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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:10325 | silicosis | HGNC:1318 | Homo sapiens (human) | 718 | C3 |
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| DOID:3008 | invasive ductal carcinoma | HGNC:7739 | Homo sapiens (human) | 4747 | NEFL |
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| DOID:2377 | multiple sclerosis | HGNC:4940 | Homo sapiens (human) | 3115 | HLA-DPB1 |
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| DOID:684 | hepatocellular carcinoma | HGNC:7218 | Homo sapiens (human) | 4353 | MPO |
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| DOID:5419 | schizophrenia | HGNC:6144 | Homo sapiens (human) | 8516 | ITGA8 |
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| DOID:2349 | arteriosclerosis | HGNC:9596 | Homo sapiens (human) | 5734 | PTGER4 |
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| DOID:10591 | pre-eclampsia | HGNC:5208 | Homo sapiens (human) | 3290 | HSD11B1 |
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| DOID:12347 | osteogenesis imperfecta | HGNC:26185 | Homo sapiens (human) | 79879 | CCDC134 |
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| DOID:4971 | myelofibrosis | HGNC:18318 | Homo sapiens (human) | 171023 | ASXL1 |
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| DOID:3910 | lung adenocarcinoma | HGNC:3236 | Homo sapiens (human) | 1956 | EGFR |
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| DOID:0112372 | Coffin-Siris syndrome 11 | HGNC:11106 | Homo sapiens (human) | 6602 | SMARCD1 |
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| DOID:13001 | carotid stenosis | HGNC:5962 | Homo sapiens (human) | 3586 | IL10 |
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| DOID:2377 | multiple sclerosis | HGNC:10907 | Homo sapiens (human) | 6556 | SLC11A1 |
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| DOID:341 | peripheral vascular disease | HGNC:6619 | Homo sapiens (human) | 3990 | LIPC |
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| DOID:9119 | acute myeloid leukemia | HGNC:10830 | Homo sapiens (human) | 6455 | SH3GL1 |
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| DOID:0111337 | Jackson-Weiss syndrome | HGNC:3688 | Homo sapiens (human) | 2260 | FGFR1 |
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| DOID:10652 | Alzheimer's disease | HGNC:11850 | Homo sapiens (human) | 7099 | TLR4 |
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| DOID:1324 | lung cancer | HGNC:7325 | Homo sapiens (human) | 4436 | MSH2 |
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| DOID:0050741 | alcohol dependence | HGNC:11048 | Homo sapiens (human) | 6530 | SLC6A2 |
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| DOID:3908 | lung non-small cell carcinoma | HGNC:5383 | Homo sapiens (human) | 3418 | IDH2 |
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| DOID:5426 | primary ovarian insufficiency | HGNC:1068 | Homo sapiens (human) | 9210 | BMP15 |
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| DOID:0050580 | hereditary lymphedema | HGNC:16709 | Homo sapiens (human) | 10203 | CALCRL |
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| DOID:0001816 | angiosarcoma | HGNC:7553 | Homo sapiens (human) | 4609 | MYC |
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| DOID:0080233 | autosomal dominant intellectual developmental disorder 50 | HGNC:30782 | Homo sapiens (human) | 80155 | NAA15 |
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| DOID:14021 | Tietze's syndrome | HGNC:7105 | Homo sapiens (human) | 4286 | MITF |
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