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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:936 | brain disease | FB:FBgn0035383 | Drosophila melanogaster (fruit fly) | 38355 | CPT2 |
|
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| DOID:0080000 | muscular disease | HGNC:2330 | Homo sapiens (human) | 1376 | CPT2 |
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| DOID:936 | brain disease | HGNC:2330 | Homo sapiens (human) | 1376 | CPT2 |
|
||
| DOID:0080000 | muscular disease | FB:FBgn0035383 | Drosophila melanogaster (fruit fly) | 38355 | CPT2 |
|
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| DOID:3146 | lipid metabolism disorder | HGNC:2330 | Homo sapiens (human) | 1376 | CPT2 |
|
||
| DOID:0110818 | hereditary spastic paraplegia 73 | HGNC:18540 | Homo sapiens (human) | 126129 | CPT1C |
|
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| DOID:9970 | obesity | HGNC:2328 | Homo sapiens (human) | 1374 | CPT1A |
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| DOID:0080547 | metabolic dysfunction-associated steatohepatitis | HGNC:2328 | Homo sapiens (human) | 1374 | CPT1A |
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| DOID:0090129 | carnitine palmitoyltransferase I deficiency | HGNC:2328 | Homo sapiens (human) | 1374 | CPT1A |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:2328 | Homo sapiens (human) | 1374 | CPT1A |
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| DOID:3319 | lymphangioleiomyomatosis | HGNC:2328 | Homo sapiens (human) | 1374 | CPT1A |
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| DOID:12351 | alcoholic hepatitis | HGNC:2328 | Homo sapiens (human) | 1374 | CPT1A |
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| DOID:3146 | lipid metabolism disorder | HGNC:2328 | Homo sapiens (human) | 1374 | CPT1A |
|
||
| DOID:783 | end stage renal disease | HGNC:2328 | Homo sapiens (human) | 1374 | CPT1A |
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| DOID:9970 | obesity | HGNC:2323 | Homo sapiens (human) | 1373 | CPS1 |
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| DOID:9452 | steatotic liver disease | HGNC:2323 | Homo sapiens (human) | 1373 | CPS1 |
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| DOID:10763 | hypertension | HGNC:2323 | Homo sapiens (human) | 1373 | CPS1 |
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| DOID:684 | hepatocellular carcinoma | HGNC:2323 | Homo sapiens (human) | 1373 | CPS1 |
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| DOID:178 | vascular disease | HGNC:2323 | Homo sapiens (human) | 1373 | CPS1 |
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| DOID:9280 | carbamoyl phosphate synthetase I deficiency disease | HGNC:2323 | Homo sapiens (human) | 1373 | CPS1 |
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| DOID:13042 | persistent fetal circulation syndrome | HGNC:2323 | Homo sapiens (human) | 1373 | CPS1 |
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| DOID:0110349 | osteogenesis imperfecta type 9 | SGD:S000002712 | Saccharomyces cerevisiae S288C | 851898 | CPR5 |
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| DOID:409 | liver disease | HGNC:2321 | Homo sapiens (human) | 1371 | CPOX |
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| DOID:13269 | hereditary coproporphyria | HGNC:2321 | Homo sapiens (human) | 1371 | CPOX |
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| DOID:0111583 | carboxypeptidase N deficiency | HGNC:2312 | Homo sapiens (human) | 1369 | CPN1 |
|
