID:302 | substance abuse | HGNC:281 | Homo sapiens (human) | 150 | ADRA2A |
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| DOID:10652 | Alzheimer's disease | HGNC:24864 | Homo sapiens (human) | 26330 | GAPDHS |
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| DOID:0050580 | hereditary lymphedema | HGNC:1850 | Homo sapiens (human) | 9620 | CELSR1 |
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| DOID:12236 | primary biliary cholangitis | HGNC:1983 | Homo sapiens (human) | 84916 | UTP4 |
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| DOID:3204 | schwannomatosis | HGNC:11103 | Homo sapiens (human) | 6598 | SMARCB1 |
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| DOID:0111538 | paramyotonia congenita of Von Eulenburg | HGNC:10591 | Homo sapiens (human) | 6329 | SCN4A |
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| DOID:0111214 | autosomal recessive distal hereditary motor neuronopathy 5 | HGNC:5228 | Homo sapiens (human) | 3300 | DNAJB2 |
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| DOID:0080586 | Van Maldergem syndrome 2 | HGNC:23109 | Homo sapiens (human) | 79633 | FAT4 |
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| DOID:4914 | esophagus adenocarcinoma | HGNC:3823 | Homo sapiens (human) | 27086 | FOXP1 |
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| DOID:684 | hepatocellular carcinoma | HGNC:9646 | Homo sapiens (human) | 5783 | PTPN13 |
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| DOID:4372 | intracranial embolism | HGNC:6344 | Homo sapiens (human) | 9365 | KL |
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| DOID:9952 | acute lymphoblastic leukemia | HGNC:8064 | Homo sapiens (human) | 8021 | NUP214 |
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| DOID:0080309 | fatal infantile hypertonic myofibrillar myopathy | HGNC:2389 | Homo sapiens (human) | 1410 | CRYAB |
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| DOID:8893 | psoriasis | HGNC:613 | Homo sapiens (human) | 348 | APOE |
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| DOID:633 | myositis | HGNC:4948 | Homo sapiens (human) | 3123 | HLA-DRB1 |
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| DOID:9296 | cleft lip | HGNC:4221 | Homo sapiens (human) | 392255 | GDF6 |
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| DOID:10652 | Alzheimer's disease | HGNC:6700 | Homo sapiens (human) | 7804 | LRP8 |
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| DOID:127 | leiomyoma | HGNC:12828 | Homo sapiens (human) | 7515 | XRCC1 |
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| DOID:0050941 | spastic ataxia 2 | HGNC:6317 | Homo sapiens (human) | 10749 | KIF1C |
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| DOID:12140 | Chagas disease | HGNC:11177 | Homo sapiens (human) | 6646 | SOAT1 |
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| DOID:0060256 | Dowling-Degos disease | HGNC:14988 | Homo sapiens (human) | 23509 | POFUT1 |
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| DOID:1324 | lung cancer | HGNC:8975 | Homo sapiens (human) | 5290 | PIK3CA |
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| DOID:12971 | hereditary spherocytosis | HGNC:492 | Homo sapiens (human) | 286 | ANK1 |
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