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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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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 | July 29, 2024 |
| Disease ID | Disease Name | Alliance of Genome Resources ID | Species | Gene ID ▼ | Gene Symbol | FlyGlycoDB | Evidence Code Names | References |
|---|---|---|---|---|---|---|---|---|
| DOID:11400 | pyelonephritis | RGD:619850 | Rattus norvegicus (Norway rat) | 94203 | Pgf |
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| DOID:0111070 | congenital bile acid synthesis defect 3 | HGNC:2652 | Homo sapiens (human) | 9420 | CYP7B1 |
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| DOID:0110810 | hereditary spastic paraplegia 5A | HGNC:2652 | Homo sapiens (human) | 9420 | CYP7B1 |
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| DOID:0060050 | autoimmune disease of blood | MGI:2151071 | Mus musculus (house mouse) | 94192 | C1galt1 |
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| DOID:0080576 | spondyloepimetaphyseal dysplasia, Genevieve-type | MGI:2149820 | Mus musculus (house mouse) | 94181 | Nans |
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| DOID:12930 | dilated cardiomyopathy | HGNC:3575 | Homo sapiens (human) | 9415 | FADS2 |
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| DOID:9744 | type 1 diabetes mellitus | HGNC:3575 | Homo sapiens (human) | 9415 | FADS2 |
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| DOID:6000 | congestive heart failure | HGNC:3575 | Homo sapiens (human) | 9415 | FADS2 |
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| DOID:1574 | alcohol use disorder | HGNC:3575 | Homo sapiens (human) | 9415 | FADS2 |
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| DOID:3146 | lipid metabolism disorder | HGNC:3575 | Homo sapiens (human) | 9415 | FADS2 |
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| DOID:5804 | discrete subaortic stenosis | HGNC:3575 | Homo sapiens (human) | 9415 | FADS2 |
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| DOID:2841 | asthma | HGNC:16036 | Homo sapiens (human) | 94101 | ORMDL1 |
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| DOID:0070382 | developmental and epileptic encephalopathy 95 | HGNC:14937 | Homo sapiens (human) | 94005 | PIGS |
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| DOID:1793 | pancreatic cancer | MGI:2136878 | Mus musculus (house mouse) | 93961 | B3galt5 |
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| DOID:0090075 | hypogonadotropic hypogonadism 15 with or without anosmia | HGNC:5201 | Homo sapiens (human) | 9394 | HS6ST1 |
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| DOID:10763 | hypertension | HGNC:6623 | Homo sapiens (human) | 9388 | LIPG |
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| DOID:3393 | coronary artery disease | HGNC:6623 | Homo sapiens (human) | 9388 | LIPG |
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| DOID:1287 | cardiovascular system disease | HGNC:6623 | Homo sapiens (human) | 9388 | LIPG |
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| DOID:9970 | obesity | HGNC:6623 | Homo sapiens (human) | 9388 | LIPG |
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| DOID:3526 | cerebral infarction | HGNC:6623 | Homo sapiens (human) | 9388 | LIPG |
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| DOID:5844 | myocardial infarction | HGNC:6623 | Homo sapiens (human) | 9388 | LIPG |
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| DOID:0070259 | congenital disorder of glycosylation type IIg | HGNC:6545 | Homo sapiens (human) | 9382 | COG1 |
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| DOID:0111671 | primary hyperoxaluria type 2 | HGNC:4570 | Homo sapiens (human) | 9380 | GRHPR |
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| DOID:2977 | primary hyperoxaluria | HGNC:4570 | Homo sapiens (human) | 9380 | GRHPR |
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| DOID:14503 | neuronal ceroid lipofuscinosis | HGNC:9326 | Homo sapiens (human) | 9374 | PPT2 |
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