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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:6432 | pulmonary hypertension | RGD:2536 | Rattus norvegicus (Norway rat) | 50672 | Ednrb |
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| DOID:0080855 | Parkinsonism | HGNC:4232 | Homo sapiens (human) | 2668 | GDNF |
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| DOID:6432 | pulmonary hypertension | RGD:3714 | Rattus norvegicus (Norway rat) | 25553 | Slc6a4 |
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| DOID:0050741 | alcohol dependence | RGD:2677 | Rattus norvegicus (Norway rat) | 25453 | Gdnf |
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| DOID:11721 | glycogen storage disease VII | HGNC:8877 | Homo sapiens (human) | 5213 | PFKM |
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| DOID:418 | systemic scleroderma | HGNC:3603 | Homo sapiens (human) | 2200 | FBN1 |
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| DOID:0110278 | autosomal recessive limb-girdle muscular dystrophy type 2D | HGNC:10805 | Homo sapiens (human) | 6442 | SGCA |
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| DOID:6688 | autoimmune lymphoproliferative syndrome | HGNC:11920 | Homo sapiens (human) | 355 | FAS |
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| DOID:10763 | hypertension | RGD:2041 | Rattus norvegicus (Norway rat) | 24170 | Add1 |
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| DOID:1852 | intrahepatic cholestasis | HGNC:45 | Homo sapiens (human) | 5244 | ABCB4 |
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| DOID:684 | hepatocellular carcinoma | HGNC:583 | Homo sapiens (human) | 324 | APC |
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| DOID:13636 | Fanconi anemia | HGNC:3585 | Homo sapiens (human) | 2177 | FANCD2 |
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| DOID:1270 | hereditary hemorrhagic telangiectasia | HGNC:3349 | Homo sapiens (human) | 2022 | ENG |
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| DOID:552 | pneumonia | HGNC:6000 | Homo sapiens (human) | 3557 | IL1RN |
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| DOID:9970 | obesity | HGNC:2159 | Homo sapiens (human) | 1268 | CNR1 |
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| DOID:9074 | systemic lupus erythematosus | HGNC:8760 | Homo sapiens (human) | 5133 | PDCD1 |
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| DOID:893 | Wilson disease | HGNC:870 | Homo sapiens (human) | 540 | ATP7B |
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| DOID:0050439 | Usher syndrome | HGNC:7606 | Homo sapiens (human) | 4647 | MYO7A |
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| DOID:10763 | hypertension | HGNC:6357 | Homo sapiens (human) | 3816 | KLK1 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:1667 | Homo sapiens (human) | 952 | CD38 |
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| DOID:1596 | depressive disorder | HGNC:11050 | Homo sapiens (human) | 6532 | SLC6A4 |
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| DOID:4184 | pseudohypoparathyroidism | HGNC:4392 | Homo sapiens (human) | 2778 | GNAS |
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| DOID:5419 | schizophrenia | HGNC:4586 | Homo sapiens (human) | 2904 | GRIN2B |
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| DOID:2741 | bilirubin metabolic disorder | HGNC:12530 | Homo sapiens (human) | 54658 | UGT1A1 |
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| DOID:0110279 | autosomal recessive limb-girdle muscular dystrophy type 2E | HGNC:10806 | Homo sapiens (human) | 6443 | SGCB |
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