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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:13241 | Behcet's disease | HGNC:6001 | Homo sapiens (human) | 3558 | IL2 |
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| DOID:11830 | myopia | HGNC:26575 | Homo sapiens (human) | 201973 | PRIMPOL |
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| DOID:5844 | myocardial infarction | HGNC:6667 | Homo sapiens (human) | 4018 | LPA |
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| DOID:0110553 | autosomal dominant nonsyndromic deafness 23 | HGNC:10887 | Homo sapiens (human) | 6495 | SIX1 |
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| DOID:3459 | breast carcinoma | HGNC:5951 | Homo sapiens (human) | 23705 | CADM1 |
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| DOID:10608 | celiac disease | HGNC:5351 | Homo sapiens (human) | 29851 | ICOS |
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| DOID:10283 | prostate cancer | HGNC:11848 | Homo sapiens (human) | 7097 | TLR2 |
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| DOID:0112283 | spondyloepiphyseal dysplasia Kondo-Fu type | HGNC:15456 | Homo sapiens (human) | 8720 | MBTPS1 |
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| DOID:2893 | cervix carcinoma | HGNC:587 | Homo sapiens (human) | 328 | APEX1 |
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| DOID:0070095 | oculocutaneous albinism type IB | HGNC:12442 | Homo sapiens (human) | 7299 | TYR |
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| DOID:8869 | neuromyelitis optica | HGNC:4944 | Homo sapiens (human) | 3119 | HLA-DQB1 |
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| DOID:0111998 | immunodeficiency 66 | HGNC:14334 | Homo sapiens (human) | 57591 | MRTFA |
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| DOID:0050589 | inflammatory bowel disease | HGNC:195 | Homo sapiens (human) | 6868 | ADAM17 |
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| DOID:0060936 | dystonia 28 childhood-onset | HGNC:15840 | Homo sapiens (human) | 9757 | KMT2B |
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| DOID:0080290 | familial erythrocytosis 5 | HGNC:3415 | Homo sapiens (human) | 2056 | EPO |
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| DOID:5684 | spondyloepimetaphyseal dysplasia, Sponastrime type | HGNC:7801 | Homo sapiens (human) | 4796 | TONSL |
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| DOID:161 | keratosis | HGNC:7218 | Homo sapiens (human) | 4353 | MPO |
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| DOID:0060863 | patterned macular dystrophy | HGNC:9942 | Homo sapiens (human) | 5961 | PRPH2 |
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| DOID:1338 | congenital dyserythropoietic anemia | HGNC:1713 | Homo sapiens (human) | 146059 | CDAN1 |
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| DOID:1324 | lung cancer | HGNC:3236 | Homo sapiens (human) | 1956 | EGFR |
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| DOID:2600 | laryngeal carcinoma | HGNC:12828 | Homo sapiens (human) | 7515 | XRCC1 |
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| DOID:3347 | osteosarcoma | HGNC:16627 | Homo sapiens (human) | 11200 | CHEK2 |
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| DOID:0070437 | hyperphosphatasia with impaired intellectual development syndrome 6 | HGNC:28213 | Homo sapiens (human) | 84992 | PIGY |
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| DOID:2986 | IgA glomerulonephritis | HGNC:11365 | Homo sapiens (human) | 6775 | STAT4 |
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| DOID:0050598 | extrapulmonary tuberculosis | HGNC:3443 | Homo sapiens (human) | 2069 | EREG |
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